CHD6 (chromodomain helicase DNA binding protein 6) - Rat Genome Database

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Gene: CHD6 (chromodomain helicase DNA binding protein 6) Homo sapiens
Analyze
Symbol: CHD6
Name: chromodomain helicase DNA binding protein 6
RGD ID: 1321381
HGNC Page HGNC:19057
Description: Enables ATP-dependent activity, acting on DNA and transcription coregulator binding activity. Involved in cell redox homeostasis and positive regulation of transcription by RNA polymerase II. Located in nucleoplasm.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: ATP-dependent helicase CHD6; CHD-6; CHD5; chromodomain-helicase-DNA-binding protein 6; helicase C-terminal domain- and SNF2 N-terminal domain-containing protein; KIAA1335; radiation-induced gene B protein; RIGB
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Genes
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh382041,402,083 - 41,618,377 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl2041,402,083 - 41,618,384 (-)EnsemblGRCh38hg38GRCh38
GRCh372040,030,723 - 40,247,016 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 362039,464,584 - 39,680,547 (-)NCBINCBI36Build 36hg18NCBI36
Build 342039,464,583 - 39,680,547NCBI
Celera2036,741,838 - 36,957,790 (-)NCBICelera
Cytogenetic Map20q12NCBI
HuRef2036,768,458 - 36,984,731 (-)NCBIHuRef
CHM1_12039,935,021 - 40,151,300 (-)NCBICHM1_1
T2T-CHM13v2.02043,133,884 - 43,350,249 (-)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Gene Ontology Annotations     Click to see Annotation Detail View

Biological Process

Cellular Component
chromatin  (IBA)
nucleoplasm  (IDA,IEA)
nucleus  (IBA,IEA)

Molecular Pathway Annotations     Click to see Annotation Detail View
Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype
References

References - curated
# Reference Title Reference Citation
1. GOAs Human GO annotations GOA_HUMAN data from the GO Consortium
2. The Nrf2 regulatory network provides an interface between redox and intermediary metabolism. Hayes JD and Dinkova-Kostova AT, Trends Biochem Sci. 2014 Apr;39(4):199-218. doi: 10.1016/j.tibs.2014.02.002. Epub 2014 Mar 16.
3. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
4. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:8889548   PMID:10718198   PMID:11780052   PMID:11889561   PMID:12168954   PMID:12477932   PMID:14702039   PMID:15231748   PMID:15489334   PMID:16314513   PMID:16713569   PMID:17027977  
PMID:17081983   PMID:17525332   PMID:20085707   PMID:20379614   PMID:20631145   PMID:20850016   PMID:20936779   PMID:21873635   PMID:21899694   PMID:22745009   PMID:23408615   PMID:23667531  
PMID:25281560   PMID:25631877   PMID:26487511   PMID:26496610   PMID:27634302   PMID:28065597   PMID:28416489   PMID:28533432   PMID:28611215   PMID:29507755   PMID:29676528   PMID:29845934  
PMID:30021884   PMID:30463901   PMID:30651562   PMID:30745168   PMID:30804502   PMID:31182584   PMID:31527615   PMID:33499712   PMID:33961781   PMID:34021162   PMID:34079125   PMID:34672954  
PMID:34709266   PMID:35140242   PMID:35439318   PMID:35819319   PMID:35906200   PMID:35914814   PMID:35944360   PMID:36089195   PMID:36408932   PMID:36473865   PMID:37689310  


Genomics

Comparative Map Data
CHD6
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh382041,402,083 - 41,618,377 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl2041,402,083 - 41,618,384 (-)EnsemblGRCh38hg38GRCh38
GRCh372040,030,723 - 40,247,016 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 362039,464,584 - 39,680,547 (-)NCBINCBI36Build 36hg18NCBI36
Build 342039,464,583 - 39,680,547NCBI
Celera2036,741,838 - 36,957,790 (-)NCBICelera
Cytogenetic Map20q12NCBI
HuRef2036,768,458 - 36,984,731 (-)NCBIHuRef
CHM1_12039,935,021 - 40,151,300 (-)NCBICHM1_1
T2T-CHM13v2.02043,133,884 - 43,350,249 (-)NCBIT2T-CHM13v2.0
Chd6
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm392160,788,898 - 160,951,006 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl2160,788,898 - 160,950,995 (-)EnsemblGRCm39 Ensembl
GRCm382160,946,978 - 161,109,086 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl2160,946,978 - 161,109,075 (-)EnsemblGRCm38mm10GRCm38
MGSCv372160,772,714 - 160,934,792 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv362160,638,419 - 160,800,497 (-)NCBIMGSCv36mm8
Celera2166,877,653 - 167,040,009 (-)NCBICelera
Cytogenetic Map2H2NCBI
cM Map280.98NCBI
Chd6
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr83170,016,204 - 170,177,480 (-)NCBIGRCr8
mRatBN7.23149,596,509 - 149,757,765 (-)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl3149,596,509 - 149,757,755 (-)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx3153,409,455 - 153,571,162 (-)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.03161,908,858 - 162,070,560 (-)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.03159,648,665 - 159,809,906 (-)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.03156,937,746 - 157,099,328 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl3156,937,733 - 157,099,306 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.03163,164,938 - 163,324,764 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.43151,741,389 - 151,924,668 (-)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.13151,647,823 - 151,830,771 (-)NCBI
Celera3148,269,027 - 148,429,163 (-)NCBICelera
Cytogenetic Map3q42NCBI
Chd6
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_00495544515,360,025 - 15,560,988 (+)EnsemblChiLan1.0
ChiLan1.0NW_00495544515,360,074 - 15,576,410 (+)NCBIChiLan1.0ChiLan1.0
CHD6
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v22147,144,211 - 47,354,354 (-)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan12047,137,310 - 47,347,383 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v02037,744,012 - 37,953,593 (-)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.12038,839,685 - 38,988,719 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl2038,839,685 - 38,999,501 (-)Ensemblpanpan1.1panPan2
CHD6
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.12429,397,320 - 29,601,206 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl2429,397,306 - 29,601,350 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha2429,042,568 - 29,246,480 (-)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.02430,102,193 - 30,305,887 (-)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl2430,102,811 - 30,306,032 (-)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.12429,370,977 - 29,574,934 (-)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.02429,474,474 - 29,678,500 (-)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.02429,971,008 - 30,174,849 (-)NCBIUU_Cfam_GSD_1.0
Chd6
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_024408640178,354,920 - 178,570,711 (-)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_004936561178,700 - 394,842 (+)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_004936561238,307 - 394,082 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
CHD6
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl1744,048,098 - 44,265,431 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.11744,048,056 - 44,265,472 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.21749,502,246 - 49,555,890 (-)NCBISscrofa10.2Sscrofa10.2susScr3
CHD6
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.1222,163,836 - 22,373,098 (+)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl222,223,919 - 22,373,275 (+)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366605070,981,245 - 71,189,656 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Chd6
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_00462479012,610,254 - 12,858,368 (+)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_00462479012,610,418 - 12,858,062 (+)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in CHD6
114 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
NM_032221.5(CHD6):c.451G>A (p.Ala151Thr) single nucleotide variant not provided [RCV000914429] Chr20:41533153 [GRCh38]
Chr20:40161792 [GRCh37]
Chr20:20q12		 benign
GRCh38/hg38 20q11.22-13.11(chr20:34249453-43359749)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053002]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053002]|See cases [RCV000053002] Chr20:34249453..43359749 [GRCh38]
Chr20:32837259..41988389 [GRCh37]
Chr20:32300920..41421803 [NCBI36]
Chr20:20q11.22-13.11		 pathogenic
NM_032221.4(CHD6):c.1557C>T (p.Ser519=) single nucleotide variant Malignant melanoma [RCV000072633] Chr20:41489901 [GRCh38]
Chr20:40118541 [GRCh37]
Chr20:39551955 [NCBI36]
Chr20:20q12		 not provided
NM_032221.4(CHD6):c.6221C>T (p.Pro2074Leu) single nucleotide variant Malignant melanoma [RCV000063734] Chr20:41417256 [GRCh38]
Chr20:40045896 [GRCh37]
Chr20:39479310 [NCBI36]
Chr20:20q12		 not provided
NM_032221.4(CHD6):c.4419G>A (p.Lys1473=) single nucleotide variant Malignant melanoma [RCV000063735] Chr20:41423628 [GRCh38]
Chr20:40052268 [GRCh37]
Chr20:39485682 [NCBI36]
Chr20:20q12		 not provided
NM_032221.4(CHD6):c.4402G>T (p.Val1468Phe) single nucleotide variant Malignant melanoma [RCV000063736] Chr20:41423645 [GRCh38]
Chr20:40052285 [GRCh37]
Chr20:39485699 [NCBI36]
Chr20:20q12		 not provided
NM_032221.4(CHD6):c.1545C>T (p.Ile515=) single nucleotide variant Malignant melanoma [RCV000063737] Chr20:41489913 [GRCh38]
Chr20:40118553 [GRCh37]
Chr20:39551967 [NCBI36]
Chr20:20q12		 not provided
GRCh38/hg38 20p13-q13.33(chr20:99557-64277321)x3 copy number gain See cases [RCV000135859] Chr20:99557..64277321 [GRCh38]
Chr20:80198..62908674 [GRCh37]
Chr20:28198..62379118 [NCBI36]
Chr20:20p13-q13.33		 pathogenic
GRCh38/hg38 20q12(chr20:41254206-41853686)x3 copy number gain See cases [RCV000137445] Chr20:41254206..41853686 [GRCh38]
Chr20:39882846..40482326 [GRCh37]
Chr20:39316260..39915740 [NCBI36]
Chr20:20q12		 likely benign
NM_032221.5(CHD6):c.7165C>T (p.Arg2389Cys) single nucleotide variant not specified [RCV000202929] Chr20:41412230 [GRCh38]
Chr20:40040870 [GRCh37]
Chr20:20q12		 benign
GRCh38/hg38 20q11.22-13.12(chr20:35237946-47631818)x1 copy number loss See cases [RCV000140816] Chr20:35237946..47631818 [GRCh38]
Chr20:33825749..46260562 [GRCh37]
Chr20:33289165..45693969 [NCBI36]
Chr20:20q11.22-13.12		 pathogenic
NM_032221.5(CHD6):c.4637G>A (p.Arg1546Gln) single nucleotide variant Inborn genetic diseases [RCV003245009] Chr20:41421998 [GRCh38]
Chr20:40050638 [GRCh37]
Chr20:20q12		 uncertain significance
GRCh37/hg19 20p13-q13.33(chr20:61569-62915555)x3 copy number gain See cases [RCV000510832] Chr20:61569..62915555 [GRCh37]
Chr20:20p13-q13.33		 pathogenic
NM_032221.5(CHD6):c.6755T>G (p.Leu2252Arg) single nucleotide variant Inborn genetic diseases [RCV003295736] Chr20:41415370 [GRCh38]
Chr20:40044010 [GRCh37]
Chr20:20q12		 uncertain significance
NM_032221.5(CHD6):c.4756A>G (p.Ile1586Val) single nucleotide variant Inborn genetic diseases [RCV003254305] Chr20:41421879 [GRCh38]
Chr20:40050519 [GRCh37]
Chr20:20q12		 uncertain significance
NM_032221.5(CHD6):c.3806A>T (p.Tyr1269Phe) single nucleotide variant Inborn genetic diseases [RCV003299173] Chr20:41445736 [GRCh38]
Chr20:40074376 [GRCh37]
Chr20:20q12		 uncertain significance
NM_032221.5(CHD6):c.5350A>G (p.Ile1784Val) single nucleotide variant Inborn genetic diseases [RCV003271114] Chr20:41421285 [GRCh38]
Chr20:40049925 [GRCh37]
Chr20:20q12		 uncertain significance
NM_032221.5(CHD6):c.722A>G (p.Gln241Arg) single nucleotide variant Inborn genetic diseases [RCV003265008] Chr20:41512976 [GRCh38]
Chr20:40141615 [GRCh37]
Chr20:20q12		 uncertain significance
NM_032221.5(CHD6):c.4096G>A (p.Val1366Ile) single nucleotide variant Inborn genetic diseases [RCV003254282] Chr20:41426126 [GRCh38]
Chr20:40054766 [GRCh37]
Chr20:20q12		 likely benign
NM_032221.5(CHD6):c.530C>T (p.Ala177Val) single nucleotide variant Inborn genetic diseases [RCV003299632] Chr20:41533074 [GRCh38]
Chr20:40161713 [GRCh37]
Chr20:20q12		 uncertain significance
NM_032221.5(CHD6):c.286C>T (p.Arg96Trp) single nucleotide variant Inborn genetic diseases [RCV003277846] Chr20:41533318 [GRCh38]
Chr20:40161957 [GRCh37]
Chr20:20q12		 uncertain significance
NM_032221.5(CHD6):c.835C>G (p.Leu279Val) single nucleotide variant Inborn genetic diseases [RCV003276702] Chr20:41512863 [GRCh38]
Chr20:40141502 [GRCh37]
Chr20:20q12		 uncertain significance
GRCh37/hg19 20p13-q13.33(chr20:61569-62915555) copy number gain See cases [RCV000512450] Chr20:61569..62915555 [GRCh37]
Chr20:20p13-q13.33		 pathogenic
GRCh37/hg19 20p13-q13.33(chr20:63244-62961294)x3 copy number gain not provided [RCV000741059] Chr20:63244..62961294 [GRCh37]
Chr20:20p13-q13.33		 pathogenic
GRCh37/hg19 20p13-q13.33(chr20:63244-62912463)x3 copy number gain not provided [RCV000741057] Chr20:63244..62912463 [GRCh37]
Chr20:20p13-q13.33		 pathogenic
GRCh37/hg19 20p13-q13.33(chr20:63244-62948788)x3 copy number gain not provided [RCV000741058] Chr20:63244..62948788 [GRCh37]
Chr20:20p13-q13.33		 pathogenic
NM_032221.5(CHD6):c.6939+8T>C single nucleotide variant not provided [RCV000895460] Chr20:41415178 [GRCh38]
Chr20:40043818 [GRCh37]
Chr20:20q12		 likely benign
NM_032221.5(CHD6):c.218C>G (p.Pro73Arg) single nucleotide variant Inborn genetic diseases [RCV003245398] Chr20:41533386 [GRCh38]
Chr20:40162025 [GRCh37]
Chr20:20q12		 uncertain significance
NM_032221.5(CHD6):c.7656G>A (p.Ala2552=) single nucleotide variant not provided [RCV000924039] Chr20:41405085 [GRCh38]
Chr20:40033725 [GRCh37]
Chr20:20q12		 likely benign
NM_032221.5(CHD6):c.2745C>G (p.Arg915=) single nucleotide variant not provided [RCV000903823] Chr20:41457348 [GRCh38]
Chr20:40085988 [GRCh37]
Chr20:20q12		 benign
NM_032221.5(CHD6):c.852+4T>C single nucleotide variant not provided [RCV000966491] Chr20:41512842 [GRCh38]
Chr20:40141481 [GRCh37]
Chr20:20q12		 benign
NM_032221.5(CHD6):c.7935G>A (p.Ser2645=) single nucleotide variant not provided [RCV000959968] Chr20:41404806 [GRCh38]
Chr20:40033446 [GRCh37]
Chr20:20q12		 benign
NM_032221.5(CHD6):c.6964G>A (p.Ala2322Thr) single nucleotide variant not provided [RCV000959969] Chr20:41413491 [GRCh38]
Chr20:40042131 [GRCh37]
Chr20:20q12		 benign
NM_032221.5(CHD6):c.3627C>T (p.Pro1209=) single nucleotide variant not provided [RCV000898604] Chr20:41451002 [GRCh38]
Chr20:40079642 [GRCh37]
Chr20:20q12		 benign
NM_032221.5(CHD6):c.3252C>T (p.Arg1084=) single nucleotide variant not provided [RCV000967554] Chr20:41452811 [GRCh38]
Chr20:40081451 [GRCh37]
Chr20:20q12		 benign
NM_032221.5(CHD6):c.3296G>A (p.Arg1099Gln) single nucleotide variant Adult spinal cord ependymoma [RCV000786038] Chr20:41452767 [GRCh38]
Chr20:40081407 [GRCh37]
Chr20:20q12		 uncertain significance
NM_032221.5(CHD6):c.6171A>G (p.Thr2057=) single nucleotide variant not provided [RCV000938235] Chr20:41417306 [GRCh38]
Chr20:40045946 [GRCh37]
Chr20:20q12		 likely benign
NM_032221.5(CHD6):c.5874G>T (p.Glu1958Asp) single nucleotide variant Inborn genetic diseases [RCV003249874] Chr20:41420761 [GRCh38]
Chr20:40049401 [GRCh37]
Chr20:20q12		 uncertain significance
NM_032221.5(CHD6):c.5863T>A (p.Phe1955Ile) single nucleotide variant Inborn genetic diseases [RCV003292276] Chr20:41420772 [GRCh38]
Chr20:40049412 [GRCh37]
Chr20:20q12		 uncertain significance
NM_032221.5(CHD6):c.238A>T (p.Asn80Tyr) single nucleotide variant Inborn genetic diseases [RCV003251627] Chr20:41533366 [GRCh38]
Chr20:40162005 [GRCh37]
Chr20:20q12		 uncertain significance
NM_032221.5(CHD6):c.7210G>C (p.Glu2404Gln) single nucleotide variant not provided [RCV000962739] Chr20:41412185 [GRCh38]
Chr20:40040825 [GRCh37]
Chr20:20q12		 benign
NM_032221.5(CHD6):c.6285C>T (p.Arg2095=) single nucleotide variant not provided [RCV000896062] Chr20:41416789 [GRCh38]
Chr20:40045429 [GRCh37]
Chr20:20q12		 likely benign
NM_032221.5(CHD6):c.554+5G>A single nucleotide variant not provided [RCV000955842] Chr20:41533045 [GRCh38]
Chr20:40161684 [GRCh37]
Chr20:20q12		 benign
NM_032221.5(CHD6):c.5277T>A (p.Thr1759=) single nucleotide variant not provided [RCV000958067] Chr20:41421358 [GRCh38]
Chr20:40049998 [GRCh37]
Chr20:20q12		 benign
NM_032221.5(CHD6):c.4556G>A (p.Gly1519Asp) single nucleotide variant not provided [RCV000958068] Chr20:41422079 [GRCh38]
Chr20:40050719 [GRCh37]
Chr20:20q12		 benign
NM_032221.5(CHD6):c.3813G>A (p.Glu1271=) single nucleotide variant not provided [RCV000955841] Chr20:41445729 [GRCh38]
Chr20:40074369 [GRCh37]
Chr20:20q12		 benign
NM_032221.5(CHD6):c.264A>T (p.Gly88=) single nucleotide variant not provided [RCV000955843] Chr20:41533340 [GRCh38]
Chr20:40161979 [GRCh37]
Chr20:20q12		 benign
NM_032221.5(CHD6):c.5603A>T (p.Glu1868Val) single nucleotide variant Inborn genetic diseases [RCV002836557] Chr20:41421032 [GRCh38]
Chr20:40049672 [GRCh37]
Chr20:20q12		 uncertain significance
NM_032221.5(CHD6):c.3614C>G (p.Ala1205Gly) single nucleotide variant not provided [RCV001658548] Chr20:41451015 [GRCh38]
Chr20:40079655 [GRCh37]
Chr20:20q12		 benign
NM_032221.5(CHD6):c.1858-19G>A single nucleotide variant not provided [RCV001720406] Chr20:41487827 [GRCh38]
Chr20:40116467 [GRCh37]
Chr20:20q12		 benign
Single allele deletion Focal-onset seizure [RCV001004039] Chr20:34980430..46806549 [GRCh37]
Chr20:20q11.23-13.13		 likely pathogenic
GRCh37/hg19 20q12(chr20:40092168-40193233)x1 copy number loss not provided [RCV001258906] Chr20:40092168..40193233 [GRCh37]
Chr20:20q12		 likely benign
GRCh37/hg19 20q12(chr20:40059151-40877732)x3 copy number gain not provided [RCV001258908] Chr20:40059151..40877732 [GRCh37]
Chr20:20q12		 uncertain significance
NM_032221.5(CHD6):c.3403C>T (p.Arg1135Cys) single nucleotide variant not provided [RCV001810674] Chr20:41451946 [GRCh38]
Chr20:40080586 [GRCh37]
Chr20:20q12		 uncertain significance
NM_032221.5(CHD6):c.5882_5895del (p.Lys1961fs) deletion not provided [RCV001814942] Chr20:41420740..41420753 [GRCh38]
Chr20:40049380..40049393 [GRCh37]
Chr20:20q12		 uncertain significance
NM_032221.5(CHD6):c.6284G>A (p.Arg2095His) single nucleotide variant Inborn genetic diseases [RCV003300409] Chr20:41416790 [GRCh38]
Chr20:40045430 [GRCh37]
Chr20:20q12		 uncertain significance
GRCh37/hg19 20q12(chr20:40135346-40399258)x3 copy number gain not provided [RCV002472820] Chr20:40135346..40399258 [GRCh37]
Chr20:20q12		 uncertain significance
NM_032221.5(CHD6):c.4445G>A (p.Arg1482His) single nucleotide variant Inborn genetic diseases [RCV002817503] Chr20:41423602 [GRCh38]
Chr20:40052242 [GRCh37]
Chr20:20q12		 uncertain significance
NM_032221.5(CHD6):c.6109G>A (p.Gly2037Arg) single nucleotide variant Inborn genetic diseases [RCV002774272] Chr20:41420526 [GRCh38]
Chr20:40049166 [GRCh37]
Chr20:20q12		 uncertain significance
NM_032221.5(CHD6):c.220A>T (p.Arg74Trp) single nucleotide variant Inborn genetic diseases [RCV002817522] Chr20:41533384 [GRCh38]
Chr20:40162023 [GRCh37]
Chr20:20q12		 uncertain significance
NM_032221.5(CHD6):c.7404C>A (p.Phe2468Leu) single nucleotide variant Inborn genetic diseases [RCV002779464] Chr20:41405337 [GRCh38]
Chr20:40033977 [GRCh37]
Chr20:20q12		 uncertain significance
NM_032221.5(CHD6):c.464G>A (p.Arg155Gln) single nucleotide variant Inborn genetic diseases [RCV002970480] Chr20:41533140 [GRCh38]
Chr20:40161779 [GRCh37]
Chr20:20q12		 uncertain significance
NM_032221.5(CHD6):c.5269G>C (p.Gly1757Arg) single nucleotide variant Inborn genetic diseases [RCV002901858] Chr20:41421366 [GRCh38]
Chr20:40050006 [GRCh37]
Chr20:20q12		 uncertain significance
NM_032221.5(CHD6):c.4244G>A (p.Arg1415Gln) single nucleotide variant Inborn genetic diseases [RCV002731712] Chr20:41425280 [GRCh38]
Chr20:40053920 [GRCh37]
Chr20:20q12		 uncertain significance
NM_032221.5(CHD6):c.4241G>T (p.Cys1414Phe) single nucleotide variant Inborn genetic diseases [RCV002840023] Chr20:41425283 [GRCh38]
Chr20:40053923 [GRCh37]
Chr20:20q12		 uncertain significance
NM_032221.5(CHD6):c.4601G>A (p.Arg1534His) single nucleotide variant Inborn genetic diseases [RCV002864652] Chr20:41422034 [GRCh38]
Chr20:40050674 [GRCh37]
Chr20:20q12		 uncertain significance
NM_032221.5(CHD6):c.434C>T (p.Pro145Leu) single nucleotide variant Inborn genetic diseases [RCV002738636] Chr20:41533170 [GRCh38]
Chr20:40161809 [GRCh37]
Chr20:20q12		 uncertain significance
NM_032221.5(CHD6):c.4570A>G (p.Thr1524Ala) single nucleotide variant Inborn genetic diseases [RCV002910459] Chr20:41422065 [GRCh38]
Chr20:40050705 [GRCh37]
Chr20:20q12		 uncertain significance
NM_032221.5(CHD6):c.5155T>C (p.Ser1719Pro) single nucleotide variant Inborn genetic diseases [RCV002887324] Chr20:41421480 [GRCh38]
Chr20:40050120 [GRCh37]
Chr20:20q12		 uncertain significance
NM_032221.5(CHD6):c.3813G>C (p.Glu1271Asp) single nucleotide variant Inborn genetic diseases [RCV002692908] Chr20:41445729 [GRCh38]
Chr20:40074369 [GRCh37]
Chr20:20q12		 uncertain significance
NM_032221.5(CHD6):c.536C>T (p.Thr179Met) single nucleotide variant Inborn genetic diseases [RCV002799986] Chr20:41533068 [GRCh38]
Chr20:40161707 [GRCh37]
Chr20:20q12		 uncertain significance
NM_032221.5(CHD6):c.6821A>G (p.Asn2274Ser) single nucleotide variant Inborn genetic diseases [RCV002738885] Chr20:41415304 [GRCh38]
Chr20:40043944 [GRCh37]
Chr20:20q12		 uncertain significance
NM_032221.5(CHD6):c.7340G>A (p.Arg2447Gln) single nucleotide variant Inborn genetic diseases [RCV002986321] Chr20:41405401 [GRCh38]
Chr20:40034041 [GRCh37]
Chr20:20q12		 uncertain significance
NM_032221.5(CHD6):c.6593C>G (p.Ser2198Cys) single nucleotide variant Inborn genetic diseases [RCV002742574] Chr20:41415532 [GRCh38]
Chr20:40044172 [GRCh37]
Chr20:20q12		 uncertain significance
NM_032221.5(CHD6):c.4828G>A (p.Asp1610Asn) single nucleotide variant Inborn genetic diseases [RCV002827906] Chr20:41421807 [GRCh38]
Chr20:40050447 [GRCh37]
Chr20:20q12		 uncertain significance
NM_032221.5(CHD6):c.6520G>A (p.Glu2174Lys) single nucleotide variant Inborn genetic diseases [RCV002873919] Chr20:41415605 [GRCh38]
Chr20:40044245 [GRCh37]
Chr20:20q12		 uncertain significance
NM_032221.5(CHD6):c.7326G>C (p.Arg2442Ser) single nucleotide variant Inborn genetic diseases [RCV002984265] Chr20:41405415 [GRCh38]
Chr20:40034055 [GRCh37]
Chr20:20q12		 uncertain significance
NM_032221.5(CHD6):c.365G>A (p.Arg122Gln) single nucleotide variant Inborn genetic diseases [RCV002955703] Chr20:41533239 [GRCh38]
Chr20:40161878 [GRCh37]
Chr20:20q12		 uncertain significance
NM_032221.5(CHD6):c.6191T>C (p.Ile2064Thr) single nucleotide variant Inborn genetic diseases [RCV002708797] Chr20:41417286 [GRCh38]
Chr20:40045926 [GRCh37]
Chr20:20q12		 uncertain significance
NM_032221.5(CHD6):c.6223A>G (p.Thr2075Ala) single nucleotide variant Inborn genetic diseases [RCV002788640] Chr20:41417254 [GRCh38]
Chr20:40045894 [GRCh37]
Chr20:20q12		 uncertain significance
NM_032221.5(CHD6):c.4871A>G (p.Gln1624Arg) single nucleotide variant Inborn genetic diseases [RCV002787518] Chr20:41421764 [GRCh38]
Chr20:40050404 [GRCh37]
Chr20:20q12		 uncertain significance
NM_032221.5(CHD6):c.6644C>T (p.Ser2215Leu) single nucleotide variant Inborn genetic diseases [RCV002878704] Chr20:41415481 [GRCh38]
Chr20:40044121 [GRCh37]
Chr20:20q12		 uncertain significance
NM_032221.5(CHD6):c.7326G>T (p.Arg2442Ser) single nucleotide variant Inborn genetic diseases [RCV002940015] Chr20:41405415 [GRCh38]
Chr20:40034055 [GRCh37]
Chr20:20q12		 uncertain significance
NM_032221.5(CHD6):c.5203A>G (p.Ile1735Val) single nucleotide variant Inborn genetic diseases [RCV002719350] Chr20:41421432 [GRCh38]
Chr20:40050072 [GRCh37]
Chr20:20q12		 likely benign
NM_032221.5(CHD6):c.7325G>C (p.Arg2442Thr) single nucleotide variant Inborn genetic diseases [RCV002812717] Chr20:41405416 [GRCh38]
Chr20:40034056 [GRCh37]
Chr20:20q12		 uncertain significance
NM_032221.5(CHD6):c.281A>G (p.Lys94Arg) single nucleotide variant Inborn genetic diseases [RCV002921531] Chr20:41533323 [GRCh38]
Chr20:40161962 [GRCh37]
Chr20:20q12		 uncertain significance
NM_032221.5(CHD6):c.3749A>G (p.Lys1250Arg) single nucleotide variant Inborn genetic diseases [RCV002897473] Chr20:41447906 [GRCh38]
Chr20:40076546 [GRCh37]
Chr20:20q12		 uncertain significance
NM_032221.5(CHD6):c.5279T>G (p.Phe1760Cys) single nucleotide variant Inborn genetic diseases [RCV002935983] Chr20:41421356 [GRCh38]
Chr20:40049996 [GRCh37]
Chr20:20q12		 uncertain significance
NM_032221.5(CHD6):c.8116G>A (p.Ala2706Thr) single nucleotide variant Inborn genetic diseases [RCV002831564] Chr20:41404625 [GRCh38]
Chr20:40033265 [GRCh37]
Chr20:20q12		 uncertain significance
NM_032221.5(CHD6):c.7085T>G (p.Leu2362Arg) single nucleotide variant Inborn genetic diseases [RCV002919865] Chr20:41413370 [GRCh38]
Chr20:40042010 [GRCh37]
Chr20:20q12		 uncertain significance
NM_032221.5(CHD6):c.7895T>C (p.Met2632Thr) single nucleotide variant Inborn genetic diseases [RCV002747387] Chr20:41404846 [GRCh38]
Chr20:40033486 [GRCh37]
Chr20:20q12		 uncertain significance
NM_032221.5(CHD6):c.8137G>T (p.Asp2713Tyr) single nucleotide variant Inborn genetic diseases [RCV002724269] Chr20:41404604 [GRCh38]
Chr20:40033244 [GRCh37]
Chr20:20q12		 uncertain significance
NM_032221.5(CHD6):c.5180A>G (p.Asn1727Ser) single nucleotide variant Inborn genetic diseases [RCV002655462] Chr20:41421455 [GRCh38]
Chr20:40050095 [GRCh37]
Chr20:20q12		 likely benign
NM_032221.5(CHD6):c.452C>T (p.Ala151Val) single nucleotide variant Inborn genetic diseases [RCV002680385] Chr20:41533152 [GRCh38]
Chr20:40161791 [GRCh37]
Chr20:20q12		 likely benign
NM_032221.5(CHD6):c.4745G>A (p.Arg1582Gln) single nucleotide variant Inborn genetic diseases [RCV002677482] Chr20:41421890 [GRCh38]
Chr20:40050530 [GRCh37]
Chr20:20q12		 uncertain significance
NM_032221.5(CHD6):c.5038G>A (p.Glu1680Lys) single nucleotide variant Inborn genetic diseases [RCV002723302] Chr20:41421597 [GRCh38]
Chr20:40050237 [GRCh37]
Chr20:20q12		 uncertain significance
NM_032221.5(CHD6):c.7247T>C (p.Leu2416Pro) single nucleotide variant Inborn genetic diseases [RCV002656322] Chr20:41412148 [GRCh38]
Chr20:40040788 [GRCh37]
Chr20:20q12		 uncertain significance
NM_032221.5(CHD6):c.6649A>G (p.Met2217Val) single nucleotide variant Inborn genetic diseases [RCV003297766] Chr20:41415476 [GRCh38]
Chr20:40044116 [GRCh37]
Chr20:20q12		 uncertain significance
NM_032221.5(CHD6):c.5222A>G (p.Lys1741Arg) single nucleotide variant Inborn genetic diseases [RCV003215136] Chr20:41421413 [GRCh38]
Chr20:40050053 [GRCh37]
Chr20:20q12		 likely benign
NM_032221.5(CHD6):c.7897G>A (p.Gly2633Ser) single nucleotide variant Inborn genetic diseases [RCV003186167] Chr20:41404844 [GRCh38]
Chr20:40033484 [GRCh37]
Chr20:20q12		 uncertain significance
NM_032221.5(CHD6):c.4622G>A (p.Arg1541His) single nucleotide variant Inborn genetic diseases [RCV003204646] Chr20:41422013 [GRCh38]
Chr20:40050653 [GRCh37]
Chr20:20q12		 uncertain significance
NM_032221.5(CHD6):c.7976A>C (p.Lys2659Thr) single nucleotide variant Inborn genetic diseases [RCV003260412] Chr20:41404765 [GRCh38]
Chr20:40033405 [GRCh37]
Chr20:20q12		 uncertain significance
NM_032221.5(CHD6):c.7592T>C (p.Met2531Thr) single nucleotide variant Inborn genetic diseases [RCV003215710] Chr20:41405149 [GRCh38]
Chr20:40033789 [GRCh37]
Chr20:20q12		 uncertain significance
NM_032221.5(CHD6):c.5186A>C (p.Glu1729Ala) single nucleotide variant Inborn genetic diseases [RCV003211822] Chr20:41421449 [GRCh38]
Chr20:40050089 [GRCh37]
Chr20:20q12		 uncertain significance
NM_032221.5(CHD6):c.5962C>A (p.Pro1988Thr) single nucleotide variant Inborn genetic diseases [RCV003206609] Chr20:41420673 [GRCh38]
Chr20:40049313 [GRCh37]
Chr20:20q12		 uncertain significance
NM_032221.5(CHD6):c.1370A>G (p.Asn457Ser) single nucleotide variant Inborn genetic diseases [RCV003359884] Chr20:41491764 [GRCh38]
Chr20:40120404 [GRCh37]
Chr20:20q12		 uncertain significance
NM_032221.5(CHD6):c.4094G>A (p.Gly1365Asp) single nucleotide variant Inborn genetic diseases [RCV003351201] Chr20:41426128 [GRCh38]
Chr20:40054768 [GRCh37]
Chr20:20q12		 uncertain significance
NM_032221.5(CHD6):c.215T>G (p.Phe72Cys) single nucleotide variant Inborn genetic diseases [RCV003373832] Chr20:41533389 [GRCh38]
Chr20:40162028 [GRCh37]
Chr20:20q12		 uncertain significance
NM_032221.5(CHD6):c.6499G>A (p.Ala2167Thr) single nucleotide variant Inborn genetic diseases [RCV003349899] Chr20:41415626 [GRCh38]
Chr20:40044266 [GRCh37]
Chr20:20q12		 uncertain significance
NM_032221.5(CHD6):c.4850A>G (p.Gln1617Arg) single nucleotide variant Inborn genetic diseases [RCV003367379] Chr20:41421785 [GRCh38]
Chr20:40050425 [GRCh37]
Chr20:20q12		 uncertain significance
NM_032221.5(CHD6):c.7277A>G (p.Asn2426Ser) single nucleotide variant Inborn genetic diseases [RCV003350161] Chr20:41405464 [GRCh38]
Chr20:40034104 [GRCh37]
Chr20:20q12		 uncertain significance
NM_032221.5(CHD6):c.452C>A (p.Ala151Glu) single nucleotide variant Inborn genetic diseases [RCV003361984] Chr20:41533152 [GRCh38]
Chr20:40161791 [GRCh37]
Chr20:20q12		 uncertain significance
NM_032221.5(CHD6):c.2365G>A (p.Asp789Asn) single nucleotide variant Inborn genetic diseases [RCV003385484] Chr20:41483412 [GRCh38]
Chr20:40112052 [GRCh37]
Chr20:20q12		 uncertain significance
NM_032221.5(CHD6):c.6013G>C (p.Glu2005Gln) single nucleotide variant Inborn genetic diseases [RCV003348508] Chr20:41420622 [GRCh38]
Chr20:40049262 [GRCh37]
Chr20:20q12		 uncertain significance
GRCh37/hg19 20q12(chr20:39839780-40169949)x3 copy number gain not provided [RCV003485214] Chr20:39839780..40169949 [GRCh37]
Chr20:20q12		 uncertain significance
NM_032221.5(CHD6):c.6741A>T (p.Ser2247=) single nucleotide variant not provided [RCV003440407] Chr20:41415384 [GRCh38]
Chr20:40044024 [GRCh37]
Chr20:20q12		 likely benign
NM_032221.5(CHD6):c.2997C>T (p.Ser999=) single nucleotide variant not provided [RCV003440408] Chr20:41455812 [GRCh38]
Chr20:40084452 [GRCh37]
Chr20:20q12		 likely benign
NM_032221.5(CHD6):c.1077G>A (p.Lys359=) single nucleotide variant not provided [RCV003431326] Chr20:41497399 [GRCh38]
Chr20:40126039 [GRCh37]
Chr20:20q12		 uncertain significance
NM_032221.5(CHD6):c.948G>A (p.Glu316=) single nucleotide variant not provided [RCV003431327] Chr20:41498194 [GRCh38]
Chr20:40126834 [GRCh37]
Chr20:20q12		 likely benign
NM_032221.5(CHD6):c.3858C>T (p.Leu1286=) single nucleotide variant not provided [RCV003431325] Chr20:41445684 [GRCh38]
Chr20:40074324 [GRCh37]
Chr20:20q12		 likely benign
NM_032221.5(CHD6):c.5577G>A (p.Leu1859=) single nucleotide variant not provided [RCV003885796] Chr20:41421058 [GRCh38]
Chr20:40049698 [GRCh37]
Chr20:20q12		 likely benign
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:2417
Count of miRNA genes:1168
Interacting mature miRNAs:1449
Transcripts:ENST00000309279, ENST00000373222, ENST00000373233, ENST00000440647, ENST00000440697, ENST00000470470, ENST00000476641, ENST00000480022, ENST00000482596
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.

Markers in Region
AL023701  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372040,085,401 - 40,085,497UniSTSGRCh37
Build 362039,518,815 - 39,518,911RGDNCBI36
Celera2036,796,064 - 36,796,160RGD
Cytogenetic Map20q12UniSTS
HuRef2036,823,116 - 36,823,212UniSTS
Z94510  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372040,082,514 - 40,082,640UniSTSGRCh37
Build 362039,515,928 - 39,516,054RGDNCBI36
Celera2036,793,177 - 36,793,303RGD
Cytogenetic Map20q12UniSTS
HuRef2036,820,229 - 36,820,355UniSTS
Z94307  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372040,171,954 - 40,172,100UniSTSGRCh37
Build 362039,605,368 - 39,605,514RGDNCBI36
Celera2036,882,613 - 36,882,759RGD
Cytogenetic Map20q12UniSTS
HuRef2036,909,673 - 36,909,819UniSTS
D20S997  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372040,030,979 - 40,031,075UniSTSGRCh37
Build 362039,464,393 - 39,464,489RGDNCBI36
Celera2036,741,647 - 36,741,743RGD
Cytogenetic Map20q12UniSTS
HuRef2036,768,696 - 36,768,792UniSTS
GeneMap99-GB4 RH Map20230.4UniSTS
NCBI RH Map20379.4UniSTS
SHGC-82496  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372040,081,511 - 40,081,833UniSTSGRCh37
Build 362039,514,925 - 39,515,247RGDNCBI36
Celera2036,792,174 - 36,792,496RGD
Cytogenetic Map20q12UniSTS
HuRef2036,819,226 - 36,819,548UniSTS
TNG Radiation Hybrid Map2018720.0UniSTS
Z94700  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372040,070,076 - 40,070,226UniSTSGRCh37
Build 362039,503,490 - 39,503,640RGDNCBI36
Celera2036,780,744 - 36,780,894RGD
Cytogenetic Map20q12UniSTS
HuRef2036,807,791 - 36,807,941UniSTS
WIAF-1711  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372040,031,913 - 40,032,157UniSTSGRCh37
Build 362039,465,327 - 39,465,571RGDNCBI36
Celera2036,742,581 - 36,742,825RGD
Cytogenetic Map20q12UniSTS
HuRef2036,769,630 - 36,769,874UniSTS
GeneMap99-GB4 RH Map20227.03UniSTS
Z94571  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372040,143,762 - 40,143,909UniSTSGRCh37
Build 362039,577,176 - 39,577,323RGDNCBI36
Celera2036,854,421 - 36,854,568RGD
Cytogenetic Map20q12UniSTS
HuRef2036,881,481 - 36,881,628UniSTS
D10S16   No map positions available.
L18426  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map18q12.1-q21.1UniSTS
Cytogenetic Map10q23.1UniSTS
Cytogenetic Map2q37UniSTS
Cytogenetic Map5q31.3UniSTS
Cytogenetic Map20q13.1UniSTS
Cytogenetic Map14q21UniSTS
Cytogenetic Map6p21.33UniSTS
Cytogenetic Map10p11UniSTS
Cytogenetic Map5q35.3UniSTS
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map5q12.3UniSTS
Cytogenetic Map8p21.2UniSTS
Cytogenetic Map14q21.3UniSTS
Cytogenetic Map11q12.3UniSTS
Cytogenetic Map10p13UniSTS
Cytogenetic Map3q13.31UniSTS
Cytogenetic Map15q22.2UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map1q21UniSTS
Cytogenetic Map3q21.3UniSTS
Cytogenetic Map9p13.2UniSTS
Cytogenetic Map20q13.12UniSTS
Cytogenetic Map9q34.1UniSTS
Cytogenetic Map1q21.3UniSTS
Cytogenetic Map1p22.1UniSTS
Cytogenetic Map19q13.31UniSTS
Cytogenetic Map22q11.23UniSTS
Cytogenetic Map19p13.1-p12UniSTS
Cytogenetic Map18p11.31-p11.21UniSTS
Cytogenetic Map2p23.1UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map6q25.3UniSTS
Cytogenetic Map1p34.3UniSTS
Cytogenetic Map11q14UniSTS
Cytogenetic Map9q21.32UniSTS
Cytogenetic Map1p34-p33UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map17q21.1UniSTS
Cytogenetic Map15q21UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map2q12.3UniSTS
Cytogenetic Map20q11.2-q13.2UniSTS
Cytogenetic Map15q26.3UniSTS
Cytogenetic Map8p23-p22UniSTS
Cytogenetic Map13q32.3UniSTS
Cytogenetic Map17q21-q22UniSTS
Cytogenetic Map2q36.1UniSTS
Cytogenetic Map5p13UniSTS
Cytogenetic Map5p12UniSTS
Cytogenetic Map12q21.1UniSTS
Cytogenetic Map3q26.32UniSTS
Cytogenetic Map13q11UniSTS
Cytogenetic Map1p35.3UniSTS
Cytogenetic Map7p12.3UniSTS
Cytogenetic Map17p12UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map13q14.11UniSTS
Cytogenetic Map3p25.1UniSTS
Cytogenetic MapXp22UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map17q11.2-q12UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic Map2p25UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map8p11.22UniSTS
Cytogenetic Map7p22UniSTS
Cytogenetic Map16q21UniSTS
Cytogenetic Map1p21.3UniSTS
Cytogenetic Map19q13.13UniSTS
Cytogenetic Map4q22.1UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map20q13.3UniSTS
Cytogenetic Map7q36.3UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map6p22.3-p22.1UniSTS
Cytogenetic Map1p35-p34.3UniSTS
Cytogenetic Map5q35.1UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map12p13.3UniSTS
Cytogenetic Map7q22UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic MapXp11UniSTS
Cytogenetic Map19q13UniSTS
Cytogenetic Map2q32.3UniSTS
Cytogenetic Map4q22.1-q23UniSTS
Cytogenetic Map1q22UniSTS
Cytogenetic Map17q22-q23.2UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map18q22.3UniSTS
Cytogenetic Map2p16.1UniSTS
Cytogenetic Map12q24.1-q24.3UniSTS
Cytogenetic Map11p11.2UniSTS
Cytogenetic Map1p34.1UniSTS
Cytogenetic Map22q13UniSTS
Cytogenetic Map12q22UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map11q24.2UniSTS
Cytogenetic MapXq22.3UniSTS
Cytogenetic Map3q13.13UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map3q27.3UniSTS
Cytogenetic Map17q21.32UniSTS
Cytogenetic Map2q35UniSTS
Cytogenetic Map9p24.2UniSTS
Cytogenetic Map14q32.11UniSTS
Cytogenetic Map2q21.1UniSTS
Cytogenetic Map15q23UniSTS
Cytogenetic Map16q22.2UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map3p22.1UniSTS
Cytogenetic Map19q13.33UniSTS
Cytogenetic Map3p14.3UniSTS
Cytogenetic Map1p36.21UniSTS
Cytogenetic Map1p31.3UniSTS
Cytogenetic Map12p12UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map6p25UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map14q23UniSTS
Cytogenetic Map1q42.1-q43UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic Map1p32UniSTS
Cytogenetic Map12q12UniSTS
Cytogenetic Map6q25.1-q26UniSTS
Cytogenetic Map5q13UniSTS
Cytogenetic Map12q13.11-q14.3UniSTS
Cytogenetic Map7p11UniSTS
Cytogenetic Map3p21.31UniSTS
Cytogenetic Map17q23.1UniSTS
Cytogenetic MapXq13-q21UniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map10q22.1UniSTS
Cytogenetic Map1q41UniSTS
Cytogenetic Map17p13.1UniSTS
Cytogenetic Map12p13.2UniSTS
Cytogenetic Map3q28-q29UniSTS
Cytogenetic Map7q11.21UniSTS
Cytogenetic Map1q41-q42.2UniSTS
Cytogenetic Map12q24.2-q24.31UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map11p11.11UniSTS
Cytogenetic Map11q22-q23UniSTS
Cytogenetic Map3q21UniSTS
Cytogenetic Map1q43UniSTS
Cytogenetic Map1p13.2UniSTS
Cytogenetic Map15q25.2UniSTS
Cytogenetic Map10q11.21UniSTS
Cytogenetic Map17q23.3UniSTS
Cytogenetic Map8q11.2UniSTS
Cytogenetic Map15q11-q13UniSTS
Cytogenetic Map13q12-q14UniSTS
Cytogenetic Map18q21.1UniSTS
Cytogenetic Map2p21UniSTS
Cytogenetic Map22q13.31UniSTS
Cytogenetic Map14q24.1UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map6p25.2UniSTS
Cytogenetic Map1q44UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map10q26.3UniSTS
Cytogenetic Map13q32.2UniSTS
Cytogenetic Map5q11.2UniSTS
Cytogenetic Map11p15.1UniSTS
Cytogenetic Map11q24UniSTS
Cytogenetic Map2q23.3UniSTS
Cytogenetic Map1p31.1UniSTS
Cytogenetic Map10q25.3UniSTS
Cytogenetic Map14q31UniSTS
Cytogenetic Map8p12-p11UniSTS
Cytogenetic Map11p15.4UniSTS
Cytogenetic Map8p11.2UniSTS
Cytogenetic Map7p11.2UniSTS
Cytogenetic MapXq28UniSTS
Cytogenetic Map15q26.1UniSTS
Cytogenetic Map7p15.3UniSTS
Cytogenetic Map17q23.2UniSTS
Cytogenetic MapXq25UniSTS
Cytogenetic Map21q22.1UniSTS
Cytogenetic Map4q25-q27UniSTS
Cytogenetic Map3q25.33UniSTS
Cytogenetic Map3q25.31UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map1p36.22UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic MapXp22.33UniSTS
Cytogenetic MapYp11.3UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic Map3p22-p21.3UniSTS
Cytogenetic Map2p15-p13UniSTS
Cytogenetic MapXp11.4UniSTS
Cytogenetic Map20p11UniSTS
Cytogenetic Map3p14.1UniSTS
Cytogenetic Map1q25.2UniSTS
Cytogenetic Map13q11-q12UniSTS
Cytogenetic Map9q34UniSTS
Cytogenetic Map7q21.13UniSTS
Cytogenetic Map20q13.33UniSTS
Cytogenetic Map9q33.3UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map3q12UniSTS
Cytogenetic Map2p25.1-p24.1UniSTS
Cytogenetic Map16p13.11UniSTS
Cytogenetic Map6q16.1UniSTS
Cytogenetic Map13q14.13UniSTS
Cytogenetic Map5p13.1UniSTS
Cytogenetic Map4q28-q32UniSTS
Cytogenetic Map11p15UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map1p32-p31UniSTS
Cytogenetic Map1p21UniSTS
Cytogenetic Map7p14.2UniSTS
Cytogenetic Map6q25UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map18p11.22UniSTS
Cytogenetic Map9p24.3UniSTS
Cytogenetic Map2p25.3UniSTS
Cytogenetic Map1q42.3UniSTS
Cytogenetic Map1q22-q23UniSTS
Cytogenetic Map4q21.22UniSTS
Cytogenetic Map13q14.2UniSTS
Cytogenetic Map2q24.3UniSTS
Cytogenetic Map7p22.1UniSTS
Cytogenetic Map9q31-q33UniSTS
Cytogenetic Map11q13.4UniSTS
Cytogenetic Map10p11.21UniSTS
Cytogenetic Map9q32UniSTS
Cytogenetic Map3q21.1UniSTS
Cytogenetic Map10q11.23UniSTS
Cytogenetic Map9q22.1-q22.2UniSTS
Cytogenetic Map4q26UniSTS
Cytogenetic Map4q28.1UniSTS
Cytogenetic Map9q31.3UniSTS
Cytogenetic Map6p22.3UniSTS
Cytogenetic Map21q21.1UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map18q11.2UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map15q26.2UniSTS
Cytogenetic Map14q22.1UniSTS
Cytogenetic Map12p12.3UniSTS
Cytogenetic Map12q13.12UniSTS
Cytogenetic Map20q11.23UniSTS
Cytogenetic Map12q13.11UniSTS
Cytogenetic Map9p13.3UniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic Map12q14.3UniSTS
Cytogenetic Map5q33.3UniSTS
Cytogenetic Map5p13.2UniSTS
Cytogenetic Map4q35.2UniSTS
Cytogenetic Map4q28.2UniSTS
Cytogenetic Map16q24.1UniSTS
Cytogenetic Map12q23.1UniSTS
Cytogenetic Map11q24.3UniSTS
Cytogenetic Map10q24.32UniSTS
Cytogenetic Map10q22.2UniSTS
Cytogenetic Map20p13UniSTS
Cytogenetic Map6q25.1UniSTS
Cytogenetic Map20q13.2UniSTS
Cytogenetic Map8q23.3UniSTS
Cytogenetic Map16q23.2UniSTS
Cytogenetic Map3p22.2UniSTS
Cytogenetic MapXp21.1UniSTS
Cytogenetic Map7p14.3UniSTS
Cytogenetic MapXp11.23UniSTS
Cytogenetic Map14q32.31UniSTS
Cytogenetic Map5p15.3UniSTS
Cytogenetic Map15q21.2UniSTS
Cytogenetic Map22q12UniSTS
Cytogenetic Map4q22UniSTS
Cytogenetic Map2p13.1UniSTS
Cytogenetic Map19q13.1-q13.2UniSTS
Cytogenetic Map1p36.3UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map2q32.1UniSTS
Cytogenetic Map7q31.3UniSTS
Cytogenetic Map5q33.1UniSTS
Cytogenetic Map13q13.1UniSTS
Cytogenetic Map8p23.1UniSTS
Cytogenetic Map15qUniSTS
Cytogenetic Map3p26UniSTS
Cytogenetic Map1p13-p12UniSTS
Cytogenetic Map21q22.11UniSTS
Cytogenetic Map14q32.2UniSTS
Cytogenetic Map15q24.1UniSTS
Cytogenetic Map4p16.1UniSTS
Cytogenetic Map15q11.2UniSTS
Cytogenetic Map3p25.2UniSTS
Cytogenetic Map7p22.3UniSTS
Cytogenetic Map10q21.1UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map21q22.2UniSTS
Cytogenetic Map1q23.3UniSTS
Cytogenetic Map1p36UniSTS
Cytogenetic Map1q25UniSTS
Cytogenetic Map15q24UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map2q22.3UniSTS
Cytogenetic Map20p11.21UniSTS
Cytogenetic Map12q24.1UniSTS
Cytogenetic Map5q31.2UniSTS
Cytogenetic Map2p25.2UniSTS
Cytogenetic Map17p11.2UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map2p25.1UniSTS
Cytogenetic Map4q12UniSTS
Cytogenetic Map1q12UniSTS
Cytogenetic Map22q11.22UniSTS
Cytogenetic Map20q11.22UniSTS
Cytogenetic Map8p21.3UniSTS
Cytogenetic Map14q32.3UniSTS
Cytogenetic Map7q32UniSTS
Cytogenetic Map5q14.1UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map14q23.3UniSTS
Cytogenetic Map1q24UniSTS
Cytogenetic Map7p13UniSTS
Cytogenetic Map17q25UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map5p15.33UniSTS
Cytogenetic Map3q29UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map16p13.13-p13.12UniSTS
Cytogenetic Map12p13.31UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map3q27UniSTS
Cytogenetic Map6q22UniSTS
Cytogenetic Map10p15.3UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map15q15UniSTS
Cytogenetic Map1p13.1UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map16q13UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map13q34UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map13q14.3UniSTS
Cytogenetic Map14q24UniSTS
Cytogenetic Map14q22-q24UniSTS
Cytogenetic Map19p13UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map22q12.2UniSTS
Cytogenetic Map16q24UniSTS
Cytogenetic MapXp22.2UniSTS
Cytogenetic Map8q13.1UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map12p12.1UniSTS
Cytogenetic Map14q11.2UniSTS
Cytogenetic Map4q35.1UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map1p22UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map10q11UniSTS
Cytogenetic Map8p11.21UniSTS
Cytogenetic Map8q24.11UniSTS
Cytogenetic Map2q37.3UniSTS
Cytogenetic Map9q22.33UniSTS
Cytogenetic Map9q22.31UniSTS
Cytogenetic Map11p15.5UniSTS
Cytogenetic Map20q12UniSTS
Cytogenetic Map2q13UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map2p15UniSTS
Cytogenetic Map12q21.31UniSTS
Cytogenetic Map17p13UniSTS
Cytogenetic Map19q12UniSTS
Cytogenetic Map6p22.1UniSTS
Cytogenetic Map11q14.2UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map18p11.21UniSTS
Cytogenetic Map10q22UniSTS
Cytogenetic MapXq21.1UniSTS
Cytogenetic Map9p21.1UniSTS
D8S2279  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map21q22.12UniSTS
Cytogenetic Map15q13UniSTS
Cytogenetic Map9q32UniSTS
Cytogenetic Map15q22.3UniSTS
Cytogenetic Map17p12UniSTS
Cytogenetic Map21q21.3UniSTS
Cytogenetic Map3p22-p21.3UniSTS
Cytogenetic Map1q21.1UniSTS
Cytogenetic Map2q24.2UniSTS
Cytogenetic Map17q24.2UniSTS
Cytogenetic Map1q32UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map20q13.3UniSTS
Cytogenetic Map2q31.1UniSTS
Cytogenetic Map1q21UniSTS
Cytogenetic Map3p14.1UniSTS
Cytogenetic Map2q37.3UniSTS
Cytogenetic Map7p14.1UniSTS
Cytogenetic Map2q22.3UniSTS
Cytogenetic Map15q13.2UniSTS
Cytogenetic Map12q24.1UniSTS
Cytogenetic Map7p15.2UniSTS
Cytogenetic Map5q31.2UniSTS
Cytogenetic Map2p25.2UniSTS
Cytogenetic Map3p24.3UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic Map5q14UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map1p36.32UniSTS
Cytogenetic Map1q42.12UniSTS
Cytogenetic Map7q21.11UniSTS
Cytogenetic Map9q34.2UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map8q22.3UniSTS
Cytogenetic Map6p21.1-p12UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map7q36.3UniSTS
Cytogenetic Map2p25.1UniSTS
Cytogenetic Map7p21.3UniSTS
Cytogenetic Map4q12UniSTS
Cytogenetic Map22q11.22UniSTS
Cytogenetic Map11p13UniSTS
Cytogenetic Map1q12UniSTS
Cytogenetic Map8p23UniSTS
Cytogenetic Map11q13.2-q13.3UniSTS
Cytogenetic Map13q14.1-q14.3UniSTS
Cytogenetic Map3q22-q24UniSTS
Cytogenetic Map3q13.1-q13.2UniSTS
Cytogenetic Map16q24UniSTS
Cytogenetic Map5q23.3-q31.1UniSTS
Cytogenetic Map8p21.3UniSTS
Cytogenetic Map14q32.3UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map7q32UniSTS
Cytogenetic Map14q32.33UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map1p32.3UniSTS
Cytogenetic Map17q11UniSTS
Cytogenetic Map17p13.1-p12UniSTS
Cytogenetic Map18q21.33UniSTS
Cytogenetic Map19p13.12UniSTS
Cytogenetic Map5q14.1UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map1q21-q23UniSTS
Cytogenetic MapXp11.23UniSTS
Cytogenetic Map4q21.1UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map14q23.3UniSTS
Cytogenetic Map17p12-p11.2UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map1q24UniSTS
Cytogenetic Map1q43UniSTS
Cytogenetic Map9q34.13UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map2q32UniSTS
Cytogenetic MapXp22.2UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map2q33UniSTS
Cytogenetic Map10p13UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic Map3q27UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map4p16.1UniSTS
Cytogenetic Map14q22.3UniSTS
Cytogenetic Map10q23-q24UniSTS
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map14q31-q32UniSTS
Cytogenetic Map5p15.33UniSTS
Cytogenetic Map1q23.2UniSTS
Cytogenetic Map16q24.3UniSTS
Cytogenetic Map4p14UniSTS
Cytogenetic Map2q32.3UniSTS
Cytogenetic Map15q21.1UniSTS
Cytogenetic Map4q32.2UniSTS
Cytogenetic Map10q23UniSTS
Cytogenetic Map5q14.2UniSTS
Cytogenetic Map4q32.1UniSTS
Cytogenetic Map1q25.1UniSTS
Cytogenetic Map11q14.1UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map11q23.1UniSTS
Cytogenetic Map3p21.1UniSTS
Cytogenetic Map16q22.2UniSTS
Cytogenetic Map14q32.31UniSTS
Cytogenetic Map16q11.2UniSTS
Cytogenetic Map6q22UniSTS
Cytogenetic Map10p15.3UniSTS
Cytogenetic Map11q23UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map12q12UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map19q13.11UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map15q15UniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map22q12.3UniSTS
Cytogenetic Map20q11UniSTS
Cytogenetic Map22q11.23UniSTS
Cytogenetic Map17q25UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map3p22.1UniSTS
Cytogenetic Map8q22.1UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map18p11.31UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map2p22.1UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map1p35.2UniSTS
Cytogenetic MapYp11.2UniSTS
Cytogenetic Map13q13.1UniSTS
Cytogenetic Map20q11.22UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map18q12UniSTS
Cytogenetic Map17q21.33UniSTS
Cytogenetic Map15q15.1UniSTS
Cytogenetic Map3q27.2UniSTS
Cytogenetic Map3q21.3UniSTS
Cytogenetic Map5p15.2UniSTS
Cytogenetic Map20q13.12UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map1q42UniSTS
Cytogenetic Map14q32.11UniSTS
Cytogenetic Map17q21.2-q21.3UniSTS
Cytogenetic Map5q32-q34UniSTS
Cytogenetic Map15q14UniSTS
Cytogenetic Map16q13UniSTS
Cytogenetic Map3q21.2UniSTS
Cytogenetic Map3p21.3UniSTS
Cytogenetic Map14q24.2UniSTS
Cytogenetic Map12q24.13UniSTS
Cytogenetic Map13q14.11UniSTS
Cytogenetic Map3q27.3UniSTS
Cytogenetic Map1q32.3UniSTS
Cytogenetic Map6p22.1UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map6q25.3UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map13q14.3UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map10p12UniSTS
Cytogenetic Map2q33.3UniSTS
Cytogenetic Map14q21.3UniSTS
Cytogenetic Map8p22-p21UniSTS
Cytogenetic Map18q11.2UniSTS
Cytogenetic Map2p15UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map12q21.33UniSTS
Cytogenetic Map20q13.32UniSTS
Cytogenetic Map1p34.1UniSTS
Cytogenetic Map10q26UniSTS
Cytogenetic Map8p23.1UniSTS
Cytogenetic Map19p13UniSTS
Cytogenetic Map7q21.13UniSTS
Cytogenetic Map7q31.1UniSTS
Cytogenetic Map1p33UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map22q12.2UniSTS
Cytogenetic Map9q22.3UniSTS
Cytogenetic Map8q13.1UniSTS
Cytogenetic Map3q25UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map20q13.33UniSTS
Cytogenetic Map1p31.3UniSTS
Cytogenetic Map14q31.1UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map12q13.2UniSTS
Cytogenetic Map22q13.31-q13.33UniSTS
Cytogenetic Map20q13.31UniSTS
Cytogenetic Map11p11.2UniSTS
Cytogenetic Map1q41UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map15q25.2UniSTS
Cytogenetic Map14q11.2UniSTS
Cytogenetic Map17q23.2UniSTS
Cytogenetic Map7q32.2UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map6q25.1UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map9p13.3UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map2p13.1UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map3q29UniSTS
Cytogenetic Map7p13UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic Map14q31-q32.1UniSTS
Cytogenetic Map1q42.11UniSTS
Cytogenetic Map4q35.1UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic Map2p13.3UniSTS
Cytogenetic MapXp11.3UniSTS
Cytogenetic Map2q11.2-q12.1UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map1p22UniSTS
Cytogenetic Map6q16.2UniSTS
Cytogenetic Map18q23UniSTS
Cytogenetic Map2q14UniSTS
Cytogenetic Map20p11.23-p11.21UniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map8p11.23UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic Map19q13UniSTS
Cytogenetic Map8p11.21UniSTS
Cytogenetic Map12q14.3UniSTS
Cytogenetic MapXq26.3UniSTS
Cytogenetic Map8q24.11UniSTS
Cytogenetic Map10q23.1UniSTS
Cytogenetic Map1q44UniSTS
Cytogenetic Map9q22.33UniSTS
Cytogenetic Map3p21.31UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map9q21.32UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic Map9q33.3UniSTS
Cytogenetic Map1p36.1UniSTS
Cytogenetic Map20q12UniSTS
Cytogenetic Map4q21.23UniSTS
Cytogenetic Map5q13.2UniSTS
Cytogenetic Map22q12.1UniSTS
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Cytogenetic Map7p14.3UniSTS
Cytogenetic Map12q21UniSTS
Cytogenetic Map7p15UniSTS
Cytogenetic Map7q22-q31UniSTS
Cytogenetic Map11q22UniSTS
Cytogenetic Map5p15.3UniSTS
Cytogenetic Map20q13.3-qterUniSTS
Cytogenetic Map1p35-p34UniSTS
Cytogenetic Map4p13-p12UniSTS
Cytogenetic Map10q21-q22UniSTS
Cytogenetic Map4q22UniSTS
Cytogenetic Map7p13-p11.1UniSTS
Cytogenetic Map9q31-q34UniSTS
Cytogenetic Map7q21.1-q22UniSTS
Cytogenetic Map15q26.1UniSTS
Cytogenetic Map3q13.13-q13.2UniSTS
Cytogenetic MapXp22.13UniSTS
Cytogenetic Map13q12.12UniSTS
Cytogenetic Map13q14.2UniSTS
Cytogenetic Map12qUniSTS
Cytogenetic Map1pUniSTS
Cytogenetic Map16pUniSTS
Cytogenetic Map15qUniSTS
Cytogenetic Map7qUniSTS
Cytogenetic Map2qUniSTS
Cytogenetic Map5q13.1UniSTS
Cytogenetic Map11p14.1UniSTS
Cytogenetic Map4q32UniSTS
Cytogenetic Map2p22UniSTS
Cytogenetic Map5q14.3UniSTS
Cytogenetic Map10p12.1UniSTS
Cytogenetic Map5q23.2UniSTS
Cytogenetic Map2p24.1UniSTS
Cytogenetic Map8q24.13UniSTS
Cytogenetic Map12p13.32UniSTS
Cytogenetic Map9p21.1UniSTS
Cytogenetic Map9q34.2-q34.3UniSTS
D10S16  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map3p24.2UniSTS
Cytogenetic Map21q21.3UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map16q24.1UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map17p11.2UniSTS
Cytogenetic Map11q24.2UniSTS
Cytogenetic Map5q23.3-q31.1UniSTS
Cytogenetic Map7q32UniSTS
Cytogenetic Map1q21-q23UniSTS
Cytogenetic MapXp11.23UniSTS
Cytogenetic Map2q11.2-q12UniSTS
Cytogenetic Map7p13UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map1p36.21UniSTS
Cytogenetic Map3p22UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map2p12UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map9p13.3-p12UniSTS
Cytogenetic Map3p21.1UniSTS
Cytogenetic Map5p13.1UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map2p25.2UniSTS
Cytogenetic Map5q21-q22UniSTS
Cytogenetic Map2p22.1UniSTS
Cytogenetic Map1q32.3UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map18q12UniSTS
Cytogenetic Map19q13.41UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map3q27.3UniSTS
Cytogenetic Map2q37.3UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map2p15UniSTS
Cytogenetic Map20q13.32UniSTS
Cytogenetic Map10q26UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map7q21.13UniSTS
Cytogenetic Map1p33UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map9q22.3UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map12q13.2UniSTS
Cytogenetic Map22q13.31-q13.33UniSTS
Cytogenetic Map1q24.1UniSTS
Cytogenetic Map7q32.2UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map1q42.11UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map19p13.1UniSTS
Cytogenetic Map11q13.5UniSTS
Cytogenetic Map11q24UniSTS
Cytogenetic Map2q11.2-q12.1UniSTS
Cytogenetic Map3q21.2UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic Map19p13UniSTS
Cytogenetic Map8p11.21UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map20q12UniSTS
Cytogenetic Map2q13UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic Map17q22.2UniSTS
Cytogenetic Map18q21UniSTS
Cytogenetic Map11q14.2UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map4q34UniSTS
Cytogenetic Map2p22-p21UniSTS
Cytogenetic Map10q26.3UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map11q13.4UniSTS
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map1p36.23UniSTS
Cytogenetic Map7p22.2UniSTS
Cytogenetic Map12q24.13UniSTS
Cytogenetic Map8p21.2UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map14q32.12UniSTS
Cytogenetic Map2q31.1UniSTS
Cytogenetic Map1p36.31UniSTS
Cytogenetic Map1p32.3UniSTS
Cytogenetic MapXq26.3UniSTS
Cytogenetic Map8p23.1UniSTS
Cytogenetic Map6q13UniSTS
Cytogenetic Map3p21.31UniSTS
Cytogenetic Map9p13.2UniSTS
Cytogenetic Map17q25UniSTS
Cytogenetic Map9q22.2UniSTS
Cytogenetic Map14q32.33UniSTS
Cytogenetic Map1q21.3UniSTS
Cytogenetic Map13q12.11UniSTS
Cytogenetic Map16p13.13UniSTS
Cytogenetic Map11p15.4UniSTS
Cytogenetic Map7q22UniSTS
Cytogenetic Map3q21UniSTS
Cytogenetic Map11q12.3UniSTS
Cytogenetic Map22q13UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map11p15.3-p15.1UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map10q22.2UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map7p22.3UniSTS
Cytogenetic Map3p21UniSTS
Cytogenetic MapXp22.3UniSTS
Cytogenetic Map1q42.3UniSTS
Cytogenetic Map18q11.2UniSTS
Cytogenetic Map6p24.3UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map1q25UniSTS
Cytogenetic Map15q11.2UniSTS
Cytogenetic Map19p13.12UniSTS
Cytogenetic Map3q26UniSTS
Cytogenetic Map12p12.1-p11.2UniSTS
Cytogenetic Map11q23.1UniSTS
Cytogenetic Map13q14.11UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map7p15.2UniSTS
Cytogenetic Map1q21UniSTS
Cytogenetic Map10q11.22UniSTS
Cytogenetic Map5p12UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map9q21.13UniSTS
Cytogenetic Map5q13.2UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic MapXq23UniSTS
Cytogenetic Map2p21UniSTS
Cytogenetic Map22q11.1UniSTS
Cytogenetic Map16q13UniSTS
Cytogenetic Map16pUniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic MapXp11.3UniSTS
Cytogenetic Map1q25.1UniSTS
Cytogenetic Map10q23-q24UniSTS
Cytogenetic Map20p13UniSTS
Cytogenetic Map7q31UniSTS
Cytogenetic Map6q23.3UniSTS
Cytogenetic MapXp22.2UniSTS
Cytogenetic Map9q32UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map20q11.22UniSTS
Cytogenetic Map4q35.1UniSTS
Cytogenetic Map3q21.3UniSTS
Cytogenetic Map5q12.3UniSTS
Cytogenetic Map6q25.1UniSTS
Cytogenetic Map14q24.1UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map14q23.2UniSTS
Cytogenetic Map15q24.1UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map8q23.1UniSTS
Cytogenetic Map2q14.3UniSTS
Cytogenetic Map20q13.33UniSTS
Cytogenetic Map21q22.11UniSTS
Cytogenetic Map5p15.1UniSTS
Cytogenetic Map15q13.1UniSTS
Cytogenetic Map15q26.1UniSTS
Cytogenetic Map7q32.1UniSTS
Cytogenetic Map8p21.3UniSTS
Cytogenetic Map1p31.1UniSTS
Cytogenetic Map17qterUniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map12q22UniSTS
Cytogenetic Map16q22.2UniSTS
Cytogenetic Map14q32UniSTS
Cytogenetic MapXp22.33UniSTS
Cytogenetic MapYp11.32UniSTS
Cytogenetic Map14q24.2UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map13q34UniSTS
Cytogenetic Map10p11.23UniSTS
Cytogenetic Map15q15.2UniSTS
Cytogenetic Map8p21.1UniSTS
Cytogenetic Map22q12.2UniSTS
Cytogenetic Map15q22.2UniSTS
Cytogenetic Map15q21UniSTS
Cytogenetic Map6p21.31UniSTS
Cytogenetic Map10q23.1UniSTS
Cytogenetic Map1p36.2UniSTS
Cytogenetic Map2p16.1UniSTS
Cytogenetic Map22q11.2UniSTS
Cytogenetic Map17q23.3UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map20q12-q13.12UniSTS
Cytogenetic Map3q26.33UniSTS
Cytogenetic Map5q31.2-q34UniSTS
Cytogenetic Map5q31.2UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map5q35.3UniSTS
Cytogenetic MapXq13-q21UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map1pter-q31.3UniSTS
Cytogenetic Map15q21.1UniSTS
Cytogenetic Map3q13.33UniSTS
Cytogenetic MapXq13.1UniSTS
Cytogenetic Map3p23-p21UniSTS
Cytogenetic Map11q22-q23UniSTS
Cytogenetic Map1p34.1UniSTS
Cytogenetic Map2q21.1UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map7p11.2UniSTS
Cytogenetic Map7p22.1UniSTS
Cytogenetic Map17q21.33UniSTS
Cytogenetic Map14q32.31UniSTS
Cytogenetic Map10q11.21UniSTS
Cytogenetic Map16q22UniSTS
Cytogenetic Map2q24UniSTS
Cytogenetic Map1q23.3UniSTS
Cytogenetic Map3q13.13UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map16p13.1UniSTS
Cytogenetic Map19q13.11UniSTS
Cytogenetic MapXp22.12UniSTS
Cytogenetic Map9q21.33UniSTS
Cytogenetic Map5q32UniSTS
Cytogenetic Map16q11.2UniSTS
Cytogenetic Map10p12.31UniSTS
Cytogenetic Map3q25.33UniSTS
Cytogenetic Map8q21.2UniSTS
Cytogenetic Map10q26.13UniSTS
Cytogenetic Map10q25.3UniSTS
Cytogenetic Map15q14-q15UniSTS
Cytogenetic Map8p11.2UniSTS
Cytogenetic Map1p34.3UniSTS
Cytogenetic Map4p15.2UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map7p15.3UniSTS
Cytogenetic Map7p21.1UniSTS
Cytogenetic Map1p36.32UniSTS
Cytogenetic Map1p36.1-p34UniSTS
Cytogenetic Map4p13UniSTS
Cytogenetic Map7q31.1-q31.2UniSTS
Cytogenetic Map8q22.2UniSTS
Cytogenetic Map15q21.1-q21.2UniSTS
Cytogenetic Map16q21UniSTS
Cytogenetic MapXq12UniSTS
Cytogenetic Map7q36.1UniSTS
Cytogenetic Map7p14.1UniSTS
Cytogenetic Map6p23UniSTS
Cytogenetic Map3p11.1UniSTS
Cytogenetic Map15q21.3UniSTS
Cytogenetic Map13q12UniSTS
Cytogenetic Map12q23.2UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map16q22.3UniSTS
Cytogenetic MapXq21UniSTS
Cytogenetic Map15q15UniSTS
Cytogenetic Map4q25UniSTS
Cytogenetic Map3q22.1UniSTS
Cytogenetic Map1q25.2UniSTS
Cytogenetic Map11q14.3UniSTS
Cytogenetic Map10q21.3UniSTS
Cytogenetic Map14q11.2UniSTS
Cytogenetic Map15q24.2UniSTS
Cytogenetic Map2p14UniSTS
Cytogenetic Map7q11.1UniSTS
Cytogenetic Map6p21UniSTS
Cytogenetic Map2p25.1-p24.1UniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map4q13.3UniSTS
Cytogenetic Map12p11.21UniSTS
Cytogenetic Map18q21.3UniSTS
Cytogenetic Map17p13UniSTS
Cytogenetic Map8q12UniSTS
Cytogenetic Map2q35UniSTS
Cytogenetic Map21q22.13UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map17q24.3UniSTS
Cytogenetic Map1p21UniSTS
Cytogenetic MapXq24UniSTS
Cytogenetic Map2q34UniSTS
Cytogenetic Map8p11.23UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic Map9q33.3UniSTS
Cytogenetic Map16p12UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic Map20q11.23UniSTS
Cytogenetic Map12q15UniSTS
Cytogenetic Map2q12.2UniSTS
Cytogenetic Map8p12UniSTS
Cytogenetic Map7q22.3UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map4q35UniSTS
Cytogenetic Map19q13.1-q13.2UniSTS
Cytogenetic Map16p13.12UniSTS
Cytogenetic Map9q34.1UniSTS
Cytogenetic Map7q36.2UniSTS
Cytogenetic Map3p23UniSTS
Cytogenetic Map6p25UniSTS
Cytogenetic Map9q22.1-q22.2UniSTS
Cytogenetic Map3q26.1-q26.2UniSTS
Cytogenetic Map5q31-q34UniSTS
Cytogenetic Map9q34UniSTS
Cytogenetic Map12p13UniSTS
Cytogenetic Map4q26UniSTS
Cytogenetic Map4p15.3UniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map15q15.1UniSTS
Cytogenetic Map1p32-p31UniSTS
Cytogenetic Map7q36.3UniSTS
Cytogenetic Map4q22.1UniSTS
Cytogenetic Map3q13.2UniSTS
Cytogenetic Map2q33.3UniSTS
Cytogenetic Map8p22UniSTS
Cytogenetic Map22q11.23UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map18q21.32UniSTS
Cytogenetic Map15q26.3UniSTS
Cytogenetic Map12q14.2UniSTS
Cytogenetic Map2q31.1-q31.2UniSTS
Cytogenetic Map12q13.11UniSTS
Cytogenetic Map9p13.3UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map6p12.3UniSTS
Cytogenetic Map6q22.32UniSTS
Cytogenetic Map5q15UniSTS
Cytogenetic Map3p14.2UniSTS
Cytogenetic Map3p25.1UniSTS
Cytogenetic Map3q27.1UniSTS
Cytogenetic Map2q36.1UniSTS
Cytogenetic Map2q37UniSTS
Cytogenetic Map19q13.31UniSTS
Cytogenetic Map4q23UniSTS
Cytogenetic Map16q24.3UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic Map10q22.1UniSTS
Cytogenetic Map18q11.1UniSTS
Cytogenetic Map16q23.2UniSTS
Cytogenetic Map12q13UniSTS
Cytogenetic Map18q21.1UniSTS
Cytogenetic Map12q12-q13UniSTS
Cytogenetic Map9p22.3UniSTS
Cytogenetic Map6p21.2UniSTS
Cytogenetic Map6p22.1UniSTS
Cytogenetic Map11p15.1UniSTS
Cytogenetic Map19qterUniSTS
Cytogenetic Map20q13.3-qterUniSTS
Cytogenetic Map12q14.1UniSTS
Cytogenetic Map7p11UniSTS
Cytogenetic Map7p15UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map16p12.3UniSTS
Cytogenetic Map3q29UniSTS
Cytogenetic Map3p21.3UniSTS
Cytogenetic Map13q14UniSTS
Cytogenetic Map17pUniSTS
Cytogenetic Map11p14.1UniSTS
Cytogenetic Map2p13.2UniSTS
Cytogenetic Map15q25.2UniSTS
Cytogenetic Map10q11.23UniSTS
Cytogenetic Map20q13.12UniSTS
Cytogenetic Map13q22.1UniSTS
Cytogenetic Map17p13.1UniSTS
Cytogenetic Map14q23.3UniSTS
Cytogenetic Map3q26.2UniSTS


Expression


RNA-SEQ Expression
High: > 1000 TPM value   Medium: Between 11 and 1000 TPM
Low: Between 0.5 and 10 TPM   Below Cutoff: < 0.5 TPM

alimentary part of gastrointestinal system circulatory system endocrine system exocrine system hemolymphoid system hepatobiliary system integumental system musculoskeletal system nervous system renal system reproductive system respiratory system sensory system visual system adipose tissue appendage entire extraembryonic component pharyngeal arch
High
Medium 857 1028 1014 145 810 57 2818 340 1506 167 1106 1268 105 1 545 1711 4 1
Low 1582 1869 712 479 1052 408 1539 1852 2228 252 354 345 70 659 1077 2 1
Below cutoff 94 89 5

Sequence

Nucleotide Sequences
RefSeq Transcripts NG_050686 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_032221 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_005260573 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_005260576 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011529080 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011529082 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017028099 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017028100 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017028101 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017028102 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017028103 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017028104 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047440545 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047440546 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047440547 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047440548 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047440549 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047440550 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047440551 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054324118 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054324119 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054324120 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054324121 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054324122 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054324123 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054324124 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054324125 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054324126 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054324127 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054324128 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054324129 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054324130 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054324131 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054324132 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054324133 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054324134 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054324135 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_001754421 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AB037756 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF525085 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK026022 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK091551 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK098144 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK296955 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL031667 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL031669 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL121674 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AY034072 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC012516 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC021907 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC039860 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC040016 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BF063641 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BM973992 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471077 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068258 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CR749575 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF456907 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF511304 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KT584560 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000309279   ⟹   ENSP00000308684
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2041,437,262 - 41,499,317 (-)Ensembl
RefSeq Acc Id: ENST00000373222   ⟹   ENSP00000362319
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2041,496,809 - 41,618,375 (-)Ensembl
RefSeq Acc Id: ENST00000373233   ⟹   ENSP00000362330
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2041,402,083 - 41,618,377 (-)Ensembl
RefSeq Acc Id: ENST00000440647   ⟹   ENSP00000392503
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2041,533,156 - 41,614,773 (-)Ensembl
RefSeq Acc Id: ENST00000440697   ⟹   ENSP00000404637
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2041,426,142 - 41,499,317 (-)Ensembl
RefSeq Acc Id: ENST00000470470
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2041,496,809 - 41,533,285 (-)Ensembl
RefSeq Acc Id: ENST00000476641
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2041,473,023 - 41,484,507 (-)Ensembl
RefSeq Acc Id: ENST00000480022
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2041,404,523 - 41,415,065 (-)Ensembl
RefSeq Acc Id: ENST00000482596
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2041,514,920 - 41,618,384 (-)Ensembl
RefSeq Acc Id: NM_032221   ⟹   NP_115597
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382041,402,083 - 41,618,377 (-)NCBI
GRCh372040,030,741 - 40,247,133 (-)NCBI
Build 362039,464,584 - 39,680,547 (-)NCBI Archive
Celera2036,741,838 - 36,957,790 (-)RGD
HuRef2036,768,458 - 36,984,731 (-)NCBI
CHM1_12039,935,021 - 40,151,300 (-)NCBI
T2T-CHM13v2.02043,133,884 - 43,350,174 (-)NCBI
Sequence:
RefSeq Acc Id: XM_005260576   ⟹   XP_005260633
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382041,402,083 - 41,440,058 (-)NCBI
GRCh372040,030,741 - 40,247,133 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011529080   ⟹   XP_011527382
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382041,402,083 - 41,540,759 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011529082   ⟹   XP_011527384
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382041,402,083 - 41,486,332 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017028099   ⟹   XP_016883588
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382041,402,083 - 41,540,067 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017028100   ⟹   XP_016883589
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382041,402,083 - 41,549,888 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017028101   ⟹   XP_016883590
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382041,402,083 - 41,540,067 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017028102   ⟹   XP_016883591
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382041,408,147 - 41,540,067 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017028104   ⟹   XP_016883593
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382041,414,607 - 41,540,067 (-)NCBI
Sequence:
RefSeq Acc Id: XM_047440545   ⟹   XP_047296501
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382041,402,083 - 41,618,377 (-)NCBI
RefSeq Acc Id: XM_047440546   ⟹   XP_047296502
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382041,402,083 - 41,618,377 (-)NCBI
RefSeq Acc Id: XM_047440547   ⟹   XP_047296503
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382041,402,083 - 41,618,377 (-)NCBI
RefSeq Acc Id: XM_047440548   ⟹   XP_047296504
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382041,402,083 - 41,618,377 (-)NCBI
RefSeq Acc Id: XM_047440549   ⟹   XP_047296505
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382041,402,083 - 41,618,377 (-)NCBI
RefSeq Acc Id: XM_047440550   ⟹   XP_047296506
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382041,402,083 - 41,602,926 (-)NCBI
RefSeq Acc Id: XM_047440551   ⟹   XP_047296507
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382041,425,178 - 41,540,067 (-)NCBI
RefSeq Acc Id: XM_054324118   ⟹   XP_054180093
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.02043,133,884 - 43,271,865 (-)NCBI
RefSeq Acc Id: XM_054324119   ⟹   XP_054180094
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.02043,133,884 - 43,334,727 (-)NCBI
RefSeq Acc Id: XM_054324120   ⟹   XP_054180095
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.02043,133,884 - 43,350,238 (-)NCBI
RefSeq Acc Id: XM_054324121   ⟹   XP_054180096
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.02043,133,884 - 43,334,727 (-)NCBI
RefSeq Acc Id: XM_054324122   ⟹   XP_054180097
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.02043,133,884 - 43,296,164 (-)NCBI
RefSeq Acc Id: XM_054324123   ⟹   XP_054180098
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.02043,133,884 - 43,350,226 (-)NCBI
RefSeq Acc Id: XM_054324124   ⟹   XP_054180099
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.02043,133,884 - 43,350,249 (-)NCBI
RefSeq Acc Id: XM_054324125   ⟹   XP_054180100
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.02043,133,884 - 43,350,226 (-)NCBI
RefSeq Acc Id: XM_054324126   ⟹   XP_054180101
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.02043,133,884 - 43,350,169 (-)NCBI
RefSeq Acc Id: XM_054324127   ⟹   XP_054180102
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.02043,133,884 - 43,272,557 (-)NCBI
RefSeq Acc Id: XM_054324128   ⟹   XP_054180103
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.02043,133,884 - 43,271,865 (-)NCBI
RefSeq Acc Id: XM_054324129   ⟹   XP_054180104
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.02043,133,884 - 43,334,727 (-)NCBI
RefSeq Acc Id: XM_054324130   ⟹   XP_054180105
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.02043,133,884 - 43,281,686 (-)NCBI
RefSeq Acc Id: XM_054324131   ⟹   XP_054180106
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.02043,139,948 - 43,271,865 (-)NCBI
RefSeq Acc Id: XM_054324132   ⟹   XP_054180107
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.02043,146,410 - 43,271,865 (-)NCBI
RefSeq Acc Id: XM_054324133   ⟹   XP_054180108
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.02043,133,884 - 43,218,133 (-)NCBI
RefSeq Acc Id: XM_054324134   ⟹   XP_054180109
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.02043,156,981 - 43,271,865 (-)NCBI
RefSeq Acc Id: XM_054324135   ⟹   XP_054180110
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.02043,133,884 - 43,171,858 (-)NCBI
Protein Sequences
Protein RefSeqs NP_115597 (Get FASTA)   NCBI Sequence Viewer  
  XP_005260633 (Get FASTA)   NCBI Sequence Viewer  
  XP_011527382 (Get FASTA)   NCBI Sequence Viewer  
  XP_011527384 (Get FASTA)   NCBI Sequence Viewer  
  XP_016883588 (Get FASTA)   NCBI Sequence Viewer  
  XP_016883589 (Get FASTA)   NCBI Sequence Viewer  
  XP_016883590 (Get FASTA)   NCBI Sequence Viewer  
  XP_016883591 (Get FASTA)   NCBI Sequence Viewer  
  XP_016883593 (Get FASTA)   NCBI Sequence Viewer  
  XP_047296501 (Get FASTA)   NCBI Sequence Viewer  
  XP_047296502 (Get FASTA)   NCBI Sequence Viewer  
  XP_047296503 (Get FASTA)   NCBI Sequence Viewer  
  XP_047296504 (Get FASTA)   NCBI Sequence Viewer  
  XP_047296505 (Get FASTA)   NCBI Sequence Viewer  
  XP_047296506 (Get FASTA)   NCBI Sequence Viewer  
  XP_047296507 (Get FASTA)   NCBI Sequence Viewer  
  XP_054180093 (Get FASTA)   NCBI Sequence Viewer  
  XP_054180094 (Get FASTA)   NCBI Sequence Viewer  
  XP_054180095 (Get FASTA)   NCBI Sequence Viewer  
  XP_054180096 (Get FASTA)   NCBI Sequence Viewer  
  XP_054180097 (Get FASTA)   NCBI Sequence Viewer  
  XP_054180098 (Get FASTA)   NCBI Sequence Viewer  
  XP_054180099 (Get FASTA)   NCBI Sequence Viewer  
  XP_054180100 (Get FASTA)   NCBI Sequence Viewer  
  XP_054180101 (Get FASTA)   NCBI Sequence Viewer  
  XP_054180102 (Get FASTA)   NCBI Sequence Viewer  
  XP_054180103 (Get FASTA)   NCBI Sequence Viewer  
  XP_054180104 (Get FASTA)   NCBI Sequence Viewer  
  XP_054180105 (Get FASTA)   NCBI Sequence Viewer  
  XP_054180106 (Get FASTA)   NCBI Sequence Viewer  
  XP_054180107 (Get FASTA)   NCBI Sequence Viewer  
  XP_054180108 (Get FASTA)   NCBI Sequence Viewer  
  XP_054180109 (Get FASTA)   NCBI Sequence Viewer  
  XP_054180110 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAH21907 (Get FASTA)   NCBI Sequence Viewer  
  AAK56405 (Get FASTA)   NCBI Sequence Viewer  
  AAN59903 (Get FASTA)   NCBI Sequence Viewer  
  BAA92573 (Get FASTA)   NCBI Sequence Viewer  
  BAB15325 (Get FASTA)   NCBI Sequence Viewer  
  BAG59500 (Get FASTA)   NCBI Sequence Viewer  
  EAW75974 (Get FASTA)   NCBI Sequence Viewer  
  EAW75975 (Get FASTA)   NCBI Sequence Viewer  
  EAW75976 (Get FASTA)   NCBI Sequence Viewer  
  EAW75977 (Get FASTA)   NCBI Sequence Viewer  
  EAW75978 (Get FASTA)   NCBI Sequence Viewer  
  EAW75979 (Get FASTA)   NCBI Sequence Viewer  
  EAW75980 (Get FASTA)   NCBI Sequence Viewer  
  EAW75981 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000362319.3
  ENSP00000362330
  ENSP00000362330.3
  ENSP00000392503.1
  ENSP00000404637.1
GenBank Protein Q8TD26 (Get FASTA)   NCBI Sequence Viewer  
Reference Protein Sequences
RefSeq Acc Id: NP_115597   ⟸   NM_032221
- UniProtKB: Q9NTT7 (UniProtKB/Swiss-Prot),   Q9H6D4 (UniProtKB/Swiss-Prot),   Q9H4H6 (UniProtKB/Swiss-Prot),   Q8WTY0 (UniProtKB/Swiss-Prot),   Q8IZR2 (UniProtKB/Swiss-Prot),   Q5TH01 (UniProtKB/Swiss-Prot),   Q5TH00 (UniProtKB/Swiss-Prot),   Q5TGZ9 (UniProtKB/Swiss-Prot),   Q5JYQ0 (UniProtKB/Swiss-Prot),   Q9P2L1 (UniProtKB/Swiss-Prot),   Q8TD26 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: XP_005260633   ⟸   XM_005260576
- Peptide Label: isoform X11
- Sequence:
RefSeq Acc Id: XP_011527382   ⟸   XM_011529080
- Peptide Label: isoform X3
- Sequence:
RefSeq Acc Id: XP_011527384   ⟸   XM_011529082
- Peptide Label: isoform X9
- Sequence:
RefSeq Acc Id: XP_016883589   ⟸   XM_017028100
- Peptide Label: isoform X6
- Sequence:
RefSeq Acc Id: XP_016883590   ⟸   XM_017028101
- Peptide Label: isoform X4
- Sequence:
RefSeq Acc Id: XP_016883588   ⟸   XM_017028099
- Peptide Label: isoform X1
- Sequence:
RefSeq Acc Id: XP_016883591   ⟸   XM_017028102
- Peptide Label: isoform X7
- Sequence:
RefSeq Acc Id: XP_016883593   ⟸   XM_017028104
- Peptide Label: isoform X8
- Sequence:
RefSeq Acc Id: ENSP00000362330   ⟸   ENST00000373233
RefSeq Acc Id: ENSP00000362319   ⟸   ENST00000373222
RefSeq Acc Id: ENSP00000308684   ⟸   ENST00000309279
RefSeq Acc Id: ENSP00000404637   ⟸   ENST00000440697
RefSeq Acc Id: ENSP00000392503   ⟸   ENST00000440647
RefSeq Acc Id: XP_047296505   ⟸   XM_047440549
- Peptide Label: isoform X2
- UniProtKB: Q9NTT7 (UniProtKB/Swiss-Prot),   Q9H6D4 (UniProtKB/Swiss-Prot),   Q9H4H6 (UniProtKB/Swiss-Prot),   Q8WTY0 (UniProtKB/Swiss-Prot),   Q8TD26 (UniProtKB/Swiss-Prot),   Q8IZR2 (UniProtKB/Swiss-Prot),   Q5TH01 (UniProtKB/Swiss-Prot),   Q5TH00 (UniProtKB/Swiss-Prot),   Q5TGZ9 (UniProtKB/Swiss-Prot),   Q5JYQ0 (UniProtKB/Swiss-Prot),   Q9P2L1 (UniProtKB/Swiss-Prot)
RefSeq Acc Id: XP_047296501   ⟸   XM_047440545
- Peptide Label: isoform X2
- UniProtKB: Q9NTT7 (UniProtKB/Swiss-Prot),   Q9H6D4 (UniProtKB/Swiss-Prot),   Q9H4H6 (UniProtKB/Swiss-Prot),   Q8WTY0 (UniProtKB/Swiss-Prot),   Q8TD26 (UniProtKB/Swiss-Prot),   Q8IZR2 (UniProtKB/Swiss-Prot),   Q5TH01 (UniProtKB/Swiss-Prot),   Q5TH00 (UniProtKB/Swiss-Prot),   Q5TGZ9 (UniProtKB/Swiss-Prot),   Q5JYQ0 (UniProtKB/Swiss-Prot),   Q9P2L1 (UniProtKB/Swiss-Prot)
RefSeq Acc Id: XP_047296502   ⟸   XM_047440546
- Peptide Label: isoform X2
- UniProtKB: Q9NTT7 (UniProtKB/Swiss-Prot),   Q9H6D4 (UniProtKB/Swiss-Prot),   Q9H4H6 (UniProtKB/Swiss-Prot),   Q8WTY0 (UniProtKB/Swiss-Prot),   Q8TD26 (UniProtKB/Swiss-Prot),   Q8IZR2 (UniProtKB/Swiss-Prot),   Q5TH01 (UniProtKB/Swiss-Prot),   Q5TH00 (UniProtKB/Swiss-Prot),   Q5TGZ9 (UniProtKB/Swiss-Prot),   Q5JYQ0 (UniProtKB/Swiss-Prot),   Q9P2L1 (UniProtKB/Swiss-Prot)
RefSeq Acc Id: XP_047296504   ⟸   XM_047440548
- Peptide Label: isoform X2
- UniProtKB: Q9NTT7 (UniProtKB/Swiss-Prot),   Q9H6D4 (UniProtKB/Swiss-Prot),   Q9H4H6 (UniProtKB/Swiss-Prot),   Q8WTY0 (UniProtKB/Swiss-Prot),   Q8TD26 (UniProtKB/Swiss-Prot),   Q8IZR2 (UniProtKB/Swiss-Prot),   Q5TH01 (UniProtKB/Swiss-Prot),   Q5TH00 (UniProtKB/Swiss-Prot),   Q5TGZ9 (UniProtKB/Swiss-Prot),   Q5JYQ0 (UniProtKB/Swiss-Prot),   Q9P2L1 (UniProtKB/Swiss-Prot)
RefSeq Acc Id: XP_047296503   ⟸   XM_047440547
- Peptide Label: isoform X2
- UniProtKB: Q9NTT7 (UniProtKB/Swiss-Prot),   Q9H6D4 (UniProtKB/Swiss-Prot),   Q9H4H6 (UniProtKB/Swiss-Prot),   Q8WTY0 (UniProtKB/Swiss-Prot),   Q8TD26 (UniProtKB/Swiss-Prot),   Q8IZR2 (UniProtKB/Swiss-Prot),   Q5TH01 (UniProtKB/Swiss-Prot),   Q5TH00 (UniProtKB/Swiss-Prot),   Q5TGZ9 (UniProtKB/Swiss-Prot),   Q5JYQ0 (UniProtKB/Swiss-Prot),   Q9P2L1 (UniProtKB/Swiss-Prot)
RefSeq Acc Id: XP_047296506   ⟸   XM_047440550
- Peptide Label: isoform X5
RefSeq Acc Id: XP_047296507   ⟸   XM_047440551
- Peptide Label: isoform X10
RefSeq Acc Id: XP_054180099   ⟸   XM_054324124
- Peptide Label: isoform X2
- UniProtKB: Q9NTT7 (UniProtKB/Swiss-Prot),   Q9H6D4 (UniProtKB/Swiss-Prot),   Q9H4H6 (UniProtKB/Swiss-Prot),   Q8WTY0 (UniProtKB/Swiss-Prot),   Q8TD26 (UniProtKB/Swiss-Prot),   Q8IZR2 (UniProtKB/Swiss-Prot),   Q5TH01 (UniProtKB/Swiss-Prot),   Q5TH00 (UniProtKB/Swiss-Prot),   Q5TGZ9 (UniProtKB/Swiss-Prot),   Q5JYQ0 (UniProtKB/Swiss-Prot),   Q9P2L1 (UniProtKB/Swiss-Prot)
RefSeq Acc Id: XP_054180095   ⟸   XM_054324120
- Peptide Label: isoform X2
- UniProtKB: Q9NTT7 (UniProtKB/Swiss-Prot),   Q9H6D4 (UniProtKB/Swiss-Prot),   Q9H4H6 (UniProtKB/Swiss-Prot),   Q8WTY0 (UniProtKB/Swiss-Prot),   Q8TD26 (UniProtKB/Swiss-Prot),   Q8IZR2 (UniProtKB/Swiss-Prot),   Q5TH01 (UniProtKB/Swiss-Prot),   Q5TH00 (UniProtKB/Swiss-Prot),   Q5TGZ9 (UniProtKB/Swiss-Prot),   Q5JYQ0 (UniProtKB/Swiss-Prot),   Q9P2L1 (UniProtKB/Swiss-Prot)
RefSeq Acc Id: XP_054180098   ⟸   XM_054324123
- Peptide Label: isoform X2
- UniProtKB: Q9NTT7 (UniProtKB/Swiss-Prot),   Q9H6D4 (UniProtKB/Swiss-Prot),   Q9H4H6 (UniProtKB/Swiss-Prot),   Q8WTY0 (UniProtKB/Swiss-Prot),   Q8TD26 (UniProtKB/Swiss-Prot),   Q8IZR2 (UniProtKB/Swiss-Prot),   Q5TH01 (UniProtKB/Swiss-Prot),   Q5TH00 (UniProtKB/Swiss-Prot),   Q5TGZ9 (UniProtKB/Swiss-Prot),   Q5JYQ0 (UniProtKB/Swiss-Prot),   Q9P2L1 (UniProtKB/Swiss-Prot)
RefSeq Acc Id: XP_054180100   ⟸   XM_054324125
- Peptide Label: isoform X2
- UniProtKB: Q9NTT7 (UniProtKB/Swiss-Prot),   Q9H6D4 (UniProtKB/Swiss-Prot),   Q9H4H6 (UniProtKB/Swiss-Prot),   Q8WTY0 (UniProtKB/Swiss-Prot),   Q8TD26 (UniProtKB/Swiss-Prot),   Q8IZR2 (UniProtKB/Swiss-Prot),   Q5TH01 (UniProtKB/Swiss-Prot),   Q5TH00 (UniProtKB/Swiss-Prot),   Q5TGZ9 (UniProtKB/Swiss-Prot),   Q5JYQ0 (UniProtKB/Swiss-Prot),   Q9P2L1 (UniProtKB/Swiss-Prot)
RefSeq Acc Id: XP_054180101   ⟸   XM_054324126
- Peptide Label: isoform X2
- UniProtKB: Q9NTT7 (UniProtKB/Swiss-Prot),   Q9H6D4 (UniProtKB/Swiss-Prot),   Q9H4H6 (UniProtKB/Swiss-Prot),   Q8WTY0 (UniProtKB/Swiss-Prot),   Q8TD26 (UniProtKB/Swiss-Prot),   Q8IZR2 (UniProtKB/Swiss-Prot),   Q5TH01 (UniProtKB/Swiss-Prot),   Q5TH00 (UniProtKB/Swiss-Prot),   Q5TGZ9 (UniProtKB/Swiss-Prot),   Q5JYQ0 (UniProtKB/Swiss-Prot),   Q9P2L1 (UniProtKB/Swiss-Prot)
RefSeq Acc Id: XP_054180096   ⟸   XM_054324121
- Peptide Label: isoform X2
- UniProtKB: Q9NTT7 (UniProtKB/Swiss-Prot),   Q9H6D4 (UniProtKB/Swiss-Prot),   Q9H4H6 (UniProtKB/Swiss-Prot),   Q8WTY0 (UniProtKB/Swiss-Prot),   Q8TD26 (UniProtKB/Swiss-Prot),   Q8IZR2 (UniProtKB/Swiss-Prot),   Q5TH01 (UniProtKB/Swiss-Prot),   Q5TH00 (UniProtKB/Swiss-Prot),   Q5TGZ9 (UniProtKB/Swiss-Prot),   Q5JYQ0 (UniProtKB/Swiss-Prot),   Q9P2L1 (UniProtKB/Swiss-Prot)
RefSeq Acc Id: XP_054180104   ⟸   XM_054324129
- Peptide Label: isoform X5
RefSeq Acc Id: XP_054180094   ⟸   XM_054324119
- Peptide Label: isoform X2
- UniProtKB: Q9NTT7 (UniProtKB/Swiss-Prot),   Q9H6D4 (UniProtKB/Swiss-Prot),   Q9H4H6 (UniProtKB/Swiss-Prot),   Q8WTY0 (UniProtKB/Swiss-Prot),   Q8TD26 (UniProtKB/Swiss-Prot),   Q8IZR2 (UniProtKB/Swiss-Prot),   Q5TH01 (UniProtKB/Swiss-Prot),   Q5TH00 (UniProtKB/Swiss-Prot),   Q5TGZ9 (UniProtKB/Swiss-Prot),   Q5JYQ0 (UniProtKB/Swiss-Prot),   Q9P2L1 (UniProtKB/Swiss-Prot)
RefSeq Acc Id: XP_054180097   ⟸   XM_054324122
- Peptide Label: isoform X2
- UniProtKB: Q9NTT7 (UniProtKB/Swiss-Prot),   Q9H6D4 (UniProtKB/Swiss-Prot),   Q9H4H6 (UniProtKB/Swiss-Prot),   Q8WTY0 (UniProtKB/Swiss-Prot),   Q8TD26 (UniProtKB/Swiss-Prot),   Q8IZR2 (UniProtKB/Swiss-Prot),   Q5TH01 (UniProtKB/Swiss-Prot),   Q5TH00 (UniProtKB/Swiss-Prot),   Q5TGZ9 (UniProtKB/Swiss-Prot),   Q5JYQ0 (UniProtKB/Swiss-Prot),   Q9P2L1 (UniProtKB/Swiss-Prot)
RefSeq Acc Id: XP_054180105   ⟸   XM_054324130
- Peptide Label: isoform X6
RefSeq Acc Id: XP_054180102   ⟸   XM_054324127
- Peptide Label: isoform X3
RefSeq Acc Id: XP_054180103   ⟸   XM_054324128
- Peptide Label: isoform X4
RefSeq Acc Id: XP_054180093   ⟸   XM_054324118
- Peptide Label: isoform X1
RefSeq Acc Id: XP_054180108   ⟸   XM_054324133
- Peptide Label: isoform X9
RefSeq Acc Id: XP_054180110   ⟸   XM_054324135
- Peptide Label: isoform X11
RefSeq Acc Id: XP_054180106   ⟸   XM_054324131
- Peptide Label: isoform X7
RefSeq Acc Id: XP_054180107   ⟸   XM_054324132
- Peptide Label: isoform X8
RefSeq Acc Id: XP_054180109   ⟸   XM_054324134
- Peptide Label: isoform X10
Protein Domains
Chromo   Helicase ATP-binding   Helicase C-terminal   Myb-like

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q8TD26-F1-model_v2 AlphaFold Q8TD26 1-1400 view protein structure
AF-Q8TD26-F2-model_v2 AlphaFold Q8TD26 201-1600 view protein structure
AF-Q8TD26-F3-model_v2 AlphaFold Q8TD26 401-1800 view protein structure
AF-Q8TD26-F4-model_v2 AlphaFold Q8TD26 601-2000 view protein structure
AF-Q8TD26-F5-model_v2 AlphaFold Q8TD26 801-2200 view protein structure
AF-Q8TD26-F6-model_v2 AlphaFold Q8TD26 1001-2400 view protein structure
AF-Q8TD26-F7-model_v2 AlphaFold Q8TD26 1201-2600 view protein structure
AF-Q8TD26-F8-model_v2 AlphaFold Q8TD26 1401-2715 view protein structure

Promoters
RGD ID:6798612
Promoter ID:HG_KWN:39464
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   HeLa_S3,   Jurkat,   K562,   Lymphoblastoid,   NB4
Transcripts:ENST00000309279,   OTTHUMT00000079270,   UC002XKC.2,   UC002XKD.1
Position:
Human AssemblyChrPosition (strand)Source
Build 362039,680,071 - 39,680,642 (-)MPROMDB
RGD ID:13206949
Promoter ID:EPDNEW_H27055
Type:initiation region
Name:CHD6_1
Description:chromodomain helicase DNA binding protein 6
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh382041,618,373 - 41,618,433EPDNEW

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:19057 AgrOrtholog
COSMIC CHD6 COSMIC
Ensembl Genes ENSG00000124177 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000373222.3 UniProtKB/Swiss-Prot
  ENST00000373233 ENTREZGENE
  ENST00000373233.8 UniProtKB/Swiss-Prot
  ENST00000440647.1 UniProtKB/TrEMBL
  ENST00000440697.5 UniProtKB/TrEMBL
Gene3D-CATH 2.40.50.40 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  3.40.50.10810 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  3.40.50.300 UniProtKB/Swiss-Prot
  Homeodomain-like UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000124177 GTEx
HGNC ID HGNC:19057 ENTREZGENE
Human Proteome Map CHD6 Human Proteome Map
InterPro BRK_domain UniProtKB/Swiss-Prot
  BRK_sf UniProtKB/Swiss-Prot
  Chromo-like_dom_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Chromo/chromo_shadow_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Chromo_domain UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  DNA/RNA_helicase_DEAH_CS UniProtKB/Swiss-Prot
  Helicase_ATP-bd UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Helicase_C UniProtKB/Swiss-Prot
  P-loop_NTPase UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SNF2-like_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SNF2/RAD54-like_C UniProtKB/Swiss-Prot
  SNF2_N UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:84181 UniProtKB/Swiss-Prot
NCBI Gene 84181 ENTREZGENE
OMIM 616114 OMIM
PANTHER CHROMODOMAIN-HELICASE-DNA-BINDING PROTEIN 9 UniProtKB/Swiss-Prot
  CHROMODOMAIN-HELICASE-DNA-BINDING PROTEIN 9 UniProtKB/Swiss-Prot
  CHROMODOMAIN-HELICASE-DNA-BINDING PROTEIN 9 UniProtKB/TrEMBL
  DNA HELICASE UniProtKB/TrEMBL
Pfam Chromo UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Helicase_C UniProtKB/Swiss-Prot
  SNF2_N UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA134974700 PharmGKB
PROSITE CHROMO_2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  DEAH_ATP_HELICASE UniProtKB/Swiss-Prot
  HELICASE_ATP_BIND_1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  HELICASE_CTER UniProtKB/Swiss-Prot
SMART BRK UniProtKB/Swiss-Prot
  CHROMO UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  DEXDc UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  HELICc UniProtKB/Swiss-Prot
Superfamily-SCOP SSF160481 UniProtKB/Swiss-Prot
  SSF52540 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SSF54160 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A0A075B6P4_HUMAN UniProtKB/TrEMBL
  CHD6_HUMAN UniProtKB/Swiss-Prot
  H7C294_HUMAN UniProtKB/TrEMBL
  Q5JYQ0 ENTREZGENE
  Q5TGZ9 ENTREZGENE
  Q5TH00 ENTREZGENE
  Q5TH01 ENTREZGENE
  Q8IZR2 ENTREZGENE
  Q8TD26 ENTREZGENE
  Q8WTY0 ENTREZGENE
  Q9H4H6 ENTREZGENE
  Q9H6D4 ENTREZGENE
  Q9NTT7 ENTREZGENE
  Q9P2L1 ENTREZGENE
UniProt Secondary Q5JYQ0 UniProtKB/Swiss-Prot
  Q5TGZ9 UniProtKB/Swiss-Prot
  Q5TH00 UniProtKB/Swiss-Prot
  Q5TH01 UniProtKB/Swiss-Prot
  Q8IZR2 UniProtKB/Swiss-Prot
  Q8WTY0 UniProtKB/Swiss-Prot
  Q9H4H6 UniProtKB/Swiss-Prot
  Q9H6D4 UniProtKB/Swiss-Prot
  Q9NTT7 UniProtKB/Swiss-Prot
  Q9P2L1 UniProtKB/Swiss-Prot