BCL11B (BCL11 transcription factor B) - Rat Genome Database

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Gene: BCL11B (BCL11 transcription factor B) Homo sapiens
Analyze
Symbol: BCL11B
Name: BCL11 transcription factor B
RGD ID: 1322422
HGNC Page HGNC:13222
Description: Enables sequence-specific double-stranded DNA binding activity. Involved in hematopoietic stem cell migration and lymphoid lineage cell migration into thymus. Acts upstream of or within positive regulation of transcription by RNA polymerase II. Part of SWI/SNF complex. Implicated in immunodeficiency 49.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: ATL1; ATL1 zinc finger protein; ATL1-alpha; ATL1-alpha zinc finger protein; ATL1-beta; ATL1-beta zinc finger protein; ATL1-delta; ATL1-delta zinc finger protein; ATL1-gamma; ATL1-gamma zinc finger protein; B cell CLL/lymphoma 11B; B-cell CLL/lymphoma 11B; B-cell CLL/lymphoma 11B (zinc finger protein); B-cell CLL/lymphoma 11B/T-cell receptor delta constant region fusion protein; B-cell lymphoma/leukaemia 11B; B-cell lymphoma/leukemia 11B; BAF chromatin remodeling complex subunit BCL11B; BCL-11B; BCL11B, BAF complex component; BCL11B/TRDC fusion; COUP-TF-interacting protein 2; CTIP-2; CTIP2; hRit1; hRIT1-alpha; IDDFSTA; IMD49; radiation-induced tumor suppressor gene 1 protein; RIT1; SMARCM2; zinc finger protein hRit1 alpha; ZNF856B
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Orthologs
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381499,169,287 - 99,272,197 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1499,169,287 - 99,272,197 (-)EnsemblGRCh38hg38GRCh38
GRCh371499,635,624 - 99,738,534 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361498,705,377 - 98,807,575 (-)NCBINCBI36Build 36hg18NCBI36
Build 341498,705,376 - 98,807,575NCBI
Celera1479,691,368 - 79,793,512 (-)NCBICelera
Cytogenetic Map14q32.2NCBI
HuRef1479,819,226 - 79,921,464 (-)NCBIHuRef
CHM1_11499,573,389 - 99,675,578 (-)NCBICHM1_1
T2T-CHM13v2.01493,400,844 - 93,503,767 (-)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
Gene Ontology Annotations     Click to see Annotation Detail View

Cellular Component
neuron projection  (IEA)
nucleus  (IBA,IEA)
SWI/SNF complex  (IDA,IEA)

Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype
Abnormally low T cell receptor excision circle level  (IAGP)
Absent speech  (IAGP)
Agenesis of corpus callosum  (IAGP)
Anxiety  (IAGP)
Asthma  (IAGP)
Autistic behavior  (IAGP)
Autosomal dominant inheritance  (IAGP)
Combined immunodeficiency  (IAGP)
Congenital onset  (IAGP)
Cutis laxa  (IAGP)
Decreased proportion of naive CD4 T cells  (IAGP)
Delayed ability to walk  (IAGP)
Delayed speech and language development  (IAGP)
Eosinophilia  (IAGP)
Epicanthus  (IAGP)
Feeding difficulties  (IAGP)
Generalized hypotonia  (IAGP)
Global developmental delay  (IAGP)
Hirsutism  (IAGP)
Hypermetropia  (IAGP)
Hypertelorism  (IAGP)
Hypodontia  (IAGP)
Hypotonia  (IAGP)
Impaired lymphocyte transformation with phytohemagglutinin  (IAGP)
Infantile onset  (IAGP)
Intellectual disability  (IAGP)
Long philtrum  (IAGP)
Lymphopenia  (IAGP)
Microcephaly  (IAGP)
Microdontia  (IAGP)
Micrognathia  (IAGP)
Motor delay  (IAGP)
Myopathic facies  (IAGP)
Myopia  (IAGP)
Narrow mouth  (IAGP)
Natal tooth  (IAGP)
Oligodontia  (IAGP)
Posteriorly rotated ears  (IAGP)
Prominent nose  (IAGP)
Psoriasiform dermatitis  (IAGP)
Pulmonary artery stenosis  (IAGP)
Recurrent infections  (IAGP)
Reduced cerebral white matter volume  (IAGP)
Seizure  (IAGP)
Severe combined immunodeficiency  (IAGP)
Short palpebral fissure  (IAGP)
Short philtrum  (IAGP)
Spastic tetraplegia  (IAGP)
Spasticity  (IAGP)
T lymphocytopenia  (IAGP)
Thin eyebrow  (IAGP)
Thin upper lip vermilion  (IAGP)
Umbilical hernia  (IAGP)
Unsteady gait  (IAGP)
Upslanted palpebral fissure  (IAGP)
Wormian bones  (IAGP)
References

References - curated
# Reference Title Reference Citation
1. GOAs Human GO annotations GOA_HUMAN data from the GO Consortium
2. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
3. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
4. Transcriptomic characteristics of bronchoalveolar lavage fluid and peripheral blood mononuclear cells in COVID-19 patients. Xiong Y, etal., Emerg Microbes Infect. 2020 Dec;9(1):761-770. doi: 10.1080/22221751.2020.1747363.
Additional References at PubMed
PMID:10744719   PMID:11719382   PMID:12196208   PMID:12565905   PMID:12692243   PMID:12930829   PMID:15104287   PMID:15325104   PMID:15668700   PMID:16091750   PMID:16809611   PMID:16950772  
PMID:17245431   PMID:17308084   PMID:17369851   PMID:18595722   PMID:18768194   PMID:19274049   PMID:19366371   PMID:19399189   PMID:19454010   PMID:19581932   PMID:20824091   PMID:21060114  
PMID:21080944   PMID:21873635   PMID:21878675   PMID:22067449   PMID:22068335   PMID:22077140   PMID:22245141   PMID:22450536   PMID:22700985   PMID:22969067   PMID:23022380   PMID:23040356  
PMID:23168072   PMID:23383087   PMID:23527175   PMID:23644491   PMID:23682716   PMID:23752268   PMID:23803414   PMID:23852730   PMID:24441149   PMID:24847357   PMID:24981860   PMID:25023966  
PMID:25056061   PMID:25128552   PMID:25613934   PMID:25665578   PMID:25798074   PMID:25827435   PMID:26096706   PMID:27161321   PMID:27637333   PMID:27725726   PMID:27959755   PMID:28232744  
PMID:28288848   PMID:28473536   PMID:28669733   PMID:28794504   PMID:28977666   PMID:29039465   PMID:29203643   PMID:29374058   PMID:29503088   PMID:29509190   PMID:29844126   PMID:30242241  
PMID:31067316   PMID:31253590   PMID:31347296   PMID:31447328   PMID:31479431   PMID:31511615   PMID:31673069   PMID:31753913   PMID:31828511   PMID:32255245   PMID:32393512   PMID:32588101  
PMID:32729240   PMID:32744500   PMID:33093445   PMID:33168583   PMID:33514850   PMID:33712472   PMID:33876209   PMID:33961781   PMID:34103329   PMID:34344074   PMID:34402058   PMID:34559552  
PMID:34738838   PMID:34865701   PMID:35016035   PMID:35421541   PMID:35864006   PMID:36202297   PMID:36211334   PMID:36376973   PMID:36602602   PMID:37689310   PMID:37737560   PMID:37956270  
PMID:37986346   PMID:38297188   PMID:38495886   PMID:38829888  


Genomics

Comparative Map Data
BCL11B
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381499,169,287 - 99,272,197 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1499,169,287 - 99,272,197 (-)EnsemblGRCh38hg38GRCh38
GRCh371499,635,624 - 99,738,534 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361498,705,377 - 98,807,575 (-)NCBINCBI36Build 36hg18NCBI36
Build 341498,705,376 - 98,807,575NCBI
Celera1479,691,368 - 79,793,512 (-)NCBICelera
Cytogenetic Map14q32.2NCBI
HuRef1479,819,226 - 79,921,464 (-)NCBIHuRef
CHM1_11499,573,389 - 99,675,578 (-)NCBICHM1_1
T2T-CHM13v2.01493,400,844 - 93,503,767 (-)NCBIT2T-CHM13v2.0
Bcl11b
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm3912107,876,662 - 107,970,404 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl12107,876,662 - 107,969,861 (-)EnsemblGRCm39 Ensembl
GRCm3812107,910,403 - 108,004,145 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl12107,910,403 - 108,003,602 (-)EnsemblGRCm38mm10GRCm38
MGSCv3712109,148,613 - 109,241,624 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv3612108,363,030 - 108,451,028 (-)NCBIMGSCv36mm8
Celera12109,151,974 - 109,245,238 (-)NCBICelera
Cytogenetic Map12F1NCBI
cM Map1259.1NCBI
Bcl11b
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr86132,598,968 - 132,692,123 (-)NCBIGRCr8
mRatBN7.26126,834,531 - 126,927,720 (-)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl6126,834,531 - 126,928,224 (-)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx6126,958,692 - 127,050,867 (-)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.06127,253,714 - 127,345,900 (-)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.06126,612,161 - 126,704,296 (-)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.06131,834,097 - 131,927,251 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl6131,834,097 - 131,926,272 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.06141,004,477 - 141,097,643 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.46132,292,671 - 132,384,572 (-)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.16132,296,789 - 132,389,378 (-)NCBI
Celera6124,393,881 - 124,486,186 (-)NCBICelera
Cytogenetic Map6q32NCBI
Bcl11b
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_00495543820,564,449 - 20,637,103 (-)EnsemblChiLan1.0
ChiLan1.0NW_00495543820,562,345 - 20,637,662 (-)NCBIChiLan1.0ChiLan1.0
BCL11B
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v215100,325,797 - 100,429,008 (-)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan11499,542,293 - 99,645,444 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v01479,795,262 - 79,898,472 (-)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.11499,122,231 - 99,205,962 (-)NCBIpanpan1.1PanPan1.1panPan2
BCL11B
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1867,622,592 - 67,713,922 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl867,622,708 - 67,714,404 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha867,145,953 - 67,237,226 (-)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.0867,909,299 - 68,000,574 (-)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl867,909,387 - 68,001,543 (-)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1867,570,743 - 67,661,895 (-)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.0867,636,646 - 67,728,187 (-)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0868,033,837 - 68,125,174 (-)NCBIUU_Cfam_GSD_1.0
Bcl11b
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_0244086406,972,307 - 7,063,288 (+)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_0049366043,023,844 - 3,110,083 (-)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_0049366043,023,781 - 3,110,104 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
BCL11B
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl7120,205,008 - 120,295,936 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.17120,205,008 - 120,295,737 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.27127,759,537 - 127,855,267 (-)NCBISscrofa10.2Sscrofa10.2susScr3
BCL11B
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.12477,122,591 - 77,222,562 (-)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl2477,122,689 - 77,221,454 (-)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366605364,224,342 - 64,347,710 (-)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Bcl11b
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_0046247344,560,699 - 4,647,858 (+)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_0046247344,560,362 - 4,649,219 (+)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in BCL11B
690 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
NM_138576.4(BCL11B):c.1938_1950del (p.Ala647fs) deletion Microcephaly [RCV001526554] Chr14:99174886..99174898 [GRCh38]
Chr14:99641223..99641235 [GRCh37]
Chr14:14q32.2		 likely pathogenic
GRCh38/hg38 14q32.2-32.33(chr14:97938637-106855263)x1 copy number loss See cases [RCV000050696] Chr14:97938637..106855263 [GRCh38]
Chr14:98404974..107263478 [GRCh37]
Chr14:97474727..106334523 [NCBI36]
Chr14:14q32.2-32.33		 pathogenic
GRCh38/hg38 14q32.2(chr14:96920270-100178956)x1 copy number loss See cases [RCV000051552] Chr14:96920270..100178956 [GRCh38]
Chr14:97386607..100645293 [GRCh37]
Chr14:96456360..99715046 [NCBI36]
Chr14:14q32.2		 pathogenic
GRCh38/hg38 14q32.13-32.33(chr14:94628219-106451054)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052298]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052298]|See cases [RCV000052298] Chr14:94628219..106451054 [GRCh38]
Chr14:95094556..106906960 [GRCh37]
Chr14:94164309..105978005 [NCBI36]
Chr14:14q32.13-32.33		 pathogenic
GRCh38/hg38 14q24.2-32.2(chr14:72787506-99596719)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052293]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052293]|See cases [RCV000052293] Chr14:72787506..99596719 [GRCh38]
Chr14:73254214..100063056 [GRCh37]
Chr14:72323967..99132809 [NCBI36]
Chr14:14q24.2-32.2		 pathogenic
GRCh38/hg38 14q32.2(chr14:97210132-100471765)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052090]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052090]|See cases [RCV000052090] Chr14:97210132..100471765 [GRCh38]
Chr14:97676469..100938102 [GRCh37]
Chr14:96746222..100007855 [NCBI36]
Chr14:14q32.2		 uncertain significance
GRCh38/hg38 14q31.3-32.33(chr14:86094030-106832642)x3 copy number gain See cases [RCV000052295] Chr14:86094030..106832642 [GRCh38]
Chr14:86560374..107240869 [GRCh37]
Chr14:85630127..106311914 [NCBI36]
Chr14:14q31.3-32.33		 pathogenic
GRCh38/hg38 14q31.2-32.33(chr14:83912345-106855405)x3 copy number gain See cases [RCV000052294] Chr14:83912345..106855405 [GRCh38]
Chr14:84378689..107263620 [GRCh37]
Chr14:83448442..106334665 [NCBI36]
Chr14:14q31.2-32.33		 pathogenic
GRCh38/hg38 14q32.12-32.33(chr14:91455861-106832642)x3 copy number gain See cases [RCV000052296] Chr14:91455861..106832642 [GRCh38]
Chr14:91922205..107240869 [GRCh37]
Chr14:90991958..106311914 [NCBI36]
Chr14:14q32.12-32.33		 pathogenic
NM_138576.3(BCL11B):c.303C>T (p.Ser101=) single nucleotide variant Malignant melanoma [RCV000070683] Chr14:99257595 [GRCh38]
Chr14:99723932 [GRCh37]
Chr14:98793685 [NCBI36]
Chr14:14q32.2		 not provided
NM_138576.4(BCL11B):c.1901_1906dup (p.Gly634_Asp635dup) duplication BCL11B-related disorder [RCV004528992]|not specified [RCV000203089] Chr14:99174929..99174930 [GRCh38]
Chr14:99641266..99641267 [GRCh37]
Chr14:14q32.2		 benign|uncertain significance
GRCh38/hg38 14q24.3-32.33(chr14:73655772-106879298)x3 copy number gain See cases [RCV000134000] Chr14:73655772..106879298 [GRCh38]
Chr14:74122475..107287505 [GRCh37]
Chr14:73192228..106358550 [NCBI36]
Chr14:14q24.3-32.33		 pathogenic
GRCh38/hg38 14q32.2-32.33(chr14:97638520-106855263)x3 copy number gain See cases [RCV000135400] Chr14:97638520..106855263 [GRCh38]
Chr14:98104857..107263478 [GRCh37]
Chr14:97174610..106334523 [NCBI36]
Chr14:14q32.2-32.33		 pathogenic
GRCh38/hg38 14q11.2-32.33(chr14:20151149-106855263)x3 copy number gain See cases [RCV000135543] Chr14:20151149..106855263 [GRCh38]
Chr14:20619308..107263478 [GRCh37]
Chr14:19689148..106334523 [NCBI36]
Chr14:14q11.2-32.33		 pathogenic
GRCh38/hg38 14q32.12-32.33(chr14:92540983-104863658)x3 copy number gain See cases [RCV000135896] Chr14:92540983..104863658 [GRCh38]
Chr14:93007328..105329995 [GRCh37]
Chr14:92077081..104401040 [NCBI36]
Chr14:14q32.12-32.33		 pathogenic
GRCh38/hg38 14q32.13-32.33(chr14:95524407-106879501)x1 copy number loss See cases [RCV000136032] Chr14:95524407..106879501 [GRCh38]
Chr14:95990744..107287708 [GRCh37]
Chr14:95060497..106358753 [NCBI36]
Chr14:14q32.13-32.33		 pathogenic
GRCh38/hg38 14q24.3-32.33(chr14:77222795-106879298)x3 copy number gain See cases [RCV000138230] Chr14:77222795..106879298 [GRCh38]
Chr14:77689138..107287505 [GRCh37]
Chr14:76758891..106358550 [NCBI36]
Chr14:14q24.3-32.33		 pathogenic
GRCh38/hg38 14q11.2-32.33(chr14:20043514-106877229)x3 copy number gain See cases [RCV000143373] Chr14:20043514..106877229 [GRCh38]
Chr14:20511673..107285437 [GRCh37]
Chr14:19581513..106356482 [NCBI36]
Chr14:14q11.2-32.33		 pathogenic
NM_138576.4(BCL11B):c.2671del (p.Ala891fs) deletion Intellectual developmental disorder with speech delay, dysmorphic facies, and t-cell abnormalities [RCV000678216] Chr14:99174165 [GRCh38]
Chr14:99640502 [GRCh37]
Chr14:14q32.2		 pathogenic
NM_138576.4(BCL11B):c.242del (p.Cys81fs) deletion Intellectual developmental disorder with speech delay, dysmorphic facies, and t-cell abnormalities [RCV000678217] Chr14:99257656 [GRCh38]
Chr14:99723993 [GRCh37]
Chr14:14q32.2		 pathogenic
NM_138576.4(BCL11B):c.1323T>G (p.Asn441Lys) single nucleotide variant Combined immunodeficiency [RCV000241534]|Immunodeficiency 49 [RCV000412543] Chr14:99175513 [GRCh38]
Chr14:99641850 [GRCh37]
Chr14:14q32.2		 pathogenic
NM_138576.4(BCL11B):c.1499C>T (p.Pro500Leu) single nucleotide variant not provided [RCV002284917] Chr14:99175337 [GRCh38]
Chr14:99641674 [GRCh37]
Chr14:14q32.2		 uncertain significance
GRCh37/hg19 14q32.2-32.33(chr14:98051841-107285437)x3 copy number gain See cases [RCV000446497] Chr14:98051841..107285437 [GRCh37]
Chr14:14q32.2-32.33		 likely pathogenic
GRCh37/hg19 14q11.2-32.33(chr14:19794561-107234280)x3 copy number gain See cases [RCV000446256] Chr14:19794561..107234280 [GRCh37]
Chr14:14q11.2-32.33		 pathogenic
NM_138576.4(BCL11B):c.289A>C (p.Ser97Arg) single nucleotide variant not provided [RCV000438094] Chr14:99257609 [GRCh38]
Chr14:99723946 [GRCh37]
Chr14:14q32.2		 uncertain significance
GRCh37/hg19 14q23.2-32.33(chr14:62493932-107285437)x3 copy number gain See cases [RCV000448557] Chr14:62493932..107285437 [GRCh37]
Chr14:14q23.2-32.33		 pathogenic
GRCh37/hg19 14q11.2-32.33(chr14:20511673-107285437) copy number gain See cases [RCV000512041] Chr14:20511673..107285437 [GRCh37]
Chr14:14q11.2-32.33		 pathogenic
NM_138576.4(BCL11B):c.1192_1196dup (p.Lys400fs) microsatellite Inborn genetic diseases [RCV000624196] Chr14:99175639..99175640 [GRCh38]
Chr14:99641976..99641977 [GRCh37]
Chr14:14q32.2		 pathogenic|uncertain significance
NM_138576.4(BCL11B):c.238C>T (p.Gln80Ter) single nucleotide variant Inborn genetic diseases [RCV000623070] Chr14:99257660 [GRCh38]
Chr14:99723997 [GRCh37]
Chr14:14q32.2		 pathogenic|likely pathogenic
NM_138576.4(BCL11B):c.721C>T (p.Gln241Ter) single nucleotide variant Inborn genetic diseases [RCV000623180] Chr14:99176115 [GRCh38]
Chr14:99642452 [GRCh37]
Chr14:14q32.2		 pathogenic|likely pathogenic
GRCh37/hg19 14q24.2-32.33(chr14:73750741-107285437)x3 copy number gain See cases [RCV000512497] Chr14:73750741..107285437 [GRCh37]
Chr14:14q24.2-32.33		 pathogenic
NM_138576.4(BCL11B):c.2607G>A (p.Leu869=) single nucleotide variant not provided [RCV003690851] Chr14:99174229 [GRCh38]
Chr14:99640566 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.2449_2456dup (p.Gly820fs) duplication Intellectual developmental disorder with speech delay, dysmorphic facies, and t-cell abnormalities [RCV000678215] Chr14:99174379..99174380 [GRCh38]
Chr14:99640716..99640717 [GRCh37]
Chr14:14q32.2		 pathogenic
NM_138576.4(BCL11B):c.2421C>G (p.Asn807Lys) single nucleotide variant Immunodeficiency 49 [RCV000678214]|Intellectual developmental disorder with speech delay, dysmorphic facies, and t-cell abnormalities [RCV000995706]|not provided [RCV001089771] Chr14:99174415 [GRCh38]
Chr14:99640752 [GRCh37]
Chr14:14q32.2		 pathogenic|likely pathogenic
NM_138576.4(BCL11B):c.1495G>T (p.Glu499Ter) single nucleotide variant Intellectual developmental disorder with speech delay, dysmorphic facies, and t-cell abnormalities [RCV000678218] Chr14:99175341 [GRCh38]
Chr14:99641678 [GRCh37]
Chr14:14q32.2		 pathogenic
NM_138576.4(BCL11B):c.1097G>A (p.Arg366Gln) single nucleotide variant not provided [RCV000678278] Chr14:99175739 [GRCh38]
Chr14:99642076 [GRCh37]
Chr14:14q32.2		 conflicting interpretations of pathogenicity|uncertain significance
GRCh37/hg19 14q32.2(chr14:98924025-101159952)x3 copy number gain not provided [RCV000683622] Chr14:98924025..101159952 [GRCh37]
Chr14:14q32.2		 uncertain significance
GRCh37/hg19 14q11.2-32.33(chr14:19280733-107287663)x3 copy number gain not provided [RCV000738413] Chr14:19280733..107287663 [GRCh37]
Chr14:14q11.2-32.33		 pathogenic
GRCh37/hg19 14q11.2-32.33(chr14:19327823-107287663)x3 copy number gain not provided [RCV000738414] Chr14:19327823..107287663 [GRCh37]
Chr14:14q11.2-32.33		 pathogenic
GRCh37/hg19 14q11.1-32.33(chr14:19000422-107289053)x3 copy number gain not provided [RCV000738412] Chr14:19000422..107289053 [GRCh37]
Chr14:14q11.1-32.33		 pathogenic
GRCh37/hg19 14q32.2(chr14:99640566-99642260)x1 copy number loss not provided [RCV000738582] Chr14:99640566..99642260 [GRCh37]
Chr14:14q32.2		 benign
GRCh37/hg19 14q32.2(chr14:99640618-99642260)x1 copy number loss not provided [RCV000738583] Chr14:99640618..99642260 [GRCh37]
Chr14:14q32.2		 benign
NM_138576.4(BCL11B):c.2439_2452dup (p.His818fs) duplication Intellectual developmental disorder with speech delay, dysmorphic facies, and t-cell abnormalities [RCV003984860]|not provided [RCV001882593] Chr14:99174383..99174384 [GRCh38]
Chr14:99640720..99640721 [GRCh37]
Chr14:14q32.2		 likely pathogenic|uncertain significance
NM_138576.4(BCL11B):c.2448_2461del (p.Ser817fs) deletion Intellectual developmental disorder with speech delay, dysmorphic facies, and t-cell abnormalities [RCV003984861] Chr14:99174375..99174388 [GRCh38]
Chr14:99640712..99640725 [GRCh37]
Chr14:14q32.2		 likely pathogenic
NM_138576.4(BCL11B):c.1907A>G (p.Asp636Gly) single nucleotide variant Inborn genetic diseases [RCV003245731] Chr14:99174929 [GRCh38]
Chr14:99641266 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1908C>G (p.Asp636Glu) single nucleotide variant Inborn genetic diseases [RCV003245732] Chr14:99174928 [GRCh38]
Chr14:99641265 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1283C>A (p.Ser428Ter) single nucleotide variant not provided [RCV001551913] Chr14:99175553 [GRCh38]
Chr14:99641890 [GRCh37]
Chr14:14q32.2		 likely pathogenic
NM_138576.4(BCL11B):c.307C>A (p.Arg103Ser) single nucleotide variant Immunodeficiency 49 [RCV003448818]|not provided [RCV005100109] Chr14:99257591 [GRCh38]
Chr14:99723928 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1810C>T (p.Leu604=) single nucleotide variant not provided [RCV000923932] Chr14:99175026 [GRCh38]
Chr14:99641363 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1011C>T (p.Leu337=) single nucleotide variant not provided [RCV000900308] Chr14:99175825 [GRCh38]
Chr14:99642162 [GRCh37]
Chr14:14q32.2		 benign
NM_138576.4(BCL11B):c.1944_1965del (p.Gly649fs) deletion Inborn genetic diseases [RCV001266988]|Intellectual developmental disorder with speech delay, dysmorphic facies, and t-cell abnormalities [RCV003325225]|not provided [RCV001089770] Chr14:99174871..99174892 [GRCh38]
Chr14:99641208..99641229 [GRCh37]
Chr14:14q32.2		 pathogenic|likely pathogenic
NM_138576.4(BCL11B):c.1845C>T (p.Ala615=) single nucleotide variant not provided [RCV000917119] Chr14:99174991 [GRCh38]
Chr14:99641328 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1032C>G (p.Ala344=) single nucleotide variant BCL11B-related disorder [RCV004528321]|not provided [RCV000886233] Chr14:99175804 [GRCh38]
Chr14:99642141 [GRCh37]
Chr14:14q32.2		 likely benign|uncertain significance
NM_138576.4(BCL11B):c.1518G>A (p.Ala506=) single nucleotide variant not provided [RCV000896993] Chr14:99175318 [GRCh38]
Chr14:99641655 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.543C>T (p.Leu181=) single nucleotide variant BCL11B-related disorder [RCV004530893]|not provided [RCV000879887] Chr14:99231442 [GRCh38]
Chr14:99697779 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1437C>T (p.His479=) single nucleotide variant not provided [RCV000879112] Chr14:99175399 [GRCh38]
Chr14:99641736 [GRCh37]
Chr14:14q32.2		 benign|likely benign
NM_138576.4(BCL11B):c.1535_1536del (p.Ala512fs) deletion Intellectual developmental disorder with speech delay, dysmorphic facies, and t-cell abnormalities [RCV002280363] Chr14:99175300..99175301 [GRCh38]
Chr14:99641637..99641638 [GRCh37]
Chr14:14q32.2		 likely pathogenic
GRCh37/hg19 14q32.12-32.33(chr14:91969028-107285437)x3 copy number gain not provided [RCV000848687] Chr14:91969028..107285437 [GRCh37]
Chr14:14q32.12-32.33		 pathogenic
NM_138576.4(BCL11B):c.1365_1367del (p.Tyr455_Lys456delinsTer) deletion not provided [RCV000844904] Chr14:99175469..99175471 [GRCh38]
Chr14:99641806..99641808 [GRCh37]
Chr14:14q32.2		 not provided
NM_138576.4(BCL11B):c.1077C>T (p.Pro359=) single nucleotide variant not provided [RCV000918565] Chr14:99175759 [GRCh38]
Chr14:99642096 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.2094C>T (p.Pro698=) single nucleotide variant not provided [RCV000920478] Chr14:99174742 [GRCh38]
Chr14:99641079 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.81dup (p.Ala28fs) duplication not provided [RCV001008291] Chr14:99257816..99257817 [GRCh38]
Chr14:99724153..99724154 [GRCh37]
Chr14:14q32.2		 pathogenic
NM_138576.4(BCL11B):c.1743_1746del (p.Gly582fs) deletion not provided [RCV001008851] Chr14:99175090..99175093 [GRCh38]
Chr14:99641427..99641430 [GRCh37]
Chr14:14q32.2		 pathogenic
NM_138576.4(BCL11B):c.1878_1884del (p.Gly630fs) deletion not provided [RCV001009131] Chr14:99174952..99174958 [GRCh38]
Chr14:99641289..99641295 [GRCh37]
Chr14:14q32.2		 pathogenic
GRCh37/hg19 14q32.2-32.33(chr14:96829290-107287663)x1 copy number loss See cases [RCV001195078] Chr14:96829290..107287663 [GRCh37]
Chr14:14q32.2-32.33		 pathogenic
NM_138576.4(BCL11B):c.2048del (p.Ser683fs) deletion Intellectual developmental disorder with speech delay, dysmorphic facies, and t-cell abnormalities [RCV000995707] Chr14:99174788 [GRCh38]
Chr14:99641125 [GRCh37]
Chr14:14q32.2		 pathogenic
NM_138576.4(BCL11B):c.1500dup (p.Gly501fs) duplication Intellectual developmental disorder with speech delay, dysmorphic facies, and t-cell abnormalities [RCV000995708] Chr14:99175335..99175336 [GRCh38]
Chr14:99641672..99641673 [GRCh37]
Chr14:14q32.2		 pathogenic
NM_138576.4(BCL11B):c.372T>A (p.Asp124Glu) single nucleotide variant not provided [RCV003230029] Chr14:99257526 [GRCh38]
Chr14:99723863 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1435C>T (p.His479Tyr) single nucleotide variant not provided [RCV003234416] Chr14:99175401 [GRCh38]
Chr14:99641738 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.655T>C (p.Ser219Pro) single nucleotide variant not provided [RCV003233360] Chr14:99176181 [GRCh38]
Chr14:99642518 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.2227C>A (p.His743Asn) single nucleotide variant Inborn genetic diseases [RCV004968648]|not provided [RCV004776627] Chr14:99174609 [GRCh38]
Chr14:99640946 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.784_820del (p.Arg262fs) deletion Autism spectrum disorder [RCV003128003] Chr14:99176016..99176052 [GRCh38]
Chr14:99642353..99642389 [GRCh37]
Chr14:14q32.2		 pathogenic
NM_138576.4(BCL11B):c.1311G>C (p.Lys437Asn) single nucleotide variant not provided [RCV004812663] Chr14:99175525 [GRCh38]
Chr14:99641862 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.2616_2617del (p.Met873fs) microsatellite not provided [RCV001570134] Chr14:99174219..99174220 [GRCh38]
Chr14:99640556..99640557 [GRCh37]
Chr14:14q32.2		 likely pathogenic
NM_138576.4(BCL11B):c.2448_2461dup (p.Glu821fs) duplication Immunodeficiency 49 [RCV002246460]|Intellectual developmental disorder with speech delay, dysmorphic facies, and t-cell abnormalities [RCV001717980] Chr14:99174374..99174375 [GRCh38]
Chr14:99640711..99640712 [GRCh37]
Chr14:14q32.2		 pathogenic
NM_138576.4(BCL11B):c.1911C>T (p.Asp637=) single nucleotide variant not provided [RCV000919035] Chr14:99174925 [GRCh38]
Chr14:99641262 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.363C>T (p.Pro121=) single nucleotide variant not provided [RCV000910075] Chr14:99257535 [GRCh38]
Chr14:99723872 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.2259C>T (p.Ser753=) single nucleotide variant not provided [RCV000914934] Chr14:99174577 [GRCh38]
Chr14:99640914 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.933G>T (p.Pro311=) single nucleotide variant BCL11B-related disorder [RCV004541934]|not provided [RCV000909578] Chr14:99175903 [GRCh38]
Chr14:99642240 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1474C>T (p.Leu492Phe) single nucleotide variant not specified [RCV001169887] Chr14:99175362 [GRCh38]
Chr14:99641699 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.2157G>C (p.Arg719=) single nucleotide variant not provided [RCV000911143] Chr14:99174679 [GRCh38]
Chr14:99641016 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1571C>G (p.Pro524Arg) single nucleotide variant not provided [RCV003011734] Chr14:99175265 [GRCh38]
Chr14:99641602 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1447T>G (p.Ser483Ala) single nucleotide variant See cases [RCV002252541] Chr14:99175389 [GRCh38]
Chr14:99641726 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.2443del (p.Arg815fs) deletion Intellectual developmental disorder with speech delay, dysmorphic facies, and t-cell abnormalities [RCV002471298] Chr14:99174393 [GRCh38]
Chr14:99640730 [GRCh37]
Chr14:14q32.2		 pathogenic
NM_138576.4(BCL11B):c.427+1G>A single nucleotide variant Intellectual developmental disorder with speech delay, dysmorphic facies, and t-cell abnormalities [RCV001716991] Chr14:99257470 [GRCh38]
Chr14:99723807 [GRCh37]
Chr14:14q32.2		 pathogenic
NM_138576.4(BCL11B):c.1887_1893del (p.Gly630fs) microsatellite Immunodeficiency 49 [RCV003314011]|not provided [RCV001682638] Chr14:99174943..99174949 [GRCh38]
Chr14:99641280..99641286 [GRCh37]
Chr14:14q32.2		 pathogenic
NM_138576.4(BCL11B):c.1582del (p.His528fs) deletion Intellectual developmental disorder with speech delay, dysmorphic facies, and t-cell abnormalities [RCV003333164] Chr14:99175254 [GRCh38]
Chr14:99641591 [GRCh37]
Chr14:14q32.2		 likely pathogenic
NM_138576.4(BCL11B):c.2346_2361del (p.Gly783fs) deletion Intellectual developmental disorder with speech delay, dysmorphic facies, and t-cell abnormalities [RCV001542096]|See cases [RCV002254725]|not provided [RCV004774456] Chr14:99174475..99174490 [GRCh38]
Chr14:99640812..99640827 [GRCh37]
Chr14:14q32.2		 pathogenic|likely pathogenic
NM_138576.4(BCL11B):c.1916_1917dup (p.Gly640fs) microsatellite not provided [RCV001543541] Chr14:99174918..99174919 [GRCh38]
Chr14:99641255..99641256 [GRCh37]
Chr14:14q32.2		 pathogenic
NM_138576.4(BCL11B):c.1657G>C (p.Glu553Gln) single nucleotide variant Intellectual developmental disorder with speech delay, dysmorphic facies, and t-cell abnormalities [RCV001196924]|not provided [RCV003393875] Chr14:99175179 [GRCh38]
Chr14:99641516 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.2348del (p.Gly783fs) deletion not provided [RCV001171592] Chr14:99174488 [GRCh38]
Chr14:99640825 [GRCh37]
Chr14:14q32.2		 pathogenic
NM_138576.4(BCL11B):c.1770_1771del (p.Lys591fs) microsatellite Intellectual developmental disorder with speech delay, dysmorphic facies, and t-cell abnormalities [RCV001253162] Chr14:99175065..99175066 [GRCh38]
Chr14:99641402..99641403 [GRCh37]
Chr14:14q32.2		 pathogenic
NM_138576.4(BCL11B):c.1742del (p.Gly581fs) deletion Intellectual developmental disorder with speech delay, dysmorphic facies, and t-cell abnormalities [RCV001254120] Chr14:99175094 [GRCh38]
Chr14:99641431 [GRCh37]
Chr14:14q32.2		 likely pathogenic
NM_138576.4(BCL11B):c.1858C>T (p.Arg620Cys) single nucleotide variant Intellectual developmental disorder with speech delay, dysmorphic facies, and t-cell abnormalities [RCV004799369]|not provided [RCV001879951] Chr14:99174978 [GRCh38]
Chr14:99641315 [GRCh37]
Chr14:14q32.2		 uncertain significance
GRCh37/hg19 14q32.2(chr14:99538014-100082239)x1 copy number loss not provided [RCV001259798] Chr14:99538014..100082239 [GRCh37]
Chr14:14q32.2		 pathogenic
NM_138576.4(BCL11B):c.461C>T (p.Ala154Val) single nucleotide variant not provided [RCV002280259] Chr14:99231524 [GRCh38]
Chr14:99697861 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1460_1485del (p.Arg487fs) deletion not provided [RCV001268898] Chr14:99175351..99175376 [GRCh38]
Chr14:99641688..99641713 [GRCh37]
Chr14:14q32.2		 pathogenic
NM_138576.4(BCL11B):c.682C>T (p.Gln228Ter) single nucleotide variant Intellectual developmental disorder with speech delay, dysmorphic facies, and t-cell abnormalities [RCV001270444] Chr14:99176154 [GRCh38]
Chr14:99642491 [GRCh37]
Chr14:14q32.2		 pathogenic
NM_138576.4(BCL11B):c.2231C>T (p.Ser744Leu) single nucleotide variant Inborn genetic diseases [RCV001265709] Chr14:99174605 [GRCh38]
Chr14:99640942 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.2435_2436insAA (p.Val813fs) insertion Intellectual developmental disorder with speech delay, dysmorphic facies, and t-cell abnormalities [RCV001290207] Chr14:99174400..99174401 [GRCh38]
Chr14:99640737..99640738 [GRCh37]
Chr14:14q32.2		 pathogenic
NM_138576.4(BCL11B):c.1347C>G (p.His449Gln) single nucleotide variant Inborn genetic diseases [RCV001266241] Chr14:99175489 [GRCh38]
Chr14:99641826 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1781T>C (p.Val594Ala) single nucleotide variant not provided [RCV001313992] Chr14:99175055 [GRCh38]
Chr14:99641392 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1698C>T (p.Arg566=) single nucleotide variant BCL11B-related disorder [RCV004531114]|not provided [RCV001325086] Chr14:99175138 [GRCh38]
Chr14:99641475 [GRCh37]
Chr14:14q32.2		 likely benign|uncertain significance
NM_138576.4(BCL11B):c.1003A>G (p.Met335Val) single nucleotide variant Immunodeficiency 49 [RCV001330354] Chr14:99175833 [GRCh38]
Chr14:99642170 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.2472C>A (p.Tyr824Ter) single nucleotide variant not provided [RCV001290988] Chr14:99174364 [GRCh38]
Chr14:99640701 [GRCh37]
Chr14:14q32.2		 likely pathogenic
NM_138576.4(BCL11B):c.785G>A (p.Arg262Gln) single nucleotide variant Intellectual developmental disorder with speech delay, dysmorphic facies, and t-cell abnormalities [RCV001330356]|not provided [RCV002546385] Chr14:99176051 [GRCh38]
Chr14:99642388 [GRCh37]
Chr14:14q32.2		 likely pathogenic|uncertain significance
NM_138576.4(BCL11B):c.1742G>A (p.Gly581Asp) single nucleotide variant not provided [RCV001349788] Chr14:99175094 [GRCh38]
Chr14:99641431 [GRCh37]
Chr14:14q32.2		 benign|conflicting interpretations of pathogenicity|uncertain significance
NM_138576.4(BCL11B):c.906C>A (p.His302Gln) single nucleotide variant Immunodeficiency 49 [RCV001335400] Chr14:99175930 [GRCh38]
Chr14:99642267 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.296C>T (p.Pro99Leu) single nucleotide variant Immunodeficiency 49 [RCV001330355] Chr14:99257602 [GRCh38]
Chr14:99723939 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1617G>T (p.Glu539Asp) single nucleotide variant not provided [RCV001373426] Chr14:99175219 [GRCh38]
Chr14:99641556 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1265C>T (p.Pro422Leu) single nucleotide variant not provided [RCV001369016] Chr14:99175571 [GRCh38]
Chr14:99641908 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.2036C>T (p.Pro679Leu) single nucleotide variant not provided [RCV001371447] Chr14:99174800 [GRCh38]
Chr14:99641137 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.514C>T (p.Arg172Cys) single nucleotide variant Inborn genetic diseases [RCV004035881]|not provided [RCV001339025] Chr14:99231471 [GRCh38]
Chr14:99697808 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.307C>T (p.Arg103Cys) single nucleotide variant not provided [RCV001319362] Chr14:99257591 [GRCh38]
Chr14:99723928 [GRCh37]
Chr14:14q32.2		 likely benign|uncertain significance
NM_138576.4(BCL11B):c.1524G>C (p.Glu508Asp) single nucleotide variant Inborn genetic diseases [RCV004968098]|not provided [RCV001347733] Chr14:99175312 [GRCh38]
Chr14:99641649 [GRCh37]
Chr14:14q32.2		 benign|uncertain significance
NM_138576.4(BCL11B):c.1935G>A (p.Ala645=) single nucleotide variant not provided [RCV001321079] Chr14:99174901 [GRCh38]
Chr14:99641238 [GRCh37]
Chr14:14q32.2		 benign|likely benign|uncertain significance
NM_138576.4(BCL11B):c.1620G>C (p.Glu540Asp) single nucleotide variant not provided [RCV001341073] Chr14:99175216 [GRCh38]
Chr14:99641553 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1905C>T (p.Asp635=) single nucleotide variant BCL11B-related disorder [RCV004533935]|not provided [RCV001516247] Chr14:99174931 [GRCh38]
Chr14:99641268 [GRCh37]
Chr14:14q32.2		 benign|likely benign
NM_138576.4(BCL11B):c.640+17C>T single nucleotide variant not provided [RCV001512659] Chr14:99231328 [GRCh38]
Chr14:99697665 [GRCh37]
Chr14:14q32.2		 benign
NM_138576.4(BCL11B):c.294G>A (p.Pro98=) single nucleotide variant not provided [RCV001434838] Chr14:99257604 [GRCh38]
Chr14:99723941 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.2349C>T (p.Gly783=) single nucleotide variant BCL11B-related disorder [RCV004533746]|not provided [RCV001443430] Chr14:99174487 [GRCh38]
Chr14:99640824 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.211del (p.Leu71fs) deletion Intellectual developmental disorder with speech delay, dysmorphic facies, and t-cell abnormalities [RCV003984859] Chr14:99257687 [GRCh38]
Chr14:99724024 [GRCh37]
Chr14:14q32.2		 pathogenic
NM_138576.4(BCL11B):c.885G>C (p.Thr295=) single nucleotide variant BCL11B-related disorder [RCV004531249]|not provided [RCV001410865] Chr14:99175951 [GRCh38]
Chr14:99642288 [GRCh37]
Chr14:14q32.2		 benign|likely benign
NM_138576.4(BCL11B):c.427+5G>A single nucleotide variant not provided [RCV001411813] Chr14:99257466 [GRCh38]
Chr14:99723803 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1483G>A (p.Ala495Thr) single nucleotide variant not provided [RCV001521198] Chr14:99175353 [GRCh38]
Chr14:99641690 [GRCh37]
Chr14:14q32.2		 benign|likely benign
NM_138576.4(BCL11B):c.2268C>T (p.Pro756=) single nucleotide variant not provided [RCV001518575] Chr14:99174568 [GRCh38]
Chr14:99640905 [GRCh37]
Chr14:14q32.2		 benign
NM_138576.4(BCL11B):c.246C>T (p.Gly82=) single nucleotide variant not provided [RCV001459542] Chr14:99257652 [GRCh38]
Chr14:99723989 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.2307C>T (p.Gly769=) single nucleotide variant not provided [RCV001513193] Chr14:99174529 [GRCh38]
Chr14:99640866 [GRCh37]
Chr14:14q32.2		 benign
NM_138576.4(BCL11B):c.813G>C (p.Pro271=) single nucleotide variant not provided [RCV001515010]|not specified [RCV003487341] Chr14:99176023 [GRCh38]
Chr14:99642360 [GRCh37]
Chr14:14q32.2		 benign
NM_138576.4(BCL11B):c.2222C>T (p.Ser741Phe) single nucleotide variant Intellectual developmental disorder with speech delay, dysmorphic facies, and t-cell abnormalities [RCV001449960] Chr14:99174614 [GRCh38]
Chr14:99640951 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1899G>A (p.Ala633=) single nucleotide variant not provided [RCV003108545] Chr14:99174937 [GRCh38]
Chr14:99641274 [GRCh37]
Chr14:14q32.2		 benign
NM_138576.4(BCL11B):c.732C>T (p.His244=) single nucleotide variant not provided [RCV003108756] Chr14:99176104 [GRCh38]
Chr14:99642441 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.2507G>A (p.Ser836Asn) single nucleotide variant BCL11B-related disorder [RCV004007233]|Intellectual developmental disorder with speech delay, dysmorphic facies, and t-cell abnormalities [RCV001788503]|not provided [RCV001726571] Chr14:99174329 [GRCh38]
Chr14:99640666 [GRCh37]
Chr14:14q32.2		 pathogenic|likely pathogenic|conflicting interpretations of pathogenicity
NM_138576.4(BCL11B):c.1190C>T (p.Pro397Leu) single nucleotide variant not specified [RCV004783552] Chr14:99175646 [GRCh38]
Chr14:99641983 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.925C>A (p.Arg309Ser) single nucleotide variant not provided [RCV004784682] Chr14:99175911 [GRCh38]
Chr14:99642248 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1097_1140delinsCAGC (p.Arg366fs) indel not provided [RCV001780682] Chr14:99175696..99175739 [GRCh38]
Chr14:99642033..99642076 [GRCh37]
Chr14:14q32.2		 likely pathogenic
NM_138576.4(BCL11B):c.1272_1278del (p.Lys425fs) deletion Intellectual developmental disorder with speech delay, dysmorphic facies, and t-cell abnormalities [RCV002272814] Chr14:99175558..99175564 [GRCh38]
Chr14:99641895..99641901 [GRCh37]
Chr14:14q32.2		 pathogenic
NM_138576.4(BCL11B):c.1322A>T (p.Asn441Ile) single nucleotide variant not provided [RCV001764880] Chr14:99175514 [GRCh38]
Chr14:99641851 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.2242G>A (p.Gly748Ser) single nucleotide variant not provided [RCV001774379] Chr14:99174594 [GRCh38]
Chr14:99640931 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1566C>G (p.Ser522Arg) single nucleotide variant not provided [RCV001752103] Chr14:99175270 [GRCh38]
Chr14:99641607 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1603GAG[8] (p.Glu543del) microsatellite not provided [RCV001754049] Chr14:99175207..99175209 [GRCh38]
Chr14:99641544..99641546 [GRCh37]
Chr14:14q32.2		 benign
NM_138576.4(BCL11B):c.2637G>C (p.Glu879Asp) single nucleotide variant not provided [RCV001786648] Chr14:99174199 [GRCh38]
Chr14:99640536 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1679C>T (p.Ser560Leu) single nucleotide variant Intellectual developmental disorder with speech delay, dysmorphic facies, and t-cell abnormalities [RCV001797011]|not provided [RCV002074128] Chr14:99175157 [GRCh38]
Chr14:99641494 [GRCh37]
Chr14:14q32.2		 likely benign|uncertain significance
NM_138576.4(BCL11B):c.908C>A (p.Pro303Gln) single nucleotide variant Immunodeficiency 49 [RCV001809278]|not provided [RCV003772267] Chr14:99175928 [GRCh38]
Chr14:99642265 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1904ACG[3] (p.Asp638del) microsatellite not provided [RCV001907741] Chr14:99174921..99174923 [GRCh38]
Chr14:99641258..99641260 [GRCh37]
Chr14:14q32.2		 likely benign|uncertain significance
NM_138576.4(BCL11B):c.986G>A (p.Arg329His) single nucleotide variant not provided [RCV002008877] Chr14:99175850 [GRCh38]
Chr14:99642187 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1156A>C (p.Asn386His) single nucleotide variant not provided [RCV001915470] Chr14:99175680 [GRCh38]
Chr14:99642017 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.2053G>A (p.Ala685Thr) single nucleotide variant not provided [RCV001873032] Chr14:99174783 [GRCh38]
Chr14:99641120 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1590GGA[3] (p.Glu533del) microsatellite not provided [RCV001950066] Chr14:99175235..99175237 [GRCh38]
Chr14:99641572..99641574 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1437C>A (p.His479Gln) single nucleotide variant not provided [RCV001929226] Chr14:99175399 [GRCh38]
Chr14:99641736 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.502A>G (p.Thr168Ala) single nucleotide variant not provided [RCV001988750] Chr14:99231483 [GRCh38]
Chr14:99697820 [GRCh37]
Chr14:14q32.2		 likely benign|uncertain significance
NM_138576.4(BCL11B):c.2357G>C (p.Arg786Pro) single nucleotide variant not provided [RCV002005062] Chr14:99174479 [GRCh38]
Chr14:99640816 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.2024_2025delinsTT (p.Pro675Leu) indel not provided [RCV002006967] Chr14:99174811..99174812 [GRCh38]
Chr14:99641148..99641149 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1196C>A (p.Pro399His) single nucleotide variant not provided [RCV002006684] Chr14:99175640 [GRCh38]
Chr14:99641977 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1196C>G (p.Pro399Arg) single nucleotide variant not provided [RCV001988178] Chr14:99175640 [GRCh38]
Chr14:99641977 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.2478C>T (p.Cys826=) single nucleotide variant not provided [RCV001915255] Chr14:99174358 [GRCh38]
Chr14:99640695 [GRCh37]
Chr14:14q32.2		 likely benign|uncertain significance
NM_138576.4(BCL11B):c.565C>T (p.Arg189Cys) single nucleotide variant Inborn genetic diseases [RCV004603133]|not provided [RCV001984124] Chr14:99231420 [GRCh38]
Chr14:99697757 [GRCh37]
Chr14:14q32.2		 likely benign|uncertain significance
NM_138576.4(BCL11B):c.455C>T (p.Ala152Val) single nucleotide variant Inborn genetic diseases [RCV002569182]|not provided [RCV001968581] Chr14:99231530 [GRCh38]
Chr14:99697867 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.757G>A (p.Gly253Arg) single nucleotide variant not provided [RCV002004014] Chr14:99176079 [GRCh38]
Chr14:99642416 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1978C>T (p.Pro660Ser) single nucleotide variant not provided [RCV001893110] Chr14:99174858 [GRCh38]
Chr14:99641195 [GRCh37]
Chr14:14q32.2		 uncertain significance
GRCh37/hg19 14q32.13-32.31(chr14:95871795-102457523)x1 copy number loss not provided [RCV001827727] Chr14:95871795..102457523 [GRCh37]
Chr14:14q32.13-32.31		 pathogenic
NM_138576.4(BCL11B):c.569C>T (p.Pro190Leu) single nucleotide variant not provided [RCV002003540] Chr14:99231416 [GRCh38]
Chr14:99697753 [GRCh37]
Chr14:14q32.2		 conflicting interpretations of pathogenicity|uncertain significance
NM_138576.4(BCL11B):c.1214G>A (p.Ser405Asn) single nucleotide variant not provided [RCV002021459] Chr14:99175622 [GRCh38]
Chr14:99641959 [GRCh37]
Chr14:14q32.2		 benign|uncertain significance
NM_138576.4(BCL11B):c.2653G>A (p.Asp885Asn) single nucleotide variant not provided [RCV002041365] Chr14:99174183 [GRCh38]
Chr14:99640520 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1068C>G (p.Ile356Met) single nucleotide variant not provided [RCV002039572] Chr14:99175768 [GRCh38]
Chr14:99642105 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1662_1668del (p.Ser555fs) deletion Intellectual developmental disorder with speech delay, dysmorphic facies, and t-cell abnormalities [RCV003984864] Chr14:99175168..99175174 [GRCh38]
Chr14:99641505..99641511 [GRCh37]
Chr14:14q32.2		 pathogenic
NM_138576.4(BCL11B):c.103G>T (p.Gly35Cys) single nucleotide variant not provided [RCV001982851] Chr14:99257795 [GRCh38]
Chr14:99724132 [GRCh37]
Chr14:14q32.2		 likely benign|uncertain significance
NM_138576.4(BCL11B):c.1005G>A (p.Met335Ile) single nucleotide variant not provided [RCV001894040] Chr14:99175831 [GRCh38]
Chr14:99642168 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1898C>T (p.Ala633Val) single nucleotide variant not provided [RCV001987557] Chr14:99174938 [GRCh38]
Chr14:99641275 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1807G>C (p.Gly603Arg) single nucleotide variant not provided [RCV001983376] Chr14:99175029 [GRCh38]
Chr14:99641366 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1735G>A (p.Ala579Thr) single nucleotide variant Inborn genetic diseases [RCV004603102]|not provided [RCV001985388] Chr14:99175101 [GRCh38]
Chr14:99641438 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.335C>T (p.Pro112Leu) single nucleotide variant not provided [RCV001969183] Chr14:99257563 [GRCh38]
Chr14:99723900 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.971A>G (p.His324Arg) single nucleotide variant not provided [RCV001894794] Chr14:99175865 [GRCh38]
Chr14:99642202 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.270C>G (p.Asp90Glu) single nucleotide variant not provided [RCV001889802] Chr14:99257628 [GRCh38]
Chr14:99723965 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.2147C>G (p.Ala716Gly) single nucleotide variant not provided [RCV002043393] Chr14:99174689 [GRCh38]
Chr14:99641026 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.2099C>T (p.Ala700Val) single nucleotide variant not provided [RCV001890774] Chr14:99174737 [GRCh38]
Chr14:99641074 [GRCh37]
Chr14:14q32.2		 benign|uncertain significance
NM_138576.4(BCL11B):c.392C>T (p.Thr131Met) single nucleotide variant BCL11B-related disorder [RCV004758835]|not provided [RCV001890924] Chr14:99257506 [GRCh38]
Chr14:99723843 [GRCh37]
Chr14:14q32.2		 likely benign|uncertain significance
NM_138576.4(BCL11B):c.583G>A (p.Gly195Arg) single nucleotide variant not provided [RCV001894730] Chr14:99231402 [GRCh38]
Chr14:99697739 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.980C>T (p.Pro327Leu) single nucleotide variant not provided [RCV002043413] Chr14:99175856 [GRCh38]
Chr14:99642193 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.561C>T (p.Ser187=) single nucleotide variant not provided [RCV001986436] Chr14:99231424 [GRCh38]
Chr14:99697761 [GRCh37]
Chr14:14q32.2		 likely benign|uncertain significance
NM_138576.4(BCL11B):c.1478_1479insAGA (p.Ser493_Ala494insGlu) insertion not provided [RCV001962712] Chr14:99175357..99175358 [GRCh38]
Chr14:99641694..99641695 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.2089C>T (p.Pro697Ser) single nucleotide variant not provided [RCV001973007] Chr14:99174747 [GRCh38]
Chr14:99641084 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1605G>C (p.Glu535Asp) single nucleotide variant not provided [RCV002013223] Chr14:99175231 [GRCh38]
Chr14:99641568 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.2286C>T (p.Gly762=) single nucleotide variant BCL11B-related disorder [RCV004542197]|not provided [RCV001992880] Chr14:99174550 [GRCh38]
Chr14:99640887 [GRCh37]
Chr14:14q32.2		 likely benign|uncertain significance
NM_138576.4(BCL11B):c.82G>A (p.Ala28Thr) single nucleotide variant BCL11B-related disorder [RCV004758845]|Inborn genetic diseases [RCV004970529]|not provided [RCV001943471] Chr14:99257816 [GRCh38]
Chr14:99724153 [GRCh37]
Chr14:14q32.2		 benign|uncertain significance
NM_138576.4(BCL11B):c.1745G>T (p.Gly582Val) single nucleotide variant not provided [RCV001886972] Chr14:99175091 [GRCh38]
Chr14:99641428 [GRCh37]
Chr14:14q32.2		 likely benign|uncertain significance
NM_138576.4(BCL11B):c.2193C>G (p.Asp731Glu) single nucleotide variant not provided [RCV001981140] Chr14:99174643 [GRCh38]
Chr14:99640980 [GRCh37]
Chr14:14q32.2		 benign|uncertain significance
NM_138576.4(BCL11B):c.484C>A (p.Pro162Thr) single nucleotide variant not provided [RCV001925887] Chr14:99231501 [GRCh38]
Chr14:99697838 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.2341G>C (p.Gly781Arg) single nucleotide variant not provided [RCV002036348] Chr14:99174495 [GRCh38]
Chr14:99640832 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1603GAG[5] (p.Glu540_Glu543del) microsatellite not provided [RCV001989447] Chr14:99175207..99175218 [GRCh38]
Chr14:99641544..99641555 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.263G>A (p.Cys88Tyr) single nucleotide variant not provided [RCV001898084] Chr14:99257635 [GRCh38]
Chr14:99723972 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1697G>C (p.Arg566Pro) single nucleotide variant not provided [RCV001904473] Chr14:99175139 [GRCh38]
Chr14:99641476 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.916G>T (p.Gly306Cys) single nucleotide variant Inborn genetic diseases [RCV003382768]|not provided [RCV001974138] Chr14:99175920 [GRCh38]
Chr14:99642257 [GRCh37]
Chr14:14q32.2		 benign|uncertain significance
NM_138576.4(BCL11B):c.1534G>T (p.Ala512Ser) single nucleotide variant not provided [RCV001876573] Chr14:99175302 [GRCh38]
Chr14:99641639 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.137T>C (p.Leu46Pro) single nucleotide variant not provided [RCV001975649] Chr14:99257761 [GRCh38]
Chr14:99724098 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1479G>A (p.Ser493=) single nucleotide variant not provided [RCV002047247] Chr14:99175357 [GRCh38]
Chr14:99641694 [GRCh37]
Chr14:14q32.2		 likely benign|uncertain significance
NM_138576.4(BCL11B):c.2340_2341delinsTC (p.Gly781Arg) indel not provided [RCV001954890] Chr14:99174495..99174496 [GRCh38]
Chr14:99640832..99640833 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1450C>A (p.Leu484Met) single nucleotide variant not provided [RCV001930396] Chr14:99175386 [GRCh38]
Chr14:99641723 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1726G>A (p.Val576Ile) single nucleotide variant not provided [RCV001931851] Chr14:99175110 [GRCh38]
Chr14:99641447 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1501G>A (p.Gly501Ser) single nucleotide variant not provided [RCV001918732] Chr14:99175335 [GRCh38]
Chr14:99641672 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1234_1257dup (p.Met412_Pro419dup) duplication not provided [RCV001877302] Chr14:99175578..99175579 [GRCh38]
Chr14:99641915..99641916 [GRCh37]
Chr14:14q32.2		 benign|uncertain significance
NM_138576.4(BCL11B):c.1112C>G (p.Ala371Gly) single nucleotide variant not provided [RCV001982305] Chr14:99175724 [GRCh38]
Chr14:99642061 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1130C>T (p.Pro377Leu) single nucleotide variant Intellectual developmental disorder with speech delay, dysmorphic facies, and t-cell abnormalities [RCV004784010]|not provided [RCV001954467] Chr14:99175706 [GRCh38]
Chr14:99642043 [GRCh37]
Chr14:14q32.2		 uncertain significance
NC_000014.8:g.(?_99640488)_(99737555_?)del deletion not provided [RCV001990117] Chr14:99640488..99737555 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1744G>A (p.Gly582Ser) single nucleotide variant not provided [RCV001886243] Chr14:99175092 [GRCh38]
Chr14:99641429 [GRCh37]
Chr14:14q32.2		 benign|conflicting interpretations of pathogenicity|uncertain significance
NM_138576.4(BCL11B):c.1864G>A (p.Ala622Thr) single nucleotide variant not provided [RCV001898271] Chr14:99174972 [GRCh38]
Chr14:99641309 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.2394C>T (p.Cys798=) single nucleotide variant not provided [RCV001999094] Chr14:99174442 [GRCh38]
Chr14:99640779 [GRCh37]
Chr14:14q32.2		 likely benign|uncertain significance
NM_138576.4(BCL11B):c.1381G>A (p.Asp461Asn) single nucleotide variant not provided [RCV001922060] Chr14:99175455 [GRCh38]
Chr14:99641792 [GRCh37]
Chr14:14q32.2		 uncertain significance
NC_000014.8:g.(?_99375322)_(101142891_?)dup duplication not provided [RCV004578224] Chr14:99375322..101142891 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.308G>A (p.Arg103His) single nucleotide variant not provided [RCV001939134] Chr14:99257590 [GRCh38]
Chr14:99723927 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.539G>A (p.Cys180Tyr) single nucleotide variant not provided [RCV001959988] Chr14:99231446 [GRCh38]
Chr14:99697783 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1159C>T (p.Pro387Ser) single nucleotide variant not provided [RCV002019495] Chr14:99175677 [GRCh38]
Chr14:99642014 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.619G>C (p.Gly207Arg) single nucleotide variant not provided [RCV002019670] Chr14:99231366 [GRCh38]
Chr14:99697703 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.2317G>A (p.Gly773Arg) single nucleotide variant BCL11B-related disorder [RCV004529076]|not provided [RCV001980447] Chr14:99174519 [GRCh38]
Chr14:99640856 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.685C>T (p.Pro229Ser) single nucleotide variant not provided [RCV001961230] Chr14:99176151 [GRCh38]
Chr14:99642488 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.317_334dup (p.Leu106_Glu111dup) duplication not provided [RCV001935759] Chr14:99257563..99257564 [GRCh38]
Chr14:99723900..99723901 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.605C>T (p.Thr202Met) single nucleotide variant Inborn genetic diseases [RCV004970515]|not provided [RCV001936006] Chr14:99231380 [GRCh38]
Chr14:99697717 [GRCh37]
Chr14:14q32.2		 likely benign|uncertain significance
NM_138576.4(BCL11B):c.728C>T (p.Thr243Met) single nucleotide variant Inborn genetic diseases [RCV002642015]|not provided [RCV001991926] Chr14:99176108 [GRCh38]
Chr14:99642445 [GRCh37]
Chr14:14q32.2		 likely benign|uncertain significance
NM_138576.4(BCL11B):c.2035C>T (p.Pro679Ser) single nucleotide variant Inborn genetic diseases [RCV003250440]|not provided [RCV002049056] Chr14:99174801 [GRCh38]
Chr14:99641138 [GRCh37]
Chr14:14q32.2		 likely benign|uncertain significance
NM_138576.4(BCL11B):c.247G>A (p.Gly83Ser) single nucleotide variant not provided [RCV002016696] Chr14:99257651 [GRCh38]
Chr14:99723988 [GRCh37]
Chr14:14q32.2		 benign|uncertain significance
NM_138576.4(BCL11B):c.918C>T (p.Gly306=) single nucleotide variant not provided [RCV002010124] Chr14:99175918 [GRCh38]
Chr14:99642255 [GRCh37]
Chr14:14q32.2		 likely benign|uncertain significance
NM_138576.4(BCL11B):c.1148G>A (p.Gly383Asp) single nucleotide variant BCL11B-related disorder [RCV004758844]|not provided [RCV001920914] Chr14:99175688 [GRCh38]
Chr14:99642025 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.2175C>T (p.Pro725=) single nucleotide variant not provided [RCV002146516] Chr14:99174661 [GRCh38]
Chr14:99640998 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.427+19G>T single nucleotide variant not provided [RCV002186325] Chr14:99257452 [GRCh38]
Chr14:99723789 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1872G>T (p.Leu624=) single nucleotide variant not provided [RCV002112093] Chr14:99174964 [GRCh38]
Chr14:99641301 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.820G>A (p.Val274Met) single nucleotide variant Inborn genetic diseases [RCV004970854]|not provided [RCV002206116] Chr14:99176016 [GRCh38]
Chr14:99642353 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.432G>A (p.Pro144=) single nucleotide variant not provided [RCV002186278] Chr14:99231553 [GRCh38]
Chr14:99697890 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1152C>T (p.Arg384=) single nucleotide variant not provided [RCV002088862] Chr14:99175684 [GRCh38]
Chr14:99642021 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.640+12C>T single nucleotide variant not provided [RCV002189663] Chr14:99231333 [GRCh38]
Chr14:99697670 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1603GAG[11] (p.Glu542_Glu543dup) microsatellite not provided [RCV002086113] Chr14:99175206..99175207 [GRCh38]
Chr14:99641543..99641544 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1656C>T (p.Pro552=) single nucleotide variant BCL11B-related disorder [RCV004543710]|not provided [RCV002165553] Chr14:99175180 [GRCh38]
Chr14:99641517 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.729G>A (p.Thr243=) single nucleotide variant not provided [RCV002189386] Chr14:99176107 [GRCh38]
Chr14:99642444 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.2346G>C (p.Pro782=) single nucleotide variant not provided [RCV002167686] Chr14:99174490 [GRCh38]
Chr14:99640827 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.567C>A (p.Arg189=) single nucleotide variant not provided [RCV002126093] Chr14:99231418 [GRCh38]
Chr14:99697755 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.804G>A (p.Pro268=) single nucleotide variant not provided [RCV002210029] Chr14:99176032 [GRCh38]
Chr14:99642369 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.777C>A (p.Leu259=) single nucleotide variant not provided [RCV002091729]|not specified [RCV004587311] Chr14:99176059 [GRCh38]
Chr14:99642396 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.366C>T (p.Asp122=) single nucleotide variant BCL11B-related disorder [RCV004531312]|not provided [RCV002209321] Chr14:99257532 [GRCh38]
Chr14:99723869 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.293C>T (p.Pro98Leu) single nucleotide variant BCL11B-related disorder [RCV004531321]|not provided [RCV002207510] Chr14:99257605 [GRCh38]
Chr14:99723942 [GRCh37]
Chr14:14q32.2		 benign|likely benign
NM_138576.4(BCL11B):c.1743C>T (p.Gly581=) single nucleotide variant not provided [RCV002147928] Chr14:99175093 [GRCh38]
Chr14:99641430 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1053G>A (p.Leu351=) single nucleotide variant not provided [RCV002167279] Chr14:99175783 [GRCh38]
Chr14:99642120 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1038C>T (p.Asp346=) single nucleotide variant not provided [RCV002127896] Chr14:99175798 [GRCh38]
Chr14:99642135 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.2262G>A (p.Thr754=) single nucleotide variant not provided [RCV002105564] Chr14:99174574 [GRCh38]
Chr14:99640911 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.2349C>G (p.Gly783=) single nucleotide variant BCL11B-related disorder [RCV004538770]|not provided [RCV002090133] Chr14:99174487 [GRCh38]
Chr14:99640824 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.2025G>C (p.Pro675=) single nucleotide variant not provided [RCV002145718] Chr14:99174811 [GRCh38]
Chr14:99641148 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.2538C>T (p.His846=) single nucleotide variant not provided [RCV002078298]|not specified [RCV004700606] Chr14:99174298 [GRCh38]
Chr14:99640635 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.640+9C>T single nucleotide variant not provided [RCV002212762] Chr14:99231336 [GRCh38]
Chr14:99697673 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.740G>A (p.Arg247His) single nucleotide variant Immunodeficiency 49 [RCV002210934]|not provided [RCV003093837] Chr14:99176096 [GRCh38]
Chr14:99642433 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.2622A>G (p.Lys874=) single nucleotide variant not provided [RCV002124856] Chr14:99174214 [GRCh38]
Chr14:99640551 [GRCh37]
Chr14:14q32.2		 benign
NM_138576.4(BCL11B):c.876G>A (p.Leu292=) single nucleotide variant not provided [RCV002169000] Chr14:99175960 [GRCh38]
Chr14:99642297 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.2097C>T (p.Ala699=) single nucleotide variant not provided [RCV002215508] Chr14:99174739 [GRCh38]
Chr14:99641076 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1457G>C (p.Gly486Ala) single nucleotide variant not provided [RCV002224787] Chr14:99175379 [GRCh38]
Chr14:99641716 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.2196A>T (p.Ala732=) single nucleotide variant not provided [RCV002189969] Chr14:99174640 [GRCh38]
Chr14:99640977 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.2043C>G (p.Leu681=) single nucleotide variant not provided [RCV002192812] Chr14:99174793 [GRCh38]
Chr14:99641130 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.888C>T (p.Gly296=) single nucleotide variant not provided [RCV002076889] Chr14:99175948 [GRCh38]
Chr14:99642285 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1051C>T (p.Leu351=) single nucleotide variant not provided [RCV002080712] Chr14:99175785 [GRCh38]
Chr14:99642122 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.2019C>T (p.Pro673=) single nucleotide variant not provided [RCV002171288] Chr14:99174817 [GRCh38]
Chr14:99641154 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.2223C>T (p.Ser741=) single nucleotide variant not provided [RCV002195313] Chr14:99174613 [GRCh38]
Chr14:99640950 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.427+14C>T single nucleotide variant not provided [RCV002206879] Chr14:99257457 [GRCh38]
Chr14:99723794 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1830C>T (p.Tyr610=) single nucleotide variant not provided [RCV002190444] Chr14:99175006 [GRCh38]
Chr14:99641343 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1782G>T (p.Val594=) single nucleotide variant not provided [RCV002080503] Chr14:99175054 [GRCh38]
Chr14:99641391 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.99C>T (p.Asp33=) single nucleotide variant not provided [RCV002071744] Chr14:99257799 [GRCh38]
Chr14:99724136 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.2257_2259del (p.Ser753del) deletion not provided [RCV002087413] Chr14:99174577..99174579 [GRCh38]
Chr14:99640914..99640916 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1603GAG[7] (p.Glu542_Glu543del) microsatellite BCL11B-related disorder [RCV004545244]|not provided [RCV002194341] Chr14:99175207..99175212 [GRCh38]
Chr14:99641544..99641549 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.774G>A (p.Ser258=) single nucleotide variant not provided [RCV002153620]|not specified [RCV005058110] Chr14:99176062 [GRCh38]
Chr14:99642399 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.641-4C>G single nucleotide variant not provided [RCV002135272] Chr14:99176199 [GRCh38]
Chr14:99642536 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.54C>T (p.Ile18=) single nucleotide variant not provided [RCV002134280] Chr14:99271165 [GRCh38]
Chr14:99737502 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.885G>A (p.Thr295=) single nucleotide variant not provided [RCV002213017] Chr14:99175951 [GRCh38]
Chr14:99642288 [GRCh37]
Chr14:14q32.2		 benign
NM_138576.4(BCL11B):c.1584C>T (p.His528=) single nucleotide variant not provided [RCV002193257] Chr14:99175252 [GRCh38]
Chr14:99641589 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1603GAG[10] (p.Glu543dup) microsatellite not provided [RCV002113504] Chr14:99175206..99175207 [GRCh38]
Chr14:99641543..99641544 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.90C>T (p.Leu30=) single nucleotide variant not provided [RCV002106651] Chr14:99257808 [GRCh38]
Chr14:99724145 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.2097C>G (p.Ala699=) single nucleotide variant not provided [RCV002206559] Chr14:99174739 [GRCh38]
Chr14:99641076 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.2541G>C (p.Gly847=) single nucleotide variant not provided [RCV002173058] Chr14:99174295 [GRCh38]
Chr14:99640632 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.71A>G (p.His24Arg) single nucleotide variant Inborn genetic diseases [RCV004045832]|not provided [RCV002096093] Chr14:99257827 [GRCh38]
Chr14:99724164 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.2127G>A (p.Ser709=) single nucleotide variant not provided [RCV002105363] Chr14:99174709 [GRCh38]
Chr14:99641046 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1725G>C (p.Gly575=) single nucleotide variant not provided [RCV002212651] Chr14:99175111 [GRCh38]
Chr14:99641448 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1332G>T (p.Val444=) single nucleotide variant not provided [RCV002194206] Chr14:99175504 [GRCh38]
Chr14:99641841 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.2034C>T (p.Ser678=) single nucleotide variant not provided [RCV002079641] Chr14:99174802 [GRCh38]
Chr14:99641139 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.312C>T (p.Ser104=) single nucleotide variant not provided [RCV002113570] Chr14:99257586 [GRCh38]
Chr14:99723923 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.641-19T>C single nucleotide variant not provided [RCV002172563] Chr14:99176214 [GRCh38]
Chr14:99642551 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.2108C>G (p.Pro703Arg) single nucleotide variant not provided [RCV002079712] Chr14:99174728 [GRCh38]
Chr14:99641065 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.336G>A (p.Pro112=) single nucleotide variant not provided [RCV002077851] Chr14:99257562 [GRCh38]
Chr14:99723899 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1975G>A (p.Ala659Thr) single nucleotide variant not provided [RCV002077870] Chr14:99174861 [GRCh38]
Chr14:99641198 [GRCh37]
Chr14:14q32.2		 benign
NM_138576.4(BCL11B):c.582C>T (p.Asp194=) single nucleotide variant not provided [RCV002195811] Chr14:99231403 [GRCh38]
Chr14:99697740 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.81C>T (p.Ala27=) single nucleotide variant not provided [RCV002152619] Chr14:99257817 [GRCh38]
Chr14:99724154 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1521C>T (p.Gly507=) single nucleotide variant BCL11B-related disorder [RCV004531326]|Immunodeficiency 49 [RCV003224611]|not provided [RCV002213061] Chr14:99175315 [GRCh38]
Chr14:99641652 [GRCh37]
Chr14:14q32.2		 benign|likely benign
NM_138576.4(BCL11B):c.58+14G>A single nucleotide variant not provided [RCV002218005] Chr14:99271147 [GRCh38]
Chr14:99737484 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1748C>A (p.Ala583Glu) single nucleotide variant not provided [RCV002138623] Chr14:99175088 [GRCh38]
Chr14:99641425 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.393G>A (p.Thr131=) single nucleotide variant not provided [RCV002083032] Chr14:99257505 [GRCh38]
Chr14:99723842 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1455C>T (p.Ala485=) single nucleotide variant not provided [RCV002083260] Chr14:99175381 [GRCh38]
Chr14:99641718 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.2343C>T (p.Gly781=) single nucleotide variant not provided [RCV002159712] Chr14:99174493 [GRCh38]
Chr14:99640830 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.2283C>T (p.Asp761=) single nucleotide variant not provided [RCV002120370] Chr14:99174553 [GRCh38]
Chr14:99640890 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1221G>C (p.Pro407=) single nucleotide variant not provided [RCV002102749] Chr14:99175615 [GRCh38]
Chr14:99641952 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1068C>T (p.Ile356=) single nucleotide variant not provided [RCV002220094] Chr14:99175768 [GRCh38]
Chr14:99642105 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.2604C>G (p.Thr868=) single nucleotide variant not provided [RCV002199751] Chr14:99174232 [GRCh38]
Chr14:99640569 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.87C>T (p.Ile29=) single nucleotide variant not provided [RCV002144417] Chr14:99257811 [GRCh38]
Chr14:99724148 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1904ACG[5] (p.Asp638dup) microsatellite not provided [RCV002144419] Chr14:99174920..99174921 [GRCh38]
Chr14:99641257..99641258 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.2646G>T (p.Leu882=) single nucleotide variant not provided [RCV002184602] Chr14:99174190 [GRCh38]
Chr14:99640527 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1179C>T (p.Asn393=) single nucleotide variant not provided [RCV002143002] Chr14:99175657 [GRCh38]
Chr14:99641994 [GRCh37]
Chr14:14q32.2		 benign|likely benign
NM_138576.4(BCL11B):c.1602C>T (p.Asp534=) single nucleotide variant not provided [RCV002083572] Chr14:99175234 [GRCh38]
Chr14:99641571 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1644C>T (p.Asn548=) single nucleotide variant not provided [RCV002158200] Chr14:99175192 [GRCh38]
Chr14:99641529 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.2127G>C (p.Ser709=) single nucleotide variant not provided [RCV002216929] Chr14:99174709 [GRCh38]
Chr14:99641046 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.2265G>A (p.Pro755=) single nucleotide variant not provided [RCV002123832] Chr14:99174571 [GRCh38]
Chr14:99640908 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1350G>A (p.Thr450=) single nucleotide variant not provided [RCV002163782] Chr14:99175486 [GRCh38]
Chr14:99641823 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1449G>C (p.Ser483=) single nucleotide variant not provided [RCV002098551] Chr14:99175387 [GRCh38]
Chr14:99641724 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.59-12_59-9del microsatellite not provided [RCV002163993] Chr14:99257848..99257851 [GRCh38]
Chr14:99724185..99724188 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.2559G>A (p.Val853=) single nucleotide variant not provided [RCV002178058] Chr14:99174277 [GRCh38]
Chr14:99640614 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.2436G>A (p.Thr812=) single nucleotide variant not provided [RCV002142149]|not specified [RCV004690251] Chr14:99174400 [GRCh38]
Chr14:99640737 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.345C>T (p.Ile115=) single nucleotide variant not provided [RCV002142298] Chr14:99257553 [GRCh38]
Chr14:99723890 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1506C>T (p.Thr502=) single nucleotide variant not provided [RCV002164503] Chr14:99175330 [GRCh38]
Chr14:99641667 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.552G>A (p.Pro184=) single nucleotide variant not provided [RCV002142513] Chr14:99231433 [GRCh38]
Chr14:99697770 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.2100G>A (p.Ala700=) single nucleotide variant not provided [RCV002119126] Chr14:99174736 [GRCh38]
Chr14:99641073 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1387G>A (p.Ala463Thr) single nucleotide variant not provided [RCV002254995] Chr14:99175449 [GRCh38]
Chr14:99641786 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1223C>T (p.Pro408Leu) single nucleotide variant not provided [RCV002255072] Chr14:99175613 [GRCh38]
Chr14:99641950 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.322A>G (p.Lys108Glu) single nucleotide variant not provided [RCV002122788] Chr14:99257576 [GRCh38]
Chr14:99723913 [GRCh37]
Chr14:14q32.2		 benign
NM_138576.4(BCL11B):c.723G>A (p.Gln241=) single nucleotide variant not provided [RCV002197816] Chr14:99176113 [GRCh38]
Chr14:99642450 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.640+11A>C single nucleotide variant not provided [RCV002142609] Chr14:99231334 [GRCh38]
Chr14:99697671 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.551C>T (p.Pro184Leu) single nucleotide variant Inborn genetic diseases [RCV004046314]|not provided [RCV002117863] Chr14:99231434 [GRCh38]
Chr14:99697771 [GRCh37]
Chr14:14q32.2		 benign|likely benign
NM_138576.4(BCL11B):c.2217G>A (p.Thr739=) single nucleotide variant not provided [RCV002161375] Chr14:99174619 [GRCh38]
Chr14:99640956 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1449G>A (p.Ser483=) single nucleotide variant not provided [RCV002083690] Chr14:99175387 [GRCh38]
Chr14:99641724 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.2136G>C (p.Leu712=) single nucleotide variant not provided [RCV002177639] Chr14:99174700 [GRCh38]
Chr14:99641037 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1719G>A (p.Val573=) single nucleotide variant not provided [RCV002202313] Chr14:99175117 [GRCh38]
Chr14:99641454 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.104G>T (p.Gly35Val) single nucleotide variant not provided [RCV002222844] Chr14:99257794 [GRCh38]
Chr14:99724131 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1245C>T (p.Gly415=) single nucleotide variant not provided [RCV002180855] Chr14:99175591 [GRCh38]
Chr14:99641928 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1977G>C (p.Ala659=) single nucleotide variant not provided [RCV002180952] Chr14:99174859 [GRCh38]
Chr14:99641196 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1881G>A (p.Ala627=) single nucleotide variant not provided [RCV002156188] Chr14:99174955 [GRCh38]
Chr14:99641292 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.2571C>T (p.Asp857=) single nucleotide variant not provided [RCV002137652] Chr14:99174265 [GRCh38]
Chr14:99640602 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1812A>G (p.Leu604=) single nucleotide variant not provided [RCV002120328] Chr14:99175024 [GRCh38]
Chr14:99641361 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1707C>T (p.Gly569=) single nucleotide variant not provided [RCV002163078] Chr14:99175129 [GRCh38]
Chr14:99641466 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1446C>A (p.Gly482=) single nucleotide variant not provided [RCV002083149] Chr14:99175390 [GRCh38]
Chr14:99641727 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1730C>T (p.Pro577Leu) single nucleotide variant not specified [RCV004782120] Chr14:99175106 [GRCh38]
Chr14:99641443 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.2474dup (p.Cys826fs) duplication Intellectual developmental disorder with speech delay, dysmorphic facies, and t-cell abnormalities [RCV004776531] Chr14:99174361..99174362 [GRCh38]
Chr14:99640698..99640699 [GRCh37]
Chr14:14q32.2		 likely pathogenic
NM_138576.4(BCL11B):c.2314A>C (p.Ser772Arg) single nucleotide variant Inborn genetic diseases [RCV004968649]|not provided [RCV004776628] Chr14:99174522 [GRCh38]
Chr14:99640859 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.562G>A (p.Ala188Thr) single nucleotide variant not provided [RCV003113062] Chr14:99231423 [GRCh38]
Chr14:99697760 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.915C>T (p.Phe305=) single nucleotide variant not provided [RCV003114784] Chr14:99175921 [GRCh38]
Chr14:99642258 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1991_2002del (p.Pro664_Gly667del) deletion not provided [RCV004795180] Chr14:99174834..99174845 [GRCh38]
Chr14:99641171..99641182 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1219C>T (p.Pro407Ser) single nucleotide variant Intellectual developmental disorder with speech delay, dysmorphic facies, and t-cell abnormalities [RCV004788316] Chr14:99175617 [GRCh38]
Chr14:99641954 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.182G>T (p.Cys61Phe) single nucleotide variant Intellectual developmental disorder with speech delay, dysmorphic facies, and t-cell abnormalities [RCV002272843] Chr14:99257716 [GRCh38]
Chr14:99724053 [GRCh37]
Chr14:14q32.2		 uncertain significance
GRCh37/hg19 14q13.3-32.33(chr14:37671058-106985955)x2 copy number gain See cases [RCV002286356] Chr14:37671058..106985955 [GRCh37]
Chr14:14q13.3-32.33		 pathogenic
NM_138576.4(BCL11B):c.1380C>A (p.Cys460Ter) single nucleotide variant See cases [RCV002287715] Chr14:99175456 [GRCh38]
Chr14:99641793 [GRCh37]
Chr14:14q32.2		 pathogenic
NM_138576.4(BCL11B):c.1262_1267dup (p.Pro422_Pro423insGlnPro) duplication not provided [RCV002265366] Chr14:99175568..99175569 [GRCh38]
Chr14:99641905..99641906 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.161A>T (p.Asp54Val) single nucleotide variant not provided [RCV002292189] Chr14:99257737 [GRCh38]
Chr14:99724074 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.89T>C (p.Leu30Pro) single nucleotide variant not provided [RCV003235959] Chr14:99257809 [GRCh38]
Chr14:99724146 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.427G>A (p.Gly143Arg) single nucleotide variant not provided [RCV002293954] Chr14:99257471 [GRCh38]
Chr14:99723808 [GRCh37]
Chr14:14q32.2		 uncertain significance
GRCh37/hg19 14q31.2-32.33(chr14:84537502-107285437)x3 copy number gain not provided [RCV002472581] Chr14:84537502..107285437 [GRCh37]
Chr14:14q31.2-32.33		 pathogenic
NM_138576.4(BCL11B):c.1736C>T (p.Ala579Val) single nucleotide variant Inborn genetic diseases [RCV003287266] Chr14:99175100 [GRCh38]
Chr14:99641437 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1206del (p.Phe403fs) deletion Intellectual developmental disorder with speech delay, dysmorphic facies, and t-cell abnormalities [RCV002472318] Chr14:99175630 [GRCh38]
Chr14:99641967 [GRCh37]
Chr14:14q32.2		 likely pathogenic
NM_138576.4(BCL11B):c.2513A>G (p.Lys838Arg) single nucleotide variant Intellectual developmental disorder with speech delay, dysmorphic facies, and t-cell abnormalities [RCV002468768] Chr14:99174323 [GRCh38]
Chr14:99640660 [GRCh37]
Chr14:14q32.2		 likely pathogenic
NM_138576.4(BCL11B):c.301T>A (p.Ser101Thr) single nucleotide variant not provided [RCV002469845] Chr14:99257597 [GRCh38]
Chr14:99723934 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1748C>T (p.Ala583Val) single nucleotide variant Intellectual developmental disorder with speech delay, dysmorphic facies, and t-cell abnormalities [RCV002470257] Chr14:99175088 [GRCh38]
Chr14:99641425 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.2605del (p.Leu869fs) deletion Intellectual developmental disorder with speech delay, dysmorphic facies, and t-cell abnormalities [RCV002463989] Chr14:99174231 [GRCh38]
Chr14:99640568 [GRCh37]
Chr14:14q32.2		 pathogenic
NM_138576.4(BCL11B):c.764C>G (p.Ala255Gly) single nucleotide variant not provided [RCV003229968] Chr14:99176072 [GRCh38]
Chr14:99642409 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.2060G>A (p.Arg687His) single nucleotide variant not provided [RCV002304870] Chr14:99174776 [GRCh38]
Chr14:99641113 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.2641T>G (p.Leu881Val) single nucleotide variant not provided [RCV002305167] Chr14:99174195 [GRCh38]
Chr14:99640532 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.2023C>T (p.Pro675Ser) single nucleotide variant not provided [RCV002298300] Chr14:99174813 [GRCh38]
Chr14:99641150 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.2138T>C (p.Val713Ala) single nucleotide variant not provided [RCV002296644] Chr14:99174698 [GRCh38]
Chr14:99641035 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.118G>A (p.Glu40Lys) single nucleotide variant not provided [RCV002296802] Chr14:99257780 [GRCh38]
Chr14:99724117 [GRCh37]
Chr14:14q32.2		 benign|uncertain significance
NM_138576.4(BCL11B):c.2383A>T (p.Ser795Cys) single nucleotide variant not provided [RCV002301015] Chr14:99174453 [GRCh38]
Chr14:99640790 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.538T>C (p.Cys180Arg) single nucleotide variant not provided [RCV002296654] Chr14:99231447 [GRCh38]
Chr14:99697784 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.473C>T (p.Ala158Val) single nucleotide variant Immunodeficiency 49 [RCV004729147]|not provided [RCV002300977] Chr14:99231512 [GRCh38]
Chr14:99697849 [GRCh37]
Chr14:14q32.2		 likely benign|uncertain significance
NM_138576.4(BCL11B):c.1814G>A (p.Gly605Asp) single nucleotide variant not provided [RCV002303411] Chr14:99175022 [GRCh38]
Chr14:99641359 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.321G>C (p.Arg107Ser) single nucleotide variant not provided [RCV002296008] Chr14:99257577 [GRCh38]
Chr14:99723914 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1638G>A (p.Leu546=) single nucleotide variant not provided [RCV002861949] Chr14:99175198 [GRCh38]
Chr14:99641535 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.755C>G (p.Pro252Arg) single nucleotide variant not provided [RCV002616815] Chr14:99176081 [GRCh38]
Chr14:99642418 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1415G>A (p.Arg472His) single nucleotide variant not provided [RCV002837663] Chr14:99175421 [GRCh38]
Chr14:99641758 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1131G>T (p.Pro377=) single nucleotide variant not provided [RCV002991726] Chr14:99175705 [GRCh38]
Chr14:99642042 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1940C>T (p.Ala647Val) single nucleotide variant Inborn genetic diseases [RCV002902354] Chr14:99174896 [GRCh38]
Chr14:99641233 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.260C>T (p.Ala87Val) single nucleotide variant not provided [RCV002903322] Chr14:99257638 [GRCh38]
Chr14:99723975 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1907_1908delinsGG (p.Asp636Gly) indel not provided [RCV003095383] Chr14:99174928..99174929 [GRCh38]
Chr14:99641265..99641266 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.357C>T (p.Val119=) single nucleotide variant not provided [RCV003095467] Chr14:99257541 [GRCh38]
Chr14:99723878 [GRCh37]
Chr14:14q32.2		 benign
NM_138576.4(BCL11B):c.2536C>G (p.His846Asp) single nucleotide variant not provided [RCV002462665] Chr14:99174300 [GRCh38]
Chr14:99640637 [GRCh37]
Chr14:14q32.2		 likely pathogenic
NM_138576.4(BCL11B):c.1869C>A (p.Phe623Leu) single nucleotide variant not provided [RCV002756686] Chr14:99174967 [GRCh38]
Chr14:99641304 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1239C>T (p.Pro413=) single nucleotide variant not provided [RCV002947268] Chr14:99175597 [GRCh38]
Chr14:99641934 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1544G>A (p.Gly515Asp) single nucleotide variant not provided [RCV002994020] Chr14:99175292 [GRCh38]
Chr14:99641629 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1272C>T (p.Ala424=) single nucleotide variant not provided [RCV002636254] Chr14:99175564 [GRCh38]
Chr14:99641901 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.153C>T (p.Pro51=) single nucleotide variant not provided [RCV002685473] Chr14:99257745 [GRCh38]
Chr14:99724082 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1767C>T (p.Asp589=) single nucleotide variant not provided [RCV002617078] Chr14:99175069 [GRCh38]
Chr14:99641406 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1938C>T (p.Gly646=) single nucleotide variant not provided [RCV003035043] Chr14:99174898 [GRCh38]
Chr14:99641235 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1908C>T (p.Asp636=) single nucleotide variant not provided [RCV002727010] Chr14:99174928 [GRCh38]
Chr14:99641265 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.909G>A (p.Pro303=) single nucleotide variant not provided [RCV002618764] Chr14:99175927 [GRCh38]
Chr14:99642264 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.51C>T (p.Leu17=) single nucleotide variant not provided [RCV002858157] Chr14:99271168 [GRCh38]
Chr14:99737505 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.2382C>T (p.Arg794=) single nucleotide variant not provided [RCV003014773] Chr14:99174454 [GRCh38]
Chr14:99640791 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.762G>A (p.Pro254=) single nucleotide variant not provided [RCV002751376] Chr14:99176074 [GRCh38]
Chr14:99642411 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1928_1933dup (p.Asp644_Ala645insGlyAsp) duplication not provided [RCV002685567] Chr14:99174902..99174903 [GRCh38]
Chr14:99641239..99641240 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.2443C>T (p.Arg815Trp) single nucleotide variant not provided [RCV002838263] Chr14:99174393 [GRCh38]
Chr14:99640730 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1129C>A (p.Pro377Thr) single nucleotide variant not provided [RCV003016050] Chr14:99175707 [GRCh38]
Chr14:99642044 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.939G>T (p.Thr313=) single nucleotide variant not provided [RCV002862911] Chr14:99175897 [GRCh38]
Chr14:99642234 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.130C>T (p.Leu44=) single nucleotide variant not provided [RCV002616571] Chr14:99257768 [GRCh38]
Chr14:99724105 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1575G>A (p.Ser525=) single nucleotide variant not provided [RCV002861984] Chr14:99175261 [GRCh38]
Chr14:99641598 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1758G>T (p.Ala586=) single nucleotide variant not provided [RCV002903013] Chr14:99175078 [GRCh38]
Chr14:99641415 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1725G>A (p.Gly575=) single nucleotide variant not provided [RCV002995667] Chr14:99175111 [GRCh38]
Chr14:99641448 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.272A>G (p.Lys91Arg) single nucleotide variant Inborn genetic diseases [RCV002818102] Chr14:99257626 [GRCh38]
Chr14:99723963 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.976G>T (p.Asp326Tyr) single nucleotide variant Inborn genetic diseases [RCV004966003]|not provided [RCV002622913] Chr14:99175860 [GRCh38]
Chr14:99642197 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1996C>T (p.Pro666Ser) single nucleotide variant Immunodeficiency 49 [RCV004725452]|not provided [RCV003003044] Chr14:99174840 [GRCh38]
Chr14:99641177 [GRCh37]
Chr14:14q32.2		 likely benign|uncertain significance
NM_138576.4(BCL11B):c.1479G>C (p.Ser493=) single nucleotide variant not provided [RCV003055633] Chr14:99175357 [GRCh38]
Chr14:99641694 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1943G>A (p.Gly648Asp) single nucleotide variant not provided [RCV003020629] Chr14:99174893 [GRCh38]
Chr14:99641230 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1603GAG[12] (p.Glu543_Leu544insGluGluGlu) microsatellite not provided [RCV002639189] Chr14:99175206..99175207 [GRCh38]
Chr14:99641543..99641544 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.2355G>A (p.Gly785=) single nucleotide variant not provided [RCV002740084] Chr14:99174481 [GRCh38]
Chr14:99640818 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1603GAG[13] (p.Glu543_Leu544insGluGluGluGlu) microsatellite not provided [RCV002591190] Chr14:99175206..99175207 [GRCh38]
Chr14:99641543..99641544 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.298C>G (p.Pro100Ala) single nucleotide variant Inborn genetic diseases [RCV002924265] Chr14:99257600 [GRCh38]
Chr14:99723937 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.546C>G (p.Pro182=) single nucleotide variant not provided [RCV002621857] Chr14:99231439 [GRCh38]
Chr14:99697776 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.305C>T (p.Ser102Leu) single nucleotide variant not provided [RCV002637626] Chr14:99257593 [GRCh38]
Chr14:99723930 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.525C>T (p.Gly175=) single nucleotide variant BCL11B-related disorder [RCV004545392]|not provided [RCV002781003] Chr14:99231460 [GRCh38]
Chr14:99697797 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1210C>T (p.Leu404=) single nucleotide variant not provided [RCV002885599] Chr14:99175626 [GRCh38]
Chr14:99641963 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1074G>C (p.Ser358=) single nucleotide variant not provided [RCV002705238] Chr14:99175762 [GRCh38]
Chr14:99642099 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1869C>T (p.Phe623=) single nucleotide variant not provided [RCV002909610] Chr14:99174967 [GRCh38]
Chr14:99641304 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.957C>G (p.Pro319=) single nucleotide variant not provided [RCV002592378] Chr14:99175879 [GRCh38]
Chr14:99642216 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.2338G>A (p.Gly780Ser) single nucleotide variant not provided [RCV002622719]|not specified [RCV004700798] Chr14:99174498 [GRCh38]
Chr14:99640835 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1786G>A (p.Gly596Ser) single nucleotide variant not provided [RCV002706464] Chr14:99175050 [GRCh38]
Chr14:99641387 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.640+10G>T single nucleotide variant not provided [RCV003038743] Chr14:99231335 [GRCh38]
Chr14:99697672 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1768G>A (p.Glu590Lys) single nucleotide variant not provided [RCV002735861] Chr14:99175068 [GRCh38]
Chr14:99641405 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.2005T>C (p.Phe669Leu) single nucleotide variant not provided [RCV002658719] Chr14:99174831 [GRCh38]
Chr14:99641168 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1800G>T (p.Glu600Asp) single nucleotide variant not provided [RCV002735598] Chr14:99175036 [GRCh38]
Chr14:99641373 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1575G>T (p.Ser525=) single nucleotide variant not provided [RCV002622605] Chr14:99175261 [GRCh38]
Chr14:99641598 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1922_1939del (p.Gly641_Gly646del) deletion not provided [RCV002976142] Chr14:99174897..99174914 [GRCh38]
Chr14:99641234..99641251 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.2460C>G (p.Gly820=) single nucleotide variant not provided [RCV003054774] Chr14:99174376 [GRCh38]
Chr14:99640713 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1445G>C (p.Gly482Ala) single nucleotide variant Inborn genetic diseases [RCV002910822] Chr14:99175391 [GRCh38]
Chr14:99641728 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1035C>T (p.Phe345=) single nucleotide variant not provided [RCV002695256] Chr14:99175801 [GRCh38]
Chr14:99642138 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.640+13G>A single nucleotide variant not provided [RCV002871081] Chr14:99231332 [GRCh38]
Chr14:99697669 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1432A>G (p.Met478Val) single nucleotide variant not provided [RCV003054759] Chr14:99175404 [GRCh38]
Chr14:99641741 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1192A>G (p.Ser398Gly) single nucleotide variant not provided [RCV002781543] Chr14:99175644 [GRCh38]
Chr14:99641981 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1794C>G (p.Val598=) single nucleotide variant not provided [RCV002875540] Chr14:99175042 [GRCh38]
Chr14:99641379 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.515G>A (p.Arg172His) single nucleotide variant not provided [RCV003043578] Chr14:99231470 [GRCh38]
Chr14:99697807 [GRCh37]
Chr14:14q32.2		 likely benign|uncertain significance
NM_138576.4(BCL11B):c.824C>T (p.Ala275Val) single nucleotide variant not provided [RCV003059884] Chr14:99176012 [GRCh38]
Chr14:99642349 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.460G>A (p.Ala154Thr) single nucleotide variant Inborn genetic diseases [RCV002803659] Chr14:99231525 [GRCh38]
Chr14:99697862 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.2095G>A (p.Ala699Thr) single nucleotide variant not provided [RCV002625466] Chr14:99174741 [GRCh38]
Chr14:99641078 [GRCh37]
Chr14:14q32.2		 benign|uncertain significance
NM_138576.4(BCL11B):c.1557C>A (p.His519Gln) single nucleotide variant not provided [RCV002663825] Chr14:99175279 [GRCh38]
Chr14:99641616 [GRCh37]
Chr14:14q32.2		 benign|uncertain significance
NM_138576.4(BCL11B):c.807C>T (p.Leu269=) single nucleotide variant not provided [RCV002711170] Chr14:99176029 [GRCh38]
Chr14:99642366 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1929_1943dup (p.Gly648_Gly649insAspAlaGlyAlaGly) duplication not provided [RCV002642776] Chr14:99174892..99174893 [GRCh38]
Chr14:99641229..99641230 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1869C>G (p.Phe623Leu) single nucleotide variant not provided [RCV002828523] Chr14:99174967 [GRCh38]
Chr14:99641304 [GRCh37]
Chr14:14q32.2		 benign
NM_138576.4(BCL11B):c.741C>T (p.Arg247=) single nucleotide variant not provided [RCV002851123] Chr14:99176095 [GRCh38]
Chr14:99642432 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1721C>T (p.Pro574Leu) single nucleotide variant not provided [RCV003041723] Chr14:99175115 [GRCh38]
Chr14:99641452 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1824G>A (p.Pro608=) single nucleotide variant not provided [RCV002786161] Chr14:99175012 [GRCh38]
Chr14:99641349 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.58+10T>G single nucleotide variant not provided [RCV002594755] Chr14:99271151 [GRCh38]
Chr14:99737488 [GRCh37]
Chr14:14q32.2		 benign
NM_138576.4(BCL11B):c.488A>G (p.His163Arg) single nucleotide variant Inborn genetic diseases [RCV002697432] Chr14:99231497 [GRCh38]
Chr14:99697834 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.343A>G (p.Ile115Val) single nucleotide variant not provided [RCV002667604] Chr14:99257555 [GRCh38]
Chr14:99723892 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.2293T>C (p.Ser765Pro) single nucleotide variant Inborn genetic diseases [RCV002929923] Chr14:99174543 [GRCh38]
Chr14:99640880 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1112C>T (p.Ala371Val) single nucleotide variant not provided [RCV002712029] Chr14:99175724 [GRCh38]
Chr14:99642061 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1727T>G (p.Val576Gly) single nucleotide variant Inborn genetic diseases [RCV002712426] Chr14:99175109 [GRCh38]
Chr14:99641446 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.981G>A (p.Pro327=) single nucleotide variant not provided [RCV002596081] Chr14:99175855 [GRCh38]
Chr14:99642192 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.171C>T (p.Thr57=) single nucleotide variant not provided [RCV003057571] Chr14:99257727 [GRCh38]
Chr14:99724064 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.177C>A (p.Gly59=) single nucleotide variant not provided [RCV003024587] Chr14:99257721 [GRCh38]
Chr14:99724058 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.2145C>T (p.Tyr715=) single nucleotide variant BCL11B-related disorder [RCV004536454]|not provided [RCV002932503] Chr14:99174691 [GRCh38]
Chr14:99641028 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1602C>G (p.Asp534Glu) single nucleotide variant not provided [RCV002643335] Chr14:99175234 [GRCh38]
Chr14:99641571 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.510T>C (p.Pro170=) single nucleotide variant not provided [RCV002958674] Chr14:99231475 [GRCh38]
Chr14:99697812 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1246G>A (p.Gly416Ser) single nucleotide variant Inborn genetic diseases [RCV002585332]|not provided [RCV002595098] Chr14:99175590 [GRCh38]
Chr14:99641927 [GRCh37]
Chr14:14q32.2		 likely benign|uncertain significance
NM_138576.4(BCL11B):c.1237_1243del (p.Pro413fs) deletion not provided [RCV003042629] Chr14:99175593..99175599 [GRCh38]
Chr14:99641930..99641936 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.247G>T (p.Gly83Cys) single nucleotide variant not provided [RCV003057623] Chr14:99257651 [GRCh38]
Chr14:99723988 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.48G>T (p.Glu16Asp) single nucleotide variant BCL11B-related disorder [RCV004536399]|not provided [RCV002766779] Chr14:99271171 [GRCh38]
Chr14:99737508 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.2119G>T (p.Val707Leu) single nucleotide variant not provided [RCV003059299] Chr14:99174717 [GRCh38]
Chr14:99641054 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.813G>A (p.Pro271=) single nucleotide variant not provided [RCV002890491] Chr14:99176023 [GRCh38]
Chr14:99642360 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.570G>A (p.Pro190=) single nucleotide variant not provided [RCV002623347] Chr14:99231415 [GRCh38]
Chr14:99697752 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1950G>A (p.Ala650=) single nucleotide variant not provided [RCV002581399] Chr14:99174886 [GRCh38]
Chr14:99641223 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1831G>A (p.Gly611Ser) single nucleotide variant not provided [RCV002967242] Chr14:99175005 [GRCh38]
Chr14:99641342 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.2136G>A (p.Leu712=) single nucleotide variant not provided [RCV002597605] Chr14:99174700 [GRCh38]
Chr14:99641037 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.563C>T (p.Ala188Val) single nucleotide variant not provided [RCV003088775] Chr14:99231422 [GRCh38]
Chr14:99697759 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.64G>A (p.Ala22Thr) single nucleotide variant not provided [RCV003031946] Chr14:99257834 [GRCh38]
Chr14:99724171 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.2024C>A (p.Pro675Gln) single nucleotide variant not provided [RCV003091740] Chr14:99174812 [GRCh38]
Chr14:99641149 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1558C>G (p.His520Asp) single nucleotide variant not provided [RCV002812025] Chr14:99175278 [GRCh38]
Chr14:99641615 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.64G>T (p.Ala22Ser) single nucleotide variant not provided [RCV002676659] Chr14:99257834 [GRCh38]
Chr14:99724171 [GRCh37]
Chr14:14q32.2		 benign
NM_138576.4(BCL11B):c.1741G>A (p.Gly581Ser) single nucleotide variant not provided [RCV003031162] Chr14:99175095 [GRCh38]
Chr14:99641432 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.2118C>T (p.Asn706=) single nucleotide variant not provided [RCV002922944] Chr14:99174718 [GRCh38]
Chr14:99641055 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1918G>A (p.Gly640Ser) single nucleotide variant not provided [RCV003065972] Chr14:99174918 [GRCh38]
Chr14:99641255 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.706C>T (p.Leu236=) single nucleotide variant not provided [RCV002856917] Chr14:99176130 [GRCh38]
Chr14:99642467 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.641-6C>A single nucleotide variant not provided [RCV002632601] Chr14:99176201 [GRCh38]
Chr14:99642538 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1931_1958del (p.Asp644fs) deletion not provided [RCV003029777] Chr14:99174878..99174905 [GRCh38]
Chr14:99641215..99641242 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1931A>T (p.Asp644Val) single nucleotide variant not provided [RCV002922046] Chr14:99174905 [GRCh38]
Chr14:99641242 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.428-13G>A single nucleotide variant not provided [RCV002856846] Chr14:99231570 [GRCh38]
Chr14:99697907 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.282C>A (p.Asp94Glu) single nucleotide variant not provided [RCV002579348] Chr14:99257616 [GRCh38]
Chr14:99723953 [GRCh37]
Chr14:14q32.2		 benign
NM_138576.4(BCL11B):c.1337G>A (p.Arg446Gln) single nucleotide variant not provided [RCV003027237] Chr14:99175499 [GRCh38]
Chr14:99641836 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1428G>A (p.Thr476=) single nucleotide variant not provided [RCV002597698] Chr14:99175408 [GRCh38]
Chr14:99641745 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1191C>T (p.Pro397=) single nucleotide variant not provided [RCV003026814] Chr14:99175645 [GRCh38]
Chr14:99641982 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.2457C>G (p.Thr819=) single nucleotide variant not provided [RCV002631708] Chr14:99174379 [GRCh38]
Chr14:99640716 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.2019_2020delinsTA (p.Ala674Thr) indel not provided [RCV002857684] Chr14:99174816..99174817 [GRCh38]
Chr14:99641153..99641154 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1904A>G (p.Asp635Gly) single nucleotide variant Inborn genetic diseases [RCV003250768]|not provided [RCV003088485] Chr14:99174932 [GRCh38]
Chr14:99641269 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.2265G>C (p.Pro755=) single nucleotide variant not provided [RCV002806804] Chr14:99174571 [GRCh38]
Chr14:99640908 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1943_1951dup (p.Ala650_Val651insGlyGlyAla) duplication not provided [RCV003044167] Chr14:99174884..99174885 [GRCh38]
Chr14:99641221..99641222 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.534G>A (p.Pro178=) single nucleotide variant not provided [RCV002598055] Chr14:99231451 [GRCh38]
Chr14:99697788 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1749G>A (p.Ala583=) single nucleotide variant not provided [RCV002631116] Chr14:99175087 [GRCh38]
Chr14:99641424 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.199T>C (p.Leu67=) single nucleotide variant not provided [RCV003030500] Chr14:99257699 [GRCh38]
Chr14:99724036 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.564G>A (p.Ala188=) single nucleotide variant not provided [RCV002900396] Chr14:99231421 [GRCh38]
Chr14:99697758 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.219dup (p.Ile74fs) duplication not provided [RCV003028138] Chr14:99257678..99257679 [GRCh38]
Chr14:99724015..99724016 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.2352C>T (p.Pro784=) single nucleotide variant not provided [RCV002962188] Chr14:99174484 [GRCh38]
Chr14:99640821 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1904_1945dup (p.Gly648_Gly649insAspAspAspAspAlaGlyGlyCysGlyAspAlaGlyAlaGly) duplication not provided [RCV002676331] Chr14:99174890..99174891 [GRCh38]
Chr14:99641227..99641228 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.2110T>C (p.Ser704Pro) single nucleotide variant not provided [RCV003028335] Chr14:99174726 [GRCh38]
Chr14:99641063 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.2385C>T (p.Ser795=) single nucleotide variant not provided [RCV002581781] Chr14:99174451 [GRCh38]
Chr14:99640788 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1180C>T (p.Pro394Ser) single nucleotide variant not provided [RCV003059940] Chr14:99175656 [GRCh38]
Chr14:99641993 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1104C>T (p.Arg368=) single nucleotide variant not provided [RCV002770276] Chr14:99175732 [GRCh38]
Chr14:99642069 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1143C>T (p.Ser381=) single nucleotide variant BCL11B-related disorder [RCV004545457]|not provided [RCV002966479] Chr14:99175693 [GRCh38]
Chr14:99642030 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1074G>A (p.Ser358=) single nucleotide variant not provided [RCV002602068] Chr14:99175762 [GRCh38]
Chr14:99642099 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1590G>A (p.Pro530=) single nucleotide variant not provided [RCV002578269] Chr14:99175246 [GRCh38]
Chr14:99641583 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.381G>A (p.Leu127=) single nucleotide variant not provided [RCV003092986] Chr14:99257517 [GRCh38]
Chr14:99723854 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.330C>T (p.Ser110=) single nucleotide variant not provided [RCV002680932] Chr14:99257568 [GRCh38]
Chr14:99723905 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.2274C>A (p.Asp758Glu) single nucleotide variant Inborn genetic diseases [RCV004965227] Chr14:99174562 [GRCh38]
Chr14:99640899 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1138G>C (p.Val380Leu) single nucleotide variant Inborn genetic diseases [RCV004965230] Chr14:99175698 [GRCh38]
Chr14:99642035 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.2457C>T (p.Thr819=) single nucleotide variant not provided [RCV002635652] Chr14:99174379 [GRCh38]
Chr14:99640716 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1096C>A (p.Arg366=) single nucleotide variant not provided [RCV002676782] Chr14:99175740 [GRCh38]
Chr14:99642077 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1151G>A (p.Arg384His) single nucleotide variant Inborn genetic diseases [RCV004965229] Chr14:99175685 [GRCh38]
Chr14:99642022 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.2640C>G (p.His880Gln) single nucleotide variant not provided [RCV003092641] Chr14:99174196 [GRCh38]
Chr14:99640533 [GRCh37]
Chr14:14q32.2		 benign|uncertain significance
NM_138576.4(BCL11B):c.629G>A (p.Cys210Tyr) single nucleotide variant not provided [RCV002606159] Chr14:99231356 [GRCh38]
Chr14:99697693 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1137C>G (p.Pro379=) single nucleotide variant not provided [RCV003067711] Chr14:99175699 [GRCh38]
Chr14:99642036 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.714G>C (p.Gln238His) single nucleotide variant not provided [RCV003049993] Chr14:99176122 [GRCh38]
Chr14:99642459 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.2632G>A (p.Gly878Ser) single nucleotide variant Inborn genetic diseases [RCV003358031]|not provided [RCV002943230] Chr14:99174204 [GRCh38]
Chr14:99640541 [GRCh37]
Chr14:14q32.2		 likely benign|uncertain significance
NM_138576.4(BCL11B):c.428-7del deletion not provided [RCV003049498] Chr14:99231564 [GRCh38]
Chr14:99697901 [GRCh37]
Chr14:14q32.2		 benign
NM_138576.4(BCL11B):c.1956C>T (p.Asn652=) single nucleotide variant not provided [RCV002721354] Chr14:99174880 [GRCh38]
Chr14:99641217 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1516G>A (p.Ala506Thr) single nucleotide variant Inborn genetic diseases [RCV002677775] Chr14:99175320 [GRCh38]
Chr14:99641657 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1650C>G (p.Ser550Arg) single nucleotide variant not provided [RCV003049666] Chr14:99175186 [GRCh38]
Chr14:99641523 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1216_1219dup (p.Pro407fs) duplication Intellectual developmental disorder with speech delay, dysmorphic facies, and t-cell abnormalities [RCV003149139] Chr14:99175616..99175617 [GRCh38]
Chr14:99641953..99641954 [GRCh37]
Chr14:14q32.2		 pathogenic
NM_138576.4(BCL11B):c.58+14G>C single nucleotide variant not provided [RCV002609694] Chr14:99271147 [GRCh38]
Chr14:99737484 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1708G>A (p.Gly570Ser) single nucleotide variant not provided [RCV002589817] Chr14:99175128 [GRCh38]
Chr14:99641465 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1970G>T (p.Gly657Val) single nucleotide variant not provided [RCV002606013] Chr14:99174866 [GRCh38]
Chr14:99641203 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.380T>C (p.Leu127Pro) single nucleotide variant Inborn genetic diseases [RCV002722947]|not provided [RCV005099581] Chr14:99257518 [GRCh38]
Chr14:99723855 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.428-7dup duplication not provided [RCV002606054] Chr14:99231563..99231564 [GRCh38]
Chr14:99697900..99697901 [GRCh37]
Chr14:14q32.2		 benign
NM_138576.4(BCL11B):c.640+13G>T single nucleotide variant not provided [RCV002608849] Chr14:99231332 [GRCh38]
Chr14:99697669 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.640+15C>T single nucleotide variant not provided [RCV002604726] Chr14:99231330 [GRCh38]
Chr14:99697667 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1266G>A (p.Pro422=) single nucleotide variant not provided [RCV002585504] Chr14:99175570 [GRCh38]
Chr14:99641907 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1980A>G (p.Pro660=) single nucleotide variant not provided [RCV002607204] Chr14:99174856 [GRCh38]
Chr14:99641193 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.248G>C (p.Gly83Ala) single nucleotide variant not provided [RCV002608937] Chr14:99257650 [GRCh38]
Chr14:99723987 [GRCh37]
Chr14:14q32.2		 benign|uncertain significance
NM_138576.4(BCL11B):c.2112C>G (p.Ser704=) single nucleotide variant not provided [RCV002658157] Chr14:99174724 [GRCh38]
Chr14:99641061 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1048C>T (p.Arg350Cys) single nucleotide variant Inborn genetic diseases [RCV002678834]|not provided [RCV003395635] Chr14:99175788 [GRCh38]
Chr14:99642125 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1860C>T (p.Arg620=) single nucleotide variant not provided [RCV002610085] Chr14:99174976 [GRCh38]
Chr14:99641313 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.2232G>T (p.Ser744=) single nucleotide variant not provided [RCV002610318] Chr14:99174604 [GRCh38]
Chr14:99640941 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1482C>T (p.Ala494=) single nucleotide variant not provided [RCV002582408] Chr14:99175354 [GRCh38]
Chr14:99641691 [GRCh37]
Chr14:14q32.2		 likely benign|conflicting interpretations of pathogenicity
NM_138576.4(BCL11B):c.1883C>T (p.Ala628Val) single nucleotide variant Inborn genetic diseases [RCV003175496] Chr14:99174953 [GRCh38]
Chr14:99641290 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.2108C>A (p.Pro703Gln) single nucleotide variant Immunodeficiency 49 [RCV004725686]|not provided [RCV003218868] Chr14:99174728 [GRCh38]
Chr14:99641065 [GRCh37]
Chr14:14q32.2		 likely benign|uncertain significance
NM_138576.4(BCL11B):c.992G>T (p.Ser331Ile) single nucleotide variant Immunodeficiency 49 [RCV003224727] Chr14:99175844 [GRCh38]
Chr14:99642181 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.93AGA[1] (p.Glu32del) microsatellite not provided [RCV003143761] Chr14:99257800..99257802 [GRCh38]
Chr14:99724137..99724139 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1165C>T (p.His389Tyr) single nucleotide variant Inborn genetic diseases [RCV003204124] Chr14:99175671 [GRCh38]
Chr14:99642008 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.2555A>T (p.Glu852Val) single nucleotide variant not provided [RCV003228543] Chr14:99174281 [GRCh38]
Chr14:99640618 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.346G>A (p.Gly116Arg) single nucleotide variant not provided [RCV003227448] Chr14:99257552 [GRCh38]
Chr14:99723889 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1370G>T (p.Cys457Phe) single nucleotide variant not provided [RCV003318907] Chr14:99175466 [GRCh38]
Chr14:99641803 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.566G>T (p.Arg189Leu) single nucleotide variant Inborn genetic diseases [RCV003309602] Chr14:99231419 [GRCh38]
Chr14:99697756 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1234A>G (p.Met412Val) single nucleotide variant not provided [RCV003329626] Chr14:99175602 [GRCh38]
Chr14:99641939 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.2275C>G (p.Leu759Val) single nucleotide variant Inborn genetic diseases [RCV003346075] Chr14:99174561 [GRCh38]
Chr14:99640898 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1217C>T (p.Thr406Met) single nucleotide variant not provided [RCV003332685] Chr14:99175619 [GRCh38]
Chr14:99641956 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1259C>G (p.Pro420Arg) single nucleotide variant Inborn genetic diseases [RCV003376533]|not provided [RCV003661050] Chr14:99175577 [GRCh38]
Chr14:99641914 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.2662A>G (p.Ile888Val) single nucleotide variant not provided [RCV003393596] Chr14:99174174 [GRCh38]
Chr14:99640511 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.2433G>C (p.Leu811Phe) single nucleotide variant BCL11B-related disorder [RCV004536639] Chr14:99174403 [GRCh38]
Chr14:99640740 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.2090C>T (p.Pro697Leu) single nucleotide variant not provided [RCV003873619] Chr14:99174746 [GRCh38]
Chr14:99641083 [GRCh37]
Chr14:14q32.2		 benign
NM_138576.4(BCL11B):c.539G>C (p.Cys180Ser) single nucleotide variant not provided [RCV003569979] Chr14:99231446 [GRCh38]
Chr14:99697783 [GRCh37]
Chr14:14q32.2		 likely benign|uncertain significance
NM_138576.4(BCL11B):c.2400C>T (p.Tyr800=) single nucleotide variant not provided [RCV003686279] Chr14:99174436 [GRCh38]
Chr14:99640773 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1602_1628del (p.Asp534_Glu542del) deletion not specified [RCV003388483] Chr14:99175208..99175234 [GRCh38]
Chr14:99641545..99641571 [GRCh37]
Chr14:14q32.2		 uncertain significance
GRCh37/hg19 14q23.1-32.33(chr14:58894502-107227240)x3 copy number gain not provided [RCV003485036] Chr14:58894502..107227240 [GRCh37]
Chr14:14q23.1-32.33		 pathogenic
GRCh37/hg19 14q31.3-32.33(chr14:88580184-107285437)x3 copy number gain not provided [RCV003485051] Chr14:88580184..107285437 [GRCh37]
Chr14:14q31.3-32.33		 pathogenic
NM_138576.4(BCL11B):c.537C>T (p.Pro179=) single nucleotide variant not provided [RCV003393598] Chr14:99231448 [GRCh38]
Chr14:99697785 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.2595del (p.Tyr866fs) deletion BCL11B-related disorder [RCV004528768] Chr14:99174241 [GRCh38]
Chr14:99640578 [GRCh37]
Chr14:14q32.2		 likely pathogenic
NM_138576.4(BCL11B):c.1465G>A (p.Asp489Asn) single nucleotide variant BCL11B-related disorder [RCV004529645] Chr14:99175371 [GRCh38]
Chr14:99641708 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1988_1999dup (p.Pro666_Gly667insGluProPhePro) duplication BCL11B-related disorder [RCV004531546] Chr14:99174836..99174837 [GRCh38]
Chr14:99641173..99641174 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.2458G>A (p.Gly820Ser) single nucleotide variant BCL11B-related disorder [RCV004528627] Chr14:99174378 [GRCh38]
Chr14:99640715 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1711G>A (p.Gly571Ser) single nucleotide variant Inborn genetic diseases [RCV004963650]|not provided [RCV003393597] Chr14:99175125 [GRCh38]
Chr14:99641462 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1852C>T (p.Gln618Ter) single nucleotide variant Intellectual developmental disorder with speech delay, dysmorphic facies, and t-cell abnormalities [RCV003444029] Chr14:99174984 [GRCh38]
Chr14:99641321 [GRCh37]
Chr14:14q32.2		 pathogenic
NM_138576.4(BCL11B):c.1158C>A (p.Asn386Lys) single nucleotide variant BCL11B-related disorder [RCV004527881] Chr14:99175678 [GRCh38]
Chr14:99642015 [GRCh37]
Chr14:14q32.2		 likely pathogenic
NM_138576.4(BCL11B):c.2499C>T (p.Cys833=) single nucleotide variant not provided [RCV003390442] Chr14:99174337 [GRCh38]
Chr14:99640674 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1201T>G (p.Ser401Ala) single nucleotide variant not provided [RCV003390443] Chr14:99175635 [GRCh38]
Chr14:99641972 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.2239A>C (p.Asn747His) single nucleotide variant not provided [RCV003578383] Chr14:99174597 [GRCh38]
Chr14:99640934 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.2264C>T (p.Pro755Leu) single nucleotide variant not provided [RCV003576954] Chr14:99174572 [GRCh38]
Chr14:99640909 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1320C>T (p.Ser440=) single nucleotide variant not provided [RCV003663596] Chr14:99175516 [GRCh38]
Chr14:99641853 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.690C>T (p.Phe230=) single nucleotide variant not provided [RCV003828722] Chr14:99176146 [GRCh38]
Chr14:99642483 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1086C>T (p.Asp362=) single nucleotide variant not provided [RCV003693834] Chr14:99175750 [GRCh38]
Chr14:99642087 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1053G>C (p.Leu351=) single nucleotide variant not provided [RCV003687631] Chr14:99175783 [GRCh38]
Chr14:99642120 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.897G>A (p.Leu299=) single nucleotide variant not provided [RCV003691343] Chr14:99175939 [GRCh38]
Chr14:99642276 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.640+14C>T single nucleotide variant not provided [RCV003693955] Chr14:99231331 [GRCh38]
Chr14:99697668 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1228C>G (p.Pro410Ala) single nucleotide variant not provided [RCV003715403] Chr14:99175608 [GRCh38]
Chr14:99641945 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1113G>A (p.Ala371=) single nucleotide variant not provided [RCV003695303] Chr14:99175723 [GRCh38]
Chr14:99642060 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.2376C>T (p.Gly792=) single nucleotide variant not provided [RCV003578448] Chr14:99174460 [GRCh38]
Chr14:99640797 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1152C>G (p.Arg384=) single nucleotide variant not provided [RCV003687148] Chr14:99175684 [GRCh38]
Chr14:99642021 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.2680A>C (p.Ser894Arg) single nucleotide variant not provided [RCV003689359] Chr14:99174156 [GRCh38]
Chr14:99640493 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.779C>T (p.Thr260Met) single nucleotide variant not provided [RCV003573460] Chr14:99176057 [GRCh38]
Chr14:99642394 [GRCh37]
Chr14:14q32.2		 benign
NM_138576.4(BCL11B):c.102G>A (p.Glu34=) single nucleotide variant not provided [RCV003661129] Chr14:99257796 [GRCh38]
Chr14:99724133 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.2235C>A (p.Ser745=) single nucleotide variant not provided [RCV003575604] Chr14:99174601 [GRCh38]
Chr14:99640938 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1974C>T (p.Phe658=) single nucleotide variant not provided [RCV003881609] Chr14:99174862 [GRCh38]
Chr14:99641199 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.2316C>T (p.Ser772=) single nucleotide variant not provided [RCV003829795] Chr14:99174520 [GRCh38]
Chr14:99640857 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1852C>G (p.Gln618Glu) single nucleotide variant not provided [RCV003577131] Chr14:99174984 [GRCh38]
Chr14:99641321 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1566C>A (p.Ser522Arg) single nucleotide variant not provided [RCV003687870] Chr14:99175270 [GRCh38]
Chr14:99641607 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1617G>C (p.Glu539Asp) single nucleotide variant not provided [RCV003713063] Chr14:99175219 [GRCh38]
Chr14:99641556 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1902_1929dup (p.Asp644fs) duplication not provided [RCV003547571] Chr14:99174906..99174907 [GRCh38]
Chr14:99641243..99641244 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.2032A>G (p.Ser678Gly) single nucleotide variant not provided [RCV003687330] Chr14:99174804 [GRCh38]
Chr14:99641141 [GRCh37]
Chr14:14q32.2		 benign|uncertain significance
NM_138576.4(BCL11B):c.1857G>T (p.Lys619Asn) single nucleotide variant not provided [RCV003694115] Chr14:99174979 [GRCh38]
Chr14:99641316 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.162C>T (p.Asp54=) single nucleotide variant not provided [RCV003876894] Chr14:99257736 [GRCh38]
Chr14:99724073 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.2635G>A (p.Glu879Lys) single nucleotide variant not provided [RCV003662096] Chr14:99174201 [GRCh38]
Chr14:99640538 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.428-12T>C single nucleotide variant not provided [RCV003828307] Chr14:99231569 [GRCh38]
Chr14:99697906 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1776G>A (p.Ala592=) single nucleotide variant not provided [RCV003878144] Chr14:99175060 [GRCh38]
Chr14:99641397 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1938C>G (p.Gly646=) single nucleotide variant not provided [RCV003714997] Chr14:99174898 [GRCh38]
Chr14:99641235 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.680del (p.Lys227fs) deletion not provided [RCV003691954] Chr14:99176156 [GRCh38]
Chr14:99642493 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.2664C>G (p.Ile888Met) single nucleotide variant not provided [RCV003663121] Chr14:99174172 [GRCh38]
Chr14:99640509 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.666T>C (p.Ile222=) single nucleotide variant not provided [RCV003663199] Chr14:99176170 [GRCh38]
Chr14:99642507 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1003A>T (p.Met335Leu) single nucleotide variant not provided [RCV003689563] Chr14:99175833 [GRCh38]
Chr14:99642170 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.641-115A>T single nucleotide variant not specified [RCV003489214] Chr14:99176310 [GRCh38]
Chr14:99642647 [GRCh37]
Chr14:14q32.2		 benign
NM_138576.4(BCL11B):c.1602_1610dup (p.Glu536_Glu537insAspGluGlu) duplication not provided [RCV003659717] Chr14:99175225..99175226 [GRCh38]
Chr14:99641562..99641563 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.138G>T (p.Leu46=) single nucleotide variant not provided [RCV003716771] Chr14:99257760 [GRCh38]
Chr14:99724097 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1205C>T (p.Pro402Leu) single nucleotide variant not provided [RCV003698676] Chr14:99175631 [GRCh38]
Chr14:99641968 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1064C>T (p.Ala355Val) single nucleotide variant not provided [RCV003852373] Chr14:99175772 [GRCh38]
Chr14:99642109 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.2245A>G (p.Ser749Gly) single nucleotide variant not provided [RCV003697006] Chr14:99174591 [GRCh38]
Chr14:99640928 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.908del (p.Pro303fs) deletion Intellectual developmental disorder with speech delay, dysmorphic facies, and t-cell abnormalities [RCV005087551] Chr14:99175928 [GRCh38]
Chr14:99642265 [GRCh37]
Chr14:14q32.2		 likely pathogenic
NM_138576.4(BCL11B):c.2625G>A (p.Lys875=) single nucleotide variant not provided [RCV003664693] Chr14:99174211 [GRCh38]
Chr14:99640548 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.529C>T (p.Leu177Phe) single nucleotide variant not provided [RCV003851978] Chr14:99231456 [GRCh38]
Chr14:99697793 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1313T>A (p.Phe438Tyr) single nucleotide variant not provided [RCV003549512] Chr14:99175523 [GRCh38]
Chr14:99641860 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.955C>G (p.Pro319Ala) single nucleotide variant not provided [RCV003700257] Chr14:99175881 [GRCh38]
Chr14:99642218 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.384C>G (p.Leu128=) single nucleotide variant not provided [RCV003718065] Chr14:99257514 [GRCh38]
Chr14:99723851 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.2431T>C (p.Leu811=) single nucleotide variant not provided [RCV003717584] Chr14:99174405 [GRCh38]
Chr14:99640742 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1260G>C (p.Pro420=) single nucleotide variant not provided [RCV003663694] Chr14:99175576 [GRCh38]
Chr14:99641913 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.2004C>G (p.Leu668=) single nucleotide variant not provided [RCV003580871] Chr14:99174832 [GRCh38]
Chr14:99641169 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.427+9T>G single nucleotide variant not provided [RCV003663862] Chr14:99257462 [GRCh38]
Chr14:99723799 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1218G>A (p.Thr406=) single nucleotide variant not provided [RCV003852178] Chr14:99175618 [GRCh38]
Chr14:99641955 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1125C>T (p.Ser375=) single nucleotide variant not provided [RCV003834691] Chr14:99175711 [GRCh38]
Chr14:99642048 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1572G>A (p.Pro524=) single nucleotide variant not provided [RCV003726636] Chr14:99175264 [GRCh38]
Chr14:99641601 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.487C>T (p.His163Tyr) single nucleotide variant not provided [RCV003666694] Chr14:99231498 [GRCh38]
Chr14:99697835 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.900G>C (p.Arg300=) single nucleotide variant not provided [RCV003840243] Chr14:99175936 [GRCh38]
Chr14:99642273 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.850G>T (p.Gly284Cys) single nucleotide variant Inborn genetic diseases [RCV004605054]|not provided [RCV003814949] Chr14:99175986 [GRCh38]
Chr14:99642323 [GRCh37]
Chr14:14q32.2		 benign|uncertain significance
NM_138576.4(BCL11B):c.1844C>T (p.Ala615Val) single nucleotide variant not provided [RCV003669066] Chr14:99174992 [GRCh38]
Chr14:99641329 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.2031C>G (p.Pro677=) single nucleotide variant not provided [RCV003836474] Chr14:99174805 [GRCh38]
Chr14:99641142 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1714G>A (p.Gly572Arg) single nucleotide variant not provided [RCV003703202] Chr14:99175122 [GRCh38]
Chr14:99641459 [GRCh37]
Chr14:14q32.2		 benign
NM_138576.4(BCL11B):c.1206G>A (p.Pro402=) single nucleotide variant BCL11B-related disorder [RCV004758949]|not provided [RCV003835712] Chr14:99175630 [GRCh38]
Chr14:99641967 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.890C>T (p.Pro297Leu) single nucleotide variant not provided [RCV003702979] Chr14:99175946 [GRCh38]
Chr14:99642283 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1703A>G (p.Asn568Ser) single nucleotide variant not provided [RCV003696841] Chr14:99175133 [GRCh38]
Chr14:99641470 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1217CGC[4] (p.Pro408_Leu409insPro) microsatellite not provided [RCV003668748] Chr14:99175610..99175611 [GRCh38]
Chr14:99641947..99641948 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.58+13G>T single nucleotide variant not provided [RCV003838775] Chr14:99271148 [GRCh38]
Chr14:99737485 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1236G>A (p.Met412Ile) single nucleotide variant not provided [RCV003724949] Chr14:99175600 [GRCh38]
Chr14:99641937 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1950G>T (p.Ala650=) single nucleotide variant not provided [RCV003837721] Chr14:99174886 [GRCh38]
Chr14:99641223 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.2649_2652del (p.Asn884fs) deletion not provided [RCV003699807] Chr14:99174184..99174187 [GRCh38]
Chr14:99640521..99640524 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1826A>G (p.Gln609Arg) single nucleotide variant not provided [RCV003834957] Chr14:99175010 [GRCh38]
Chr14:99641347 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.198C>T (p.Pro66=) single nucleotide variant not provided [RCV003723337] Chr14:99257700 [GRCh38]
Chr14:99724037 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1901G>A (p.Gly634Asp) single nucleotide variant not provided [RCV003580183] Chr14:99174935 [GRCh38]
Chr14:99641272 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.2226G>C (p.Glu742Asp) single nucleotide variant not provided [RCV003852054] Chr14:99174610 [GRCh38]
Chr14:99640947 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.2048G>A (p.Ser683Asn) single nucleotide variant not provided [RCV003701097] Chr14:99174788 [GRCh38]
Chr14:99641125 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1978C>G (p.Pro660Ala) single nucleotide variant not provided [RCV003855325] Chr14:99174858 [GRCh38]
Chr14:99641195 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.2008C>T (p.Pro670Ser) single nucleotide variant not provided [RCV003558063] Chr14:99174828 [GRCh38]
Chr14:99641165 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1140G>C (p.Val380=) single nucleotide variant not provided [RCV003716901] Chr14:99175696 [GRCh38]
Chr14:99642033 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.2026C>T (p.Leu676=) single nucleotide variant not provided [RCV003723826] Chr14:99174810 [GRCh38]
Chr14:99641147 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.2265G>T (p.Pro755=) single nucleotide variant not provided [RCV003707980] Chr14:99174571 [GRCh38]
Chr14:99640908 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.2542C>T (p.Gln848Ter) single nucleotide variant not provided [RCV003552011] Chr14:99174294 [GRCh38]
Chr14:99640631 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.818C>T (p.Ala273Val) single nucleotide variant not provided [RCV003567448] Chr14:99176018 [GRCh38]
Chr14:99642355 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1817C>T (p.Ala606Val) single nucleotide variant not provided [RCV003708454] Chr14:99175019 [GRCh38]
Chr14:99641356 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.2049C>T (p.Ser683=) single nucleotide variant not provided [RCV003845897] Chr14:99174787 [GRCh38]
Chr14:99641124 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.802C>A (p.Pro268Thr) single nucleotide variant not provided [RCV003708839] Chr14:99176034 [GRCh38]
Chr14:99642371 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.224A>C (p.Glu75Ala) single nucleotide variant not provided [RCV003706506] Chr14:99257674 [GRCh38]
Chr14:99724011 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.408C>T (p.Pro136=) single nucleotide variant not provided [RCV003863097] Chr14:99257490 [GRCh38]
Chr14:99723827 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.291C>G (p.Ser97Arg) single nucleotide variant not provided [RCV003565226] Chr14:99257607 [GRCh38]
Chr14:99723944 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.566G>A (p.Arg189His) single nucleotide variant not provided [RCV003858224] Chr14:99231419 [GRCh38]
Chr14:99697756 [GRCh37]
Chr14:14q32.2		 benign
NM_138576.4(BCL11B):c.2328C>G (p.Thr776=) single nucleotide variant not provided [RCV003732981] Chr14:99174508 [GRCh38]
Chr14:99640845 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.2319A>G (p.Gly773=) single nucleotide variant not provided [RCV003732982] Chr14:99174517 [GRCh38]
Chr14:99640854 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.2357G>A (p.Arg786Gln) single nucleotide variant not provided [RCV003552951] Chr14:99174479 [GRCh38]
Chr14:99640816 [GRCh37]
Chr14:14q32.2		 benign
NM_138576.4(BCL11B):c.558C>T (p.Cys186=) single nucleotide variant not provided [RCV003729179] Chr14:99231427 [GRCh38]
Chr14:99697764 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1284G>C (p.Ser428=) single nucleotide variant not provided [RCV003676151] Chr14:99175552 [GRCh38]
Chr14:99641889 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1916C>T (p.Ala639Val) single nucleotide variant not provided [RCV003848177] Chr14:99174920 [GRCh38]
Chr14:99641257 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.2565C>T (p.Arg855=) single nucleotide variant not provided [RCV003706043] Chr14:99174271 [GRCh38]
Chr14:99640608 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.979C>G (p.Pro327Ala) single nucleotide variant not provided [RCV003865657] Chr14:99175857 [GRCh38]
Chr14:99642194 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1599G>A (p.Glu533=) single nucleotide variant not provided [RCV003734281] Chr14:99175237 [GRCh38]
Chr14:99641574 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1795A>G (p.Met599Val) single nucleotide variant Inborn genetic diseases [RCV004374231]|not provided [RCV003734294]|not specified [RCV004701816] Chr14:99175041 [GRCh38]
Chr14:99641378 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.512T>C (p.Leu171Pro) single nucleotide variant not provided [RCV003680821] Chr14:99231473 [GRCh38]
Chr14:99697810 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.2460C>T (p.Gly820=) single nucleotide variant not provided [RCV003730924] Chr14:99174376 [GRCh38]
Chr14:99640713 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.2235C>T (p.Ser745=) single nucleotide variant not provided [RCV003824278] Chr14:99174601 [GRCh38]
Chr14:99640938 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.29A>G (p.Gln10Arg) single nucleotide variant not provided [RCV003719354] Chr14:99271190 [GRCh38]
Chr14:99737527 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.198C>G (p.Pro66=) single nucleotide variant not provided [RCV003869561] Chr14:99257700 [GRCh38]
Chr14:99724037 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1015G>A (p.Ala339Thr) single nucleotide variant not provided [RCV003866847] Chr14:99175821 [GRCh38]
Chr14:99642158 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1998C>T (p.Pro666=) single nucleotide variant not provided [RCV003871411] Chr14:99174838 [GRCh38]
Chr14:99641175 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.39C>T (p.Ser13=) single nucleotide variant not provided [RCV003845643] Chr14:99271180 [GRCh38]
Chr14:99737517 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.2379C>T (p.Arg793=) single nucleotide variant not provided [RCV003684326] Chr14:99174457 [GRCh38]
Chr14:99640794 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.641-14G>C single nucleotide variant not provided [RCV003846320] Chr14:99176209 [GRCh38]
Chr14:99642546 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1725G>T (p.Gly575=) single nucleotide variant not provided [RCV003685627] Chr14:99175111 [GRCh38]
Chr14:99641448 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.2096C>G (p.Ala699Gly) single nucleotide variant not provided [RCV003823795] Chr14:99174740 [GRCh38]
Chr14:99641077 [GRCh37]
Chr14:14q32.2		 benign
NM_138576.4(BCL11B):c.1697G>A (p.Arg566His) single nucleotide variant not provided [RCV003734465] Chr14:99175139 [GRCh38]
Chr14:99641476 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.2446C>T (p.Arg816Trp) single nucleotide variant not provided [RCV003718922] Chr14:99174390 [GRCh38]
Chr14:99640727 [GRCh37]
Chr14:14q32.2		 uncertain significance
GRCh37/hg19 14q32.2-32.32(chr14:97705251-103682578)x3 copy number gain not specified [RCV003987047] Chr14:97705251..103682578 [GRCh37]
Chr14:14q32.2-32.32		 uncertain significance
NM_138576.4(BCL11B):c.1944C>T (p.Gly648=) single nucleotide variant not provided [RCV003848740] Chr14:99174892 [GRCh38]
Chr14:99641229 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1467C>G (p.Asp489Glu) single nucleotide variant not provided [RCV003707692] Chr14:99175369 [GRCh38]
Chr14:99641706 [GRCh37]
Chr14:14q32.2		 benign
NM_138576.4(BCL11B):c.1861G>T (p.Gly621Cys) single nucleotide variant not provided [RCV003721346] Chr14:99174975 [GRCh38]
Chr14:99641312 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.2211C>T (p.Phe737=) single nucleotide variant not provided [RCV003728287] Chr14:99174625 [GRCh38]
Chr14:99640962 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.884C>T (p.Thr295Met) single nucleotide variant not provided [RCV003847092] Chr14:99175952 [GRCh38]
Chr14:99642289 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.533C>T (p.Pro178Leu) single nucleotide variant not provided [RCV003731614] Chr14:99231452 [GRCh38]
Chr14:99697789 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.129C>T (p.Gly43=) single nucleotide variant not provided [RCV003853524] Chr14:99257769 [GRCh38]
Chr14:99724106 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1221G>A (p.Pro407=) single nucleotide variant not provided [RCV003684357] Chr14:99175615 [GRCh38]
Chr14:99641952 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1563G>C (p.Glu521Asp) single nucleotide variant BCL11B-related disorder [RCV004540723]|not provided [RCV003566955] Chr14:99175273 [GRCh38]
Chr14:99641610 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.684_685delinsAG (p.Pro229Ala) indel not provided [RCV003712407] Chr14:99176151..99176152 [GRCh38]
Chr14:99642488..99642489 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1599G>C (p.Glu533Asp) single nucleotide variant not provided [RCV003684434] Chr14:99175237 [GRCh38]
Chr14:99641574 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.2193C>T (p.Asp731=) single nucleotide variant not provided [RCV003710780] Chr14:99174643 [GRCh38]
Chr14:99640980 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1296C>T (p.Cys432=) single nucleotide variant not provided [RCV003854075] Chr14:99175540 [GRCh38]
Chr14:99641877 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.113T>C (p.Ile38Thr) single nucleotide variant not provided [RCV003854163] Chr14:99257785 [GRCh38]
Chr14:99724122 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1212G>C (p.Leu404=) single nucleotide variant not provided [RCV003737805] Chr14:99175624 [GRCh38]
Chr14:99641961 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.933G>A (p.Pro311=) single nucleotide variant not provided [RCV003844202] Chr14:99175903 [GRCh38]
Chr14:99642240 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1920C>T (p.Gly640=) single nucleotide variant not provided [RCV003821659] Chr14:99174916 [GRCh38]
Chr14:99641253 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1271C>A (p.Ala424Asp) single nucleotide variant Inborn genetic diseases [RCV004968504]|not provided [RCV003841616] Chr14:99175565 [GRCh38]
Chr14:99641902 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1816G>T (p.Ala606Ser) single nucleotide variant not provided [RCV003567347] Chr14:99175020 [GRCh38]
Chr14:99641357 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1878T>G (p.Arg626=) single nucleotide variant not provided [RCV003710400] Chr14:99174958 [GRCh38]
Chr14:99641295 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1950G>C (p.Ala650=) single nucleotide variant not provided [RCV003822147] Chr14:99174886 [GRCh38]
Chr14:99641223 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.334C>A (p.Pro112Thr) single nucleotide variant not provided [RCV003552906] Chr14:99257564 [GRCh38]
Chr14:99723901 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1634T>C (p.Leu545Pro) single nucleotide variant not provided [RCV003732374] Chr14:99175202 [GRCh38]
Chr14:99641539 [GRCh37]
Chr14:14q32.2		 benign|uncertain significance
NM_138576.4(BCL11B):c.1598A>C (p.Glu533Ala) single nucleotide variant not provided [RCV003706170] Chr14:99175238 [GRCh38]
Chr14:99641575 [GRCh37]
Chr14:14q32.2		 likely benign|uncertain significance
NM_138576.4(BCL11B):c.1540G>A (p.Asp514Asn) single nucleotide variant not provided [RCV003861089] Chr14:99175296 [GRCh38]
Chr14:99641633 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1267_1268insTTGCTCTCCCATGCCCCCTGGCGGCACGCCGCCCCCGCAGCCGC (p.Pro423fs) insertion not provided [RCV003567450] Chr14:99175568..99175569 [GRCh38]
Chr14:99641905..99641906 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.828G>A (p.Gln276=) single nucleotide variant not provided [RCV003853587] Chr14:99176008 [GRCh38]
Chr14:99642345 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.924C>T (p.Gly308=) single nucleotide variant not provided [RCV003818368] Chr14:99175912 [GRCh38]
Chr14:99642249 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.2088G>A (p.Leu696=) single nucleotide variant not provided [RCV003705281] Chr14:99174748 [GRCh38]
Chr14:99641085 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1287C>T (p.Cys429=) single nucleotide variant not provided [RCV003820887] Chr14:99175549 [GRCh38]
Chr14:99641886 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1904_1939del (p.Asp635_Gly646del) deletion not provided [RCV003730648] Chr14:99174897..99174932 [GRCh38]
Chr14:99641234..99641269 [GRCh37]
Chr14:14q32.2		 conflicting interpretations of pathogenicity|uncertain significance
NM_138576.4(BCL11B):c.797C>T (p.Pro266Leu) single nucleotide variant not provided [RCV003735837] Chr14:99176039 [GRCh38]
Chr14:99642376 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1632G>C (p.Leu544=) single nucleotide variant not provided [RCV003822130] Chr14:99175204 [GRCh38]
Chr14:99641541 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1509C>T (p.Ser503=) single nucleotide variant not provided [RCV003728477] Chr14:99175327 [GRCh38]
Chr14:99641664 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.2454C>T (p.His818=) single nucleotide variant not provided [RCV003821165] Chr14:99174382 [GRCh38]
Chr14:99640719 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1627G>C (p.Glu543Gln) single nucleotide variant not provided [RCV003731292] Chr14:99175209 [GRCh38]
Chr14:99641546 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.2364C>T (p.Ser788=) single nucleotide variant not provided [RCV003843741] Chr14:99174472 [GRCh38]
Chr14:99640809 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1644C>A (p.Asn548Lys) single nucleotide variant Immunodeficiency 49 [RCV003993635] Chr14:99175192 [GRCh38]
Chr14:99641529 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.2007C>A (p.Phe669Leu) single nucleotide variant Inborn genetic diseases [RCV004426277] Chr14:99174829 [GRCh38]
Chr14:99641166 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.2299C>T (p.Arg767Cys) single nucleotide variant Inborn genetic diseases [RCV004426278] Chr14:99174537 [GRCh38]
Chr14:99640874 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1105G>A (p.Glu369Lys) single nucleotide variant Inborn genetic diseases [RCV004426274] Chr14:99175731 [GRCh38]
Chr14:99642068 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1468G>A (p.Asp490Asn) single nucleotide variant Inborn genetic diseases [RCV004426276] Chr14:99175368 [GRCh38]
Chr14:99641705 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.*2C>T single nucleotide variant BCL11B-related disorder [RCV004540940] Chr14:99174149 [GRCh38]
Chr14:99640486 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.123A>G (p.Pro41=) single nucleotide variant not provided [RCV005103152]|not specified [RCV003988195] Chr14:99257775 [GRCh38]
Chr14:99724112 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.2403C>A (p.Cys801Ter) single nucleotide variant not provided [RCV003887588] Chr14:99174433 [GRCh38]
Chr14:99640770 [GRCh37]
Chr14:14q32.2		 likely pathogenic
NM_138576.4(BCL11B):c.886G>A (p.Gly296Ser) single nucleotide variant not provided [RCV003884067] Chr14:99175950 [GRCh38]
Chr14:99642287 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1358A>G (p.Lys453Arg) single nucleotide variant Inborn genetic diseases [RCV004426275] Chr14:99175478 [GRCh38]
Chr14:99641815 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.2518_2519del (p.Thr840fs) deletion Inborn genetic diseases [RCV004426279] Chr14:99174317..99174318 [GRCh38]
Chr14:99640654..99640655 [GRCh37]
Chr14:14q32.2		 likely pathogenic
NM_138576.4(BCL11B):c.814G>C (p.Glu272Gln) single nucleotide variant Intellectual developmental disorder with speech delay, dysmorphic facies, and t-cell abnormalities [RCV004547272] Chr14:99176022 [GRCh38]
Chr14:99642359 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.301T>G (p.Ser101Ala) single nucleotide variant Inborn genetic diseases [RCV004605834] Chr14:99257597 [GRCh38]
Chr14:99723934 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.682C>G (p.Gln228Glu) single nucleotide variant not provided [RCV004592414] Chr14:99176154 [GRCh38]
Chr14:99642491 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.334C>G (p.Pro112Ala) single nucleotide variant Intellectual developmental disorder with speech delay, dysmorphic facies, and t-cell abnormalities [RCV004594826] Chr14:99257564 [GRCh38]
Chr14:99723901 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1705G>A (p.Gly569Ser) single nucleotide variant Inborn genetic diseases [RCV004607005] Chr14:99175131 [GRCh38]
Chr14:99641468 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.2T>C (p.Met1Thr) single nucleotide variant Inborn genetic diseases [RCV004605835] Chr14:99271217 [GRCh38]
Chr14:99737554 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1707del (p.Gly570fs) deletion Immunodeficiency 49 [RCV004797147] Chr14:99175129 [GRCh38]
Chr14:99641466 [GRCh37]
Chr14:14q32.2		 likely pathogenic
NM_138576.4(BCL11B):c.958C>T (p.Pro320Ser) single nucleotide variant not provided [RCV004774932] Chr14:99175878 [GRCh38]
Chr14:99642215 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.739C>T (p.Arg247Cys) single nucleotide variant not provided [RCV004766244] Chr14:99176097 [GRCh38]
Chr14:99642434 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.2378G>A (p.Arg793His) single nucleotide variant not provided [RCV004771314] Chr14:99174458 [GRCh38]
Chr14:99640795 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1975_1995del (p.Ala659_Phe665del) deletion not provided [RCV004768425] Chr14:99174841..99174861 [GRCh38]
Chr14:99641178..99641198 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.756_765del (p.Gly253fs) deletion BCL11B-related disorder [RCV004730658] Chr14:99176071..99176080 [GRCh38]
Chr14:99642408..99642417 [GRCh37]
Chr14:14q32.2		 pathogenic
NM_138576.4(BCL11B):c.2534C>T (p.Thr845Met) single nucleotide variant not provided [RCV004721959] Chr14:99174302 [GRCh38]
Chr14:99640639 [GRCh37]
Chr14:14q32.2		 likely pathogenic
NM_138576.4(BCL11B):c.320G>C (p.Arg107Thr) single nucleotide variant not provided [RCV004811517] Chr14:99257578 [GRCh38]
Chr14:99723915 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.784C>T (p.Arg262Trp) single nucleotide variant not provided [RCV004769242] Chr14:99176052 [GRCh38]
Chr14:99642389 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1444G>T (p.Gly482Cys) single nucleotide variant Inborn genetic diseases [RCV004965231] Chr14:99175392 [GRCh38]
Chr14:99641729 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.884C>G (p.Thr295Arg) single nucleotide variant Inborn genetic diseases [RCV004965233] Chr14:99175952 [GRCh38]
Chr14:99642289 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.653C>T (p.Pro218Leu) single nucleotide variant not provided [RCV004726040] Chr14:99176183 [GRCh38]
Chr14:99642520 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.2456C>T (p.Thr819Ile) single nucleotide variant not provided [RCV004769837] Chr14:99174380 [GRCh38]
Chr14:99640717 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1784T>C (p.Leu595Pro) single nucleotide variant Inborn genetic diseases [RCV004965232] Chr14:99175052 [GRCh38]
Chr14:99641389 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1351G>T (p.Gly451Cys) single nucleotide variant BCL11B-related disorder [RCV004758963] Chr14:99175485 [GRCh38]
Chr14:99641822 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1080C>T (p.Ala360=) single nucleotide variant BCL11B-related disorder [RCV004759119] Chr14:99175756 [GRCh38]
Chr14:99642093 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.842A>G (p.Asn281Ser) single nucleotide variant not provided [RCV004766308] Chr14:99175994 [GRCh38]
Chr14:99642331 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.2275C>A (p.Leu759Met) single nucleotide variant not provided [RCV005052651] Chr14:99174561 [GRCh38]
Chr14:99640898 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1219C>G (p.Pro407Ala) single nucleotide variant Immunodeficiency 49 [RCV005005714] Chr14:99175617 [GRCh38]
Chr14:99641954 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1666T>C (p.Phe556Leu) single nucleotide variant not provided [RCV004823371] Chr14:99175170 [GRCh38]
Chr14:99641507 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.708G>C (p.Leu236=) single nucleotide variant not provided [RCV005106209] Chr14:99176128 [GRCh38]
Chr14:99642465 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.2079C>T (p.Asp693=) single nucleotide variant not provided [RCV005173758] Chr14:99174757 [GRCh38]
Chr14:99641094 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.2479G>A (p.Glu827Lys) single nucleotide variant not provided [RCV005145887] Chr14:99174357 [GRCh38]
Chr14:99640694 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.586A>G (p.Thr196Ala) single nucleotide variant not provided [RCV005063433] Chr14:99231399 [GRCh38]
Chr14:99697736 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.2037C>G (p.Pro679=) single nucleotide variant not provided [RCV005085589] Chr14:99174799 [GRCh38]
Chr14:99641136 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1420A>G (p.Met474Val) single nucleotide variant not provided [RCV005172407] Chr14:99175416 [GRCh38]
Chr14:99641753 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.641-14G>A single nucleotide variant not provided [RCV005065436] Chr14:99176209 [GRCh38]
Chr14:99642546 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.555C>G (p.Cys185Trp) single nucleotide variant not provided [RCV005086201] Chr14:99231430 [GRCh38]
Chr14:99697767 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1793T>C (p.Val598Ala) single nucleotide variant not provided [RCV005085163] Chr14:99175043 [GRCh38]
Chr14:99641380 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.764C>T (p.Ala255Val) single nucleotide variant not provided [RCV005174355] Chr14:99176072 [GRCh38]
Chr14:99642409 [GRCh37]
Chr14:14q32.2		 benign
NM_138576.4(BCL11B):c.1108C>T (p.Leu370=) single nucleotide variant not provided [RCV005066231] Chr14:99175728 [GRCh38]
Chr14:99642065 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1842G>A (p.Leu614=) single nucleotide variant not provided [RCV005066957] Chr14:99174994 [GRCh38]
Chr14:99641331 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.2121G>A (p.Val707=) single nucleotide variant not provided [RCV005087036] Chr14:99174715 [GRCh38]
Chr14:99641052 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.864C>T (p.Pro288=) single nucleotide variant not specified [RCV005087615] Chr14:99175972 [GRCh38]
Chr14:99642309 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.2476T>C (p.Cys826Arg) single nucleotide variant not provided [RCV005227204] Chr14:99174360 [GRCh38]
Chr14:99640697 [GRCh37]
Chr14:14q32.2		 pathogenic
NM_138576.4(BCL11B):c.1762G>A (p.Ala588Thr) single nucleotide variant not provided [RCV005171788] Chr14:99175074 [GRCh38]
Chr14:99641411 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.800C>T (p.Pro267Leu) single nucleotide variant not provided [RCV005174690] Chr14:99176036 [GRCh38]
Chr14:99642373 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.2020_2021delinsTT (p.Ala674Leu) indel not provided [RCV005087313] Chr14:99174815..99174816 [GRCh38]
Chr14:99641152..99641153 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.928C>G (p.Leu310Val) single nucleotide variant not provided [RCV005127494] Chr14:99175908 [GRCh38]
Chr14:99642245 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.376C>T (p.His126Tyr) single nucleotide variant not provided [RCV005202514] Chr14:99257522 [GRCh38]
Chr14:99723859 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.899G>T (p.Arg300Leu) single nucleotide variant not provided [RCV005157013] Chr14:99175937 [GRCh38]
Chr14:99642274 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.991A>G (p.Ser331Gly) single nucleotide variant not provided [RCV005135854] Chr14:99175845 [GRCh38]
Chr14:99642182 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1602_1622dup (p.Glu540_Glu541insAspGluGluGluGluGluGlu) duplication not provided [RCV005074007] Chr14:99175213..99175214 [GRCh38]
Chr14:99641550..99641551 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1471G>A (p.Gly491Arg) single nucleotide variant not provided [RCV005130600] Chr14:99175365 [GRCh38]
Chr14:99641702 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1500C>T (p.Pro500=) single nucleotide variant not provided [RCV005186908] Chr14:99175336 [GRCh38]
Chr14:99641673 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1715G>C (p.Gly572Ala) single nucleotide variant not specified [RCV005238449] Chr14:99175121 [GRCh38]
Chr14:99641458 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1227G>A (p.Leu409=) single nucleotide variant not provided [RCV005072521] Chr14:99175609 [GRCh38]
Chr14:99641946 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.372T>C (p.Asp124=) single nucleotide variant not provided [RCV005158408] Chr14:99257526 [GRCh38]
Chr14:99723863 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1903G>A (p.Asp635Asn) single nucleotide variant not provided [RCV005140641] Chr14:99174933 [GRCh38]
Chr14:99641270 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1245C>G (p.Gly415=) single nucleotide variant not provided [RCV005123285] Chr14:99175591 [GRCh38]
Chr14:99641928 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1972T>A (p.Phe658Ile) single nucleotide variant not specified [RCV005238486] Chr14:99174864 [GRCh38]
Chr14:99641201 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.2310G>A (p.Thr770=) single nucleotide variant not provided [RCV005076599] Chr14:99174526 [GRCh38]
Chr14:99640863 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.2502G>A (p.Ala834=) single nucleotide variant not provided [RCV005075808] Chr14:99174334 [GRCh38]
Chr14:99640671 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1579G>A (p.Gly527Ser) single nucleotide variant not provided [RCV005074094] Chr14:99175257 [GRCh38]
Chr14:99641594 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1131G>A (p.Pro377=) single nucleotide variant not provided [RCV005244077] Chr14:99175705 [GRCh38]
Chr14:99642042 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1977G>A (p.Ala659=) single nucleotide variant not provided [RCV005244078] Chr14:99174859 [GRCh38]
Chr14:99641196 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.719C>T (p.Ala240Val) single nucleotide variant not provided [RCV005168164] Chr14:99176117 [GRCh38]
Chr14:99642454 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.537C>G (p.Pro179=) single nucleotide variant not provided [RCV005129734] Chr14:99231448 [GRCh38]
Chr14:99697785 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.2337G>A (p.Leu779=) single nucleotide variant not provided [RCV005190364] Chr14:99174499 [GRCh38]
Chr14:99640836 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.990C>T (p.Leu330=) single nucleotide variant not provided [RCV005202675] Chr14:99175846 [GRCh38]
Chr14:99642183 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1524G>A (p.Glu508=) single nucleotide variant not provided [RCV005166478] Chr14:99175312 [GRCh38]
Chr14:99641649 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.808G>A (p.Gly270Arg) single nucleotide variant not provided [RCV005234060] Chr14:99176028 [GRCh38]
Chr14:99642365 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1737G>A (p.Ala579=) single nucleotide variant not provided [RCV005161869] Chr14:99175099 [GRCh38]
Chr14:99641436 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1584C>G (p.His528Gln) single nucleotide variant not provided [RCV005193810] Chr14:99175252 [GRCh38]
Chr14:99641589 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1904_1921del (p.Asp635_Gly640del) deletion not provided [RCV005154042] Chr14:99174915..99174932 [GRCh38]
Chr14:99641252..99641269 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1224G>A (p.Pro408=) single nucleotide variant not provided [RCV005073407] Chr14:99175612 [GRCh38]
Chr14:99641949 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1914C>G (p.Asp638Glu) single nucleotide variant not provided [RCV005156184] Chr14:99174922 [GRCh38]
Chr14:99641259 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1652G>T (p.Arg551Leu) single nucleotide variant not provided [RCV005233347] Chr14:99175184 [GRCh38]
Chr14:99641521 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1317G>A (p.Gln439=) single nucleotide variant not provided [RCV005115987] Chr14:99175519 [GRCh38]
Chr14:99641856 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1335C>T (p.His445=) single nucleotide variant not provided [RCV005178635] Chr14:99175501 [GRCh38]
Chr14:99641838 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.59-14_59-12del microsatellite not provided [RCV005132709] Chr14:99257851..99257853 [GRCh38]
Chr14:99724188..99724190 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1531A>C (p.Lys511Gln) single nucleotide variant not provided [RCV005167882] Chr14:99175305 [GRCh38]
Chr14:99641642 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1833C>G (p.Gly611=) single nucleotide variant not provided [RCV005138605] Chr14:99175003 [GRCh38]
Chr14:99641340 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1590GGA[5] (p.Glu533_Asp534insGlu) microsatellite not provided [RCV005200108] Chr14:99175234..99175235 [GRCh38]
Chr14:99641571..99641572 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1137C>T (p.Pro379=) single nucleotide variant not provided [RCV005192907] Chr14:99175699 [GRCh38]
Chr14:99642036 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.2044A>C (p.Asn682His) single nucleotide variant not provided [RCV005186562] Chr14:99174792 [GRCh38]
Chr14:99641129 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.2220G>A (p.Ser740=) single nucleotide variant not provided [RCV005141610] Chr14:99174616 [GRCh38]
Chr14:99640953 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1230G>C (p.Pro410=) single nucleotide variant not provided [RCV005084294] Chr14:99175606 [GRCh38]
Chr14:99641943 [GRCh37]
Chr14:14q32.2		 benign
NM_138576.4(BCL11B):c.1561G>A (p.Glu521Lys) single nucleotide variant not provided [RCV005071398] Chr14:99175275 [GRCh38]
Chr14:99641612 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.2107C>T (p.Pro703Ser) single nucleotide variant not provided [RCV005111079] Chr14:99174729 [GRCh38]
Chr14:99641066 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.64G>C (p.Ala22Pro) single nucleotide variant not provided [RCV005076882] Chr14:99257834 [GRCh38]
Chr14:99724171 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.2363G>A (p.Ser788Asn) single nucleotide variant not provided [RCV005119650] Chr14:99174473 [GRCh38]
Chr14:99640810 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.933G>C (p.Pro311=) single nucleotide variant not provided [RCV005191348] Chr14:99175903 [GRCh38]
Chr14:99642240 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.97G>T (p.Asp33Tyr) single nucleotide variant not provided [RCV005111177] Chr14:99257801 [GRCh38]
Chr14:99724138 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1098G>C (p.Arg366=) single nucleotide variant not provided [RCV005119758] Chr14:99175738 [GRCh38]
Chr14:99642075 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.834G>A (p.Pro278=) single nucleotide variant not provided [RCV005081991] Chr14:99176002 [GRCh38]
Chr14:99642339 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1460_1461insT (p.Ser488fs) insertion not provided [RCV005205696] Chr14:99175375..99175376 [GRCh38]
Chr14:99641712..99641713 [GRCh37]
Chr14:14q32.2		 likely pathogenic
NM_138576.4(BCL11B):c.1969G>A (p.Gly657Ser) single nucleotide variant not provided [RCV005190497] Chr14:99174867 [GRCh38]
Chr14:99641204 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.827_835del (p.Gln276_Pro278del) deletion not provided [RCV005140275] Chr14:99176001..99176009 [GRCh38]
Chr14:99642338..99642346 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.211C>T (p.Leu71=) single nucleotide variant not provided [RCV005166614] Chr14:99257687 [GRCh38]
Chr14:99724024 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.2179C>T (p.Leu727=) single nucleotide variant not provided [RCV005165116] Chr14:99174657 [GRCh38]
Chr14:99640994 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.2055C>G (p.Ala685=) single nucleotide variant not provided [RCV005161631] Chr14:99174781 [GRCh38]
Chr14:99641118 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.29A>T (p.Gln10Leu) single nucleotide variant not provided [RCV005082218] Chr14:99271190 [GRCh38]
Chr14:99737527 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.964C>T (p.Arg322Cys) single nucleotide variant not provided [RCV005116418] Chr14:99175872 [GRCh38]
Chr14:99642209 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1822C>T (p.Pro608Ser) single nucleotide variant not provided [RCV005124910] Chr14:99175014 [GRCh38]
Chr14:99641351 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.586A>C (p.Thr196Pro) single nucleotide variant not provided [RCV005198037] Chr14:99231399 [GRCh38]
Chr14:99697736 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.2673C>T (p.Ala891=) single nucleotide variant not provided [RCV005069221] Chr14:99174163 [GRCh38]
Chr14:99640500 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.2573T>C (p.Ile858Thr) single nucleotide variant not provided [RCV005123330] Chr14:99174263 [GRCh38]
Chr14:99640600 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.2068G>A (p.Val690Met) single nucleotide variant not provided [RCV005130891] Chr14:99174768 [GRCh38]
Chr14:99641105 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1278C>G (p.Ser426Arg) single nucleotide variant not provided [RCV005177017] Chr14:99175558 [GRCh38]
Chr14:99641895 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.2329C>T (p.Pro777Ser) single nucleotide variant not provided [RCV005127409] Chr14:99174507 [GRCh38]
Chr14:99640844 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.766A>G (p.Ser256Gly) single nucleotide variant not provided [RCV005154286] Chr14:99176070 [GRCh38]
Chr14:99642407 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1943G>T (p.Gly648Val) single nucleotide variant not provided [RCV005180423] Chr14:99174893 [GRCh38]
Chr14:99641230 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1712G>A (p.Gly571Asp) single nucleotide variant not provided [RCV005202530] Chr14:99175124 [GRCh38]
Chr14:99641461 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.612T>C (p.Ala204=) single nucleotide variant not provided [RCV005131055] Chr14:99231373 [GRCh38]
Chr14:99697710 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1834G>A (p.Glu612Lys) single nucleotide variant not provided [RCV005152324] Chr14:99175002 [GRCh38]
Chr14:99641339 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.1494C>T (p.Pro498=) single nucleotide variant not provided [RCV005183198] Chr14:99175342 [GRCh38]
Chr14:99641679 [GRCh37]
Chr14:14q32.2		 likely benign
NM_138576.4(BCL11B):c.1934CGGGCG[1] (p.645AG[1]) microsatellite not provided [RCV005068489] Chr14:99174891..99174896 [GRCh38]
Chr14:99641228..99641233 [GRCh37]
Chr14:14q32.2		 uncertain significance
NM_138576.4(BCL11B):c.2613A>G (p.Lys871=) single nucleotide variant not provided [RCV005073114] Chr14:99174223 [GRCh38]
Chr14:99640560 [GRCh37]
Chr14:14q32.2		 likely benign
miRNA Target Status (No longer updated)

Predicted Target Of
Summary Value
Count of predictions:4245
Count of miRNA genes:1086
Interacting mature miRNAs:1335
Transcripts:ENST00000345514, ENST00000357195, ENST00000443726
Prediction methods:Miranda, Rnahybrid, Targetscan
Result types:miRGate_prediction

The detailed report is available here: Full Report CSV TAB Printer

miRNA Target Status data imported from miRGate (http://mirgate.bioinfo.cnio.es/).
For more information about miRGate, see PMID:25858286 or access the full paper here.


QTLs in Region (GRCh38)
The following QTLs overlap with this region.    Full Report CSV TAB Printer Gviewer
RGD IDSymbolNameLODP ValueTraitSub TraitChrStartStopSpecies
597102359GWAS1198433_Herythrocyte count QTL GWAS1198433 (human)3e-14erythrocyte countred blood cell count (CMO:0000025)149922087499220875Human
597291288GWAS1387362_Hbody mass index QTL GWAS1387362 (human)1e-10body mass indexbody mass index (BMI) (CMO:0000105)149920545199205452Human
597603231GWAS1660091_Htype 2 diabetes mellitus QTL GWAS1660091 (human)2e-10type 2 diabetes mellitus149923374399233744Human
597255576GWAS1351650_Hbipolar disorder QTL GWAS1351650 (human)9e-09bipolar disorder149924660899246609Human
597052178GWAS1148252_Herythrocyte count QTL GWAS1148252 (human)4e-12erythrocyte countred blood cell count (CMO:0000025)149923259499232595Human
597614747GWAS1671607_Hcellulitis, abscess QTL GWAS1671607 (human)1e-12cellulitis, abscess149923899499238995Human
597349151GWAS1445225_Hrestless legs syndrome QTL GWAS1445225 (human)8e-15restless legs syndrome149926889699268897Human
406979652GWAS628628_Hschizophrenia QTL GWAS628628 (human)9e-10schizophrenia149925288299252883Human
597310877GWAS1406951_Hbody mass index QTL GWAS1406951 (human)4e-09body mass indexbody mass index (BMI) (CMO:0000105)149920445499204455Human
406946374GWAS595350_Hhematocrit QTL GWAS595350 (human)4e-13hematocrithematocrit (CMO:0000037)149923259499232595Human
597186321GWAS1282395_Hbody mass index QTL GWAS1282395 (human)1e-16body mass indexbody mass index (BMI) (CMO:0000105)149923374399233744Human
597287699GWAS1383773_Hhemoglobin measurement QTL GWAS1383773 (human)5e-10hemoglobin measurementhemoglobin measurement (CMO:0000508)149923259499232595Human
597098140GWAS1194214_Htestosterone measurement QTL GWAS1194214 (human)9e-12testosterone measurementserum testosterone level (CMO:0000568)149925183699251837Human
597288597GWAS1384671_Hbody mass index QTL GWAS1384671 (human)1e-09body mass indexbody mass index (BMI) (CMO:0000105)149923374399233744Human
597059736GWAS1155810_Hmetabolic syndrome QTL GWAS1155810 (human)1e-10metabolic syndrome149923374399233744Human
597235734GWAS1331808_Hbiological sex QTL GWAS1331808 (human)2e-11biological sex149924159699241597Human
597109383GWAS1205457_Hmathematical ability QTL GWAS1205457 (human)7e-21mathematical ability149926889699268897Human
597307784GWAS1403858_Herythrocyte count QTL GWAS1403858 (human)1e-12erythrocyte countred blood cell count (CMO:0000025)149923259499232595Human
597213962GWAS1310036_Hschizophrenia QTL GWAS1310036 (human)2e-08schizophrenia149924569599245696Human
597036928GWAS1133002_Hbody mass index QTL GWAS1133002 (human)7e-13body mass indexbody mass index (BMI) (CMO:0000105)149923374399233744Human
597317389GWAS1413463_Hbody surface area QTL GWAS1413463 (human)6e-10body surface area149923374399233744Human
596985870GWAS1105389_Hbody mass index QTL GWAS1105389 (human)1e-10body mass index149920545199205452Human
597323450GWAS1419524_Hschizophrenia QTL GWAS1419524 (human)1e-08schizophrenia149920445499204455Human
597170105GWAS1266179_Hbody mass index QTL GWAS1266179 (human)7e-12body mass indexbody mass index (BMI) (CMO:0000105)149920545199205452Human
597254584GWAS1350658_Hthalamus volume QTL GWAS1350658 (human)2e-10thalamus volume149924336599243366Human
597290298GWAS1386372_Hbody weight QTL GWAS1386372 (human)1e-10body mass (VT:0001259)body weight (CMO:0000012)149921467599214676Human
597039422GWAS1135496_Hbipolar disorder QTL GWAS1135496 (human)5e-08bipolar disorder149924660899246609Human
406943853GWAS592829_Hhematocrit QTL GWAS592829 (human)2e-12hematocrithematocrit (CMO:0000037)149923259499232595Human
597254580GWAS1350654_Hthalamus volume QTL GWAS1350654 (human)3e-09thalamus volume149925288299252883Human
597031589GWAS1127663_Hbody mass index QTL GWAS1127663 (human)6e-11body mass indexbody mass index (BMI) (CMO:0000105)149920646099206461Human
597321134GWAS1417208_Hdiastolic blood pressure, systolic blood pressure QTL GWAS1417208 (human)0.0000001diastolic blood pressure, systolic blood pressuresystolic blood pressure (CMO:0000004)149922143699221437Human
596956321GWAS1075840_Hschizophrenia QTL GWAS1075840 (human)2e-08schizophrenia149925288299252883Human
597324332GWAS1420406_Hdiastolic blood pressure, systolic blood pressure QTL GWAS1420406 (human)4e-11diastolic blood pressure, systolic blood pressuresystolic blood pressure (CMO:0000004)149922143699221437Human
597323683GWAS1419757_Hschizophrenia QTL GWAS1419757 (human)2e-10schizophrenia149926704799267048Human
597117741GWAS1213815_Hcognitive function measurement QTL GWAS1213815 (human)3e-09cognitive behavior trait (VT:0010450)149926889699268897Human
597213733GWAS1309807_Hschizophrenia QTL GWAS1309807 (human)3e-08schizophrenia149925288299252883Human
597098538GWAS1194612_Hschizophrenia QTL GWAS1194612 (human)3e-08schizophrenia149925334399253344Human
597318951GWAS1415025_Hsmoking initiation QTL GWAS1415025 (human)1e-16smoking initiation149926038299260383Human
597298778GWAS1394852_Hhematocrit QTL GWAS1394852 (human)3e-10hematocrithematocrit (CMO:0000037)149923259499232595Human
407154439GWAS803415_Hgut microbiome measurement QTL GWAS803415 (human)0.000006gut microbiome measurement149918622499186225Human
597195995GWAS1292069_Hlean body mass QTL GWAS1292069 (human)3e-08body lean mass (VT:0010483)total body lean mass (CMO:0003950)149921467599214676Human
406938245GWAS587221_Hhemoglobin measurement QTL GWAS587221 (human)3e-16red blood cell density measurementhemoglobin measurement (CMO:0000508)149924159699241597Human
597026256GWAS1122330_Hschizophrenia QTL GWAS1122330 (human)5e-08schizophrenia149925288299252883Human
597231327GWAS1327401_Hsmoking status measurement QTL GWAS1327401 (human)3e-08smoking status measurement149922750699227507Human
597328349GWAS1424423_Hbody mass index QTL GWAS1424423 (human)9e-12body mass indexbody mass index (BMI) (CMO:0000105)149923374399233744Human
597073116GWAS1169190_Hschizophrenia QTL GWAS1169190 (human)2e-08bipolar disorder149925288299252883Human
597228244GWAS1324318_Hsmoking initiation QTL GWAS1324318 (human)3e-08smoking initiation149926074999260750Human
597228374GWAS1324448_Hsmoking status measurement QTL GWAS1324448 (human)1e-11smoking status measurement149922233399222334Human
597618000GWAS1674860_Hbody weight QTL GWAS1674860 (human)5e-14body mass (VT:0001259)body weight (CMO:0000012)149923809099238091Human
597252566GWAS1348640_Hschizophrenia QTL GWAS1348640 (human)8e-09schizophrenia149925288299252883Human
597084998GWAS1181072_Hbody mass index QTL GWAS1181072 (human)1e-08body mass indexbody mass index (BMI) (CMO:0000105)149920694199206942Human
597175624GWAS1271698_HTinnitus QTL GWAS1271698 (human)0.00001Tinnitus149923763199237632Human
407125008GWAS773984_Hschizophrenia QTL GWAS773984 (human)5e-09schizophrenia149925288299252883Human
597096003GWAS1192077_Htestosterone measurement QTL GWAS1192077 (human)7e-16testosterone measurementserum testosterone level (CMO:0000568)149926125499261255Human
597051712GWAS1147786_Hhematocrit QTL GWAS1147786 (human)5e-14hematocrithematocrit (CMO:0000037)149924159699241597Human
597033920GWAS1129994_Hrisk-taking behaviour QTL GWAS1129994 (human)4e-09risk-taking behaviour149924336599243366Human
597211470GWAS1307544_Hobsessive-compulsive disorder, attention deficit hyperactivity disorder, Tourette syndrome, bipolar disorder, autism spectrum disorder, schizophrenia, anorexia nervosa, major depressive disorder QTL GWAS1307544 (human)3e-10obsessive-compulsive disorder, attention deficit hyperactivity disorder, Tourette syndrome, bipolar disorder, autism spectrum disorder, schizophrenia, anorexia nervosa, major depressive disorder149925288299252883Human
596961741GWAS1081260_Hmetabolic syndrome QTL GWAS1081260 (human)1e-10metabolic syndrome149923374399233744Human
597080394GWAS1176468_Hbipolar disorder QTL GWAS1176468 (human)3e-09bipolar disorder149924660899246609Human
597277816GWAS1373890_Hdiet measurement QTL GWAS1373890 (human)9e-10eating behavior trait (VT:0001431)food intake measurement (CMO:0000772)149920658099206581Human
596966007GWAS1085526_Hbody mass index QTL GWAS1085526 (human)4e-09body mass index149920445499204455Human
407067936GWAS716912_Hobsessive-compulsive disorder, attention deficit hyperactivity disorder, Tourette syndrome, unipolar depression, bipolar disorder, autism spectrum disorder, schizophrenia, anorexia nervosa QTL GWAS716912 (human)3e-10obsessive-compulsive disorder, attention deficit hyperactivity disorder, Tourette syndrome, unipolar depression, bipolar disorder, autism spectrum disorder, schizophrenia, anorexia nervosa149925288299252883Human
406983590GWAS632566_Hhemoglobin measurement QTL GWAS632566 (human)3e-12hemoglobin measurementhemoglobin measurement (CMO:0000508)149923259499232595Human
406981156GWAS630132_Hhemoglobin measurement QTL GWAS630132 (human)6e-15hemoglobin measurementhemoglobin measurement (CMO:0000508)149923259499232595Human
597096561GWAS1192635_Hbipolar disorder QTL GWAS1192635 (human)1e-08bipolar disorder149923763199237632Human
597094398GWAS1190472_Hschizophrenia QTL GWAS1190472 (human)1e-08schizophrenia149925288299252883Human
596972414GWAS1091933_Hobsessive-compulsive disorder, attention deficit hyperactivity disorder, Tourette syndrome, bipolar disorder, autism spectrum disorder, schizophrenia, anorexia nervosa, major depressive disorder QTL GWAS1091933 (human)3e-10obsessive-compulsive disorder, attention deficit hyperactivity disorder, Tourette syndrome, bipolar disorder, autism spectrum disorder, schizophrenia, anorexia nervosa, major depressive disorder149925288299252883Human
597108216GWAS1204290_Hmathematical ability QTL GWAS1204290 (human)7e-12mathematical ability149926761799267618Human
597208552GWAS1304626_Hmathematical ability QTL GWAS1304626 (human)5e-15mathematical ability149926761799267618Human
597195744GWAS1291818_Hlean body mass QTL GWAS1291818 (human)1e-08body lean mass (VT:0010483)total body lean mass (CMO:0003950)149923374399233744Human
597088366GWAS1184440_Hschizophrenia QTL GWAS1184440 (human)4e-08schizophrenia149925595399255954Human
597600996GWAS1657856_Hbody mass index QTL GWAS1657856 (human)5e-13body mass indexbody mass index (BMI) (CMO:0000105)149923809099238091Human
597336548GWAS1432622_Hdyslexia QTL GWAS1432622 (human)6e-09dyslexia149926952499269526Human

Markers in Region
RH66257  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,662,069 - 99,662,208UniSTSGRCh37
Build 361498,731,822 - 98,731,961RGDNCBI36
Celera1479,717,819 - 79,717,958RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,845,664 - 79,845,803UniSTS
GeneMap99-GB4 RH Map14269.93UniSTS
RH102937  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,635,676 - 99,635,762UniSTSGRCh37
Build 361498,705,429 - 98,705,515RGDNCBI36
Celera1479,691,420 - 79,691,506RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,819,278 - 79,819,364UniSTS
GeneMap99-GB4 RH Map14269.93UniSTS
SHGC-105284  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,689,690 - 99,689,963UniSTSGRCh37
Build 361498,759,443 - 98,759,716RGDNCBI36
Celera1479,745,429 - 79,745,702RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,873,256 - 79,873,529UniSTS
TNG Radiation Hybrid Map1440278.0UniSTS
SHGC-147186  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,677,931 - 99,678,214UniSTSGRCh37
Build 361498,747,684 - 98,747,967RGDNCBI36
Celera1479,733,660 - 79,733,943RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,861,492 - 79,861,775UniSTS
TNG Radiation Hybrid Map1440271.0UniSTS
SHGC-147980  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,683,980 - 99,684,256UniSTSGRCh37
Build 361498,753,733 - 98,754,009RGDNCBI36
Celera1479,739,721 - 79,739,997RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,867,548 - 79,867,824UniSTS
TNG Radiation Hybrid Map1440290.0UniSTS
ECD00608  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,694,185 - 99,695,082UniSTSGRCh37
Build 361498,763,938 - 98,764,835RGDNCBI36
Celera1479,749,924 - 79,750,821RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,877,751 - 79,878,648UniSTS
ECD00834  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,706,595 - 99,707,483UniSTSGRCh37
Build 361498,776,348 - 98,777,236RGDNCBI36
Celera1479,762,285 - 79,763,173RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,890,160 - 79,891,048UniSTS
ECD00854  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,710,290 - 99,711,177UniSTSGRCh37
Build 361498,780,043 - 98,780,930RGDNCBI36
Celera1479,765,980 - 79,766,867RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,893,848 - 79,894,735UniSTS
ECD00919  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,652,931 - 99,653,815UniSTSGRCh37
Build 361498,722,684 - 98,723,568RGDNCBI36
Celera1479,708,676 - 79,709,560RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,836,537 - 79,837,421UniSTS
ECD01250  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,688,240 - 99,689,111UniSTSGRCh37
Build 361498,757,993 - 98,758,864RGDNCBI36
Celera1479,743,980 - 79,744,850RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,871,807 - 79,872,677UniSTS
ECD01421  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,653,860 - 99,654,725UniSTSGRCh37
Build 361498,723,613 - 98,724,478RGDNCBI36
Celera1479,709,605 - 79,710,480RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,837,466 - 79,838,331UniSTS
ECD01656  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,730,113 - 99,730,891UniSTSGRCh37
GRCh371499,730,034 - 99,730,891UniSTSGRCh37
Build 361498,799,787 - 98,800,644RGDNCBI36
Celera1479,785,726 - 79,786,583RGD
Celera1479,785,805 - 79,786,583UniSTS
Cytogenetic Map14q32.2UniSTS
HuRef1479,913,594 - 79,914,450UniSTS
HuRef1479,913,673 - 79,914,450UniSTS
ECD01684  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,721,787 - 99,722,643UniSTSGRCh37
Build 361498,791,540 - 98,792,396RGDNCBI36
Celera1479,777,479 - 79,778,335RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,905,347 - 79,906,203UniSTS
ECD01718  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,698,601 - 99,699,456UniSTSGRCh37
Build 361498,768,354 - 98,769,209RGDNCBI36
Celera1479,754,292 - 79,755,147RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,882,167 - 79,883,022UniSTS
ECD02053  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,728,290 - 99,729,133UniSTSGRCh37
Build 361498,798,043 - 98,798,886RGDNCBI36
Celera1479,783,982 - 79,784,825RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,911,850 - 79,912,693UniSTS
ECD02178  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,639,031 - 99,639,869UniSTSGRCh37
Build 361498,708,784 - 98,709,622RGDNCBI36
Celera1479,694,775 - 79,695,613RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,822,633 - 79,823,471UniSTS
ECD02211  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,719,962 - 99,720,799UniSTSGRCh37
Build 361498,789,715 - 98,790,552RGDNCBI36
Celera1479,775,655 - 79,776,492RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,903,523 - 79,904,360UniSTS
ECD02268  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,712,996 - 99,713,831UniSTSGRCh37
Build 361498,782,749 - 98,783,584RGDNCBI36
Celera1479,768,687 - 79,769,523RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,896,555 - 79,897,391UniSTS
ECD02302  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,738,792 - 99,739,626UniSTSGRCh37
Build 361498,808,545 - 98,809,379RGDNCBI36
Celera1479,794,482 - 79,795,316RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,922,436 - 79,923,270UniSTS
ECD02331  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,730,931 - 99,731,764UniSTSGRCh37
Build 361498,800,684 - 98,801,517RGDNCBI36
Celera1479,786,623 - 79,787,456RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,914,490 - 79,915,322UniSTS
ECD02332  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,732,764 - 99,733,597UniSTSGRCh37
Build 361498,802,517 - 98,803,350RGDNCBI36
Celera1479,788,456 - 79,789,289RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,916,322 - 79,917,155UniSTS
ECD02476  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,720,844 - 99,721,672UniSTSGRCh37
Build 361498,790,597 - 98,791,425RGDNCBI36
Celera1479,776,537 - 79,777,365RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,904,405 - 79,905,233UniSTS
ECD02507  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,670,844 - 99,671,671UniSTSGRCh37
Build 361498,740,597 - 98,741,424RGDNCBI36
Celera1479,726,573 - 79,727,400RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,854,405 - 79,855,232UniSTS
ECD02508  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,697,718 - 99,698,545UniSTSGRCh37
Build 361498,767,471 - 98,768,298RGDNCBI36
Celera1479,753,409 - 79,754,236RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,881,284 - 79,882,111UniSTS
ECD02572  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,670,008 - 99,670,833UniSTSGRCh37
Build 361498,739,761 - 98,740,586RGDNCBI36
Celera1479,725,737 - 79,726,562RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,853,569 - 79,854,394UniSTS
ECD02587  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,677,988 - 99,678,812UniSTSGRCh37
Build 361498,747,741 - 98,748,565RGDNCBI36
Celera1479,733,717 - 79,734,541RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,861,549 - 79,862,370UniSTS
ECD02588  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,731,863 - 99,732,687UniSTSGRCh37
Build 361498,801,616 - 98,802,440RGDNCBI36
Celera1479,787,555 - 79,788,379RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,915,421 - 79,916,245UniSTS
ECD02614  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,729,136 - 99,729,959UniSTSGRCh37
Build 361498,798,889 - 98,799,712RGDNCBI36
Celera1479,784,828 - 79,785,651RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,912,696 - 79,913,519UniSTS
ECD02747  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,679,746 - 99,680,564UniSTSGRCh37
Build 361498,749,499 - 98,750,317RGDNCBI36
Celera1479,735,475 - 79,736,293RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,863,304 - 79,864,122UniSTS
ECD02841  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,713,895 - 99,714,710UniSTSGRCh37
Build 361498,783,648 - 98,784,463RGDNCBI36
Celera1479,769,587 - 79,770,402RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,897,455 - 79,898,270UniSTS
ECD03005  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,676,585 - 99,677,394UniSTSGRCh37
Build 361498,746,338 - 98,747,147RGDNCBI36
Celera1479,732,314 - 79,733,123RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,860,146 - 79,860,955UniSTS
ECD03006  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,699,507 - 99,700,316UniSTSGRCh37
Build 361498,769,260 - 98,770,069RGDNCBI36
Celera1479,755,198 - 79,756,007RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,883,073 - 79,883,882UniSTS
ECD03110  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,671,694 - 99,672,499UniSTSGRCh37
Build 361498,741,447 - 98,742,252RGDNCBI36
Celera1479,727,423 - 79,728,228RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,855,255 - 79,856,060UniSTS
ECD03261  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,695,898 - 99,696,698UniSTSGRCh37
Build 361498,765,651 - 98,766,451RGDNCBI36
Celera1479,751,589 - 79,752,389RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,879,464 - 79,880,264UniSTS
ECD03303  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,711,258 - 99,712,057UniSTSGRCh37
Build 361498,781,011 - 98,781,810RGDNCBI36
Celera1479,766,948 - 79,767,748RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,894,816 - 79,895,616UniSTS
ECD03518  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,678,859 - 99,679,651UniSTSGRCh37
Build 361498,748,612 - 98,749,404RGDNCBI36
Celera1479,734,588 - 79,735,380RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,862,417 - 79,863,209UniSTS
ECD03729  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,704,491 - 99,705,276UniSTSGRCh37
Build 361498,774,244 - 98,775,029RGDNCBI36
Celera1479,760,181 - 79,760,966RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,888,056 - 79,888,841UniSTS
ECD03769  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,703,601 - 99,704,385UniSTSGRCh37
Build 361498,773,354 - 98,774,138RGDNCBI36
Celera1479,759,291 - 79,760,075RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,887,166 - 79,887,950UniSTS
ECD04672  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,654,956 - 99,655,713UniSTSGRCh37
Build 361498,724,709 - 98,725,466RGDNCBI36
Celera1479,710,711 - 79,711,468RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,838,556 - 79,839,313UniSTS
ECD05015  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,675,598 - 99,676,345UniSTSGRCh37
Build 361498,745,351 - 98,746,098RGDNCBI36
Celera1479,731,327 - 79,732,074RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,859,159 - 79,859,906UniSTS
ECD05223  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,692,020 - 99,692,761UniSTSGRCh37
Build 361498,761,773 - 98,762,514RGDNCBI36
Celera1479,747,759 - 79,748,500RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,875,586 - 79,876,327UniSTS
ECD05755  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,644,008 - 99,644,735UniSTSGRCh37
Build 361498,713,761 - 98,714,488RGDNCBI36
Celera1479,699,754 - 79,700,481RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,827,614 - 79,828,341UniSTS
ECD05898  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,735,251 - 99,735,974UniSTSGRCh37
Build 361498,805,004 - 98,805,727RGDNCBI36
Celera1479,790,943 - 79,791,666RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,918,811 - 79,919,535UniSTS
ECD05961  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,655,746 - 99,656,467UniSTSGRCh37
Build 361498,725,499 - 98,726,220RGDNCBI36
Celera1479,711,501 - 79,712,222RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,839,346 - 79,840,067UniSTS
ECD05985  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,692,862 - 99,693,582UniSTSGRCh37
Build 361498,762,615 - 98,763,335RGDNCBI36
Celera1479,748,601 - 79,749,321RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,876,428 - 79,877,148UniSTS
ECD06185  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,647,038 - 99,647,753UniSTSGRCh37
Build 361498,716,791 - 98,717,506RGDNCBI36
Celera1479,702,783 - 79,703,498RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,830,645 - 79,831,360UniSTS
ECD06186  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,701,231 - 99,701,946UniSTSGRCh37
Build 361498,770,984 - 98,771,699RGDNCBI36
Celera1479,756,922 - 79,757,637RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,884,797 - 79,885,512UniSTS
ECD06187  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,708,340 - 99,709,055UniSTSGRCh37
Build 361498,778,093 - 98,778,808RGDNCBI36
Celera1479,764,030 - 79,764,745RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,891,905 - 79,892,620UniSTS
ECD06287  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,707,582 - 99,708,294UniSTSGRCh37
Build 361498,777,335 - 98,778,047RGDNCBI36
Celera1479,763,272 - 79,763,984RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,891,147 - 79,891,859UniSTS
ECD06323  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,696,845 - 99,697,556UniSTSGRCh37
Build 361498,766,598 - 98,767,309RGDNCBI36
Celera1479,752,536 - 79,753,247RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,880,411 - 79,881,122UniSTS
ECD06362  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,724,739 - 99,725,449UniSTSGRCh37
Build 361498,794,492 - 98,795,202RGDNCBI36
Celera1479,780,431 - 79,781,141RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,908,299 - 79,909,009UniSTS
ECD06407  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,734,383 - 99,735,092UniSTSGRCh37
Build 361498,804,136 - 98,804,845RGDNCBI36
Celera1479,790,075 - 79,790,784RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,917,943 - 79,918,652UniSTS
ECD06444  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,643,210 - 99,643,918UniSTSGRCh37
Build 361498,712,963 - 98,713,671RGDNCBI36
Celera1479,698,956 - 79,699,664RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,826,816 - 79,827,524UniSTS
ECD06445  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,644,798 - 99,645,506UniSTSGRCh37
Build 361498,714,551 - 98,715,259RGDNCBI36
Celera1479,700,544 - 79,701,252RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,828,404 - 79,829,112UniSTS
ECD06747  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,709,157 - 99,709,857UniSTSGRCh37
Build 361498,778,910 - 98,779,610RGDNCBI36
Celera1479,764,847 - 79,765,547RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,892,722 - 79,893,422UniSTS
ECD06839  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,726,256 - 99,726,953UniSTSGRCh37
Build 361498,796,009 - 98,796,706RGDNCBI36
Celera1479,781,948 - 79,782,645RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,909,816 - 79,910,513UniSTS
ECD07076  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,725,499 - 99,726,190UniSTSGRCh37
Build 361498,795,252 - 98,795,943RGDNCBI36
Celera1479,781,191 - 79,781,882RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,909,059 - 79,909,750UniSTS
ECD07215  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,736,395 - 99,737,082UniSTSGRCh37
Build 361498,806,148 - 98,806,835RGDNCBI36
Celera1479,792,077 - 79,792,764RGD
Cytogenetic Map14q32.2UniSTS
ECD07358  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,650,092 - 99,650,775UniSTSGRCh37
Build 361498,719,845 - 98,720,528RGDNCBI36
Celera1479,705,837 - 79,706,520RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,833,699 - 79,834,382UniSTS
ECD07359  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,681,791 - 99,682,474UniSTSGRCh37
Build 361498,751,544 - 98,752,227RGDNCBI36
Celera1479,737,520 - 79,738,203RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,865,349 - 79,866,032UniSTS
ECD07656  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,635,450 - 99,636,125UniSTSGRCh37
Build 361498,705,203 - 98,705,878RGDNCBI36
Celera1479,691,194 - 79,691,869RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,819,052 - 79,819,727UniSTS
ECD07657  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,662,000 - 99,662,675UniSTSGRCh37
Build 361498,731,753 - 98,732,428RGDNCBI36
Celera1479,717,750 - 79,718,425RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,845,595 - 79,846,270UniSTS
ECD07658  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,681,103 - 99,681,778UniSTSGRCh37
Build 361498,750,856 - 98,751,531RGDNCBI36
Celera1479,736,832 - 79,737,507RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,864,661 - 79,865,336UniSTS
ECD07841  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,733,699 - 99,734,369UniSTSGRCh37
Build 361498,803,452 - 98,804,122RGDNCBI36
Celera1479,789,391 - 79,790,061RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,917,257 - 79,917,929UniSTS
ECD07875  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,674,034 - 99,674,703UniSTSGRCh37
Build 361498,743,787 - 98,744,456RGDNCBI36
Celera1479,729,763 - 79,730,432RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,857,595 - 79,858,264UniSTS
ECD08040  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,674,725 - 99,675,390UniSTSGRCh37
Build 361498,744,478 - 98,745,143RGDNCBI36
Celera1479,730,454 - 79,731,119RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,858,286 - 79,858,951UniSTS
ECD08228  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,716,824 - 99,717,484UniSTSGRCh37
Build 361498,786,577 - 98,787,237RGDNCBI36
Celera1479,772,516 - 79,773,177RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,900,384 - 79,901,045UniSTS
ECD08516  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,673,330 - 99,673,982UniSTSGRCh37
Build 361498,743,083 - 98,743,735RGDNCBI36
Celera1479,729,059 - 79,729,711RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,856,891 - 79,857,543UniSTS
ECD08831  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,662,732 - 99,663,376UniSTSGRCh37
Build 361498,732,485 - 98,733,129RGDNCBI36
Celera1479,718,482 - 79,719,125RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,846,327 - 79,846,971UniSTS
ECD09124  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,636,176 - 99,636,812UniSTSGRCh37
Build 361498,705,929 - 98,706,565RGDNCBI36
Celera1479,691,920 - 79,692,556RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,819,778 - 79,820,414UniSTS
ECD09724  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,642,301 - 99,642,922UniSTSGRCh37
Build 361498,712,054 - 98,712,675RGDNCBI36
Celera1479,698,047 - 79,698,668RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,825,907 - 79,826,528UniSTS
ECD09725  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,647,869 - 99,648,490UniSTSGRCh37
Build 361498,717,622 - 98,718,243RGDNCBI36
Celera1479,703,614 - 79,704,235RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,831,476 - 79,832,097UniSTS
ECD10120  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,702,277 - 99,702,887UniSTSGRCh37
Build 361498,772,030 - 98,772,640RGDNCBI36
Celera1479,757,967 - 79,758,577RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,885,842 - 79,886,452UniSTS
ECD10452  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,718,785 - 99,719,386UniSTSGRCh37
Build 361498,788,538 - 98,789,139RGDNCBI36
Celera1479,774,478 - 79,775,079RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,902,346 - 79,902,947UniSTS
ECD10588  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,702,916 - 99,703,513UniSTSGRCh37
Build 361498,772,669 - 98,773,266RGDNCBI36
Celera1479,758,606 - 79,759,203RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,886,481 - 79,887,078UniSTS
ECD10644  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,638,301 - 99,638,896UniSTSGRCh37
Build 361498,708,054 - 98,708,649RGDNCBI36
Celera1479,694,045 - 79,694,640RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,821,903 - 79,822,498UniSTS
ECD10715  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,683,755 - 99,684,348UniSTSGRCh37
Build 361498,753,508 - 98,754,101RGDNCBI36
Celera1479,739,496 - 79,740,089RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,867,323 - 79,867,916UniSTS
ECD10781  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,687,545 - 99,688,136UniSTSGRCh37
Build 361498,757,298 - 98,757,889RGDNCBI36
Celera1479,743,285 - 79,743,876RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,871,112 - 79,871,703UniSTS
ECD10912  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,637,642 - 99,638,229UniSTSGRCh37
Build 361498,707,395 - 98,707,982RGDNCBI36
Celera1479,693,386 - 79,693,973RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,821,244 - 79,821,831UniSTS
ECD10953  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,668,628 - 99,669,214UniSTSGRCh37
Build 361498,738,381 - 98,738,967RGDNCBI36
Celera1479,724,357 - 79,724,943RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,852,189 - 79,852,775UniSTS
ECD11165  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,648,695 - 99,649,275UniSTSGRCh37
Build 361498,718,448 - 98,719,028RGDNCBI36
Celera1479,704,440 - 79,705,020RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,832,302 - 79,832,882UniSTS
ECD11300  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,669,261 - 99,669,837UniSTSGRCh37
Build 361498,739,014 - 98,739,590RGDNCBI36
Celera1479,724,990 - 79,725,566RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,852,822 - 79,853,398UniSTS
ECD11631  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,727,615 - 99,728,181UniSTSGRCh37
Build 361498,797,368 - 98,797,934RGDNCBI36
Celera1479,783,307 - 79,783,873RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,911,175 - 79,911,741UniSTS
ECD11698  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,712,348 - 99,712,912UniSTSGRCh37
Build 361498,782,101 - 98,782,665RGDNCBI36
Celera1479,768,039 - 79,768,603RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,895,907 - 79,896,471UniSTS
ECD11699  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,727,036 - 99,727,600UniSTSGRCh37
Build 361498,796,789 - 98,797,353RGDNCBI36
Celera1479,782,728 - 79,783,292RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,910,596 - 79,911,160UniSTS
ECD12700  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,657,880 - 99,658,416UniSTSGRCh37
Build 361498,727,633 - 98,728,169RGDNCBI36
Celera1479,713,634 - 79,714,170RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,841,479 - 79,842,015UniSTS
ECD12701  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,659,715 - 99,660,251UniSTSGRCh37
Build 361498,729,468 - 98,730,004RGDNCBI36
Celera1479,715,465 - 79,716,001RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,843,310 - 79,843,846UniSTS
ECD12738  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,660,285 - 99,660,820UniSTSGRCh37
Build 361498,730,038 - 98,730,573RGDNCBI36
Celera1479,716,035 - 79,716,570RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,843,880 - 79,844,415UniSTS
ECD12781  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,658,429 - 99,658,963UniSTSGRCh37
Build 361498,728,182 - 98,728,716RGDNCBI36
Celera1479,714,183 - 79,714,717RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,842,028 - 79,842,562UniSTS
ECD12870  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,705,399 - 99,705,931UniSTSGRCh37
Build 361498,775,152 - 98,775,684RGDNCBI36
Celera1479,761,089 - 79,761,621RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,888,964 - 79,889,496UniSTS
ECD12957  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,705,944 - 99,706,474UniSTSGRCh37
Build 361498,775,697 - 98,776,227RGDNCBI36
Celera1479,761,634 - 79,762,164RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,889,509 - 79,890,039UniSTS
ECD13018  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,637,039 - 99,637,567UniSTSGRCh37
Build 361498,706,792 - 98,707,320RGDNCBI36
Celera1479,692,783 - 79,693,311RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,820,641 - 79,821,169UniSTS
ECD13366  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,723,460 - 99,723,979UniSTSGRCh37
Build 361498,793,213 - 98,793,732RGDNCBI36
Celera1479,779,152 - 79,779,671RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,907,020 - 79,907,539UniSTS
ECD13525  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,639,927 - 99,640,442UniSTSGRCh37
Build 361498,709,680 - 98,710,195RGDNCBI36
Celera1479,695,673 - 79,696,188RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,823,531 - 79,824,046UniSTS
ECD13561  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,664,907 - 99,665,421UniSTSGRCh37
Build 361498,734,660 - 98,735,174RGDNCBI36
Celera1479,720,656 - 79,721,170RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,848,502 - 79,849,016UniSTS
ECD13649  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,723,989 - 99,724,501UniSTSGRCh37
Build 361498,793,742 - 98,794,254RGDNCBI36
Celera1479,779,681 - 79,780,193RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,907,549 - 79,908,061UniSTS
ECD13810  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,665,468 - 99,665,976UniSTSGRCh37
Build 361498,735,221 - 98,735,729RGDNCBI36
Celera1479,721,217 - 79,721,725RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,849,063 - 79,849,571UniSTS
ECD14126  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,664,001 - 99,664,501UniSTSGRCh37
Build 361498,733,754 - 98,734,254RGDNCBI36
Celera1479,719,750 - 79,720,250RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,847,596 - 79,848,096UniSTS
ECD14350  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,663,483 - 99,663,978UniSTSGRCh37
Build 361498,733,236 - 98,733,731RGDNCBI36
Celera1479,719,232 - 79,719,727RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,847,078 - 79,847,573UniSTS
ECD14351  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,666,598 - 99,667,093UniSTSGRCh37
Build 361498,736,351 - 98,736,846RGDNCBI36
Celera1479,722,327 - 79,722,822RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,850,159 - 79,850,654UniSTS
ECD14484  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,689,300 - 99,689,792UniSTSGRCh37
Build 361498,759,053 - 98,759,545RGDNCBI36
Celera1479,745,039 - 79,745,531RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,872,866 - 79,873,358UniSTS
ECD14532  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,689,837 - 99,690,328UniSTSGRCh37
Build 361498,759,590 - 98,760,081RGDNCBI36
Celera1479,745,576 - 79,746,067RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,873,403 - 79,873,894UniSTS
ECD14795  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,651,826 - 99,652,311UniSTSGRCh37
Build 361498,721,579 - 98,722,064RGDNCBI36
Celera1479,707,571 - 79,708,056RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,835,432 - 79,835,917UniSTS
ECD14837  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,650,984 - 99,651,468UniSTSGRCh37
Build 361498,720,737 - 98,721,221RGDNCBI36
Celera1479,706,729 - 79,707,213RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,834,591 - 79,835,075UniSTS
ECD14934  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,666,092 - 99,666,574UniSTSGRCh37
Build 361498,735,845 - 98,736,327RGDNCBI36
Celera1479,721,821 - 79,722,303RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,849,653 - 79,850,135UniSTS
ECD15048  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,667,271 - 99,667,750UniSTSGRCh37
Build 361498,737,024 - 98,737,503RGDNCBI36
Celera1479,723,000 - 79,723,479RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,850,832 - 79,851,311UniSTS
ECD15332  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,646,407 - 99,646,879UniSTSGRCh37
Build 361498,716,160 - 98,716,632RGDNCBI36
Celera1479,702,152 - 79,702,624RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,830,014 - 79,830,486UniSTS
ECD15414  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,645,857 - 99,646,327UniSTSGRCh37
Build 361498,715,610 - 98,716,080RGDNCBI36
Celera1479,701,602 - 79,702,072RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,829,464 - 79,829,934UniSTS
ECD16498  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,657,001 - 99,657,438UniSTSGRCh37
Build 361498,726,754 - 98,727,191RGDNCBI36
Celera1479,712,756 - 79,713,193RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,840,600 - 79,841,038UniSTS
ECD16547  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,667,862 - 99,668,297UniSTSGRCh37
Build 361498,737,615 - 98,738,050RGDNCBI36
Celera1479,723,591 - 79,724,026RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,851,423 - 79,851,858UniSTS
ECD17061  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,641,732 - 99,642,146UniSTSGRCh37
Build 361498,711,485 - 98,711,899RGDNCBI36
Celera1479,697,478 - 79,697,892RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,825,338 - 79,825,752UniSTS
ECD17926  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,737,204 - 99,737,583UniSTSGRCh37
Build 361498,806,957 - 98,807,336RGDNCBI36
Celera1479,792,886 - 79,793,265RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,920,837 - 79,921,216UniSTS
ECD18269  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,717,855 - 99,718,221UniSTSGRCh37
Build 361498,787,608 - 98,787,974RGDNCBI36
Celera1479,773,548 - 79,773,914RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,901,416 - 79,901,782UniSTS
ECD18658  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,685,748 - 99,686,099UniSTSGRCh37
Build 361498,755,501 - 98,755,852RGDNCBI36
Celera1479,741,488 - 79,741,839RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,869,315 - 79,869,666UniSTS
ECD18803  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,691,133 - 99,691,479UniSTSGRCh37
Build 361498,760,886 - 98,761,232RGDNCBI36
Celera1479,746,872 - 79,747,218RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,874,699 - 79,875,045UniSTS
ECD18821  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,661,474 - 99,661,819UniSTSGRCh37
Build 361498,731,227 - 98,731,572RGDNCBI36
Celera1479,717,224 - 79,717,569RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,845,069 - 79,845,414UniSTS
ECD18912  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,684,738 - 99,685,080UniSTSGRCh37
Build 361498,754,491 - 98,754,833RGDNCBI36
Celera1479,740,479 - 79,740,821RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,868,306 - 79,868,648UniSTS
ECD19694  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,709,942 - 99,710,254UniSTSGRCh37
Build 361498,779,695 - 98,780,007RGDNCBI36
Celera1479,765,632 - 79,765,944RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,893,507 - 79,893,819UniSTS
ECD19857  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,715,312 - 99,715,618UniSTSGRCh37
Build 361498,785,065 - 98,785,371RGDNCBI36
Celera1479,771,004 - 79,771,310RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,898,872 - 79,899,178UniSTS
ECD20115  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,718,382 - 99,718,678UniSTSGRCh37
Build 361498,788,135 - 98,788,431RGDNCBI36
Celera1479,774,075 - 79,774,371RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,901,943 - 79,902,239UniSTS
ECD20162  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,659,329 - 99,659,623UniSTSGRCh37
Build 361498,729,082 - 98,729,376RGDNCBI36
Celera1479,715,079 - 79,715,373RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,842,924 - 79,843,218UniSTS
ECD20454  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,690,761 - 99,691,044UniSTSGRCh37
Build 361498,760,514 - 98,760,797RGDNCBI36
Celera1479,746,500 - 79,746,783RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,874,327 - 79,874,610UniSTS
ECD20505  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,722,897 - 99,723,178UniSTSGRCh37
Build 361498,792,650 - 98,792,931RGDNCBI36
Celera1479,778,589 - 79,778,870RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,906,457 - 79,906,738UniSTS
ECD20575  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,682,832 - 99,683,111UniSTSGRCh37
Build 361498,752,585 - 98,752,864RGDNCBI36
Celera1479,738,561 - 79,738,840RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,866,390 - 79,866,669UniSTS
ECD20744  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,640,505 - 99,640,778UniSTSGRCh37
Build 361498,710,258 - 98,710,531RGDNCBI36
Celera1479,696,251 - 79,696,524RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,824,109 - 79,824,384UniSTS
ECD21126  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,677,582 - 99,677,842UniSTSGRCh37
Build 361498,747,335 - 98,747,595RGDNCBI36
Celera1479,733,311 - 79,733,571RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,861,143 - 79,861,403UniSTS
ECD21249  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,691,690 - 99,691,945UniSTSGRCh37
Build 361498,761,443 - 98,761,698RGDNCBI36
Celera1479,747,429 - 79,747,684RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,875,256 - 79,875,511UniSTS
ECD21571  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,649,410 - 99,649,655UniSTSGRCh37
Build 361498,719,163 - 98,719,408RGDNCBI36
Celera1479,705,155 - 79,705,400RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,833,017 - 79,833,262UniSTS
ECD21572  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,719,592 - 99,719,837UniSTSGRCh37
Build 361498,789,345 - 98,789,590RGDNCBI36
Celera1479,775,285 - 79,775,530RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,903,153 - 79,903,398UniSTS
ECD21757  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,686,162 - 99,686,402UniSTSGRCh37
Build 361498,755,915 - 98,756,155RGDNCBI36
Celera1479,741,902 - 79,742,142RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,869,729 - 79,869,969UniSTS
ECD22064  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,661,098 - 99,661,328UniSTSGRCh37
Build 361498,730,851 - 98,731,081RGDNCBI36
Celera1479,716,848 - 79,717,078RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,844,693 - 79,844,923UniSTS
ECD22286  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,693,768 - 99,693,991UniSTSGRCh37
Build 361498,763,521 - 98,763,744RGDNCBI36
Celera1479,749,507 - 79,749,730RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,877,334 - 79,877,557UniSTS
ECD22801  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,738,456 - 99,738,663UniSTSGRCh37
Build 361498,808,209 - 98,808,416RGDNCBI36
Celera1479,794,146 - 79,794,353RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,922,100 - 79,922,307UniSTS
ECD23275  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,700,989 - 99,701,182UniSTSGRCh37
Build 361498,770,742 - 98,770,935RGDNCBI36
Celera1479,756,680 - 79,756,873RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,884,555 - 79,884,748UniSTS
ECD23276  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,714,941 - 99,715,134UniSTSGRCh37
Build 361498,784,694 - 98,784,887RGDNCBI36
Celera1479,770,633 - 79,770,826RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,898,501 - 79,898,694UniSTS
ECD23841  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,737,883 - 99,738,056UniSTSGRCh37
Build 361498,807,636 - 98,807,809RGDNCBI36
Celera1479,793,573 - 79,793,746RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,921,527 - 79,921,700UniSTS
REN47683  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,635,200 - 99,635,458UniSTSGRCh37
Build 361498,704,953 - 98,705,211RGDNCBI36
Celera1479,690,944 - 79,691,202RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,818,802 - 79,819,060UniSTS
REN47684  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,635,455 - 99,635,703UniSTSGRCh37
Build 361498,705,208 - 98,705,456RGDNCBI36
Celera1479,691,199 - 79,691,447RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,819,057 - 79,819,305UniSTS
REN47685  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,635,672 - 99,635,898UniSTSGRCh37
Build 361498,705,425 - 98,705,651RGDNCBI36
Celera1479,691,416 - 79,691,642RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,819,274 - 79,819,500UniSTS
REN47686  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,635,872 - 99,636,133UniSTSGRCh37
Build 361498,705,625 - 98,705,886RGDNCBI36
Celera1479,691,616 - 79,691,877RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,819,474 - 79,819,735UniSTS
REN47687  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,636,125 - 99,636,380UniSTSGRCh37
Build 361498,705,878 - 98,706,133RGDNCBI36
Celera1479,691,869 - 79,692,124RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,819,727 - 79,819,982UniSTS
REN47688  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,636,376 - 99,636,642UniSTSGRCh37
Build 361498,706,129 - 98,706,395RGDNCBI36
Celera1479,692,120 - 79,692,386RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,819,978 - 79,820,244UniSTS
REN47689  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,636,634 - 99,636,880UniSTSGRCh37
Build 361498,706,387 - 98,706,633RGDNCBI36
Celera1479,692,378 - 79,692,624RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,820,236 - 79,820,482UniSTS
REN47690  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,636,863 - 99,637,094UniSTSGRCh37
Build 361498,706,616 - 98,706,847RGDNCBI36
Celera1479,692,607 - 79,692,838RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,820,465 - 79,820,696UniSTS
REN47691  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,637,067 - 99,637,327UniSTSGRCh37
Build 361498,706,820 - 98,707,080RGDNCBI36
Celera1479,692,811 - 79,693,071RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,820,669 - 79,820,929UniSTS
REN47692  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,637,304 - 99,637,560UniSTSGRCh37
Build 361498,707,057 - 98,707,313RGDNCBI36
Celera1479,693,048 - 79,693,304RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,820,906 - 79,821,162UniSTS
REN47693  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,637,453 - 99,637,723UniSTSGRCh37
Build 361498,707,206 - 98,707,476RGDNCBI36
Celera1479,693,197 - 79,693,467RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,821,055 - 79,821,325UniSTS
REN47694  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,637,696 - 99,637,950UniSTSGRCh37
Build 361498,707,449 - 98,707,703RGDNCBI36
Celera1479,693,440 - 79,693,694RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,821,298 - 79,821,552UniSTS
REN47695  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,637,905 - 99,638,157UniSTSGRCh37
Build 361498,707,658 - 98,707,910RGDNCBI36
Celera1479,693,649 - 79,693,901RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,821,507 - 79,821,759UniSTS
REN47696  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,638,151 - 99,638,407UniSTSGRCh37
Build 361498,707,904 - 98,708,160RGDNCBI36
Celera1479,693,895 - 79,694,151RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,821,753 - 79,822,009UniSTS
REN47697  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,638,384 - 99,638,646UniSTSGRCh37
Build 361498,708,137 - 98,708,399RGDNCBI36
Celera1479,694,128 - 79,694,390RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,821,986 - 79,822,248UniSTS
REN47698  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,638,645 - 99,638,894UniSTSGRCh37
Build 361498,708,398 - 98,708,647RGDNCBI36
Celera1479,694,389 - 79,694,638RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,822,247 - 79,822,496UniSTS
REN47699  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,638,891 - 99,639,127UniSTSGRCh37
Build 361498,708,644 - 98,708,880RGDNCBI36
Celera1479,694,635 - 79,694,871RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,822,493 - 79,822,729UniSTS
REN47700  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,639,113 - 99,639,374UniSTSGRCh37
Build 361498,708,866 - 98,709,127RGDNCBI36
Celera1479,694,857 - 79,695,118RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,822,715 - 79,822,976UniSTS
REN47701  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,639,367 - 99,639,612UniSTSGRCh37
Build 361498,709,120 - 98,709,365RGDNCBI36
Celera1479,695,111 - 79,695,356RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,822,969 - 79,823,214UniSTS
REN47702  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,639,598 - 99,639,829UniSTSGRCh37
Build 361498,709,351 - 98,709,582RGDNCBI36
Celera1479,695,342 - 79,695,573RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,823,200 - 79,823,431UniSTS
REN47703  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,639,823 - 99,640,065UniSTSGRCh37
Build 361498,709,576 - 98,709,818RGDNCBI36
Celera1479,695,567 - 79,695,811RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,823,425 - 79,823,669UniSTS
REN47704  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,640,012 - 99,640,285UniSTSGRCh37
Build 361498,709,765 - 98,710,038RGDNCBI36
Celera1479,695,758 - 79,696,031RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,823,616 - 79,823,889UniSTS
REN47705  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,640,267 - 99,640,529UniSTSGRCh37
Build 361498,710,020 - 98,710,282RGDNCBI36
Celera1479,696,013 - 79,696,275RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,823,871 - 79,824,133UniSTS
REN47706  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,640,510 - 99,640,764UniSTSGRCh37
Build 361498,710,263 - 98,710,517RGDNCBI36
Celera1479,696,256 - 79,696,510RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,824,114 - 79,824,370UniSTS
REN47707  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,640,740 - 99,641,002UniSTSGRCh37
Build 361498,710,493 - 98,710,755RGDNCBI36
Celera1479,696,486 - 79,696,748RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,824,346 - 79,824,608UniSTS
REN47708  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,641,367 - 99,641,626UniSTSGRCh37
Build 361498,711,120 - 98,711,379RGDNCBI36
Celera1479,697,113 - 79,697,372RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,824,973 - 79,825,232UniSTS
REN47709  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,641,608 - 99,641,867UniSTSGRCh37
Build 361498,711,361 - 98,711,620RGDNCBI36
Celera1479,697,354 - 79,697,613RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,825,214 - 79,825,473UniSTS
REN47710  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,641,746 - 99,642,003UniSTSGRCh37
GRCh371499,640,639 - 99,642,003UniSTSGRCh37
Build 361498,711,499 - 98,711,756RGDNCBI36
Celera1479,696,385 - 79,697,749UniSTS
Celera1479,697,492 - 79,697,749RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,825,352 - 79,825,609UniSTS
HuRef1479,824,244 - 79,825,609UniSTS
REN47711  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,641,984 - 99,642,236UniSTSGRCh37
Build 361498,711,737 - 98,711,989RGDNCBI36
Celera1479,697,730 - 79,697,982RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,825,590 - 79,825,842UniSTS
REN47712  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,642,297 - 99,642,523UniSTSGRCh37
Build 361498,712,050 - 98,712,276RGDNCBI36
Celera1479,698,043 - 79,698,269RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,825,903 - 79,826,129UniSTS
REN47713  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,642,506 - 99,642,737UniSTSGRCh37
Build 361498,712,259 - 98,712,490RGDNCBI36
Celera1479,698,252 - 79,698,483RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,826,112 - 79,826,343UniSTS
REN47714  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,642,718 - 99,642,977UniSTSGRCh37
Build 361498,712,471 - 98,712,730RGDNCBI36
Celera1479,698,464 - 79,698,723RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,826,324 - 79,826,583UniSTS
REN47715  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,642,967 - 99,643,225UniSTSGRCh37
Build 361498,712,720 - 98,712,978RGDNCBI36
Celera1479,698,713 - 79,698,971RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,826,573 - 79,826,831UniSTS
REN47716  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,643,211 - 99,643,437UniSTSGRCh37
Build 361498,712,964 - 98,713,190RGDNCBI36
Celera1479,698,957 - 79,699,183RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,826,817 - 79,827,043UniSTS
REN47717  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,643,411 - 99,643,681UniSTSGRCh37
Build 361498,713,164 - 98,713,434RGDNCBI36
Celera1479,699,157 - 79,699,427RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,827,017 - 79,827,287UniSTS
REN47718  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,643,658 - 99,643,917UniSTSGRCh37
Build 361498,713,411 - 98,713,670RGDNCBI36
Celera1479,699,404 - 79,699,663RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,827,264 - 79,827,523UniSTS
REN47719  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,643,913 - 99,644,158UniSTSGRCh37
Build 361498,713,666 - 98,713,911RGDNCBI36
Celera1479,699,659 - 79,699,904RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,827,519 - 79,827,764UniSTS
REN47720  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,644,143 - 99,644,385UniSTSGRCh37
Build 361498,713,896 - 98,714,138RGDNCBI36
Celera1479,699,889 - 79,700,131RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,827,749 - 79,827,991UniSTS
REN47721  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,644,337 - 99,644,597UniSTSGRCh37
Build 361498,714,090 - 98,714,350RGDNCBI36
Celera1479,700,083 - 79,700,343RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,827,943 - 79,828,203UniSTS
REN47722  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,644,574 - 99,644,822UniSTSGRCh37
Build 361498,714,327 - 98,714,575RGDNCBI36
Celera1479,700,320 - 79,700,568RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,828,180 - 79,828,428UniSTS
REN47723  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,644,763 - 99,645,021UniSTSGRCh37
Build 361498,714,516 - 98,714,774RGDNCBI36
Celera1479,700,509 - 79,700,767RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,828,369 - 79,828,627UniSTS
REN47724  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,644,998 - 99,645,264UniSTSGRCh37
Build 361498,714,751 - 98,715,017RGDNCBI36
Celera1479,700,744 - 79,701,010RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,828,604 - 79,828,870UniSTS
REN47725  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,645,211 - 99,645,460UniSTSGRCh37
Build 361498,714,964 - 98,715,213RGDNCBI36
Celera1479,700,957 - 79,701,206RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,828,817 - 79,829,066UniSTS
REN47726  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,645,276 - 99,645,533UniSTSGRCh37
Build 361498,715,029 - 98,715,286RGDNCBI36
Celera1479,701,022 - 79,701,279RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,828,882 - 79,829,139UniSTS
REN47727  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,645,843 - 99,646,068UniSTSGRCh37
Build 361498,715,596 - 98,715,821RGDNCBI36
Celera1479,701,588 - 79,701,813RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,829,450 - 79,829,675UniSTS
REN47728  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,646,059 - 99,646,325UniSTSGRCh37
Build 361498,715,812 - 98,716,078RGDNCBI36
Celera1479,701,804 - 79,702,070RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,829,666 - 79,829,932UniSTS
REN47729  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,646,313 - 99,646,559UniSTSGRCh37
Build 361498,716,066 - 98,716,312RGDNCBI36
Celera1479,702,058 - 79,702,304RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,829,920 - 79,830,166UniSTS
REN47730  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,646,534 - 99,646,773UniSTSGRCh37
Build 361498,716,287 - 98,716,526RGDNCBI36
Celera1479,702,279 - 79,702,518RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,830,141 - 79,830,380UniSTS
REN47731  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,646,743 - 99,646,993UniSTSGRCh37
Build 361498,716,496 - 98,716,746RGDNCBI36
Celera1479,702,488 - 79,702,738RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,830,350 - 79,830,600UniSTS
REN47732  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,646,970 - 99,647,211UniSTSGRCh37
Build 361498,716,723 - 98,716,964RGDNCBI36
Celera1479,702,715 - 79,702,956RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,830,577 - 79,830,818UniSTS
REN47733  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,647,188 - 99,647,437UniSTSGRCh37
Build 361498,716,941 - 98,717,190RGDNCBI36
Celera1479,702,933 - 79,703,182RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,830,795 - 79,831,044UniSTS
REN47734  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,647,411 - 99,647,656UniSTSGRCh37
Build 361498,717,164 - 98,717,409RGDNCBI36
Celera1479,703,156 - 79,703,401RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,831,018 - 79,831,263UniSTS
REN47735  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,647,633 - 99,647,883UniSTSGRCh37
Build 361498,717,386 - 98,717,636RGDNCBI36
Celera1479,703,378 - 79,703,628RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,831,240 - 79,831,490UniSTS
REN47736  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,647,850 - 99,648,100UniSTSGRCh37
Build 361498,717,603 - 98,717,853RGDNCBI36
Celera1479,703,595 - 79,703,845RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,831,457 - 79,831,707UniSTS
REN47737  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,648,097 - 99,648,344UniSTSGRCh37
Build 361498,717,850 - 98,718,097RGDNCBI36
Celera1479,703,842 - 79,704,089RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,831,704 - 79,831,951UniSTS
REN47738  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,648,332 - 99,648,586UniSTSGRCh37
Build 361498,718,085 - 98,718,339RGDNCBI36
Celera1479,704,077 - 79,704,331RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,831,939 - 79,832,193UniSTS
REN47739  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,648,563 - 99,648,830UniSTSGRCh37
Build 361498,718,316 - 98,718,583RGDNCBI36
Celera1479,704,308 - 79,704,575RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,832,170 - 79,832,437UniSTS
REN47740  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,648,807 - 99,649,036UniSTSGRCh37
Build 361498,718,560 - 98,718,789RGDNCBI36
Celera1479,704,552 - 79,704,781RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,832,414 - 79,832,643UniSTS
REN47741  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,649,014 - 99,649,260UniSTSGRCh37
Build 361498,718,767 - 98,719,013RGDNCBI36
Celera1479,704,759 - 79,705,005RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,832,621 - 79,832,867UniSTS
REN47742  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,649,237 - 99,649,495UniSTSGRCh37
Build 361498,718,990 - 98,719,248RGDNCBI36
Celera1479,704,982 - 79,705,240RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,832,844 - 79,833,102UniSTS
REN47743  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,649,487 - 99,649,741UniSTSGRCh37
Build 361498,719,240 - 98,719,494RGDNCBI36
Celera1479,705,232 - 79,705,486RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,833,094 - 79,833,348UniSTS
REN47744  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,649,672 - 99,649,945UniSTSGRCh37
Build 361498,719,425 - 98,719,698RGDNCBI36
Celera1479,705,417 - 79,705,690RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,833,279 - 79,833,552UniSTS
REN47745  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,649,932 - 99,650,199UniSTSGRCh37
Build 361498,719,685 - 98,719,952RGDNCBI36
Celera1479,705,677 - 79,705,944RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,833,539 - 79,833,806UniSTS
REN47746  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,650,179 - 99,650,403UniSTSGRCh37
Build 361498,719,932 - 98,720,156RGDNCBI36
Celera1479,705,924 - 79,706,148RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,833,786 - 79,834,010UniSTS
REN47747  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,650,371 - 99,650,599UniSTSGRCh37
Build 361498,720,124 - 98,720,352RGDNCBI36
Celera1479,706,116 - 79,706,344RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,833,978 - 79,834,206UniSTS
REN47748  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,650,571 - 99,650,805UniSTSGRCh37
Build 361498,720,324 - 98,720,558RGDNCBI36
Celera1479,706,316 - 79,706,550RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,834,178 - 79,834,412UniSTS
REN47749  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,650,782 - 99,651,047UniSTSGRCh37
Build 361498,720,535 - 98,720,800RGDNCBI36
Celera1479,706,527 - 79,706,792RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,834,389 - 79,834,654UniSTS
REN47750  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,651,029 - 99,651,278UniSTSGRCh37
Build 361498,720,782 - 98,721,031RGDNCBI36
Celera1479,706,774 - 79,707,023RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,834,636 - 79,834,885UniSTS
REN47751  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,651,273 - 99,651,497UniSTSGRCh37
Build 361498,721,026 - 98,721,250RGDNCBI36
Celera1479,707,018 - 79,707,242RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,834,880 - 79,835,104UniSTS
REN47752  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,651,804 - 99,652,034UniSTSGRCh37
Build 361498,721,557 - 98,721,787RGDNCBI36
Celera1479,707,549 - 79,707,779RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,835,410 - 79,835,640UniSTS
REN47753  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,652,018 - 99,652,267UniSTSGRCh37
Build 361498,721,771 - 98,722,020RGDNCBI36
Celera1479,707,763 - 79,708,012RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,835,624 - 79,835,873UniSTS
REN47754  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,652,244 - 99,652,505UniSTSGRCh37
Build 361498,721,997 - 98,722,258RGDNCBI36
Celera1479,707,989 - 79,708,250RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,835,850 - 79,836,111UniSTS
REN47755  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,652,391 - 99,652,641UniSTSGRCh37
Build 361498,722,144 - 98,722,394RGDNCBI36
Celera1479,708,136 - 79,708,386RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,835,997 - 79,836,247UniSTS
REN47756  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,652,895 - 99,653,120UniSTSGRCh37
Build 361498,722,648 - 98,722,873RGDNCBI36
Celera1479,708,640 - 79,708,865RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,836,501 - 79,836,726UniSTS
REN47757  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,653,097 - 99,653,344UniSTSGRCh37
Build 361498,722,850 - 98,723,097RGDNCBI36
Celera1479,708,842 - 79,709,089RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,836,703 - 79,836,950UniSTS
REN47758  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,653,340 - 99,653,589UniSTSGRCh37
Build 361498,723,093 - 98,723,342RGDNCBI36
Celera1479,709,085 - 79,709,334RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,836,946 - 79,837,195UniSTS
REN47759  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,653,566 - 99,653,812UniSTSGRCh37
Build 361498,723,319 - 98,723,565RGDNCBI36
Celera1479,709,311 - 79,709,557RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,837,172 - 79,837,418UniSTS
REN47760  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,653,748 - 99,653,999UniSTSGRCh37
Build 361498,723,501 - 98,723,752RGDNCBI36
Celera1479,709,493 - 79,709,744RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,837,354 - 79,837,605UniSTS
REN47761  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,653,979 - 99,654,245UniSTSGRCh37
Build 361498,723,732 - 98,723,998RGDNCBI36
Celera1479,709,724 - 79,710,000RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,837,585 - 79,837,851UniSTS
REN47762  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,654,234 - 99,654,474UniSTSGRCh37
Build 361498,723,987 - 98,724,227RGDNCBI36
Celera1479,709,989 - 79,710,229RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,837,840 - 79,838,080UniSTS
REN47763  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,654,472 - 99,654,728UniSTSGRCh37
Build 361498,724,225 - 98,724,481RGDNCBI36
Celera1479,710,227 - 79,710,483RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,838,078 - 79,838,334UniSTS
REN47764  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,654,706 - 99,654,954UniSTSGRCh37
Build 361498,724,459 - 98,724,707RGDNCBI36
Celera1479,710,461 - 79,710,709RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,838,312 - 79,838,554UniSTS
REN47765  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,654,827 - 99,655,063UniSTSGRCh37
Build 361498,724,580 - 98,724,816RGDNCBI36
Celera1479,710,582 - 79,710,818RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,838,433 - 79,838,663UniSTS
REN47766  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,655,055 - 99,655,302UniSTSGRCh37
Build 361498,724,808 - 98,725,055RGDNCBI36
Celera1479,710,810 - 79,711,057RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,838,655 - 79,838,902UniSTS
REN47767  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,655,266 - 99,655,514UniSTSGRCh37
Build 361498,725,019 - 98,725,267RGDNCBI36
Celera1479,711,021 - 79,711,269RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,838,866 - 79,839,114UniSTS
REN47768  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,655,491 - 99,655,747UniSTSGRCh37
Build 361498,725,244 - 98,725,500RGDNCBI36
Celera1479,711,246 - 79,711,502RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,839,091 - 79,839,347UniSTS
REN47769  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,655,688 - 99,655,948UniSTSGRCh37
Build 361498,725,441 - 98,725,701RGDNCBI36
Celera1479,711,443 - 79,711,703RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,839,288 - 79,839,548UniSTS
REN47770  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,655,937 - 99,656,205UniSTSGRCh37
Build 361498,725,690 - 98,725,958RGDNCBI36
Celera1479,711,692 - 79,711,960RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,839,537 - 79,839,805UniSTS
REN47771  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,656,201 - 99,656,434UniSTSGRCh37
Build 361498,725,954 - 98,726,187RGDNCBI36
Celera1479,711,956 - 79,712,189RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,839,801 - 79,840,034UniSTS
REN47772  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,656,325 - 99,656,549UniSTSGRCh37
Build 361498,726,078 - 98,726,302RGDNCBI36
Celera1479,712,080 - 79,712,304RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,839,925 - 79,840,149UniSTS
REN47773  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,656,808 - 99,657,035UniSTSGRCh37
Build 361498,726,561 - 98,726,788RGDNCBI36
Celera1479,712,563 - 79,712,790RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,840,407 - 79,840,634UniSTS
REN47774  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,657,034 - 99,657,284UniSTSGRCh37
Build 361498,726,787 - 98,727,037RGDNCBI36
Celera1479,712,789 - 79,713,039RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,840,633 - 79,840,884UniSTS
REN47775  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,657,256 - 99,657,523UniSTSGRCh37
Build 361498,727,009 - 98,727,276RGDNCBI36
Celera1479,713,011 - 79,713,278RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,840,856 - 79,841,123UniSTS
REN47776  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,657,498 - 99,657,722UniSTSGRCh37
Build 361498,727,251 - 98,727,475RGDNCBI36
Celera1479,713,253 - 79,713,476RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,841,098 - 79,841,321UniSTS
REN47777  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,657,701 - 99,657,948UniSTSGRCh37
Build 361498,727,454 - 98,727,701RGDNCBI36
Celera1479,713,455 - 79,713,702RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,841,300 - 79,841,547UniSTS
REN47778  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,657,909 - 99,658,157UniSTSGRCh37
Build 361498,727,662 - 98,727,910RGDNCBI36
Celera1479,713,663 - 79,713,911RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,841,508 - 79,841,756UniSTS
REN47779  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,658,132 - 99,658,382UniSTSGRCh37
Build 361498,727,885 - 98,728,135RGDNCBI36
Celera1479,713,886 - 79,714,136RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,841,731 - 79,841,981UniSTS
REN47780  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,658,359 - 99,658,614UniSTSGRCh37
Build 361498,728,112 - 98,728,367RGDNCBI36
Celera1479,714,113 - 79,714,368RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,841,958 - 79,842,213UniSTS
REN47781  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,658,598 - 99,658,862UniSTSGRCh37
Build 361498,728,351 - 98,728,615RGDNCBI36
Celera1479,714,352 - 79,714,616RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,842,197 - 79,842,461UniSTS
REN47782  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,658,840 - 99,659,088UniSTSGRCh37
Build 361498,728,593 - 98,728,841RGDNCBI36
Celera1479,714,594 - 79,714,842RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,842,439 - 79,842,687UniSTS
REN47783  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,659,082 - 99,659,336UniSTSGRCh37
Build 361498,728,835 - 98,729,089RGDNCBI36
Celera1479,714,836 - 79,715,086RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,842,681 - 79,842,931UniSTS
REN47784  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,659,311 - 99,659,540UniSTSGRCh37
Build 361498,729,064 - 98,729,293RGDNCBI36
Celera1479,715,061 - 79,715,290RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,842,906 - 79,843,135UniSTS
REN47785  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,659,516 - 99,659,762UniSTSGRCh37
Build 361498,729,269 - 98,729,515RGDNCBI36
Celera1479,715,266 - 79,715,512RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,843,111 - 79,843,357UniSTS
REN47786  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,659,739 - 99,659,994UniSTSGRCh37
Build 361498,729,492 - 98,729,747RGDNCBI36
Celera1479,715,489 - 79,715,744RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,843,334 - 79,843,589UniSTS
REN47787  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,659,903 - 99,660,159UniSTSGRCh37
Build 361498,729,656 - 98,729,912RGDNCBI36
Celera1479,715,653 - 79,715,909RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,843,498 - 79,843,754UniSTS
REN47788  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,660,154 - 99,660,413UniSTSGRCh37
Build 361498,729,907 - 98,730,166RGDNCBI36
Celera1479,715,904 - 79,716,163RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,843,749 - 79,844,008UniSTS
REN47789  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,660,403 - 99,660,675UniSTSGRCh37
Build 361498,730,156 - 98,730,428RGDNCBI36
Celera1479,716,153 - 79,716,425RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,843,998 - 79,844,270UniSTS
REN47790  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,660,656 - 99,660,898UniSTSGRCh37
Build 361498,730,409 - 98,730,651RGDNCBI36
Celera1479,716,406 - 79,716,648RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,844,251 - 79,844,493UniSTS
REN47791  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,660,856 - 99,661,106UniSTSGRCh37
Build 361498,730,609 - 98,730,859RGDNCBI36
Celera1479,716,606 - 79,716,856RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,844,451 - 79,844,701UniSTS
REN47792  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,661,083 - 99,661,337UniSTSGRCh37
Build 361498,730,836 - 98,731,090RGDNCBI36
Celera1479,716,833 - 79,717,087RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,844,678 - 79,844,932UniSTS
REN47793  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,661,318 - 99,661,567UniSTSGRCh37
Build 361498,731,071 - 98,731,320RGDNCBI36
Celera1479,717,068 - 79,717,317RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,844,913 - 79,845,162UniSTS
REN47794  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,661,526 - 99,661,778UniSTSGRCh37
Build 361498,731,279 - 98,731,531RGDNCBI36
Celera1479,717,276 - 79,717,528RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,845,121 - 79,845,373UniSTS
REN47795  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,661,777 - 99,662,023UniSTSGRCh37
Build 361498,731,530 - 98,731,776RGDNCBI36
Celera1479,717,527 - 79,717,773RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,845,372 - 79,845,618UniSTS
REN47796  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,661,965 - 99,662,225UniSTSGRCh37
Build 361498,731,718 - 98,731,978RGDNCBI36
Celera1479,717,715 - 79,717,975RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,845,560 - 79,845,820UniSTS
REN47797  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,662,204 - 99,662,464UniSTSGRCh37
Build 361498,731,957 - 98,732,217RGDNCBI36
Celera1479,717,954 - 79,718,214RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,845,799 - 79,846,059UniSTS
REN47798  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,662,460 - 99,662,708UniSTSGRCh37
Build 361498,732,213 - 98,732,461RGDNCBI36
Celera1479,718,210 - 79,718,458RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,846,055 - 79,846,303UniSTS
REN47799  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,662,685 - 99,662,950UniSTSGRCh37
Build 361498,732,438 - 98,732,703RGDNCBI36
Celera1479,718,435 - 79,718,699RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,846,280 - 79,846,545UniSTS
REN47800  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,662,929 - 99,663,174UniSTSGRCh37
Build 361498,732,682 - 98,732,927RGDNCBI36
Celera1479,718,678 - 79,718,923RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,846,524 - 79,846,769UniSTS
REN47801  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,663,145 - 99,663,392UniSTSGRCh37
Build 361498,732,898 - 98,733,145RGDNCBI36
Celera1479,718,894 - 79,719,141RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,846,740 - 79,846,987UniSTS
REN47802  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,663,369 - 99,663,611UniSTSGRCh37
Build 361498,733,122 - 98,733,364RGDNCBI36
Celera1479,719,118 - 79,719,360RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,846,964 - 79,847,206UniSTS
REN47803  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,663,605 - 99,663,831UniSTSGRCh37
Build 361498,733,358 - 98,733,584RGDNCBI36
Celera1479,719,354 - 79,719,580RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,847,200 - 79,847,426UniSTS
REN47804  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,663,803 - 99,664,064UniSTSGRCh37
Build 361498,733,556 - 98,733,817RGDNCBI36
Celera1479,719,552 - 79,719,813RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,847,398 - 79,847,659UniSTS
REN47805  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,664,041 - 99,664,287UniSTSGRCh37
Build 361498,733,794 - 98,734,040RGDNCBI36
Celera1479,719,790 - 79,720,036RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,847,636 - 79,847,882UniSTS
REN47806  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,664,270 - 99,664,525UniSTSGRCh37
Build 361498,734,023 - 98,734,278RGDNCBI36
Celera1479,720,019 - 79,720,274RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,847,865 - 79,848,120UniSTS
REN47807  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,664,520 - 99,664,771UniSTSGRCh37
Build 361498,734,273 - 98,734,524RGDNCBI36
Celera1479,720,269 - 79,720,520RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,848,115 - 79,848,366UniSTS
REN47808  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,664,763 - 99,664,990UniSTSGRCh37
Build 361498,734,516 - 98,734,743RGDNCBI36
Celera1479,720,512 - 79,720,739RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,848,358 - 79,848,585UniSTS
REN47809  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,664,983 - 99,665,227UniSTSGRCh37
Build 361498,734,736 - 98,734,980RGDNCBI36
Celera1479,720,732 - 79,720,976RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,848,578 - 79,848,822UniSTS
REN47810  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,665,221 - 99,665,488UniSTSGRCh37
Build 361498,734,974 - 98,735,241RGDNCBI36
Celera1479,720,970 - 79,721,237RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,848,816 - 79,849,083UniSTS
REN47811  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,665,464 - 99,665,720UniSTSGRCh37
Build 361498,735,217 - 98,735,473RGDNCBI36
Celera1479,721,213 - 79,721,469RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,849,059 - 79,849,315UniSTS
REN47812  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,665,715 - 99,665,964UniSTSGRCh37
Build 361498,735,468 - 98,735,717RGDNCBI36
Celera1479,721,464 - 79,721,713RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,849,310 - 79,849,559UniSTS
REN47813  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,665,963 - 99,666,233UniSTSGRCh37
Build 361498,735,716 - 98,735,986RGDNCBI36
Celera1479,721,712 - 79,721,962RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,849,558 - 79,849,794UniSTS
REN47814  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,666,210 - 99,666,439UniSTSGRCh37
Build 361498,735,963 - 98,736,192RGDNCBI36
Celera1479,721,939 - 79,722,168RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,849,771 - 79,850,000UniSTS
REN47815  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,666,418 - 99,666,681UniSTSGRCh37
Build 361498,736,171 - 98,736,434RGDNCBI36
Celera1479,722,147 - 79,722,410RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,849,979 - 79,850,242UniSTS
REN47816  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,666,668 - 99,666,901UniSTSGRCh37
Build 361498,736,421 - 98,736,654RGDNCBI36
Celera1479,722,397 - 79,722,630RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,850,229 - 79,850,462UniSTS
REN47817  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,666,871 - 99,667,121UniSTSGRCh37
Build 361498,736,624 - 98,736,874RGDNCBI36
Celera1479,722,600 - 79,722,850RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,850,432 - 79,850,682UniSTS
REN47818  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,667,117 - 99,667,362UniSTSGRCh37
Build 361498,736,870 - 98,737,115RGDNCBI36
Celera1479,722,846 - 79,723,091RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,850,678 - 79,850,923UniSTS
REN47819  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,667,341 - 99,667,584UniSTSGRCh37
Build 361498,737,094 - 98,737,337RGDNCBI36
Celera1479,723,070 - 79,723,313RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,850,902 - 79,851,145UniSTS
REN47820  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,667,561 - 99,667,817UniSTSGRCh37
Build 361498,737,314 - 98,737,570RGDNCBI36
Celera1479,723,290 - 79,723,546RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,851,122 - 79,851,378UniSTS
REN47821  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,667,773 - 99,668,034UniSTSGRCh37
Build 361498,737,526 - 98,737,787RGDNCBI36
Celera1479,723,502 - 79,723,763RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,851,334 - 79,851,595UniSTS
REN47822  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,668,022 - 99,668,263UniSTSGRCh37
Build 361498,737,775 - 98,738,016RGDNCBI36
Celera1479,723,751 - 79,723,992RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,851,583 - 79,851,824UniSTS
REN47823  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,668,161 - 99,668,393UniSTSGRCh37
Build 361498,737,914 - 98,738,146RGDNCBI36
Celera1479,723,890 - 79,724,122RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,851,722 - 79,851,954UniSTS
REN47824  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,668,278 - 99,668,538UniSTSGRCh37
Build 361498,738,031 - 98,738,291RGDNCBI36
Celera1479,724,007 - 79,724,267RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,851,839 - 79,852,099UniSTS
REN47825  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,668,457 - 99,668,698UniSTSGRCh37
Build 361498,738,210 - 98,738,451RGDNCBI36
Celera1479,724,186 - 79,724,427RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,852,018 - 79,852,259UniSTS
REN47826  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,668,682 - 99,668,932UniSTSGRCh37
Build 361498,738,435 - 98,738,685RGDNCBI36
Celera1479,724,411 - 79,724,661RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,852,243 - 79,852,493UniSTS
REN47827  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,668,924 - 99,669,189UniSTSGRCh37
Build 361498,738,677 - 98,738,942RGDNCBI36
Celera1479,724,653 - 79,724,918RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,852,485 - 79,852,750UniSTS
REN47828  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,669,187 - 99,669,434UniSTSGRCh37
Build 361498,738,940 - 98,739,187RGDNCBI36
Celera1479,724,916 - 79,725,163RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,852,748 - 79,852,995UniSTS
REN47829  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,669,432 - 99,669,701UniSTSGRCh37
Build 361498,739,185 - 98,739,454RGDNCBI36
Celera1479,725,161 - 79,725,430RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,852,993 - 79,853,262UniSTS
REN47830  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,669,697 - 99,669,962UniSTSGRCh37
Build 361498,739,450 - 98,739,715RGDNCBI36
Celera1479,725,426 - 79,725,691RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,853,258 - 79,853,523UniSTS
REN47831  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,669,941 - 99,670,165UniSTSGRCh37
Build 361498,739,694 - 98,739,918RGDNCBI36
Celera1479,725,670 - 79,725,894RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,853,502 - 79,853,726UniSTS
REN47832  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,670,133 - 99,670,367UniSTSGRCh37
Build 361498,739,886 - 98,740,120RGDNCBI36
Celera1479,725,862 - 79,726,096RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,853,694 - 79,853,928UniSTS
REN47833  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,670,342 - 99,670,613UniSTSGRCh37
Build 361498,740,095 - 98,740,366RGDNCBI36
Celera1479,726,071 - 79,726,342RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,853,903 - 79,854,174UniSTS
REN47834  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,670,594 - 99,670,860UniSTSGRCh37
Build 361498,740,347 - 98,740,613RGDNCBI36
Celera1479,726,323 - 79,726,589RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,854,155 - 79,854,421UniSTS
REN47835  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,670,837 - 99,671,079UniSTSGRCh37
Build 361498,740,590 - 98,740,832RGDNCBI36
Celera1479,726,566 - 79,726,808RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,854,398 - 79,854,640UniSTS
REN47836  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,671,076 - 99,671,322UniSTSGRCh37
Build 361498,740,829 - 98,741,075RGDNCBI36
Celera1479,726,805 - 79,727,051RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,854,637 - 79,854,883UniSTS
REN47837  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,671,299 - 99,671,564UniSTSGRCh37
Build 361498,741,052 - 98,741,317RGDNCBI36
Celera1479,727,028 - 79,727,293RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,854,860 - 79,855,125UniSTS
REN47838  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,671,551 - 99,671,790UniSTSGRCh37
Build 361498,741,304 - 98,741,543RGDNCBI36
Celera1479,727,280 - 79,727,519RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,855,112 - 79,855,351UniSTS
REN47839  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,671,767 - 99,672,017UniSTSGRCh37
Build 361498,741,520 - 98,741,770RGDNCBI36
Celera1479,727,496 - 79,727,746RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,855,328 - 79,855,578UniSTS
REN47840  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,671,994 - 99,672,233UniSTSGRCh37
Build 361498,741,747 - 98,741,986RGDNCBI36
Celera1479,727,723 - 79,727,962RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,855,555 - 79,855,794UniSTS
REN47841  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,672,228 - 99,672,476UniSTSGRCh37
Build 361498,741,981 - 98,742,229RGDNCBI36
Celera1479,727,957 - 79,728,205RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,855,789 - 79,856,037UniSTS
REN47842  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,672,458 - 99,672,701UniSTSGRCh37
Build 361498,742,211 - 98,742,454RGDNCBI36
Celera1479,728,187 - 79,728,430RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,856,019 - 79,856,262UniSTS
REN47843  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,672,692 - 99,672,947UniSTSGRCh37
Build 361498,742,445 - 98,742,700RGDNCBI36
Celera1479,728,421 - 79,728,676RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,856,253 - 79,856,508UniSTS
REN47844  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,672,924 - 99,673,167UniSTSGRCh37
Build 361498,742,677 - 98,742,920RGDNCBI36
Celera1479,728,653 - 79,728,896RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,856,485 - 79,856,728UniSTS
REN47845  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,673,144 - 99,673,412UniSTSGRCh37
Build 361498,742,897 - 98,743,165RGDNCBI36
Celera1479,728,873 - 79,729,141RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,856,705 - 79,856,973UniSTS
REN47846  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,673,388 - 99,673,634UniSTSGRCh37
Build 361498,743,141 - 98,743,387RGDNCBI36
Celera1479,729,117 - 79,729,363RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,856,949 - 79,857,195UniSTS
REN47847  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,673,608 - 99,673,873UniSTSGRCh37
Build 361498,743,361 - 98,743,626RGDNCBI36
Celera1479,729,337 - 79,729,602RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,857,169 - 79,857,434UniSTS
REN47848  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,673,850 - 99,674,102UniSTSGRCh37
Build 361498,743,603 - 98,743,855RGDNCBI36
Celera1479,729,579 - 79,729,831RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,857,411 - 79,857,663UniSTS
REN47849  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,674,031 - 99,674,285UniSTSGRCh37
Build 361498,743,784 - 98,744,038RGDNCBI36
Celera1479,729,760 - 79,730,014RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,857,592 - 79,857,846UniSTS
REN47850  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,674,266 - 99,674,493UniSTSGRCh37
Build 361498,744,019 - 98,744,246RGDNCBI36
Celera1479,729,995 - 79,730,222RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,857,827 - 79,858,054UniSTS
REN47851  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,674,470 - 99,674,704UniSTSGRCh37
Build 361498,744,223 - 98,744,457RGDNCBI36
Celera1479,730,199 - 79,730,433RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,858,031 - 79,858,265UniSTS
REN47852  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,674,691 - 99,674,937UniSTSGRCh37
Build 361498,744,444 - 98,744,690RGDNCBI36
Celera1479,730,420 - 79,730,666RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,858,252 - 79,858,498UniSTS
REN47853  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,674,913 - 99,675,137UniSTSGRCh37
Build 361498,744,666 - 98,744,890RGDNCBI36
Celera1479,730,642 - 79,730,866RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,858,474 - 79,858,698UniSTS
REN47854  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,675,108 - 99,675,366UniSTSGRCh37
Build 361498,744,861 - 98,745,119RGDNCBI36
Celera1479,730,837 - 79,731,095RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,858,669 - 79,858,927UniSTS
REN47855  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,675,343 - 99,675,575UniSTSGRCh37
Build 361498,745,096 - 98,745,328RGDNCBI36
Celera1479,731,072 - 79,731,304RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,858,904 - 79,859,136UniSTS
REN47856  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,675,552 - 99,675,807UniSTSGRCh37
Build 361498,745,305 - 98,745,560RGDNCBI36
Celera1479,731,281 - 79,731,536RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,859,113 - 79,859,368UniSTS
REN47857  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,675,755 - 99,676,019UniSTSGRCh37
Build 361498,745,508 - 98,745,772RGDNCBI36
Celera1479,731,484 - 79,731,748RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,859,316 - 79,859,580UniSTS
REN47858  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,675,994 - 99,676,242UniSTSGRCh37
Build 361498,745,747 - 98,745,995RGDNCBI36
Celera1479,731,723 - 79,731,971RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,859,555 - 79,859,803UniSTS
REN47859  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,676,221 - 99,676,462UniSTSGRCh37
Build 361498,745,974 - 98,746,215RGDNCBI36
Celera1479,731,950 - 79,732,191RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,859,782 - 79,860,023UniSTS
REN47860  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,676,440 - 99,676,665UniSTSGRCh37
Build 361498,746,193 - 98,746,418RGDNCBI36
Celera1479,732,169 - 79,732,394RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,860,001 - 79,860,226UniSTS
REN47861  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,676,639 - 99,676,901UniSTSGRCh37
Build 361498,746,392 - 98,746,654RGDNCBI36
Celera1479,732,368 - 79,732,630RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,860,200 - 79,860,462UniSTS
REN47862  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,676,879 - 99,677,124UniSTSGRCh37
Build 361498,746,632 - 98,746,877RGDNCBI36
Celera1479,732,608 - 79,732,853RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,860,440 - 79,860,685UniSTS
REN47863  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,677,103 - 99,677,357UniSTSGRCh37
Build 361498,746,856 - 98,747,110RGDNCBI36
Celera1479,732,832 - 79,733,086RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,860,664 - 79,860,918UniSTS
REN47864  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,677,322 - 99,677,586UniSTSGRCh37
GRCh371499,677,273 - 99,677,586UniSTSGRCh37
Build 361498,747,026 - 98,747,339RGDNCBI36
Celera1479,733,002 - 79,733,315RGD
Celera1479,733,051 - 79,733,315UniSTS
Cytogenetic Map14q32.2UniSTS
HuRef1479,860,834 - 79,861,147UniSTS
HuRef1479,860,883 - 79,861,147UniSTS
REN47865  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,677,581 - 99,677,826UniSTSGRCh37
Build 361498,747,334 - 98,747,579RGDNCBI36
Celera1479,733,310 - 79,733,555RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,861,142 - 79,861,387UniSTS
REN47866  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,677,798 - 99,678,061UniSTSGRCh37
Build 361498,747,551 - 98,747,814RGDNCBI36
Celera1479,733,527 - 79,733,790RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,861,359 - 79,861,622UniSTS
REN47867  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,678,038 - 99,678,292UniSTSGRCh37
Build 361498,747,791 - 98,748,045RGDNCBI36
Celera1479,733,767 - 79,734,021RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,861,599 - 79,861,853UniSTS
REN47868  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,678,278 - 99,678,507UniSTSGRCh37
Build 361498,748,031 - 98,748,260RGDNCBI36
Celera1479,734,007 - 79,734,236RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,861,839 - 79,862,068UniSTS
REN47869  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,678,473 - 99,678,724UniSTSGRCh37
Build 361498,748,226 - 98,748,477RGDNCBI36
Celera1479,734,202 - 79,734,453RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,862,034 - 79,862,282UniSTS
REN47870  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,678,713 - 99,678,963UniSTSGRCh37
Build 361498,748,466 - 98,748,716RGDNCBI36
Celera1479,734,442 - 79,734,692RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,862,271 - 79,862,521UniSTS
REN47871  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,678,934 - 99,679,179UniSTSGRCh37
Build 361498,748,687 - 98,748,932RGDNCBI36
Celera1479,734,663 - 79,734,908RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,862,492 - 79,862,737UniSTS
REN47872  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,679,157 - 99,679,414UniSTSGRCh37
Build 361498,748,910 - 98,749,167RGDNCBI36
Celera1479,734,886 - 79,735,143RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,862,715 - 79,862,972UniSTS
REN47873  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,679,354 - 99,679,619UniSTSGRCh37
Build 361498,749,107 - 98,749,372RGDNCBI36
Celera1479,735,083 - 79,735,348RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,862,912 - 79,863,177UniSTS
REN47874  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,679,597 - 99,679,854UniSTSGRCh37
Build 361498,749,350 - 98,749,607RGDNCBI36
Celera1479,735,326 - 79,735,583RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,863,155 - 79,863,412UniSTS
REN47875  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,679,850 - 99,680,100UniSTSGRCh37
Build 361498,749,603 - 98,749,853RGDNCBI36
Celera1479,735,579 - 79,735,829RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,863,408 - 79,863,658UniSTS
REN47876  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,680,081 - 99,680,323UniSTSGRCh37
Build 361498,749,834 - 98,750,076RGDNCBI36
Celera1479,735,810 - 79,736,052RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,863,639 - 79,863,881UniSTS
REN47877  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,680,292 - 99,680,519UniSTSGRCh37
Build 361498,750,045 - 98,750,272RGDNCBI36
Celera1479,736,021 - 79,736,248RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,863,850 - 79,864,077UniSTS
REN47878  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,680,487 - 99,680,712UniSTSGRCh37
Build 361498,750,240 - 98,750,465RGDNCBI36
Celera1479,736,216 - 79,736,441RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,864,045 - 79,864,270UniSTS
REN47879  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,680,962 - 99,681,210UniSTSGRCh37
Build 361498,750,715 - 98,750,963RGDNCBI36
Celera1479,736,691 - 79,736,939RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,864,520 - 79,864,768UniSTS
REN47880  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,681,200 - 99,681,434UniSTSGRCh37
Build 361498,750,953 - 98,751,187RGDNCBI36
Celera1479,736,929 - 79,737,163RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,864,758 - 79,864,992UniSTS
REN47881  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,681,413 - 99,681,660UniSTSGRCh37
Build 361498,751,166 - 98,751,413RGDNCBI36
Celera1479,737,142 - 79,737,389RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,864,971 - 79,865,218UniSTS
REN47882  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,681,634 - 99,681,874UniSTSGRCh37
Build 361498,751,387 - 98,751,627RGDNCBI36
Celera1479,737,363 - 79,737,603RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,865,192 - 79,865,432UniSTS
REN47883  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,681,851 - 99,682,075UniSTSGRCh37
Build 361498,751,604 - 98,751,828RGDNCBI36
Celera1479,737,580 - 79,737,804RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,865,409 - 79,865,633UniSTS
REN47884  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,682,054 - 99,682,295UniSTSGRCh37
Build 361498,751,807 - 98,752,048RGDNCBI36
Celera1479,737,783 - 79,738,024RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,865,612 - 79,865,853UniSTS
REN47885  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,682,290 - 99,682,526UniSTSGRCh37
Build 361498,752,043 - 98,752,279RGDNCBI36
Celera1479,738,019 - 79,738,255RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,865,848 - 79,866,084UniSTS
REN47886  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,682,503 - 99,682,764UniSTSGRCh37
Build 361498,752,256 - 98,752,517RGDNCBI36
Celera1479,738,232 - 79,738,493RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,866,061 - 79,866,322UniSTS
REN47887  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,682,737 - 99,683,000UniSTSGRCh37
Build 361498,752,490 - 98,752,753RGDNCBI36
Celera1479,738,466 - 79,738,729RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,866,295 - 79,866,558UniSTS
REN47888  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,682,940 - 99,683,201UniSTSGRCh37
Build 361498,752,693 - 98,752,954RGDNCBI36
Celera1479,738,669 - 79,738,930RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,866,498 - 79,866,759UniSTS
REN47889  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,683,156 - 99,683,418UniSTSGRCh37
Build 361498,752,909 - 98,753,171RGDNCBI36
Celera1479,738,885 - 79,739,147RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,866,714 - 79,866,978UniSTS
REN47890  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,683,215 - 99,683,453UniSTSGRCh37
Build 361498,752,968 - 98,753,206RGDNCBI36
Celera1479,738,944 - 79,739,182RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,866,773 - 79,867,013UniSTS
REN47891  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,683,534 - 99,683,768UniSTSGRCh37
Build 361498,753,287 - 98,753,521RGDNCBI36
Celera1479,739,263 - 79,739,509RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,867,094 - 79,867,336UniSTS
REN47892  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,683,744 - 99,684,001UniSTSGRCh37
Build 361498,753,497 - 98,753,754RGDNCBI36
Celera1479,739,485 - 79,739,742RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,867,312 - 79,867,569UniSTS
REN47893  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,683,978 - 99,684,234UniSTSGRCh37
Build 361498,753,731 - 98,753,987RGDNCBI36
Celera1479,739,719 - 79,739,975RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,867,546 - 79,867,802UniSTS
REN47894  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,684,157 - 99,684,382UniSTSGRCh37
Build 361498,753,910 - 98,754,135RGDNCBI36
Celera1479,739,898 - 79,740,123RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,867,725 - 79,867,950UniSTS
REN47895  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,684,740 - 99,684,970UniSTSGRCh37
Build 361498,754,493 - 98,754,723RGDNCBI36
Celera1479,740,481 - 79,740,711RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,868,308 - 79,868,538UniSTS
REN47896  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,684,967 - 99,685,203UniSTSGRCh37
Build 361498,754,720 - 98,754,956RGDNCBI36
Celera1479,740,708 - 79,740,944RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,868,535 - 79,868,771UniSTS
REN47897  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,685,121 - 99,685,346UniSTSGRCh37
Build 361498,754,874 - 98,755,099RGDNCBI36
Celera1479,740,862 - 79,741,087RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,868,689 - 79,868,914UniSTS
REN47898  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,685,313 - 99,685,548UniSTSGRCh37
Build 361498,755,066 - 98,755,301RGDNCBI36
Celera1479,741,054 - 79,741,288RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,868,881 - 79,869,115UniSTS
REN47899  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,685,517 - 99,685,770UniSTSGRCh37
Build 361498,755,270 - 98,755,523RGDNCBI36
Celera1479,741,257 - 79,741,510RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,869,084 - 79,869,337UniSTS
REN47900  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,685,747 - 99,685,984UniSTSGRCh37
Build 361498,755,500 - 98,755,737RGDNCBI36
Celera1479,741,487 - 79,741,724RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,869,314 - 79,869,551UniSTS
REN47901  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,685,956 - 99,686,196UniSTSGRCh37
Build 361498,755,709 - 98,755,949RGDNCBI36
Celera1479,741,696 - 79,741,936RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,869,523 - 79,869,763UniSTS
REN47902  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,686,166 - 99,686,414UniSTSGRCh37
Build 361498,755,919 - 98,756,167RGDNCBI36
Celera1479,741,906 - 79,742,154RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,869,733 - 79,869,981UniSTS
REN47903  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,686,391 - 99,686,639UniSTSGRCh37
Build 361498,756,144 - 98,756,392RGDNCBI36
Celera1479,742,131 - 79,742,379RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,869,958 - 79,870,206UniSTS
REN47904  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,686,634 - 99,686,898UniSTSGRCh37
Build 361498,756,387 - 98,756,651RGDNCBI36
Celera1479,742,374 - 79,742,638RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,870,201 - 79,870,465UniSTS
REN47905  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,686,878 - 99,687,130UniSTSGRCh37
Build 361498,756,631 - 98,756,883RGDNCBI36
Celera1479,742,618 - 79,742,870RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,870,445 - 79,870,697UniSTS
REN47906  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,686,929 - 99,687,173UniSTSGRCh37
Build 361498,756,682 - 98,756,926RGDNCBI36
Celera1479,742,669 - 79,742,913RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,870,496 - 79,870,740UniSTS
REN47907  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,687,485 - 99,687,709UniSTSGRCh37
Build 361498,757,238 - 98,757,462RGDNCBI36
Celera1479,743,225 - 79,743,449RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,871,052 - 79,871,276UniSTS
REN47908  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,687,676 - 99,687,900UniSTSGRCh37
Build 361498,757,429 - 98,757,653RGDNCBI36
Celera1479,743,416 - 79,743,640RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,871,243 - 79,871,467UniSTS
REN47909  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,687,873 - 99,688,105UniSTSGRCh37
Build 361498,757,626 - 98,757,858RGDNCBI36
Celera1479,743,613 - 79,743,845RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,871,440 - 79,871,672UniSTS
REN47910  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,688,086 - 99,688,315UniSTSGRCh37
Build 361498,757,839 - 98,758,068RGDNCBI36
Celera1479,743,826 - 79,744,055RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,871,653 - 79,871,882UniSTS
REN47911  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,688,273 - 99,688,524UniSTSGRCh37
Build 361498,758,026 - 98,758,277RGDNCBI36
Celera1479,744,013 - 79,744,264RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,871,840 - 79,872,091UniSTS
REN47912  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,688,501 - 99,688,735UniSTSGRCh37
Build 361498,758,254 - 98,758,488RGDNCBI36
Celera1479,744,241 - 79,744,474RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,872,068 - 79,872,301UniSTS
REN47913  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,688,704 - 99,688,949UniSTSGRCh37
Build 361498,758,457 - 98,758,702RGDNCBI36
Celera1479,744,443 - 79,744,688RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,872,270 - 79,872,515UniSTS
REN47914  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,688,921 - 99,689,166UniSTSGRCh37
Build 361498,758,674 - 98,758,919RGDNCBI36
Celera1479,744,660 - 79,744,905RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,872,487 - 79,872,732UniSTS
REN47915  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,689,143 - 99,689,411UniSTSGRCh37
Build 361498,758,896 - 98,759,164RGDNCBI36
Celera1479,744,882 - 79,745,150RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,872,709 - 79,872,977UniSTS
REN47916  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,689,385 - 99,689,639UniSTSGRCh37
Build 361498,759,138 - 98,759,392RGDNCBI36
Celera1479,745,124 - 79,745,378RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,872,951 - 79,873,205UniSTS
REN47917  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,689,617 - 99,689,879UniSTSGRCh37
Build 361498,759,370 - 98,759,632RGDNCBI36
Celera1479,745,356 - 79,745,618RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,873,183 - 79,873,445UniSTS
REN47918  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,689,854 - 99,690,107UniSTSGRCh37
Build 361498,759,607 - 98,759,860RGDNCBI36
Celera1479,745,593 - 79,745,846RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,873,420 - 79,873,673UniSTS
REN47919  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,690,083 - 99,690,318UniSTSGRCh37
Build 361498,759,836 - 98,760,071RGDNCBI36
Celera1479,745,822 - 79,746,057RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,873,649 - 79,873,884UniSTS
REN47920  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,690,290 - 99,690,523UniSTSGRCh37
Build 361498,760,043 - 98,760,276RGDNCBI36
Celera1479,746,029 - 79,746,262RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,873,856 - 79,874,089UniSTS
REN47921  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,690,496 - 99,690,745UniSTSGRCh37
Build 361498,760,249 - 98,760,498RGDNCBI36
Celera1479,746,235 - 79,746,484RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,874,062 - 79,874,311UniSTS
REN47922  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,690,715 - 99,690,942UniSTSGRCh37
Build 361498,760,468 - 98,760,695RGDNCBI36
Celera1479,746,454 - 79,746,681RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,874,281 - 79,874,508UniSTS
REN47923  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,690,921 - 99,691,154UniSTSGRCh37
Build 361498,760,674 - 98,760,907RGDNCBI36
Celera1479,746,660 - 79,746,893RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,874,487 - 79,874,720UniSTS
REN47924  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,691,141 - 99,691,403UniSTSGRCh37
Build 361498,760,894 - 98,761,156RGDNCBI36
Celera1479,746,880 - 79,747,142RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,874,707 - 79,874,969UniSTS
REN47925  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,691,396 - 99,691,646UniSTSGRCh37
Build 361498,761,149 - 98,761,399RGDNCBI36
Celera1479,747,135 - 79,747,385RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,874,962 - 79,875,212UniSTS
REN47926  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,691,644 - 99,691,868UniSTSGRCh37
Build 361498,761,397 - 98,761,621RGDNCBI36
Celera1479,747,383 - 79,747,607RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,875,210 - 79,875,434UniSTS
REN47927  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,691,837 - 99,692,105UniSTSGRCh37
Build 361498,761,590 - 98,761,858RGDNCBI36
Celera1479,747,576 - 79,747,844RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,875,403 - 79,875,671UniSTS
REN47928  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,692,082 - 99,692,326UniSTSGRCh37
Build 361498,761,835 - 98,762,079RGDNCBI36
Celera1479,747,821 - 79,748,065RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,875,648 - 79,875,892UniSTS
REN47929  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,692,291 - 99,692,532UniSTSGRCh37
Build 361498,762,044 - 98,762,285RGDNCBI36
Celera1479,748,030 - 79,748,271RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,875,857 - 79,876,098UniSTS
REN47930  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,692,520 - 99,692,752UniSTSGRCh37
Build 361498,762,273 - 98,762,505RGDNCBI36
Celera1479,748,259 - 79,748,491RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,876,086 - 79,876,318UniSTS
REN47931  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,692,733 - 99,692,979UniSTSGRCh37
Build 361498,762,486 - 98,762,732RGDNCBI36
Celera1479,748,472 - 79,748,718RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,876,299 - 79,876,545UniSTS
REN47932  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,692,929 - 99,693,188UniSTSGRCh37
Build 361498,762,682 - 98,762,941RGDNCBI36
Celera1479,748,668 - 79,748,927RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,876,495 - 79,876,754UniSTS
REN47933  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,693,186 - 99,693,434UniSTSGRCh37
Build 361498,762,939 - 98,763,187RGDNCBI36
Celera1479,748,925 - 79,749,173RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,876,752 - 79,877,000UniSTS
REN47934  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,693,399 - 99,693,642UniSTSGRCh37
Build 361498,763,152 - 98,763,395RGDNCBI36
Celera1479,749,138 - 79,749,381RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,876,965 - 79,877,208UniSTS
REN47935  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,693,629 - 99,693,891UniSTSGRCh37
Build 361498,763,382 - 98,763,644RGDNCBI36
Celera1479,749,368 - 79,749,630RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,877,195 - 79,877,457UniSTS
REN47936  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,693,875 - 99,694,126UniSTSGRCh37
Build 361498,763,628 - 98,763,879RGDNCBI36
Celera1479,749,614 - 79,749,865RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,877,441 - 79,877,692UniSTS
REN47937  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,694,052 - 99,694,293UniSTSGRCh37
Build 361498,763,805 - 98,764,046RGDNCBI36
Celera1479,749,791 - 79,750,032RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,877,618 - 79,877,859UniSTS
REN47938  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,694,273 - 99,694,531UniSTSGRCh37
Build 361498,764,026 - 98,764,284RGDNCBI36
Celera1479,750,012 - 79,750,270RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,877,839 - 79,878,097UniSTS
REN47939  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,694,472 - 99,694,731UniSTSGRCh37
Build 361498,764,225 - 98,764,484RGDNCBI36
Celera1479,750,211 - 79,750,470RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,878,038 - 79,878,297UniSTS
REN47940  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,694,713 - 99,694,959UniSTSGRCh37
Build 361498,764,466 - 98,764,712RGDNCBI36
Celera1479,750,452 - 79,750,698RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,878,279 - 79,878,525UniSTS
REN47941  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,694,920 - 99,695,156UniSTSGRCh37
Build 361498,764,673 - 98,764,909RGDNCBI36
Celera1479,750,659 - 79,750,895RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,878,486 - 79,878,722UniSTS
REN47942  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,695,098 - 99,695,350UniSTSGRCh37
Build 361498,764,851 - 98,765,103RGDNCBI36
Celera1479,750,837 - 79,751,089RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,878,664 - 79,878,916UniSTS
REN47943  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,695,324 - 99,695,591UniSTSGRCh37
Build 361498,765,077 - 98,765,344RGDNCBI36
Celera1479,751,063 - 79,751,286RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,878,890 - 79,879,157UniSTS
REN47944  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,695,580 - 99,695,825UniSTSGRCh37
Build 361498,765,333 - 98,765,578RGDNCBI36
Celera1479,751,275 - 79,751,516RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,879,146 - 79,879,391UniSTS
REN47945  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,695,803 - 99,696,056UniSTSGRCh37
Build 361498,765,556 - 98,765,809RGDNCBI36
Celera1479,751,494 - 79,751,747RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,879,369 - 79,879,622UniSTS
REN47946  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,696,028 - 99,696,258UniSTSGRCh37
Build 361498,765,781 - 98,766,011RGDNCBI36
Celera1479,751,719 - 79,751,949RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,879,594 - 79,879,824UniSTS
REN47947  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,696,254 - 99,696,490UniSTSGRCh37
Build 361498,766,007 - 98,766,243RGDNCBI36
Celera1479,751,945 - 79,752,181RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,879,820 - 79,880,056UniSTS
REN47948  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,696,480 - 99,696,706UniSTSGRCh37
Build 361498,766,233 - 98,766,459RGDNCBI36
Celera1479,752,171 - 79,752,397RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,880,046 - 79,880,272UniSTS
REN47949  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,696,696 - 99,696,944UniSTSGRCh37
Build 361498,766,449 - 98,766,697RGDNCBI36
Celera1479,752,387 - 79,752,635RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,880,262 - 79,880,510UniSTS
REN47950  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,696,932 - 99,697,156UniSTSGRCh37
Build 361498,766,685 - 98,766,909RGDNCBI36
Celera1479,752,623 - 79,752,847RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,880,498 - 79,880,722UniSTS
REN47951  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,697,134 - 99,697,403UniSTSGRCh37
Build 361498,766,887 - 98,767,156RGDNCBI36
Celera1479,752,825 - 79,753,094RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,880,700 - 79,880,969UniSTS
REN47952  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,697,284 - 99,697,550UniSTSGRCh37
Build 361498,767,037 - 98,767,303RGDNCBI36
Celera1479,752,975 - 79,753,241RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,880,850 - 79,881,116UniSTS
REN47953  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,697,527 - 99,697,751UniSTSGRCh37
Build 361498,767,280 - 98,767,504RGDNCBI36
Celera1479,753,218 - 79,753,442RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,881,093 - 79,881,317UniSTS
REN47954  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,697,717 - 99,697,953UniSTSGRCh37
Build 361498,767,470 - 98,767,706RGDNCBI36
Celera1479,753,408 - 79,753,644RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,881,283 - 79,881,519UniSTS
REN47955  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,697,838 - 99,698,069UniSTSGRCh37
Build 361498,767,591 - 98,767,822RGDNCBI36
Celera1479,753,529 - 79,753,760RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,881,404 - 79,881,635UniSTS
REN47956  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,698,039 - 99,698,281UniSTSGRCh37
Build 361498,767,792 - 98,768,034RGDNCBI36
Celera1479,753,730 - 79,753,972RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,881,605 - 79,881,847UniSTS
REN47957  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,698,249 - 99,698,510UniSTSGRCh37
Build 361498,768,002 - 98,768,263RGDNCBI36
Celera1479,753,940 - 79,754,201RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,881,815 - 79,882,076UniSTS
REN47958  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,698,491 - 99,698,729UniSTSGRCh37
Build 361498,768,244 - 98,768,482RGDNCBI36
Celera1479,754,182 - 79,754,420RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,882,057 - 79,882,295UniSTS
REN47959  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,698,603 - 99,698,847UniSTSGRCh37
Build 361498,768,356 - 98,768,600RGDNCBI36
Celera1479,754,294 - 79,754,538RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,882,169 - 79,882,413UniSTS
REN47960  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,698,824 - 99,699,068UniSTSGRCh37
Build 361498,768,577 - 98,768,821RGDNCBI36
Celera1479,754,515 - 79,754,759RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,882,390 - 79,882,634UniSTS
REN47961  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,699,045 - 99,699,289UniSTSGRCh37
Build 361498,768,798 - 98,769,042RGDNCBI36
Celera1479,754,736 - 79,754,980RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,882,611 - 79,882,855UniSTS
REN47962  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,699,266 - 99,699,512UniSTSGRCh37
Build 361498,769,019 - 98,769,265RGDNCBI36
Celera1479,754,957 - 79,755,203RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,882,832 - 79,883,078UniSTS
REN47963  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,699,491 - 99,699,726UniSTSGRCh37
Build 361498,769,244 - 98,769,479RGDNCBI36
Celera1479,755,182 - 79,755,417RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,883,057 - 79,883,292UniSTS
REN47964  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,699,723 - 99,699,980UniSTSGRCh37
Build 361498,769,476 - 98,769,733RGDNCBI36
Celera1479,755,414 - 79,755,671RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,883,289 - 79,883,546UniSTS
REN47965  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,699,972 - 99,700,196UniSTSGRCh37
Build 361498,769,725 - 98,769,949RGDNCBI36
Celera1479,755,663 - 79,755,887RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,883,538 - 79,883,762UniSTS
REN47966  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,700,160 - 99,700,409UniSTSGRCh37
Build 361498,769,913 - 98,770,162RGDNCBI36
Celera1479,755,851 - 79,756,100RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,883,726 - 79,883,975UniSTS
REN47967  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,700,386 - 99,700,624UniSTSGRCh37
Build 361498,770,139 - 98,770,377RGDNCBI36
Celera1479,756,077 - 79,756,315RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,883,952 - 79,884,190UniSTS
REN47968  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,700,589 - 99,700,838UniSTSGRCh37
Build 361498,770,342 - 98,770,591RGDNCBI36
Celera1479,756,280 - 79,756,529RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,884,155 - 79,884,404UniSTS
REN47969  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,700,795 - 99,701,046UniSTSGRCh37
Build 361498,770,548 - 98,770,799RGDNCBI36
Celera1479,756,486 - 79,756,737RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,884,361 - 79,884,612UniSTS
REN47970  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,701,022 - 99,701,282UniSTSGRCh37
Build 361498,770,775 - 98,771,035RGDNCBI36
Celera1479,756,713 - 79,756,973RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,884,588 - 79,884,848UniSTS
REN47971  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,701,229 - 99,701,453UniSTSGRCh37
Build 361498,770,982 - 98,771,206RGDNCBI36
Celera1479,756,920 - 79,757,144RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,884,795 - 79,885,019UniSTS
REN47972  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,701,417 - 99,701,660UniSTSGRCh37
Build 361498,771,170 - 98,771,413RGDNCBI36
Celera1479,757,108 - 79,757,351RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,884,983 - 79,885,226UniSTS
REN47973  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,701,604 - 99,701,861UniSTSGRCh37
Build 361498,771,357 - 98,771,614RGDNCBI36
Celera1479,757,295 - 79,757,552RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,885,170 - 79,885,427UniSTS
REN47974  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,701,761 - 99,702,010UniSTSGRCh37
Build 361498,771,514 - 98,771,763RGDNCBI36
Celera1479,757,452 - 79,757,701RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,885,327 - 79,885,576UniSTS
REN47975  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,701,985 - 99,702,224UniSTSGRCh37
Build 361498,771,738 - 98,771,977RGDNCBI36
Celera1479,757,676 - 79,757,915RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,885,551 - 79,885,790UniSTS
REN47976  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,702,193 - 99,702,465UniSTSGRCh37
Build 361498,771,946 - 98,772,218RGDNCBI36
Celera1479,757,884 - 79,758,155RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,885,759 - 79,886,030UniSTS
REN47977  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,702,454 - 99,702,709UniSTSGRCh37
Build 361498,772,207 - 98,772,462RGDNCBI36
Celera1479,758,144 - 79,758,399RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,886,019 - 79,886,274UniSTS
REN47978  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,702,698 - 99,702,940UniSTSGRCh37
Build 361498,772,451 - 98,772,693RGDNCBI36
Celera1479,758,388 - 79,758,630RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,886,263 - 79,886,505UniSTS
REN47979  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,702,930 - 99,703,179UniSTSGRCh37
Build 361498,772,683 - 98,772,932RGDNCBI36
Celera1479,758,620 - 79,758,869RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,886,495 - 79,886,744UniSTS
REN47980  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,703,147 - 99,703,391UniSTSGRCh37
Build 361498,772,900 - 98,773,144RGDNCBI36
Celera1479,758,837 - 79,759,081RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,886,712 - 79,886,956UniSTS
REN47981  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,703,354 - 99,703,620UniSTSGRCh37
Build 361498,773,107 - 98,773,373RGDNCBI36
Celera1479,759,044 - 79,759,310RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,886,919 - 79,887,185UniSTS
REN47982  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,703,597 - 99,703,842UniSTSGRCh37
Build 361498,773,350 - 98,773,595RGDNCBI36
Celera1479,759,287 - 79,759,532RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,887,162 - 79,887,407UniSTS
REN47983  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,703,798 - 99,704,040UniSTSGRCh37
Build 361498,773,551 - 98,773,793RGDNCBI36
Celera1479,759,488 - 79,759,730RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,887,363 - 79,887,605UniSTS
REN47984  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,704,012 - 99,704,260UniSTSGRCh37
Build 361498,773,765 - 98,774,013RGDNCBI36
Celera1479,759,702 - 79,759,950RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,887,577 - 79,887,825UniSTS
REN47985  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,704,230 - 99,704,480UniSTSGRCh37
Build 361498,773,983 - 98,774,233RGDNCBI36
Celera1479,759,920 - 79,760,170RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,887,795 - 79,888,045UniSTS
REN47986  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,704,450 - 99,704,678UniSTSGRCh37
Build 361498,774,203 - 98,774,431RGDNCBI36
Celera1479,760,140 - 79,760,368RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,888,015 - 79,888,243UniSTS
REN47987  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,704,621 - 99,704,881UniSTSGRCh37
Build 361498,774,374 - 98,774,634RGDNCBI36
Celera1479,760,311 - 79,760,571RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,888,186 - 79,888,446UniSTS
REN47988  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,704,868 - 99,705,122UniSTSGRCh37
Build 361498,774,621 - 98,774,875RGDNCBI36
Celera1479,760,558 - 79,760,812RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,888,433 - 79,888,687UniSTS
REN47989  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,705,043 - 99,705,267UniSTSGRCh37
Build 361498,774,796 - 98,775,020RGDNCBI36
Celera1479,760,733 - 79,760,957RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,888,608 - 79,888,832UniSTS
REN47990  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,705,254 - 99,705,493UniSTSGRCh37
Build 361498,775,007 - 98,775,246RGDNCBI36
Celera1479,760,944 - 79,761,183RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,888,819 - 79,889,058UniSTS
REN47991  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,705,470 - 99,705,716UniSTSGRCh37
Build 361498,775,223 - 98,775,469RGDNCBI36
Celera1479,761,160 - 79,761,406RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,889,035 - 79,889,281UniSTS
REN47992  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,705,691 - 99,705,953UniSTSGRCh37
Build 361498,775,444 - 98,775,706RGDNCBI36
Celera1479,761,381 - 79,761,643RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,889,256 - 79,889,518UniSTS
REN47993  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,705,945 - 99,706,204UniSTSGRCh37
Build 361498,775,698 - 98,775,957RGDNCBI36
Celera1479,761,635 - 79,761,894RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,889,510 - 79,889,769UniSTS
REN47994  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,706,183 - 99,706,436UniSTSGRCh37
Build 361498,775,936 - 98,776,189RGDNCBI36
Celera1479,761,873 - 79,762,126RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,889,748 - 79,890,001UniSTS
REN47995  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,706,419 - 99,706,684UniSTSGRCh37
Build 361498,776,172 - 98,776,437RGDNCBI36
Celera1479,762,109 - 79,762,374RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,889,984 - 79,890,249UniSTS
REN47996  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,706,661 - 99,706,916UniSTSGRCh37
Build 361498,776,414 - 98,776,669RGDNCBI36
Celera1479,762,351 - 79,762,606RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,890,226 - 79,890,481UniSTS
REN47997  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,706,851 - 99,707,119UniSTSGRCh37
Build 361498,776,604 - 98,776,872RGDNCBI36
Celera1479,762,541 - 79,762,809RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,890,416 - 79,890,684UniSTS
REN47998  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,707,096 - 99,707,351UniSTSGRCh37
Build 361498,776,849 - 98,777,104RGDNCBI36
Celera1479,762,786 - 79,763,041RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,890,661 - 79,890,916UniSTS
REN47999  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,707,325 - 99,707,573UniSTSGRCh37
Build 361498,777,078 - 98,777,326RGDNCBI36
Celera1479,763,015 - 79,763,263RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,890,890 - 79,891,138UniSTS
REN48000  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,707,550 - 99,707,809UniSTSGRCh37
Build 361498,777,303 - 98,777,562RGDNCBI36
Celera1479,763,240 - 79,763,499RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,891,115 - 79,891,374UniSTS
REN48001  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,707,784 - 99,708,050UniSTSGRCh37
Build 361498,777,537 - 98,777,803RGDNCBI36
Celera1479,763,474 - 79,763,740RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,891,349 - 79,891,615UniSTS
REN48002  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,708,049 - 99,708,297UniSTSGRCh37
Build 361498,777,802 - 98,778,050RGDNCBI36
Celera1479,763,739 - 79,763,987RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,891,614 - 79,891,862UniSTS
REN48003  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,708,280 - 99,708,507UniSTSGRCh37
Build 361498,778,033 - 98,778,260RGDNCBI36
Celera1479,763,970 - 79,764,197RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,891,845 - 79,892,072UniSTS
REN48004  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,708,484 - 99,708,738UniSTSGRCh37
Build 361498,778,237 - 98,778,491RGDNCBI36
Celera1479,764,174 - 79,764,428RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,892,049 - 79,892,303UniSTS
REN48005  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,708,727 - 99,708,970UniSTSGRCh37
Build 361498,778,480 - 98,778,723RGDNCBI36
Celera1479,764,417 - 79,764,660RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,892,292 - 79,892,535UniSTS
REN48006  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,708,949 - 99,709,191UniSTSGRCh37
Build 361498,778,702 - 98,778,944RGDNCBI36
Celera1479,764,639 - 79,764,881RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,892,514 - 79,892,756UniSTS
REN48007  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,709,175 - 99,709,401UniSTSGRCh37
Build 361498,778,928 - 98,779,154RGDNCBI36
Celera1479,764,865 - 79,765,091RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,892,740 - 79,892,966UniSTS
REN48008  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,709,362 - 99,709,606UniSTSGRCh37
Build 361498,779,115 - 98,779,359RGDNCBI36
Celera1479,765,052 - 79,765,296RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,892,927 - 79,893,171UniSTS
REN48009  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,709,578 - 99,709,827UniSTSGRCh37
Build 361498,779,331 - 98,779,580RGDNCBI36
Celera1479,765,268 - 79,765,517RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,893,143 - 79,893,392UniSTS
REN48010  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,709,803 - 99,710,056UniSTSGRCh37
Build 361498,779,556 - 98,779,809RGDNCBI36
Celera1479,765,493 - 79,765,746RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,893,368 - 79,893,621UniSTS
REN48011  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,710,032 - 99,710,258UniSTSGRCh37
Build 361498,779,785 - 98,780,011RGDNCBI36
Celera1479,765,722 - 79,765,948RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,893,597 - 79,893,823UniSTS
REN48012  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,710,236 - 99,710,492UniSTSGRCh37
Build 361498,779,989 - 98,780,245RGDNCBI36
Celera1479,765,926 - 79,766,182RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,893,801 - 79,894,050UniSTS
REN48013  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,710,469 - 99,710,716UniSTSGRCh37
Build 361498,780,222 - 98,780,469RGDNCBI36
Celera1479,766,159 - 79,766,406RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,894,027 - 79,894,274UniSTS
REN48014  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,710,692 - 99,710,931UniSTSGRCh37
Build 361498,780,445 - 98,780,684RGDNCBI36
Celera1479,766,382 - 79,766,621RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,894,250 - 79,894,489UniSTS
REN48015  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,710,930 - 99,711,176UniSTSGRCh37
Build 361498,780,683 - 98,780,929RGDNCBI36
Celera1479,766,620 - 79,766,866RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,894,488 - 79,894,734UniSTS
REN48016  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,711,171 - 99,711,426UniSTSGRCh37
Build 361498,780,924 - 98,781,179RGDNCBI36
Celera1479,766,861 - 79,767,116RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,894,729 - 79,894,984UniSTS
REN48017  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,711,397 - 99,711,646UniSTSGRCh37
Build 361498,781,150 - 98,781,399RGDNCBI36
Celera1479,767,087 - 79,767,336RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,894,955 - 79,895,204UniSTS
REN48018  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,711,624 - 99,711,852UniSTSGRCh37
Build 361498,781,377 - 98,781,605RGDNCBI36
Celera1479,767,314 - 79,767,542RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,895,182 - 79,895,410UniSTS
REN48019  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,711,803 - 99,712,059UniSTSGRCh37
Build 361498,781,556 - 98,781,812RGDNCBI36
Celera1479,767,493 - 79,767,750RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,895,361 - 79,895,618UniSTS
REN48020  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,711,923 - 99,712,191UniSTSGRCh37
Build 361498,781,676 - 98,781,944RGDNCBI36
Celera1479,767,613 - 79,767,882RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,895,481 - 79,895,750UniSTS
REN48021  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,712,185 - 99,712,433UniSTSGRCh37
Build 361498,781,938 - 98,782,186RGDNCBI36
Celera1479,767,876 - 79,768,124RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,895,744 - 79,895,992UniSTS
REN48022  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,712,413 - 99,712,657UniSTSGRCh37
Build 361498,782,166 - 98,782,410RGDNCBI36
Celera1479,768,104 - 79,768,348RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,895,972 - 79,896,216UniSTS
REN48023  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,712,516 - 99,712,745UniSTSGRCh37
Build 361498,782,269 - 98,782,498RGDNCBI36
Celera1479,768,207 - 79,768,436RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,896,075 - 79,896,304UniSTS
REN48024  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,712,679 - 99,712,912UniSTSGRCh37
Build 361498,782,432 - 98,782,665RGDNCBI36
Celera1479,768,370 - 79,768,603RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,896,238 - 79,896,471UniSTS
REN48025  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,712,888 - 99,713,136UniSTSGRCh37
Build 361498,782,641 - 98,782,889RGDNCBI36
Celera1479,768,579 - 79,768,828RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,896,447 - 79,896,696UniSTS
REN48026  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,713,102 - 99,713,326UniSTSGRCh37
Build 361498,782,855 - 98,783,079RGDNCBI36
Celera1479,768,794 - 79,769,018RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,896,662 - 79,896,886UniSTS
REN48027  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,713,278 - 99,713,540UniSTSGRCh37
Build 361498,783,031 - 98,783,293RGDNCBI36
Celera1479,768,970 - 79,769,232RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,896,838 - 79,897,100UniSTS
REN48028  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,713,516 - 99,713,764UniSTSGRCh37
Build 361498,783,269 - 98,783,517RGDNCBI36
Celera1479,769,208 - 79,769,456RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,897,076 - 79,897,324UniSTS
REN48029  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,713,762 - 99,714,025UniSTSGRCh37
Build 361498,783,515 - 98,783,778RGDNCBI36
Celera1479,769,454 - 79,769,717RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,897,322 - 79,897,585UniSTS
REN48030  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,714,003 - 99,714,262UniSTSGRCh37
Build 361498,783,756 - 98,784,015RGDNCBI36
Celera1479,769,695 - 79,769,954RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,897,563 - 79,897,822UniSTS
REN48031  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,714,252 - 99,714,486UniSTSGRCh37
Build 361498,784,005 - 98,784,239RGDNCBI36
Celera1479,769,944 - 79,770,178RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,897,812 - 79,898,046UniSTS
REN48032  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,714,453 - 99,714,711UniSTSGRCh37
Build 361498,784,206 - 98,784,464RGDNCBI36
Celera1479,770,145 - 79,770,403RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,898,013 - 79,898,271UniSTS
REN48033  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,714,688 - 99,714,949UniSTSGRCh37
Build 361498,784,441 - 98,784,702RGDNCBI36
Celera1479,770,380 - 79,770,641RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,898,248 - 79,898,509UniSTS
REN48034  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,714,926 - 99,715,161UniSTSGRCh37
Build 361498,784,679 - 98,784,914RGDNCBI36
Celera1479,770,618 - 79,770,853RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,898,486 - 79,898,721UniSTS
REN48035  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,715,130 - 99,715,383UniSTSGRCh37
Build 361498,784,883 - 98,785,136RGDNCBI36
Celera1479,770,822 - 79,771,075RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,898,690 - 79,898,943UniSTS
REN48036  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,715,377 - 99,715,618UniSTSGRCh37
Build 361498,785,130 - 98,785,371RGDNCBI36
Celera1479,771,069 - 79,771,310RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,898,937 - 79,899,178UniSTS
REN48037  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,715,601 - 99,715,851UniSTSGRCh37
Build 361498,785,354 - 98,785,604RGDNCBI36
Celera1479,771,293 - 79,771,543RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,899,161 - 79,899,411UniSTS
REN48038  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,715,830 - 99,716,080UniSTSGRCh37
Build 361498,785,583 - 98,785,833RGDNCBI36
Celera1479,771,522 - 79,771,772RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,899,390 - 79,899,640UniSTS
REN48039  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,715,931 - 99,716,192UniSTSGRCh37
Build 361498,785,684 - 98,785,945RGDNCBI36
Celera1479,771,623 - 79,771,884RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,899,491 - 79,899,752UniSTS
REN48040  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,716,082 - 99,716,310UniSTSGRCh37
Build 361498,785,835 - 98,786,063RGDNCBI36
Celera1479,771,774 - 79,772,002RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,899,642 - 79,899,870UniSTS
REN48041  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,716,813 - 99,717,070UniSTSGRCh37
Build 361498,786,566 - 98,786,823RGDNCBI36
Celera1479,772,505 - 79,772,762RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,900,373 - 79,900,630UniSTS
REN48042  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,717,053 - 99,717,287UniSTSGRCh37
Build 361498,786,806 - 98,787,040RGDNCBI36
Celera1479,772,745 - 79,772,980RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,900,613 - 79,900,848UniSTS
REN48043  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,717,263 - 99,717,517UniSTSGRCh37
Build 361498,787,016 - 98,787,270RGDNCBI36
Celera1479,772,956 - 79,773,210RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,900,824 - 79,901,078UniSTS
REN48044  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,717,509 - 99,717,747UniSTSGRCh37
Build 361498,787,262 - 98,787,500RGDNCBI36
Celera1479,773,202 - 79,773,440RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,901,070 - 79,901,308UniSTS
REN48045  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,717,720 - 99,717,981UniSTSGRCh37
Build 361498,787,473 - 98,787,734RGDNCBI36
Celera1479,773,413 - 79,773,674RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,901,281 - 79,901,542UniSTS
REN48046  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,717,964 - 99,718,193UniSTSGRCh37
Build 361498,787,717 - 98,787,946RGDNCBI36
Celera1479,773,657 - 79,773,886RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,901,525 - 79,901,754UniSTS
REN48047  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,718,172 - 99,718,396UniSTSGRCh37
Build 361498,787,925 - 98,788,149RGDNCBI36
Celera1479,773,865 - 79,774,089RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,901,733 - 79,901,957UniSTS
REN48048  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,718,382 - 99,718,617UniSTSGRCh37
Build 361498,788,135 - 98,788,370RGDNCBI36
Celera1479,774,075 - 79,774,310RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,901,943 - 79,902,178UniSTS
REN48049  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,718,601 - 99,718,849UniSTSGRCh37
Build 361498,788,354 - 98,788,602RGDNCBI36
Celera1479,774,294 - 79,774,542RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,902,162 - 79,902,410UniSTS
REN48050  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,718,841 - 99,719,085UniSTSGRCh37
Build 361498,788,594 - 98,788,838RGDNCBI36
Celera1479,774,534 - 79,774,778RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,902,402 - 79,902,646UniSTS
REN48051  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,719,049 - 99,719,293UniSTSGRCh37
Build 361498,788,802 - 98,789,046RGDNCBI36
Celera1479,774,742 - 79,774,986RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,902,610 - 79,902,854UniSTS
REN48052  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,719,261 - 99,719,496UniSTSGRCh37
Build 361498,789,014 - 98,789,249RGDNCBI36
Celera1479,774,954 - 79,775,189RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,902,822 - 79,903,057UniSTS
REN48053  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,719,489 - 99,719,730UniSTSGRCh37
Build 361498,789,242 - 98,789,483RGDNCBI36
Celera1479,775,182 - 79,775,423RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,903,050 - 79,903,291UniSTS
REN48054  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,719,669 - 99,719,915UniSTSGRCh37
Build 361498,789,422 - 98,789,668RGDNCBI36
Celera1479,775,362 - 79,775,608RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,903,230 - 79,903,476UniSTS
REN48055  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,719,892 - 99,720,138UniSTSGRCh37
Build 361498,789,645 - 98,789,891RGDNCBI36
Celera1479,775,585 - 79,775,831RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,903,453 - 79,903,699UniSTS
REN48056  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,720,109 - 99,720,356UniSTSGRCh37
Build 361498,789,862 - 98,790,109RGDNCBI36
Celera1479,775,802 - 79,776,049RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,903,670 - 79,903,917UniSTS
REN48057  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,720,338 - 99,720,581UniSTSGRCh37
Build 361498,790,091 - 98,790,334RGDNCBI36
Celera1479,776,031 - 79,776,274RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,903,899 - 79,904,142UniSTS
REN48058  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,720,559 - 99,720,800UniSTSGRCh37
Build 361498,790,312 - 98,790,553RGDNCBI36
Celera1479,776,252 - 79,776,493RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,904,120 - 79,904,361UniSTS
REN48059  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,720,776 - 99,721,015UniSTSGRCh37
Build 361498,790,529 - 98,790,768RGDNCBI36
Celera1479,776,469 - 79,776,708RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,904,337 - 79,904,576UniSTS
REN48060  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,721,011 - 99,721,260UniSTSGRCh37
Build 361498,790,764 - 98,791,013RGDNCBI36
Celera1479,776,704 - 79,776,953RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,904,572 - 79,904,821UniSTS
REN48061  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,721,231 - 99,721,472UniSTSGRCh37
Build 361498,790,984 - 98,791,225RGDNCBI36
Celera1479,776,924 - 79,777,165RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,904,792 - 79,905,033UniSTS
REN48062  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,721,449 - 99,721,696UniSTSGRCh37
Build 361498,791,202 - 98,791,449RGDNCBI36
Celera1479,777,142 - 79,777,389RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,905,010 - 79,905,257UniSTS
REN48063  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,721,674 - 99,721,922UniSTSGRCh37
Build 361498,791,427 - 98,791,675RGDNCBI36
Celera1479,777,367 - 79,777,614RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,905,235 - 79,905,482UniSTS
REN48064  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,721,912 - 99,722,171UniSTSGRCh37
Build 361498,791,665 - 98,791,924RGDNCBI36
Celera1479,777,604 - 79,777,863RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,905,472 - 79,905,731UniSTS
REN48065  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,722,151 - 99,722,395UniSTSGRCh37
Build 361498,791,904 - 98,792,148RGDNCBI36
Celera1479,777,843 - 79,778,087RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,905,711 - 79,905,955UniSTS
REN48066  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,722,375 - 99,722,645UniSTSGRCh37
Build 361498,792,128 - 98,792,398RGDNCBI36
Celera1479,778,067 - 79,778,337RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,905,935 - 79,906,205UniSTS
REN48067  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,722,632 - 99,722,873UniSTSGRCh37
Build 361498,792,385 - 98,792,626RGDNCBI36
Celera1479,778,324 - 79,778,565RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,906,192 - 79,906,433UniSTS
REN48068  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,722,821 - 99,723,093UniSTSGRCh37
Build 361498,792,574 - 98,792,846RGDNCBI36
Celera1479,778,513 - 79,778,785RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,906,381 - 79,906,653UniSTS
REN48069  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,723,061 - 99,723,291UniSTSGRCh37
Build 361498,792,814 - 98,793,044RGDNCBI36
Celera1479,778,753 - 79,778,983RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,906,621 - 79,906,851UniSTS
REN48070  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,723,262 - 99,723,506UniSTSGRCh37
Build 361498,793,015 - 98,793,259RGDNCBI36
Celera1479,778,954 - 79,779,198RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,906,822 - 79,907,066UniSTS
REN48071  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,723,469 - 99,723,713UniSTSGRCh37
Build 361498,793,222 - 98,793,466RGDNCBI36
Celera1479,779,161 - 79,779,405RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,907,029 - 79,907,273UniSTS
REN48072  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,723,694 - 99,723,926UniSTSGRCh37
Build 361498,793,447 - 98,793,679RGDNCBI36
Celera1479,779,386 - 79,779,618RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,907,254 - 79,907,486UniSTS
REN48073  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,723,917 - 99,724,142UniSTSGRCh37
Build 361498,793,670 - 98,793,895RGDNCBI36
Celera1479,779,609 - 79,779,834RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,907,477 - 79,907,702UniSTS
REN48074  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,724,119 - 99,724,385UniSTSGRCh37
Build 361498,793,872 - 98,794,138RGDNCBI36
Celera1479,779,811 - 79,780,077RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,907,679 - 79,907,945UniSTS
REN48075  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,724,351 - 99,724,581UniSTSGRCh37
Build 361498,794,104 - 98,794,334RGDNCBI36
Celera1479,780,043 - 79,780,273RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,907,911 - 79,908,141UniSTS
REN48076  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,724,565 - 99,724,806UniSTSGRCh37
Build 361498,794,318 - 98,794,559RGDNCBI36
Celera1479,780,257 - 79,780,498RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,908,125 - 79,908,366UniSTS
REN48077  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,724,783 - 99,725,008UniSTSGRCh37
Build 361498,794,536 - 98,794,761RGDNCBI36
Celera1479,780,475 - 79,780,700RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,908,343 - 79,908,568UniSTS
REN48078  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,724,982 - 99,725,229UniSTSGRCh37
Build 361498,794,735 - 98,794,982RGDNCBI36
Celera1479,780,674 - 79,780,921RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,908,542 - 79,908,789UniSTS
REN48079  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,725,211 - 99,725,449UniSTSGRCh37
Build 361498,794,964 - 98,795,202RGDNCBI36
Celera1479,780,903 - 79,781,141RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,908,771 - 79,909,009UniSTS
REN48080  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,725,443 - 99,725,701UniSTSGRCh37
Build 361498,795,196 - 98,795,454RGDNCBI36
Celera1479,781,135 - 79,781,393RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,909,003 - 79,909,261UniSTS
REN48081  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,725,677 - 99,725,927UniSTSGRCh37
Build 361498,795,430 - 98,795,680RGDNCBI36
Celera1479,781,369 - 79,781,619RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,909,237 - 79,909,487UniSTS
REN48082  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,725,903 - 99,726,132UniSTSGRCh37
Build 361498,795,656 - 98,795,885RGDNCBI36
Celera1479,781,595 - 79,781,824RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,909,463 - 79,909,692UniSTS
REN48083  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,726,108 - 99,726,368UniSTSGRCh37
Build 361498,795,861 - 98,796,121RGDNCBI36
Celera1479,781,800 - 79,782,060RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,909,668 - 79,909,928UniSTS
REN48084  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,726,345 - 99,726,601UniSTSGRCh37
Build 361498,796,098 - 98,796,354RGDNCBI36
Celera1479,782,037 - 79,782,293RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,909,905 - 79,910,161UniSTS
REN48085  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,726,600 - 99,726,824UniSTSGRCh37
Build 361498,796,353 - 98,796,577RGDNCBI36
Celera1479,782,292 - 79,782,516RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,910,160 - 79,910,384UniSTS
REN48086  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,726,809 - 99,727,062UniSTSGRCh37
Build 361498,796,562 - 98,796,815RGDNCBI36
Celera1479,782,501 - 79,782,754RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,910,369 - 79,910,622UniSTS
REN48087  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,727,038 - 99,727,285UniSTSGRCh37
Build 361498,796,791 - 98,797,038RGDNCBI36
Celera1479,782,730 - 79,782,977RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,910,598 - 79,910,845UniSTS
REN48088  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,727,283 - 99,727,545UniSTSGRCh37
Build 361498,797,036 - 98,797,298RGDNCBI36
Celera1479,782,975 - 79,783,237RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,910,843 - 79,911,105UniSTS
REN48089  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,727,516 - 99,727,767UniSTSGRCh37
Build 361498,797,269 - 98,797,520RGDNCBI36
Celera1479,783,208 - 79,783,459RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,911,076 - 79,911,327UniSTS
REN48090  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,727,732 - 99,727,981UniSTSGRCh37
Build 361498,797,485 - 98,797,734RGDNCBI36
Celera1479,783,424 - 79,783,673RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,911,292 - 79,911,541UniSTS
REN48091  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,727,959 - 99,728,208UniSTSGRCh37
Build 361498,797,712 - 98,797,961RGDNCBI36
Celera1479,783,651 - 79,783,900RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,911,519 - 79,911,768UniSTS
REN48092  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,728,185 - 99,728,432UniSTSGRCh37
Build 361498,797,938 - 98,798,185RGDNCBI36
Celera1479,783,877 - 79,784,124RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,911,745 - 79,911,992UniSTS
REN48093  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,728,408 - 99,728,637UniSTSGRCh37
Build 361498,798,161 - 98,798,390RGDNCBI36
Celera1479,784,100 - 79,784,329RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,911,968 - 79,912,197UniSTS
REN48094  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,728,618 - 99,728,881UniSTSGRCh37
Build 361498,798,371 - 98,798,634RGDNCBI36
Celera1479,784,310 - 79,784,573RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,912,178 - 79,912,441UniSTS
REN48095  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,728,858 - 99,729,124UniSTSGRCh37
Build 361498,798,611 - 98,798,877RGDNCBI36
Celera1479,784,550 - 79,784,816RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,912,418 - 79,912,684UniSTS
REN48096  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,729,119 - 99,729,362UniSTSGRCh37
Build 361498,798,872 - 98,799,115RGDNCBI36
Celera1479,784,811 - 79,785,054RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,912,679 - 79,912,922UniSTS
REN48097  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,729,348 - 99,729,611UniSTSGRCh37
Build 361498,799,101 - 98,799,364RGDNCBI36
Celera1479,785,040 - 79,785,303RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,912,908 - 79,913,171UniSTS
REN48098  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,729,596 - 99,729,844UniSTSGRCh37
Build 361498,799,349 - 98,799,597RGDNCBI36
Celera1479,785,288 - 79,785,536RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,913,156 - 79,913,404UniSTS
REN48099  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,729,835 - 99,730,159UniSTSGRCh37
GRCh371499,729,835 - 99,730,080UniSTSGRCh37
Build 361498,799,588 - 98,799,833RGDNCBI36
Celera1479,785,527 - 79,785,772RGD
Celera1479,785,527 - 79,785,851UniSTS
Cytogenetic Map14q32.2UniSTS
HuRef1479,913,395 - 79,913,640UniSTS
HuRef1479,913,395 - 79,913,719UniSTS
REN48100  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,730,145 - 99,730,323UniSTSGRCh37
GRCh371499,730,066 - 99,730,323UniSTSGRCh37
Build 361498,799,819 - 98,800,076RGDNCBI36
Celera1479,785,758 - 79,786,015RGD
Celera1479,785,837 - 79,786,015UniSTS
Cytogenetic Map14q32.2UniSTS
HuRef1479,913,626 - 79,913,883UniSTS
HuRef1479,913,705 - 79,913,883UniSTS
REN48101  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,730,313 - 99,730,557UniSTSGRCh37
Build 361498,800,066 - 98,800,310RGDNCBI36
Celera1479,786,005 - 79,786,249RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,913,873 - 79,914,116UniSTS
REN48102  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,730,526 - 99,730,766UniSTSGRCh37
Build 361498,800,279 - 98,800,519RGDNCBI36
Celera1479,786,218 - 79,786,458RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,914,085 - 79,914,325UniSTS
REN48103  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,730,735 - 99,730,994UniSTSGRCh37
Build 361498,800,488 - 98,800,747RGDNCBI36
Celera1479,786,427 - 79,786,686RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,914,294 - 79,914,553UniSTS
REN48104  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,730,985 - 99,731,231UniSTSGRCh37
Build 361498,800,738 - 98,800,984RGDNCBI36
Celera1479,786,677 - 79,786,923RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,914,544 - 79,914,790UniSTS
REN48105  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,731,214 - 99,731,474UniSTSGRCh37
Build 361498,800,967 - 98,801,227RGDNCBI36
Celera1479,786,906 - 79,787,166RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,914,773 - 79,915,033UniSTS
REN48106  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,731,435 - 99,731,683UniSTSGRCh37
Build 361498,801,188 - 98,801,436RGDNCBI36
Celera1479,787,127 - 79,787,375RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,914,951 - 79,915,241UniSTS
HuRef1479,914,994 - 79,915,241UniSTS
REN48107  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,731,671 - 99,731,914UniSTSGRCh37
Build 361498,801,424 - 98,801,667RGDNCBI36
Celera1479,787,363 - 79,787,606RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,915,229 - 79,915,472UniSTS
REN48108  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,731,891 - 99,732,122UniSTSGRCh37
Build 361498,801,644 - 98,801,875RGDNCBI36
Celera1479,787,583 - 79,787,814RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,915,449 - 79,915,680UniSTS
REN48109  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,732,089 - 99,732,332UniSTSGRCh37
Build 361498,801,842 - 98,802,085RGDNCBI36
Celera1479,787,781 - 79,788,024RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,915,647 - 79,915,890UniSTS
REN48110  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,732,309 - 99,732,561UniSTSGRCh37
Build 361498,802,062 - 98,802,314RGDNCBI36
Celera1479,788,001 - 79,788,253RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,915,867 - 79,916,119UniSTS
REN48111  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,732,548 - 99,732,796UniSTSGRCh37
Build 361498,802,301 - 98,802,549RGDNCBI36
Celera1479,788,240 - 79,788,488RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,916,106 - 79,916,354UniSTS
REN48112  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,732,768 - 99,732,995UniSTSGRCh37
Build 361498,802,521 - 98,802,748RGDNCBI36
Celera1479,788,460 - 79,788,687RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,916,326 - 79,916,553UniSTS
REN48113  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,732,965 - 99,733,214UniSTSGRCh37
Build 361498,802,718 - 98,802,967RGDNCBI36
Celera1479,788,657 - 79,788,906RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,916,523 - 79,916,772UniSTS
REN48114  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,733,191 - 99,733,444UniSTSGRCh37
Build 361498,802,944 - 98,803,197RGDNCBI36
Celera1479,788,883 - 79,789,136RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,916,749 - 79,917,002UniSTS
REN48115  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,733,358 - 99,733,611UniSTSGRCh37
Build 361498,803,111 - 98,803,364RGDNCBI36
Celera1479,789,050 - 79,789,303RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,916,916 - 79,917,169UniSTS
REN48116  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,733,589 - 99,733,854UniSTSGRCh37
Build 361498,803,342 - 98,803,607RGDNCBI36
Celera1479,789,281 - 79,789,546RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,917,147 - 79,917,412UniSTS
REN48117  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,733,836 - 99,734,074UniSTSGRCh37
Build 361498,803,589 - 98,803,827RGDNCBI36
Celera1479,789,528 - 79,789,766RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,917,394 - 79,917,634UniSTS
REN48118  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,734,065 - 99,734,309UniSTSGRCh37
Build 361498,803,818 - 98,804,062RGDNCBI36
Celera1479,789,757 - 79,790,001RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,917,625 - 79,917,869UniSTS
REN48119  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,734,299 - 99,734,550UniSTSGRCh37
Build 361498,804,052 - 98,804,303RGDNCBI36
Celera1479,789,991 - 79,790,242RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,917,859 - 79,918,110UniSTS
REN48120  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,734,545 - 99,734,781UniSTSGRCh37
Build 361498,804,298 - 98,804,534RGDNCBI36
Celera1479,790,237 - 79,790,473RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,918,105 - 79,918,341UniSTS
REN48121  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,734,773 - 99,735,005UniSTSGRCh37
Build 361498,804,526 - 98,804,758RGDNCBI36
Celera1479,790,465 - 79,790,697RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,918,333 - 79,918,565UniSTS
REN48122  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,734,984 - 99,735,225UniSTSGRCh37
Build 361498,804,737 - 98,804,978RGDNCBI36
Celera1479,790,676 - 79,790,917RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,918,544 - 79,918,785UniSTS
REN48123  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,735,205 - 99,735,437UniSTSGRCh37
Build 361498,804,958 - 98,805,190RGDNCBI36
Celera1479,790,897 - 79,791,129RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,918,765 - 79,918,997UniSTS
REN48124  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,735,412 - 99,735,651UniSTSGRCh37
Build 361498,805,165 - 98,805,404RGDNCBI36
Celera1479,791,104 - 79,791,343RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,918,972 - 79,919,211UniSTS
REN48125  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,735,597 - 99,735,847UniSTSGRCh37
Build 361498,805,350 - 98,805,600RGDNCBI36
Celera1479,791,289 - 79,791,539RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,919,157 - 79,919,407UniSTS
REN48126  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,735,826 - 99,736,051UniSTSGRCh37
Build 361498,805,579 - 98,805,804RGDNCBI36
Celera1479,791,518 - 79,791,743RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,919,386 - 79,919,612UniSTS
REN48127  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,735,950 - 99,736,209UniSTSGRCh37
Build 361498,805,703 - 98,805,962RGDNCBI36
Celera1479,791,642 - 79,791,901RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,919,511 - 79,919,770UniSTS
REN48128  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,736,183 - 99,736,453UniSTSGRCh37
Build 361498,805,936 - 98,806,206RGDNCBI36
Celera1479,791,875 - 79,792,135RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,919,744 - 79,920,004UniSTS
REN48129  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,736,436 - 99,736,705UniSTSGRCh37
Build 361498,806,189 - 98,806,458RGDNCBI36
Celera1479,792,118 - 79,792,387RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,919,987 - 79,920,256UniSTS
REN48130  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,736,672 - 99,736,897UniSTSGRCh37
Build 361498,806,425 - 98,806,650RGDNCBI36
Celera1479,792,354 - 79,792,579RGD
Cytogenetic Map14q32.2UniSTS
REN48131  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,736,856 - 99,737,084UniSTSGRCh37
Build 361498,806,609 - 98,806,837RGDNCBI36
Celera1479,792,538 - 79,792,766RGD
Cytogenetic Map14q32.2UniSTS
REN48132  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,737,309 - 99,737,571UniSTSGRCh37
Build 361498,807,062 - 98,807,324RGDNCBI36
Celera1479,792,991 - 79,793,253RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,920,942 - 79,921,204UniSTS
REN48133  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,737,734 - 99,737,958UniSTSGRCh37
Build 361498,807,487 - 98,807,711RGDNCBI36
Celera1479,793,424 - 79,793,648RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,921,376 - 79,921,602UniSTS
REN48134  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,737,927 - 99,738,153UniSTSGRCh37
Build 361498,807,680 - 98,807,906RGDNCBI36
Celera1479,793,617 - 79,793,843RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,921,571 - 79,921,797UniSTS
REN48135  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,738,018 - 99,738,280UniSTSGRCh37
Build 361498,807,771 - 98,808,033RGDNCBI36
Celera1479,793,708 - 79,793,970RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,921,662 - 79,921,924UniSTS
REN48136  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,738,261 - 99,738,493UniSTSGRCh37
Build 361498,808,014 - 98,808,246RGDNCBI36
Celera1479,793,951 - 79,794,183RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,921,905 - 79,922,137UniSTS
REN48137  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,738,456 - 99,738,705UniSTSGRCh37
Build 361498,808,209 - 98,808,458RGDNCBI36
Celera1479,794,146 - 79,794,395RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,922,100 - 79,922,349UniSTS
REN48138  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,738,677 - 99,738,917UniSTSGRCh37
Build 361498,808,430 - 98,808,670RGDNCBI36
Celera1479,794,367 - 79,794,607RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,922,321 - 79,922,561UniSTS
REN48139  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,738,901 - 99,739,142UniSTSGRCh37
Build 361498,808,654 - 98,808,895RGDNCBI36
Celera1479,794,591 - 79,794,832RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,922,545 - 79,922,786UniSTS
REN48140  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,739,096 - 99,739,351UniSTSGRCh37
Build 361498,808,849 - 98,809,104RGDNCBI36
Celera1479,794,786 - 79,795,041RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,922,740 - 79,922,995UniSTS
REN48141  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,739,326 - 99,739,569UniSTSGRCh37
Build 361498,809,079 - 98,809,322RGDNCBI36
Celera1479,795,016 - 79,795,259RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,922,970 - 79,923,213UniSTS
REN48142  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,739,544 - 99,739,787UniSTSGRCh37
Build 361498,809,297 - 98,809,540RGDNCBI36
Celera1479,795,234 - 79,795,477RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,923,188 - 79,923,431UniSTS
BCL11B_101.2  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,638,623 - 99,639,429UniSTSGRCh37
Build 361498,708,376 - 98,709,182RGDNCBI36
Celera1479,694,367 - 79,695,173RGD
HuRef1479,822,225 - 79,823,031UniSTS
SHGC-57955  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,643,646 - 99,643,752UniSTSGRCh37
Build 361498,713,399 - 98,713,505RGDNCBI36
Celera1479,699,392 - 79,699,498RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,827,252 - 79,827,358UniSTS
TNG Radiation Hybrid Map1440244.0UniSTS
stSG632077  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,636,109 - 99,636,305UniSTSGRCh37
Build 361498,705,862 - 98,706,058RGDNCBI36
Celera1479,691,853 - 79,692,049RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,819,711 - 79,819,907UniSTS
stSG632078  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,636,313 - 99,637,536UniSTSGRCh37
Build 361498,706,066 - 98,707,289RGDNCBI36
Celera1479,692,057 - 79,693,280RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,819,915 - 79,821,138UniSTS
stSG632079  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,637,518 - 99,638,980UniSTSGRCh37
Build 361498,707,271 - 98,708,733RGDNCBI36
Celera1479,693,262 - 79,694,724RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,821,120 - 79,822,582UniSTS
stSG632080  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,638,961 - 99,640,338UniSTSGRCh37
Build 361498,708,714 - 98,710,091RGDNCBI36
Celera1479,694,705 - 79,696,084RGD
Cytogenetic Map14q32.2UniSTS
HuRef1479,822,563 - 79,823,942UniSTS
stSG632083  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,642,903 - 99,644,212UniSTSGRCh37
Build 361498,712,656 - 98,713,965RGDNCBI36
Celera1479,698,649 - 79,699,958RGD
HuRef1479,826,509 - 79,827,818UniSTS
stSG632084  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,644,193 - 99,645,379UniSTSGRCh37
Build 361498,713,946 - 98,715,132RGDNCBI36
Celera1479,699,939 - 79,701,125RGD
HuRef1479,827,799 - 79,828,985UniSTS
stSG632085  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,645,411 - 99,646,800UniSTSGRCh37
Build 361498,715,164 - 98,716,553RGDNCBI36
Celera1479,701,157 - 79,702,545RGD
HuRef1479,829,017 - 79,830,407UniSTS
stSG632086  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,646,781 - 99,648,252UniSTSGRCh37
Build 361498,716,534 - 98,718,005RGDNCBI36
Celera1479,702,526 - 79,703,997RGD
HuRef1479,830,388 - 79,831,859UniSTS
stSG632087  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,648,233 - 99,649,568UniSTSGRCh37
Build 361498,717,986 - 98,719,321RGDNCBI36
Celera1479,703,978 - 79,705,313RGD
HuRef1479,831,840 - 79,833,175UniSTS
stSG632088  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,649,549 - 99,650,964UniSTSGRCh37
Build 361498,719,302 - 98,720,717RGDNCBI36
Celera1479,705,294 - 79,706,709RGD
HuRef1479,833,156 - 79,834,571UniSTS
stSG632089  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,650,945 - 99,652,311UniSTSGRCh37
Build 361498,720,698 - 98,722,064RGDNCBI36
Celera1479,706,690 - 79,708,056RGD
HuRef1479,834,552 - 79,835,917UniSTS
stSG632090  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,652,292 - 99,653,392UniSTSGRCh37
Build 361498,722,045 - 98,723,145RGDNCBI36
Celera1479,708,037 - 79,709,137RGD
HuRef1479,835,898 - 79,836,998UniSTS
stSG632091  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,653,373 - 99,654,725UniSTSGRCh37
Build 361498,723,126 - 98,724,478RGDNCBI36
Celera1479,709,118 - 79,710,480RGD
HuRef1479,836,979 - 79,838,331UniSTS
stSG632092  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,654,706 - 99,655,882UniSTSGRCh37
Build 361498,724,459 - 98,725,635RGDNCBI36
Celera1479,710,461 - 79,711,637RGD
HuRef1479,838,312 - 79,839,482UniSTS
stSG632093  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,655,863 - 99,657,018UniSTSGRCh37
Build 361498,725,616 - 98,726,771RGDNCBI36
Celera1479,711,618 - 79,712,773RGD
HuRef1479,839,463 - 79,840,617UniSTS
stSG632094  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,657,001 - 99,658,261UniSTSGRCh37
Build 361498,726,754 - 98,728,014RGDNCBI36
Celera1479,712,756 - 79,714,015RGD
HuRef1479,840,600 - 79,841,860UniSTS
stSG632095  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,658,242 - 99,659,559UniSTSGRCh37
Build 361498,727,995 - 98,729,312RGDNCBI36
Celera1479,713,996 - 79,715,309RGD
HuRef1479,841,841 - 79,843,154UniSTS
stSG632096  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,659,540 - 99,660,722UniSTSGRCh37
Build 361498,729,293 - 98,730,475RGDNCBI36
Celera1479,715,290 - 79,716,472RGD
HuRef1479,843,135 - 79,844,317UniSTS
stSG632097  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,660,703 - 99,662,115UniSTSGRCh37
Build 361498,730,456 - 98,731,868RGDNCBI36
Celera1479,716,453 - 79,717,865RGD
HuRef1479,844,298 - 79,845,710UniSTS
stSG632098  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,662,096 - 99,663,563UniSTSGRCh37
Build 361498,731,849 - 98,733,316RGDNCBI36
Celera1479,717,846 - 79,719,312RGD
HuRef1479,845,691 - 79,847,158UniSTS
stSG632099  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,663,544 - 99,664,926UniSTSGRCh37
Build 361498,733,297 - 98,734,679RGDNCBI36
Celera1479,719,293 - 79,720,675RGD
HuRef1479,847,139 - 79,848,521UniSTS
stSG632100  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,664,907 - 99,666,350UniSTSGRCh37
Build 361498,734,660 - 98,736,103RGDNCBI36
Celera1479,720,656 - 79,722,079RGD
HuRef1479,848,502 - 79,849,911UniSTS
stSG632101  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,666,331 - 99,667,606UniSTSGRCh37
Build 361498,736,084 - 98,737,359RGDNCBI36
Celera1479,722,060 - 79,723,335RGD
HuRef1479,849,892 - 79,851,167UniSTS
stSG632102  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,667,655 - 99,668,804UniSTSGRCh37
Build 361498,737,408 - 98,738,557RGDNCBI36
Celera1479,723,384 - 79,724,533RGD
HuRef1479,851,216 - 79,852,365UniSTS
stSG632103  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,668,784 - 99,669,837UniSTSGRCh37
Build 361498,738,537 - 98,739,590RGDNCBI36
Celera1479,724,513 - 79,725,566RGD
HuRef1479,852,345 - 79,853,398UniSTS
stSG632104  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,669,819 - 99,671,128UniSTSGRCh37
Build 361498,739,572 - 98,740,881RGDNCBI36
Celera1479,725,548 - 79,726,857RGD
HuRef1479,853,380 - 79,854,689UniSTS
stSG632105  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,671,109 - 99,672,457UniSTSGRCh37
Build 361498,740,862 - 98,742,210RGDNCBI36
Celera1479,726,838 - 79,728,186RGD
HuRef1479,854,670 - 79,856,018UniSTS
stSG632106  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,672,438 - 99,673,883UniSTSGRCh37
Build 361498,742,191 - 98,743,636RGDNCBI36
Celera1479,728,167 - 79,729,612RGD
HuRef1479,855,999 - 79,857,444UniSTS
stSG632107  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,673,864 - 99,675,305UniSTSGRCh37
Build 361498,743,617 - 98,745,058RGDNCBI36
Celera1479,729,593 - 79,731,034RGD
HuRef1479,857,425 - 79,858,866UniSTS
stSG632108  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,675,286 - 99,675,577UniSTSGRCh37
Build 361498,745,039 - 98,745,330RGDNCBI36
Celera1479,731,015 - 79,731,306RGD
HuRef1479,858,847 - 79,859,138UniSTS
stSG632109  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,675,598 - 99,676,715UniSTSGRCh37
Build 361498,745,351 - 98,746,468RGDNCBI36
Celera1479,731,327 - 79,732,444RGD
HuRef1479,859,159 - 79,860,276UniSTS
stSG632110  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,676,882 - 99,678,203UniSTSGRCh37
Build 361498,746,635 - 98,747,956RGDNCBI36
Celera1479,732,611 - 79,733,932RGD
HuRef1479,860,443 - 79,861,764UniSTS
stSG632111  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,678,187 - 99,679,488UniSTSGRCh37
Build 361498,747,940 - 98,749,241RGDNCBI36
Celera1479,733,916 - 79,735,217RGD
HuRef1479,861,748 - 79,863,046UniSTS
stSG632112  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,679,469 - 99,680,472UniSTSGRCh37
Build 361498,749,222 - 98,750,225RGDNCBI36
Celera1479,735,198 - 79,736,201RGD
HuRef1479,863,027 - 79,864,030UniSTS
stSG632114  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,681,943 - 99,683,055UniSTSGRCh37
Build 361498,751,696 - 98,752,808RGDNCBI36
Celera1479,737,672 - 79,738,784RGD
HuRef1479,865,501 - 79,866,613UniSTS
stSG632115  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,683,036 - 99,684,106UniSTSGRCh37
Build 361498,752,789 - 98,753,859RGDNCBI36
Celera1479,738,765 - 79,739,847RGD
HuRef1479,866,594 - 79,867,674UniSTS
stSG632116  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,684,061 - 99,685,068UniSTSGRCh37
Build 361498,753,814 - 98,754,821RGDNCBI36
Celera1479,739,802 - 79,740,809RGD
HuRef1479,867,629 - 79,868,636UniSTS
stSG632117  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,685,052 - 99,686,180UniSTSGRCh37
Build 361498,754,805 - 98,755,933RGDNCBI36
Celera1479,740,793 - 79,741,920RGD
HuRef1479,868,620 - 79,869,747UniSTS
stSG632118  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,686,162 - 99,687,565UniSTSGRCh37
Build 361498,755,915 - 98,757,318RGDNCBI36
Celera1479,741,902 - 79,743,305RGD
HuRef1479,869,729 - 79,871,132UniSTS
stSG632119  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,687,548 - 99,687,825UniSTSGRCh37
Build 361498,757,301 - 98,757,578RGDNCBI36
Celera1479,743,288 - 79,743,565RGD
HuRef1479,871,115 - 79,871,392UniSTS
stSG632120  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,687,854 - 99,689,024UniSTSGRCh37
Build 361498,757,607 - 98,758,777RGDNCBI36
Celera1479,743,594 - 79,744,763RGD
HuRef1479,871,421 - 79,872,590UniSTS
stSG632121  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,689,005 - 99,690,226UniSTSGRCh37
Build 361498,758,758 - 98,759,979RGDNCBI36
Celera1479,744,744 - 79,745,965RGD
HuRef1479,872,571 - 79,873,792UniSTS
stSG632122  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,690,437 - 99,691,498UniSTSGRCh37
Build 361498,760,190 - 98,761,251RGDNCBI36
Celera1479,746,176 - 79,747,237RGD
HuRef1479,874,003 - 79,875,064UniSTS
stSG632123  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,691,479 - 99,692,478UniSTSGRCh37
Build 361498,761,232 - 98,762,231RGDNCBI36
Celera1479,747,218 - 79,748,217RGD
HuRef1479,875,045 - 79,876,044UniSTS
stSG632124  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,692,530 - 99,693,582UniSTSGRCh37
Build 361498,762,283 - 98,763,335RGDNCBI36
Celera1479,748,269 - 79,749,321RGD
HuRef1479,876,096 - 79,877,148UniSTS
stSG632125  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,693,563 - 99,693,887UniSTSGRCh37
Build 361498,763,316 - 98,763,640RGDNCBI36
Celera1479,749,302 - 79,749,626RGD
HuRef1479,877,129 - 79,877,453UniSTS
stSG632126  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,693,919 - 99,695,021UniSTSGRCh37
Build 361498,763,672 - 98,764,774RGDNCBI36
Celera1479,749,658 - 79,750,760RGD
HuRef1479,877,485 - 79,878,587UniSTS
stSG632127  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,695,003 - 99,696,452UniSTSGRCh37
Build 361498,764,756 - 98,766,205RGDNCBI36
Celera1479,750,742 - 79,752,143RGD
HuRef1479,878,569 - 79,880,018UniSTS
stSG632128  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,696,520 - 99,697,687UniSTSGRCh37
Build 361498,766,273 - 98,767,440RGDNCBI36
Celera1479,752,211 - 79,753,378RGD
HuRef1479,880,086 - 79,881,253UniSTS
stSG632129  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,697,718 - 99,698,745UniSTSGRCh37
Build 361498,767,471 - 98,768,498RGDNCBI36
Celera1479,753,409 - 79,754,436RGD
HuRef1479,881,284 - 79,882,311UniSTS
stSG632130  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,698,726 - 99,699,729UniSTSGRCh37
Build 361498,768,479 - 98,769,482RGDNCBI36
Celera1479,754,417 - 79,755,420RGD
HuRef1479,882,292 - 79,883,295UniSTS
stSG632131  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,699,710 - 99,701,016UniSTSGRCh37
Build 361498,769,463 - 98,770,769RGDNCBI36
Celera1479,755,401 - 79,756,707RGD
HuRef1479,883,276 - 79,884,582UniSTS
stSG632132  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,700,997 - 99,702,203UniSTSGRCh37
Build 361498,770,750 - 98,771,956RGDNCBI36
Celera1479,756,688 - 79,757,894RGD
HuRef1479,884,563 - 79,885,769UniSTS
stSG632133  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,702,185 - 99,703,345UniSTSGRCh37
Build 361498,771,938 - 98,773,098RGDNCBI36
Celera1479,757,876 - 79,759,035RGD
HuRef1479,885,751 - 79,886,910UniSTS
stSG632134  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,703,326 - 99,704,549UniSTSGRCh37
Build 361498,773,079 - 98,774,302RGDNCBI36
Celera1479,759,016 - 79,760,239RGD
HuRef1479,886,891 - 79,888,114UniSTS
stSG632135  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,704,530 - 99,706,007UniSTSGRCh37
Build 361498,774,283 - 98,775,760RGDNCBI36
Celera1479,760,220 - 79,761,697RGD
HuRef1479,888,095 - 79,889,572UniSTS
stSG632136  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,705,988 - 99,707,405UniSTSGRCh37
Build 361498,775,741 - 98,777,158RGDNCBI36
Celera1479,761,678 - 79,763,095RGD
HuRef1479,889,553 - 79,890,970UniSTS
stSG632137  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,707,386 - 99,708,644UniSTSGRCh37
Build 361498,777,139 - 98,778,397RGDNCBI36
Celera1479,763,076 - 79,764,334RGD
HuRef1479,890,951 - 79,892,209UniSTS
stSG632138  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,708,625 - 99,710,058UniSTSGRCh37
Build 361498,778,378 - 98,779,811RGDNCBI36
Celera1479,764,315 - 79,765,748RGD
HuRef1479,892,190 - 79,893,623UniSTS
stSG632139  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,710,039 - 99,711,177UniSTSGRCh37
Build 361498,779,792 - 98,780,930RGDNCBI36
Celera1479,765,729 - 79,766,867RGD
HuRef1479,893,604 - 79,894,735UniSTS
stSG632140  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,711,158 - 99,712,645UniSTSGRCh37
Build 361498,780,911 - 98,782,398RGDNCBI36
Celera1479,766,848 - 79,768,336RGD
HuRef1479,894,716 - 79,896,204UniSTS
stSG632141  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,712,624 - 99,713,831UniSTSGRCh37
Build 361498,782,377 - 98,783,584RGDNCBI36
Celera1479,768,315 - 79,769,523RGD
HuRef1479,896,183 - 79,897,391UniSTS
stSG632142  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,713,880 - 99,714,941UniSTSGRCh37
Build 361498,783,633 - 98,784,694RGDNCBI36
Celera1479,769,572 - 79,770,633RGD
HuRef1479,897,440 - 79,898,501UniSTS
stSG632143  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,714,926 - 99,715,937UniSTSGRCh37
Build 361498,784,679 - 98,785,690RGDNCBI36
Celera1479,770,618 - 79,771,629RGD
HuRef1479,898,486 - 79,899,497UniSTS
stSG632145  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,717,322 - 99,718,506UniSTSGRCh37
Build 361498,787,075 - 98,788,259RGDNCBI36
Celera1479,773,015 - 79,774,199RGD
HuRef1479,900,883 - 79,902,067UniSTS
stSG632146  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,718,650 - 99,719,780UniSTSGRCh37
Build 361498,788,403 - 98,789,533RGDNCBI36
Celera1479,774,343 - 79,775,473RGD
HuRef1479,902,211 - 79,903,341UniSTS
stSG632147  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,719,761 - 99,720,902UniSTSGRCh37
Build 361498,789,514 - 98,790,655RGDNCBI36
Celera1479,775,454 - 79,776,595RGD
HuRef1479,903,322 - 79,904,463UniSTS
stSG632148  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,720,883 - 99,721,980UniSTSGRCh37
Build 361498,790,636 - 98,791,733RGDNCBI36
Celera1479,776,576 - 79,777,672RGD
HuRef1479,904,444 - 79,905,540UniSTS
stSG632149  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,721,961 - 99,723,336UniSTSGRCh37
Build 361498,791,714 - 98,793,089RGDNCBI36
Celera1479,777,653 - 79,779,028RGD
HuRef1479,905,521 - 79,906,896UniSTS
stSG632150  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,723,533 - 99,724,771UniSTSGRCh37
Build 361498,793,286 - 98,794,524RGDNCBI36
Celera1479,779,225 - 79,780,463RGD
HuRef1479,907,093 - 79,908,331UniSTS
stSG632151  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,724,752 - 99,726,203UniSTSGRCh37
Build 361498,794,505 - 98,795,956RGDNCBI36
Celera1479,780,444 - 79,781,895RGD
HuRef1479,908,312 - 79,909,763UniSTS
stSG632152  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,726,184 - 99,727,600UniSTSGRCh37
Build 361498,795,937 - 98,797,353RGDNCBI36
Celera1479,781,876 - 79,783,292RGD
HuRef1479,909,744 - 79,911,160UniSTS
stSG632153  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,727,741 - 99,729,025UniSTSGRCh37
Build 361498,797,494 - 98,798,778RGDNCBI36
Celera1479,783,433 - 79,784,717RGD
HuRef1479,911,301 - 79,912,585UniSTS
stSG632154  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,729,006 - 99,730,132UniSTSGRCh37
GRCh371499,729,006 - 99,730,053UniSTSGRCh37
Build 361498,798,759 - 98,799,806RGDNCBI36
Celera1479,784,698 - 79,785,745RGD
Celera1479,784,698 - 79,785,824UniSTS
HuRef1479,912,566 - 79,913,613UniSTS
HuRef1479,912,566 - 79,913,692UniSTS
stSG632156  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,731,430 - 99,732,414UniSTSGRCh37
GRCh371499,731,388 - 99,732,414UniSTSGRCh37
Build 361498,801,141 - 98,802,167RGDNCBI36
Celera1479,787,080 - 79,788,106RGD
Celera1479,787,122 - 79,788,106UniSTS
HuRef1479,914,947 - 79,915,972UniSTS
HuRef1479,914,989 - 79,915,972UniSTS
stSG632158  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,732,639 - 99,733,776UniSTSGRCh37
Build 361498,802,392 - 98,803,529RGDNCBI36
Celera1479,788,331 - 79,789,468RGD
HuRef1479,916,197 - 79,917,334UniSTS
stSG632161  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,736,179 - 99,737,222UniSTSGRCh37
Build 361498,805,932 - 98,806,975RGDNCBI36
Celera1479,791,871 - 79,792,904RGD
HuRef1479,919,740 - 79,920,855UniSTS
stSG632163  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371499,738,517 - 99,739,572UniSTSGRCh37
Build 361498,808,270 - 98,809,325RGDNCBI36
Celera1479,794,207 - 79,795,262RGD
HuRef1479,922,161 - 79,923,216UniSTS
WI-19381  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map14q32.2UniSTS
HuRef1479,845,653 - 79,845,903UniSTS
GeneMap99-GB4 RH Map14269.66UniSTS
Whitehead-RH Map14347.8UniSTS


Expression

RNA-SEQ Expression

adipose tissue
alimentary part of gastrointestinal system
appendage
circulatory system
ectoderm
endocrine system
endoderm
entire extraembryonic component
exocrine system
hemolymphoid system
hepatobiliary system
integumental system
mesenchyme
mesoderm
musculoskeletal system
nervous system
pharyngeal arch
renal system
reproductive system
respiratory system
sensory system
1204 2411 2748 2186 4878 1706 2262 2 608 1681 449 2214 6913 6155 44 3692 1 821 1685 1543 172

Sequence

Nucleotide Sequences
RefSeq Transcripts NG_027894 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001282237 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001282238 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_022898 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_138576 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047431707 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047431708 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054376623 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054376624 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AB041218 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AB041222 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AB043584 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AB057668 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AB057669 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AB057670 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF086271 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AJ404614 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL109767 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL162151 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL359681 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471061 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068264 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  FB736423 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  JQ861941 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Ensembl Acc Id: ENST00000345514   ⟹   ENSP00000280435
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1499,169,287 - 99,271,485 (-)Ensembl
Ensembl Acc Id: ENST00000357195   ⟹   ENSP00000349723
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1499,169,287 - 99,272,197 (-)Ensembl
Ensembl Acc Id: ENST00000443726   ⟹   ENSP00000387419
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1499,173,961 - 99,271,524 (-)Ensembl
RefSeq Acc Id: NM_001282237   ⟹   NP_001269166
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381499,169,287 - 99,272,197 (-)NCBI
HuRef1479,819,226 - 79,921,694 (-)NCBI
CHM1_11499,573,389 - 99,675,806 (-)NCBI
T2T-CHM13v2.01493,400,844 - 93,503,767 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001282238   ⟹   NP_001269167
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381499,169,287 - 99,272,197 (-)NCBI
HuRef1479,819,226 - 79,921,694 (-)NCBI
CHM1_11499,573,389 - 99,675,806 (-)NCBI
T2T-CHM13v2.01493,400,844 - 93,503,767 (-)NCBI
Sequence:
RefSeq Acc Id: NM_022898   ⟹   NP_075049
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381499,169,287 - 99,272,197 (-)NCBI
GRCh371499,635,624 - 99,738,514 (-)NCBI
Build 361498,705,377 - 98,807,575 (-)NCBI Archive
HuRef1479,819,226 - 79,921,694 (-)NCBI
CHM1_11499,573,389 - 99,675,806 (-)NCBI
T2T-CHM13v2.01493,400,844 - 93,503,767 (-)NCBI
Sequence:
RefSeq Acc Id: NM_138576   ⟹   NP_612808
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381499,169,287 - 99,272,197 (-)NCBI
GRCh371499,635,624 - 99,738,514 (-)NCBI
Build 361498,705,377 - 98,807,575 (-)NCBI Archive
HuRef1479,819,226 - 79,921,694 (-)NCBI
CHM1_11499,573,389 - 99,675,806 (-)NCBI
T2T-CHM13v2.01493,400,844 - 93,503,767 (-)NCBI
Sequence:
RefSeq Acc Id: XM_047431707   ⟹   XP_047287663
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381499,169,287 - 99,269,100 (-)NCBI
RefSeq Acc Id: XM_047431708   ⟹   XP_047287664
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381499,169,287 - 99,272,197 (-)NCBI
RefSeq Acc Id: XM_054376623   ⟹   XP_054232598
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01493,400,844 - 93,500,671 (-)NCBI
RefSeq Acc Id: XM_054376624   ⟹   XP_054232599
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01493,400,844 - 93,503,767 (-)NCBI
RefSeq Acc Id: NP_075049   ⟸   NM_022898
- Peptide Label: isoform 2
- UniProtKB: L8B567 (UniProtKB/TrEMBL),   D3YTK1 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_612808   ⟸   NM_138576
- Peptide Label: isoform 1
- UniProtKB: Q9H162 (UniProtKB/Swiss-Prot),   Q9C0K0 (UniProtKB/Swiss-Prot),   L8B7P7 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001269167   ⟸   NM_001282238
- Peptide Label: isoform 4
- UniProtKB: L8B862 (UniProtKB/TrEMBL),   D3YTK1 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001269166   ⟸   NM_001282237
- Peptide Label: isoform 3
- UniProtKB: L8B8F6 (UniProtKB/TrEMBL)
- Sequence:
Ensembl Acc Id: ENSP00000280435   ⟸   ENST00000345514
Ensembl Acc Id: ENSP00000387419   ⟸   ENST00000443726
Ensembl Acc Id: ENSP00000349723   ⟸   ENST00000357195
RefSeq Acc Id: XP_047287664   ⟸   XM_047431708
- Peptide Label: isoform X2
- UniProtKB: D3YTK1 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_047287663   ⟸   XM_047431707
- Peptide Label: isoform X1
- UniProtKB: D3YTK1 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054232599   ⟸   XM_054376624
- Peptide Label: isoform X2
- UniProtKB: D3YTK1 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054232598   ⟸   XM_054376623
- Peptide Label: isoform X1
- UniProtKB: D3YTK1 (UniProtKB/TrEMBL)
Protein Domains
C2H2-type

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q9C0K0-F1-model_v2 AlphaFold Q9C0K0 1-894 view protein structure

Promoters
RGD ID:6791289
Promoter ID:HG_KWN:20143
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   CD4+TCell_2Hour,   Jurkat,   K562,   Lymphoblastoid,   NB4
Transcripts:ENST00000345514,   ENST00000357195,   ENST00000392980
Position:
Human AssemblyChrPosition (strand)Source
Build 361498,807,176 - 98,808,387 (-)MPROMDB
RGD ID:7228599
Promoter ID:EPDNEW_H20046
Type:initiation region
Name:BCL11B_2
Description:B-cell CLL/lymphoma 11B
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H20047  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381499,271,316 - 99,271,376EPDNEW
RGD ID:7228603
Promoter ID:EPDNEW_H20047
Type:initiation region
Name:BCL11B_1
Description:B-cell CLL/lymphoma 11B
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H20046  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381499,271,514 - 99,271,574EPDNEW

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:13222 AgrOrtholog
COSMIC BCL11B COSMIC
Ensembl Genes ENSG00000127152 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript ENST00000345514 ENTREZGENE
  ENST00000345514.2 UniProtKB/Swiss-Prot
  ENST00000357195 ENTREZGENE
  ENST00000357195.8 UniProtKB/Swiss-Prot
Gene3D-CATH Classic Zinc Finger UniProtKB/Swiss-Prot
GTEx ENSG00000127152 GTEx
HGNC ID HGNC:13222 ENTREZGENE
Human Proteome Map BCL11B Human Proteome Map
InterPro Dev/Hematopoietic_TF UniProtKB/Swiss-Prot
  Znf_C2H2_sf UniProtKB/Swiss-Prot
  Znf_C2H2_type UniProtKB/Swiss-Prot
KEGG Report hsa:64919 UniProtKB/Swiss-Prot
NCBI Gene 64919 ENTREZGENE
OMIM 606558 OMIM
PANTHER B-CELL LYMPHOMA/LEUKEMIA 11 UniProtKB/Swiss-Prot
  B-CELL LYMPHOMA/LEUKEMIA 11B UniProtKB/Swiss-Prot
Pfam zf-C2H2 UniProtKB/Swiss-Prot
PharmGKB PA25301 PharmGKB
PROSITE ZINC_FINGER_C2H2_1 UniProtKB/Swiss-Prot
  ZINC_FINGER_C2H2_2 UniProtKB/Swiss-Prot
SMART ZnF_C2H2 UniProtKB/Swiss-Prot
Superfamily-SCOP SSF57667 UniProtKB/Swiss-Prot
UniProt BC11B_HUMAN UniProtKB/Swiss-Prot
  D3YTK1 ENTREZGENE, UniProtKB/TrEMBL
  L8B567 ENTREZGENE, UniProtKB/TrEMBL
  L8B7P7 ENTREZGENE, UniProtKB/TrEMBL
  L8B862 ENTREZGENE, UniProtKB/TrEMBL
  L8B8F6 ENTREZGENE, UniProtKB/TrEMBL
  Q9C0K0 ENTREZGENE
  Q9H162 ENTREZGENE
UniProt Secondary Q9H162 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2022-10-31 BCL11B  BCL11 transcription factor B  BCL11B  BAF chromatin remodeling complex subunit BCL11B  Symbol and/or name change 19259463 PROVISIONAL
2019-01-29 BCL11B  BAF chromatin remodeling complex subunit BCL11B  BCL11B  BCL11B, BAF complex component  Symbol and/or name change 5135510 APPROVED
2018-11-06 BCL11B  BCL11B, BAF complex component  BCL11B  B cell CLL/lymphoma 11B  Symbol and/or name change 5135510 APPROVED
2017-12-19 BCL11B  B cell CLL/lymphoma 11B  BCL11B  B-cell CLL/lymphoma 11B  Symbol and/or name change 5135510 APPROVED
2016-01-12 BCL11B  B-cell CLL/lymphoma 11B  BCL11B  B-cell CLL/lymphoma 11B (zinc finger protein)  Symbol and/or name change 5135510 APPROVED