HOXA13 (homeobox A13) - Rat Genome Database

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Gene: HOXA13 (homeobox A13) Homo sapiens
Analyze
Symbol: HOXA13
Name: homeobox A13
RGD ID: 1346914
HGNC Page HGNC:5102
Description: Enables sequence-specific double-stranded DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to act upstream of or within several processes, including circulatory system development; endothelial cell differentiation; and reproductive structure development. Located in chromosome; intermediate filament cytoskeleton; and nucleoplasm. Implicated in Guttmacher syndrome and hand-foot-genital syndrome.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: homeo box 1J; homeo box A13; homeobox protein Hox-1J; homeobox protein Hox-A13; homeobox protein HOXA13; HOX1; HOX1J; transcription factor HOXA13
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
GRCh38727,194,364 - 27,200,091 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl727,193,503 - 27,200,091 (-)EnsemblGRCh38hg38GRCh38
GRCh37727,233,983 - 27,239,710 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36727,203,024 - 27,206,250 (-)NCBINCBI36Build 36hg18NCBI36
Build 34727,009,738 - 27,012,936NCBI
Celera727,225,437 - 27,228,662 (-)NCBICelera
Cytogenetic Map7p15.2NCBI
HuRef727,117,064 - 27,119,882 (-)NCBIHuRef
CHM1_1727,236,223 - 27,239,448 (-)NCBICHM1_1
T2T-CHM13v2.0727,330,371 - 27,336,079 (-)NCBIT2T-CHM13v2.0
CRA_TCAGchr7v2727,287,684 - 27,290,909 (-)NCBI
JBrowse: View Region in Genome Browser (JBrowse)
Model


Gene Ontology Annotations     Click to see Annotation Detail View

Cellular Component

Phenotype Annotations     Click to see Annotation Detail View
References

References - curated
# Reference Title Reference Citation
1. GOAs Human GO annotations GOA_HUMAN data from the GO Consortium
2. Sonic hedgehog, BMP4, and Hox genes in the development of anorectal malformations in Ethylenethiourea-exposed fetal rats. Mandhan P, etal., J Pediatr Surg. 2006 Dec;41(12):2041-5.
3. Mutation of HOXA13 in hand-foot-genital syndrome. Mortlock DP and Innis JW, Nat Genet. 1997 Feb;15(2):179-80.
4. OMIM Disease Annotation Pipeline OMIM Disease Annotation Pipeline
5. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
6. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
7. RGD HPO Phenotype Annotation Pipeline RGD automated import pipeline for human HPO-to-gene-to-disease annotations
8. Maternal exposure to di-n-butyl phthalate (DBP) induces combined anorectal and urogenital malformations in male rat offspring. Zhu YP, etal., Reprod Toxicol. 2016 Jun;61:169-76. doi: 10.1016/j.reprotox.2016.04.007. Epub 2016 Apr 11.
Additional References at PubMed
PMID:1358459   PMID:1973146   PMID:2574852   PMID:8646877   PMID:9847074   PMID:10569982   PMID:10656931   PMID:10835276   PMID:10839976   PMID:11206481   PMID:11688568   PMID:11830496  
PMID:11857506   PMID:11968094   PMID:12073020   PMID:12112533   PMID:12414828   PMID:12477932   PMID:12690205   PMID:12853948   PMID:14675924   PMID:15617687   PMID:16087734   PMID:17274802  
PMID:17935235   PMID:18245445   PMID:18483557   PMID:19145497   PMID:19274049   PMID:19423998   PMID:19453261   PMID:19491265   PMID:19591980   PMID:19997598   PMID:20301596   PMID:21626505  
PMID:21829694   PMID:21873635   PMID:21893383   PMID:21971947   PMID:23332764   PMID:23376215   PMID:23532960   PMID:23592225   PMID:24114970   PMID:24626613   PMID:25341685   PMID:25472883  
PMID:25665578   PMID:25889214   PMID:26043692   PMID:26356815   PMID:26485220   PMID:26590955   PMID:26695677   PMID:26982635   PMID:27064878   PMID:27108607   PMID:27144338   PMID:27176855  
PMID:27684187   PMID:27830363   PMID:28384324   PMID:28473536   PMID:28534516   PMID:28766961   PMID:28782268   PMID:28947713   PMID:29035381   PMID:29436749   PMID:29678634   PMID:29757528  
PMID:29844126   PMID:30550979   PMID:30649340   PMID:31957853   PMID:32076268   PMID:32222541   PMID:32444962   PMID:32589328   PMID:32822724   PMID:33629307   PMID:33896818   PMID:34075028  
PMID:34079125   PMID:34099670   PMID:34140506   PMID:34189442   PMID:34979376   PMID:35076814   PMID:35271311   PMID:35785414   PMID:36129980   PMID:36190650   PMID:36373674   PMID:36411030  
PMID:36702441   PMID:36724073   PMID:37392284   PMID:37563232   PMID:37704626   PMID:38129477  


Genomics

Comparative Map Data
HOXA13
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38727,194,364 - 27,200,091 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl727,193,503 - 27,200,091 (-)EnsemblGRCh38hg38GRCh38
GRCh37727,233,983 - 27,239,710 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36727,203,024 - 27,206,250 (-)NCBINCBI36Build 36hg18NCBI36
Build 34727,009,738 - 27,012,936NCBI
Celera727,225,437 - 27,228,662 (-)NCBICelera
Cytogenetic Map7p15.2NCBI
HuRef727,117,064 - 27,119,882 (-)NCBIHuRef
CHM1_1727,236,223 - 27,239,448 (-)NCBICHM1_1
T2T-CHM13v2.0727,330,371 - 27,336,079 (-)NCBIT2T-CHM13v2.0
CRA_TCAGchr7v2727,287,684 - 27,290,909 (-)NCBI
Hoxa13
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm39652,235,833 - 52,237,865 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl652,234,674 - 52,237,788 (-)EnsemblGRCm39 Ensembl
GRCm38652,258,853 - 52,260,880 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl652,257,694 - 52,260,880 (-)EnsemblGRCm38mm10GRCm38
MGSCv37652,208,852 - 52,210,874 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv36652,188,436 - 52,190,458 (-)NCBIMGSCv36mm8
Celera652,780,486 - 52,782,142 (-)NCBICelera
Cytogenetic Map6B3NCBI
cM Map625.41NCBI
Hoxa13
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr8482,689,566 - 82,691,701 (-)NCBIGRCr8
mRatBN7.2481,358,956 - 81,361,091 (-)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl481,358,956 - 81,361,091 (-)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx486,580,795 - 86,582,928 (-)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0482,356,180 - 82,358,313 (-)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0480,783,284 - 80,785,419 (-)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.0482,313,383 - 82,315,550 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl482,228,017 - 82,229,397 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.04146,980,144 - 146,982,279 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.4480,558,841 - 80,561,053NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
Celera476,249,534 - 76,251,232 (-)NCBICelera
Cytogenetic Map4q24NCBI
Hoxa13
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_00495541028,890,171 - 28,893,515 (-)EnsemblChiLan1.0
ChiLan1.0NW_00495541028,887,952 - 28,893,515 (-)NCBIChiLan1.0ChiLan1.0
HOXA13
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v2632,026,168 - 32,029,267 (-)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan1780,346,803 - 80,353,992 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v0727,838,656 - 27,844,562 (-)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.1727,441,171 - 27,443,793 (-)NCBIpanpan1.1PanPan1.1panPan2
HOXA13
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.11440,371,234 - 40,375,261 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl1440,373,059 - 40,375,980 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha1439,801,720 - 39,806,138 (-)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.01440,309,583 - 40,314,003 (-)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl1440,311,665 - 40,314,704 (-)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.11440,423,492 - 40,427,909 (-)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.01440,108,556 - 40,112,977 (-)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.01440,467,202 - 40,471,624 (-)NCBIUU_Cfam_GSD_1.0
Hoxa13
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440511884,612,984 - 84,615,546 (-)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_0049364783,824,715 - 3,827,277 (-)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_0049364783,824,715 - 3,827,277 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
HOXA13
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl1845,373,440 - 45,376,325 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.11845,373,340 - 45,379,046 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.21850,007,054 - 50,008,334 (+)NCBISscrofa10.2Sscrofa10.2susScr3
HOXA13
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.12131,168,239 - 31,175,960 (+)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl2131,168,793 - 31,173,056 (+)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366604273,559,316 - 73,565,124 (-)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Hoxa13
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_0046247393,406,436 - 3,410,851 (+)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_0046247393,405,860 - 3,410,426 (+)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in HOXA13
125 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
HOXA13, GLN50LEU AND 2-BP DEL, -79GC, PROMOTER single nucleotide variant Guttmacher syndrome [RCV000016022] Chr7:7p15-p14.2 pathogenic
NM_000522.5(HOXA13):c.421_422insAGGCGGGCC (p.Gly140_Pro141insGlnAlaGly) insertion not provided [RCV000723201] Chr7:27199656..27199657 [GRCh38]
Chr7:27239275..27239276 [GRCh37]
Chr7:7p15.2		 benign|uncertain significance
NM_000522.5(HOXA13):c.960G>C (p.Arg320Ser) single nucleotide variant not provided [RCV000722821] Chr7:27198405 [GRCh38]
Chr7:27238024 [GRCh37]
Chr7:7p15.2		 uncertain significance
NM_000522.5(HOXA13):c.351_377del (p.Ala125_Ala133del) deletion Guttmacher syndrome [RCV002485839]|not provided [RCV000722997] Chr7:27199701..27199727 [GRCh38]
Chr7:27239320..27239346 [GRCh37]
Chr7:7p15.2		 likely benign|uncertain significance
NM_000522.5(HOXA13):c.1107G>A (p.Trp369Ter) single nucleotide variant Hand-foot-genital syndrome [RCV000016018] Chr7:27198258 [GRCh38]
Chr7:27237877 [GRCh37]
Chr7:7p15.2		 pathogenic
NM_000522.5(HOXA13):c.407C>A (p.Ser136Ter) single nucleotide variant Hand-foot-genital syndrome [RCV000016019] Chr7:27199671 [GRCh38]
Chr7:27239290 [GRCh37]
Chr7:7p15.2		 pathogenic
NM_000522.5(HOXA13):c.366_389dup (p.Ala133_Ser134insAlaAlaAlaAlaAlaAlaAlaAla) duplication Hand-foot-genital syndrome [RCV000016020] Chr7:27199688..27199689 [GRCh38]
Chr7:27239307..27239308 [GRCh37]
Chr7:7p15.2		 pathogenic
NM_000522.5(HOXA13):c.1114A>C (p.Asn372His) single nucleotide variant Hand-foot-genital syndrome [RCV000016021] Chr7:27198251 [GRCh38]
Chr7:27237870 [GRCh37]
Chr7:7p15.2		 pathogenic
HOXA13, 18-BP DUP, ALANINE TRACT EXPANSION insertion Hand-foot-genital syndrome [RCV000016023] Chr7:7p15-p14.2 pathogenic
NM_000522.5(HOXA13):c.366_392dup (p.Ala133_Ser134insAlaAlaAlaAlaAlaAlaAlaAlaAla) duplication Hand-foot-genital syndrome [RCV000016024] Chr7:27199685..27199686 [GRCh38]
Chr7:27239304..27239305 [GRCh37]
Chr7:7p15.2		 pathogenic
NM_000522.5(HOXA13):c.355_406dup (p.Ser136fs) duplication Hand-foot-genital syndrome [RCV000016025] Chr7:27199671..27199672 [GRCh38]
Chr7:27239290..27239291 [GRCh37]
Chr7:7p15.2		 pathogenic
GRCh38/hg38 7p22.3-14.1(chr7:54185-41875885)x3 copy number gain See cases [RCV000051159] Chr7:54185..41875885 [GRCh38]
Chr7:54185..41915483 [GRCh37]
Chr7:149268..41882008 [NCBI36]
Chr7:7p22.3-14.1		 pathogenic
GRCh38/hg38 7p22.3-q36.3(chr7:53985-159282531)x1 copy number loss See cases [RCV000052250] Chr7:53985..159282531 [GRCh38]
Chr7:53985..159075220 [GRCh37]
Chr7:149068..158767981 [NCBI36]
Chr7:7p22.3-q36.3		 pathogenic
GRCh38/hg38 7p15.2(chr7:27154807-27422335)x1 copy number loss See cases [RCV000052313] Chr7:27154807..27422335 [GRCh38]
Chr7:27194426..27461954 [GRCh37]
Chr7:27160951..27428479 [NCBI36]
Chr7:7p15.2		 pathogenic
GRCh38/hg38 7p15.2-14.3(chr7:25511691-30421133)x1 copy number loss See cases [RCV000052310] Chr7:25511691..30421133 [GRCh38]
Chr7:25551310..30460749 [GRCh37]
Chr7:25517835..30427274 [NCBI36]
Chr7:7p15.2-14.3		 pathogenic
GRCh38/hg38 7p15.2(chr7:27107301-27314586)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053436]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053436]|See cases [RCV000053436] Chr7:27107301..27314586 [GRCh38]
Chr7:27146920..27354205 [GRCh37]
Chr7:27113445..27320730 [NCBI36]
Chr7:7p15.2		 uncertain significance
GRCh38/hg38 7p22.3-14.2(chr7:54185-37089712)x3 copy number gain See cases [RCV000053530] Chr7:54185..37089712 [GRCh38]
Chr7:54185..37129317 [GRCh37]
Chr7:149268..37095842 [NCBI36]
Chr7:7p22.3-14.2		 pathogenic
GRCh38/hg38 7p21.1-15.2(chr7:20210912-27849400)x1 copy number loss See cases [RCV000134333] Chr7:20210912..27849400 [GRCh38]
Chr7:20250535..27889019 [GRCh37]
Chr7:20217060..27855544 [NCBI36]
Chr7:7p21.1-15.2		 pathogenic
GRCh38/hg38 7p22.3-q36.3(chr7:54185-159282390)x1 copy number loss See cases [RCV000135401] Chr7:54185..159282390 [GRCh38]
Chr7:54185..159075079 [GRCh37]
Chr7:149268..158767840 [NCBI36]
Chr7:7p22.3-q36.3		 pathogenic
GRCh38/hg38 7p21.1-14.3(chr7:20561456-32005143)x1 copy number loss See cases [RCV000136775] Chr7:20561456..32005143 [GRCh38]
Chr7:20601079..32044755 [GRCh37]
Chr7:20567604..32011280 [NCBI36]
Chr7:7p21.1-14.3		 pathogenic
GRCh38/hg38 7p22.1-15.2(chr7:5682209-27230311)x3 copy number gain See cases [RCV000136649] Chr7:5682209..27230311 [GRCh38]
Chr7:5721840..27269930 [GRCh37]
Chr7:5688366..27236455 [NCBI36]
Chr7:7p22.1-15.2		 pathogenic
GRCh38/hg38 7p22.3-15.2(chr7:1698124-27207295)x3 copy number gain See cases [RCV000143060] Chr7:1698124..27207295 [GRCh38]
Chr7:1737760..27246914 [GRCh37]
Chr7:1704286..27213439 [NCBI36]
Chr7:7p22.3-15.2		 pathogenic
GRCh37/hg19 7p15.3-14.3(chr7:22935369-32621975)x1 copy number loss See cases [RCV000240125] Chr7:22935369..32621975 [GRCh37]
Chr7:7p15.3-14.3		 pathogenic
NM_000522.5(HOXA13):c.357_395del (p.Ala121_Ala133del) deletion HOXA13-related disorder [RCV003945772]|not provided [RCV000722970] Chr7:27199683..27199721 [GRCh38]
Chr7:27239302..27239340 [GRCh37]
Chr7:7p15.2		 uncertain significance
NM_000522.5(HOXA13):c.360_377del (p.Ala128_Ala133del) deletion Guttmacher syndrome [RCV002499335]|HOXA13-related disorder [RCV003980357]|not provided [RCV000722612] Chr7:27199701..27199718 [GRCh38]
Chr7:27239320..27239337 [GRCh37]
Chr7:7p15.2		 likely benign|uncertain significance
NM_000522.5(HOXA13):c.357_392del (p.Ala122_Ala133del) deletion not provided [RCV000723095] Chr7:27199686..27199721 [GRCh38]
Chr7:27239305..27239340 [GRCh37]
Chr7:7p15.2		 uncertain significance
TMEM106B-BRAF fusion deletion Pleomorphic xanthoastrocytoma [RCV000454357] Chr7:12258147..140494267 [GRCh37]
Chr7:7p21.3-q34		 pathogenic
GRCh37/hg19 7p21.3-14.2(chr7:11562624-36395416)x3 copy number gain See cases [RCV000446478] Chr7:11562624..36395416 [GRCh37]
Chr7:7p21.3-14.2		 pathogenic
GRCh37/hg19 7p22.3-q36.3(chr7:43360-159119707)x1 copy number loss See cases [RCV000446044] Chr7:43360..159119707 [GRCh37]
Chr7:7p22.3-q36.3		 pathogenic
NM_000522.5(HOXA13):c.633G>T (p.Met211Ile) single nucleotide variant not provided [RCV000436352] Chr7:27199445 [GRCh38]
Chr7:27239064 [GRCh37]
Chr7:7p15.2		 benign|likely benign
GRCh37/hg19 7p15.3-15.2(chr7:25448425-27578387)x3 copy number gain See cases [RCV000447735] Chr7:25448425..27578387 [GRCh37]
Chr7:7p15.3-15.2		 likely pathogenic
GRCh37/hg19 7p21.3-12.1(chr7:11048840-52863626)x3 copy number gain See cases [RCV000512091] Chr7:11048840..52863626 [GRCh37]
Chr7:7p21.3-12.1		 pathogenic
GRCh37/hg19 7p22.3-q36.3(chr7:43361-159119707) copy number gain See cases [RCV000510686] Chr7:43361..159119707 [GRCh37]
Chr7:7p22.3-q36.3		 pathogenic
NM_000522.5(HOXA13):c.150T>G (p.Ala50=) single nucleotide variant not provided [RCV004705627]|not specified [RCV000503653] Chr7:27199928 [GRCh38]
Chr7:27239547 [GRCh37]
Chr7:7p15.2		 likely benign
NM_000522.5(HOXA13):c.159C>G (p.Ala53=) single nucleotide variant not specified [RCV000501567] Chr7:27199919 [GRCh38]
Chr7:27239538 [GRCh37]
Chr7:7p15.2		 likely benign
GRCh37/hg19 7p22.3-14.3(chr7:704573-29257946)x3 copy number gain See cases [RCV000510275] Chr7:704573..29257946 [GRCh37]
Chr7:7p22.3-14.3		 pathogenic
GRCh37/hg19 7p15.3-14.3(chr7:24344104-28879357)x1 copy number loss See cases [RCV000510695] Chr7:24344104..28879357 [GRCh37]
Chr7:7p15.3-14.3		 pathogenic
GRCh37/hg19 7p22.3-q36.3(chr7:43361-159119707)x3 copy number gain See cases [RCV000511549] Chr7:43361..159119707 [GRCh37]
Chr7:7p22.3-q36.3		 pathogenic
NM_000522.5(HOXA13):c.476C>T (p.Ala159Val) single nucleotide variant Inborn genetic diseases [RCV003261736] Chr7:27199602 [GRCh38]
Chr7:27239221 [GRCh37]
Chr7:7p15.2		 uncertain significance
NM_000522.5(HOXA13):c.1058G>A (p.Arg353Lys) single nucleotide variant Inborn genetic diseases [RCV003297754] Chr7:27198307 [GRCh38]
Chr7:27237926 [GRCh37]
Chr7:7p15.2		 uncertain significance
NM_000522.5(HOXA13):c.191C>T (p.Ala64Val) single nucleotide variant Inborn genetic diseases [RCV003245335] Chr7:27199887 [GRCh38]
Chr7:27239506 [GRCh37]
Chr7:7p15.2		 uncertain significance
NC_000007.13:g.(20954043_21001537)_(114528369_114556605)inv inversion Childhood apraxia of speech [RCV000234948] Chr7:21001537..114528369 [GRCh37]
Chr7:7p15.3-q31.1		 pathogenic
GRCh37/hg19 7p22.3-q36.3(chr7:44935-159126310)x3 copy number gain not provided [RCV000746280] Chr7:44935..159126310 [GRCh37]
Chr7:7p22.3-q36.3		 pathogenic
GRCh37/hg19 7p22.3-q36.3(chr7:10704-159122532)x3 copy number gain not provided [RCV000746278] Chr7:10704..159122532 [GRCh37]
Chr7:7p22.3-q36.3		 pathogenic
GRCh37/hg19 7p15.2(chr7:27026872-27322106)x3 copy number gain not provided [RCV000746569] Chr7:27026872..27322106 [GRCh37]
Chr7:7p15.2		 benign
GRCh37/hg19 7p15.2(chr7:27065705-27286796)x1 copy number loss not provided [RCV000746570] Chr7:27065705..27286796 [GRCh37]
Chr7:7p15.2		 benign
GRCh37/hg19 7p15.2(chr7:27089764-27322106)x3 copy number gain not provided [RCV000746571] Chr7:27089764..27322106 [GRCh37]
Chr7:7p15.2		 benign
GRCh37/hg19 7p15.2(chr7:27118974-27264337)x3 copy number gain not provided [RCV000746572] Chr7:27118974..27264337 [GRCh37]
Chr7:7p15.2		 benign
GRCh37/hg19 7p15.2(chr7:27118974-27286796)x3 copy number gain not provided [RCV000746573] Chr7:27118974..27286796 [GRCh37]
Chr7:7p15.2		 benign
GRCh37/hg19 7p15.2(chr7:27123880-27286796)x1 copy number loss not provided [RCV000746574] Chr7:27123880..27286796 [GRCh37]
Chr7:7p15.2		 benign
GRCh37/hg19 7p15.2(chr7:27130276-27286796)x3 copy number gain not provided [RCV000746575] Chr7:27130276..27286796 [GRCh37]
Chr7:7p15.2		 benign
GRCh37/hg19 7p15.2(chr7:27135314-27264337)x3 copy number gain not provided [RCV000746576] Chr7:27135314..27264337 [GRCh37]
Chr7:7p15.2		 benign
GRCh37/hg19 7p15.2(chr7:27135314-27286796)x3 copy number gain not provided [RCV000746577] Chr7:27135314..27286796 [GRCh37]
Chr7:7p15.2		 benign
NC_000007.14:g.27200398dup duplication not provided [RCV001667298] Chr7:27200396..27200397 [GRCh38]
Chr7:27240015..27240016 [GRCh37]
Chr7:7p15.2		 benign
NM_000522.5(HOXA13):c.496C>A (p.Pro166Thr) single nucleotide variant Guttmacher syndrome [RCV002488462]|not provided [RCV001679968] Chr7:27199582 [GRCh38]
Chr7:27239201 [GRCh37]
Chr7:7p15.2		 benign
NM_000522.5(HOXA13):c.887C>A (p.Ala296Glu) single nucleotide variant Inborn genetic diseases [RCV003245977] Chr7:27199191 [GRCh38]
Chr7:27238810 [GRCh37]
Chr7:7p15.2		 uncertain significance
NM_000522.5(HOXA13):c.591C>A (p.Pro197=) single nucleotide variant not provided [RCV000906704] Chr7:27199487 [GRCh38]
Chr7:27239106 [GRCh37]
Chr7:7p15.2		 benign
NM_000522.5(HOXA13):c.342G>A (p.Pro114=) single nucleotide variant HOXA13-related disorder [RCV003975732]|not provided [RCV000900759] Chr7:27199736 [GRCh38]
Chr7:27239355 [GRCh37]
Chr7:7p15.2		 likely benign
NM_000522.5(HOXA13):c.357_386del (p.Ala124_Ala133del) deletion not provided [RCV000950156] Chr7:27199692..27199721 [GRCh38]
Chr7:27239311..27239340 [GRCh37]
Chr7:7p15.2		 likely benign
NM_000522.5(HOXA13):c.575A>G (p.Lys192Arg) single nucleotide variant not provided [RCV000904568] Chr7:27199503 [GRCh38]
Chr7:27239122 [GRCh37]
Chr7:7p15.2		 likely benign
NM_000522.5(HOXA13):c.357T>C (p.Ala119=) single nucleotide variant not provided [RCV000983480] Chr7:27199721 [GRCh38]
Chr7:27239340 [GRCh37]
Chr7:7p15.2		 likely benign
GRCh37/hg19 7p22.3-q36.3(chr7:10365-159119707)x3 copy number gain not provided [RCV000848126] Chr7:10365..159119707 [GRCh37]
Chr7:7p22.3-q36.3		 pathogenic
GRCh37/hg19 7p15.3-14.3(chr7:23877135-33139446)x1 copy number loss not provided [RCV001005924] Chr7:23877135..33139446 [GRCh37]
Chr7:7p15.3-14.3		 pathogenic
GRCh38/hg38 7p22.3-15.2(chr7:43360-27196404)x3 copy number gain See cases [RCV000143586] Chr7:43360..27196404 [GRCh38]
Chr7:43360..27236023 [GRCh37]
Chr7:138443..27202548 [NCBI36]
Chr7:7p22.3-15.2		 pathogenic
NC_000007.13:g.23236782_30690453del7453672 deletion Silver Russell Syndrome-related disorder [RCV000785664] Chr7:23236782..30690453 [GRCh37]
Chr7:7p15.3-14.3		 pathogenic
NM_000522.5(HOXA13):c.561C>T (p.His187=) single nucleotide variant not provided [RCV000919937] Chr7:27199517 [GRCh38]
Chr7:27239136 [GRCh37]
Chr7:7p15.2		 likely benign
NM_000522.5(HOXA13):c.480G>A (p.Ala160=) single nucleotide variant Guttmacher syndrome [RCV002501486]|not provided [RCV000893672]|not specified [RCV001729738] Chr7:27199598 [GRCh38]
Chr7:27239217 [GRCh37]
Chr7:7p15.2		 benign|likely benign
NM_000522.5(HOXA13):c.360_377dup (p.Ala133_Ser134insAlaAlaAlaAlaAlaAla) duplication Hand-foot-genital syndrome [RCV001568360] Chr7:27199700..27199701 [GRCh38]
Chr7:27239319..27239320 [GRCh37]
Chr7:7p15.2		 pathogenic|likely pathogenic
NM_000522.5(HOXA13):c.662T>A (p.Phe221Tyr) single nucleotide variant Inborn genetic diseases [RCV003377919]|not provided [RCV003106617] Chr7:27199416 [GRCh38]
Chr7:27239035 [GRCh37]
Chr7:7p15.2		 uncertain significance
NM_000522.5(HOXA13):c.234T>A (p.Ala78=) single nucleotide variant Guttmacher syndrome [RCV002505334]|not provided [RCV000910589] Chr7:27199844 [GRCh38]
Chr7:27239463 [GRCh37]
Chr7:7p15.2		 likely benign
NM_000522.5(HOXA13):c.1002A>G (p.Leu334=) single nucleotide variant not provided [RCV000886022] Chr7:27198363 [GRCh38]
Chr7:27237982 [GRCh37]
Chr7:7p15.2		 benign|likely benign
NM_000522.5(HOXA13):c.366G>T (p.Ala122=) single nucleotide variant not provided [RCV000910437] Chr7:27199712 [GRCh38]
Chr7:27239331 [GRCh37]
Chr7:7p15.2		 likely benign
NM_000522.5(HOXA13):c.922+84G>C single nucleotide variant not provided [RCV001721759] Chr7:27199072 [GRCh38]
Chr7:27238691 [GRCh37]
Chr7:7p15.2		 benign
NM_000522.5(HOXA13):c.504G>A (p.Ala168=) single nucleotide variant not provided [RCV001673344] Chr7:27199574 [GRCh38]
Chr7:27239193 [GRCh37]
Chr7:7p15.2		 benign
NM_000522.5(HOXA13):c.126_152del (p.Ala43_Ala51del) deletion not provided [RCV001354585] Chr7:27199926..27199952 [GRCh38]
Chr7:27239545..27239571 [GRCh37]
Chr7:7p15.2		 likely benign
NM_000522.5(HOXA13):c.381CGC[5] (p.Ala133del) microsatellite HOXA13-related disorder [RCV003933709]|not specified [RCV002248989] Chr7:27199680..27199682 [GRCh38]
Chr7:27239299..27239301 [GRCh37]
Chr7:7p15.2		 benign|likely benign
NM_000522.5(HOXA13):c.263G>A (p.Arg88His) single nucleotide variant Guttmacher syndrome [RCV002489757]|Inborn genetic diseases [RCV003355531]|not provided [RCV001763204] Chr7:27199815 [GRCh38]
Chr7:27239434 [GRCh37]
Chr7:7p15.2		 uncertain significance
NM_000522.5(HOXA13):c.193G>A (p.Ala65Thr) single nucleotide variant Inborn genetic diseases [RCV003295247] Chr7:27199885 [GRCh38]
Chr7:27239504 [GRCh37]
Chr7:7p15.2		 uncertain significance
NM_000522.5(HOXA13):c.499G>T (p.Ala167Ser) single nucleotide variant Guttmacher syndrome [RCV002503204]|not provided [RCV001767092] Chr7:27199579 [GRCh38]
Chr7:27239198 [GRCh37]
Chr7:7p15.2		 uncertain significance
NM_000522.5(HOXA13):c.527G>A (p.Ser176Asn) single nucleotide variant Guttmacher syndrome [RCV002496096]|not provided [RCV001770868] Chr7:27199551 [GRCh38]
Chr7:27239170 [GRCh37]
Chr7:7p15.2		 uncertain significance
NM_000522.5(HOXA13):c.481C>T (p.Gln161Ter) single nucleotide variant not provided [RCV001765752] Chr7:27199597 [GRCh38]
Chr7:27239216 [GRCh37]
Chr7:7p15.2		 uncertain significance
NM_000522.5(HOXA13):c.962G>A (p.Arg321Lys) single nucleotide variant not provided [RCV001757994] Chr7:27198403 [GRCh38]
Chr7:27238022 [GRCh37]
Chr7:7p15.2		 uncertain significance
NM_000522.5(HOXA13):c.603C>T (p.Ala201=) single nucleotide variant not specified [RCV001820559] Chr7:27199475 [GRCh38]
Chr7:27239094 [GRCh37]
Chr7:7p15.2		 uncertain significance
NM_000522.5(HOXA13):c.373G>A (p.Ala125Thr) single nucleotide variant not provided [RCV002005700] Chr7:27199705 [GRCh38]
Chr7:27239324 [GRCh37]
Chr7:7p15.2		 uncertain significance
GRCh37/hg19 7p21.3-14.2(chr7:10745750-35305167) copy number gain not specified [RCV002053668] Chr7:10745750..35305167 [GRCh37]
Chr7:7p21.3-14.2		 likely pathogenic
NM_000522.5(HOXA13):c.357_389del (p.Ala123_Ala133del) deletion not provided [RCV001936651] Chr7:27199689..27199721 [GRCh38]
Chr7:27239308..27239340 [GRCh37]
Chr7:7p15.2		 uncertain significance
NM_000522.5(HOXA13):c.175C>T (p.Pro59Ser) single nucleotide variant Guttmacher syndrome [RCV002479518]|Inborn genetic diseases [RCV002562162]|not provided [RCV001934329] Chr7:27199903 [GRCh38]
Chr7:27239522 [GRCh37]
Chr7:7p15.2		 uncertain significance
NM_000522.5(HOXA13):c.280C>G (p.Pro94Ala) single nucleotide variant not provided [RCV001954605] Chr7:27199798 [GRCh38]
Chr7:27239417 [GRCh37]
Chr7:7p15.2		 uncertain significance
NM_000522.5(HOXA13):c.140C>T (p.Ala47Val) single nucleotide variant not provided [RCV001995801] Chr7:27199938 [GRCh38]
Chr7:27239557 [GRCh37]
Chr7:7p15.2		 uncertain significance
NM_000522.5(HOXA13):c.431C>T (p.Pro144Leu) single nucleotide variant not provided [RCV001934016] Chr7:27199647 [GRCh38]
Chr7:27239266 [GRCh37]
Chr7:7p15.2		 uncertain significance
NM_000522.5(HOXA13):c.46G>A (p.Val16Ile) single nucleotide variant Guttmacher syndrome [RCV002490001]|HOXA13-related disorder [RCV004756301]|not provided [RCV001899805] Chr7:27200032 [GRCh38]
Chr7:27239651 [GRCh37]
Chr7:7p15.2		 uncertain significance
NM_000522.5(HOXA13):c.921C>G (p.Pro307=) single nucleotide variant not provided [RCV001996336] Chr7:27199157 [GRCh38]
Chr7:27238776 [GRCh37]
Chr7:7p15.2		 uncertain significance
NM_000522.5(HOXA13):c.598GCC[4] (p.Ala204_Ala205del) microsatellite not provided [RCV002049459] Chr7:27199463..27199468 [GRCh38]
Chr7:27239082..27239087 [GRCh37]
Chr7:7p15.2		 uncertain significance
NM_000522.5(HOXA13):c.175C>G (p.Pro59Ala) single nucleotide variant HOXA13-related disorder [RCV003951330]|not provided [RCV002210401] Chr7:27199903 [GRCh38]
Chr7:27239522 [GRCh37]
Chr7:7p15.2		 likely benign
NM_000522.5(HOXA13):c.678G>A (p.Lys226=) single nucleotide variant not provided [RCV002128672] Chr7:27199400 [GRCh38]
Chr7:27239019 [GRCh37]
Chr7:7p15.2		 likely benign
NM_000522.5(HOXA13):c.456A>G (p.Gln152=) single nucleotide variant not provided [RCV002167485] Chr7:27199622 [GRCh38]
Chr7:27239241 [GRCh37]
Chr7:7p15.2		 likely benign
NM_000522.5(HOXA13):c.25C>T (p.Pro9Ser) single nucleotide variant not provided [RCV002128859] Chr7:27200053 [GRCh38]
Chr7:27239672 [GRCh37]
Chr7:7p15.2		 likely benign
NM_000522.5(HOXA13):c.897C>T (p.Pro299=) single nucleotide variant not provided [RCV002145864] Chr7:27199181 [GRCh38]
Chr7:27238800 [GRCh37]
Chr7:7p15.2		 benign
NM_000522.5(HOXA13):c.147G>A (p.Ala49=) single nucleotide variant not provided [RCV002193236] Chr7:27199931 [GRCh38]
Chr7:27239550 [GRCh37]
Chr7:7p15.2		 benign
Single allele complex Ring chromosome 7 [RCV002280646] Chr7:43360..159119707 [GRCh37]
Chr7:7p22.3-q36.3		 pathogenic
NM_000522.5(HOXA13):c.591C>G (p.Pro197=) single nucleotide variant not provided [RCV003121204] Chr7:27199487 [GRCh38]
Chr7:27239106 [GRCh37]
Chr7:7p15.2		 likely benign
GRCh37/hg19 7p15.3-14.3(chr7:25451740-33864069) copy number loss Cyclical vomiting syndrome [RCV002280775] Chr7:25451740..33864069 [GRCh37]
Chr7:7p15.3-14.3		 pathogenic
NM_000522.5(HOXA13):c.363C>T (p.Ala121=) single nucleotide variant not provided [RCV003872576] Chr7:27199715 [GRCh38]
Chr7:27239334 [GRCh37]
Chr7:7p15.2		 likely benign
GRCh37/hg19 7p22.3-q36.3(chr7:56604613-96692931)x1 copy number loss See cases [RCV002287832] Chr7:56604613..96692931 [GRCh37]
Chr7:7p22.3-q36.3		 uncertain significance
GRCh37/hg19 7p15.2-15.1(chr7:26418391-28323299)x3 copy number gain not provided [RCV002474593] Chr7:26418391..28323299 [GRCh37]
Chr7:7p15.2-15.1		 uncertain significance
NM_000522.5(HOXA13):c.869A>C (p.Tyr290Ser) single nucleotide variant Hand-foot-genital syndrome [RCV002463573] Chr7:27199209 [GRCh38]
Chr7:27238828 [GRCh37]
Chr7:7p15.2		 likely pathogenic
NM_000522.5(HOXA13):c.741dup (p.Gly248fs) duplication Hand-foot-genital syndrome [RCV002472165] Chr7:27199336..27199337 [GRCh38]
Chr7:27238955..27238956 [GRCh37]
Chr7:7p15.2		 likely pathogenic
NM_000522.5(HOXA13):c.538C>T (p.Pro180Ser) single nucleotide variant Inborn genetic diseases [RCV002859238] Chr7:27199540 [GRCh38]
Chr7:27239159 [GRCh37]
Chr7:7p15.2		 uncertain significance
NM_000522.5(HOXA13):c.270G>A (p.Leu90=) single nucleotide variant not provided [RCV002617785] Chr7:27199808 [GRCh38]
Chr7:27239427 [GRCh37]
Chr7:7p15.2		 likely benign
NM_000522.5(HOXA13):c.500C>G (p.Ala167Gly) single nucleotide variant Inborn genetic diseases [RCV002884062] Chr7:27199578 [GRCh38]
Chr7:27239197 [GRCh37]
Chr7:7p15.2		 uncertain significance
NM_000522.5(HOXA13):c.157G>A (p.Ala53Thr) single nucleotide variant Inborn genetic diseases [RCV002687689] Chr7:27199921 [GRCh38]
Chr7:27239540 [GRCh37]
Chr7:7p15.2		 uncertain significance
NM_000522.5(HOXA13):c.294G>T (p.Ala98=) single nucleotide variant not provided [RCV003097511] Chr7:27199784 [GRCh38]
Chr7:27239403 [GRCh37]
Chr7:7p15.2		 likely benign
NM_000522.5(HOXA13):c.950G>C (p.Ser317Thr) single nucleotide variant Inborn genetic diseases [RCV002748995]|not provided [RCV003730380] Chr7:27198415 [GRCh38]
Chr7:27238034 [GRCh37]
Chr7:7p15.2		 uncertain significance
GRCh37/hg19 7p15.2-14.3(chr7:27133786-34466477)x1 copy number loss not provided [RCV002475752] Chr7:27133786..34466477 [GRCh37]
Chr7:7p15.2-14.3		 pathogenic
NM_000522.5(HOXA13):c.850G>A (p.Gly284Ser) single nucleotide variant not provided [RCV002775810] Chr7:27199228 [GRCh38]
Chr7:27238847 [GRCh37]
Chr7:7p15.2		 uncertain significance
NM_000522.5(HOXA13):c.132G>C (p.Ala44=) single nucleotide variant not provided [RCV003052981] Chr7:27199946 [GRCh38]
Chr7:27239565 [GRCh37]
Chr7:7p15.2		 likely benign
NM_000522.5(HOXA13):c.614C>T (p.Ala205Val) single nucleotide variant Inborn genetic diseases [RCV002911612] Chr7:27199464 [GRCh38]
Chr7:27239083 [GRCh37]
Chr7:7p15.2		 uncertain significance
NM_000522.5(HOXA13):c.544G>T (p.Ala182Ser) single nucleotide variant Inborn genetic diseases [RCV002661251] Chr7:27199534 [GRCh38]
Chr7:27239153 [GRCh37]
Chr7:7p15.2		 uncertain significance
NM_000522.5(HOXA13):c.956A>G (p.Tyr319Cys) single nucleotide variant not provided [RCV002690872] Chr7:27198409 [GRCh38]
Chr7:27238028 [GRCh37]
Chr7:7p15.2		 uncertain significance
NM_000522.5(HOXA13):c.196G>T (p.Ala66Ser) single nucleotide variant HOXA13-related disorder [RCV004756444]|not provided [RCV002923727] Chr7:27199882 [GRCh38]
Chr7:27239501 [GRCh37]
Chr7:7p15.2		 likely benign|uncertain significance
NM_000522.5(HOXA13):c.126_152dup (p.Ala51_Gly52insAlaAlaAlaAlaAlaAlaAlaAlaAla) duplication not provided [RCV002867925] Chr7:27199925..27199926 [GRCh38]
Chr7:27239544..27239545 [GRCh37]
Chr7:7p15.2		 uncertain significance
NM_000522.5(HOXA13):c.418G>T (p.Gly140Cys) single nucleotide variant not provided [RCV002621952] Chr7:27199660 [GRCh38]
Chr7:27239279 [GRCh37]
Chr7:7p15.2		 uncertain significance
NM_000522.5(HOXA13):c.423G>A (p.Pro141=) single nucleotide variant not provided [RCV002735840] Chr7:27199655 [GRCh38]
Chr7:27239274 [GRCh37]
Chr7:7p15.2		 likely benign
NM_000522.5(HOXA13):c.496C>T (p.Pro166Ser) single nucleotide variant not provided [RCV002781180] Chr7:27199582 [GRCh38]
Chr7:27239201 [GRCh37]
Chr7:7p15.2		 likely benign
NM_000522.5(HOXA13):c.360T>A (p.Ala120=) single nucleotide variant not provided [RCV002667474] Chr7:27199718 [GRCh38]
Chr7:27239337 [GRCh37]
Chr7:7p15.2		 likely benign
NM_000522.5(HOXA13):c.598GCC[7] (p.Ala205_Phe206insAla) microsatellite not provided [RCV002932729] Chr7:27199462..27199463 [GRCh38]
Chr7:27239081..27239082 [GRCh37]
Chr7:7p15.2		 likely benign
NM_000522.5(HOXA13):c.588G>A (p.Gln196=) single nucleotide variant not provided [RCV003007159] Chr7:27199490 [GRCh38]
Chr7:27239109 [GRCh37]
Chr7:7p15.2		 likely benign
NM_000522.5(HOXA13):c.470C>T (p.Ser157Leu) single nucleotide variant not provided [RCV003005316] Chr7:27199608 [GRCh38]
Chr7:27239227 [GRCh37]
Chr7:7p15.2		 uncertain significance
NM_000522.5(HOXA13):c.375_398dup (p.Ala133_Ser134insAlaAlaAlaAlaAlaAlaAlaAla) duplication not provided [RCV003040322] Chr7:27199679..27199680 [GRCh38]
Chr7:27239298..27239299 [GRCh37]
Chr7:7p15.2		 uncertain significance
NM_000522.5(HOXA13):c.24C>A (p.His8Gln) single nucleotide variant not provided [RCV003022510] Chr7:27200054 [GRCh38]
Chr7:27239673 [GRCh37]
Chr7:7p15.2		 uncertain significance
NM_000522.5(HOXA13):c.112G>A (p.Ala38Thr) single nucleotide variant Inborn genetic diseases [RCV002763211] Chr7:27199966 [GRCh38]
Chr7:27239585 [GRCh37]
Chr7:7p15.2		 uncertain significance
NM_000522.5(HOXA13):c.505C>G (p.Leu169Val) single nucleotide variant Inborn genetic diseases [RCV002664627] Chr7:27199573 [GRCh38]
Chr7:27239192 [GRCh37]
Chr7:7p15.2		 uncertain significance
NM_000522.5(HOXA13):c.421C>T (p.Pro141Ser) single nucleotide variant Inborn genetic diseases [RCV002763555] Chr7:27199657 [GRCh38]
Chr7:27239276 [GRCh37]
Chr7:7p15.2		 uncertain significance
NM_000522.5(HOXA13):c.848A>G (p.Asn283Ser) single nucleotide variant Inborn genetic diseases [RCV002916610] Chr7:27199230 [GRCh38]
Chr7:27238849 [GRCh37]
Chr7:7p15.2		 uncertain significance
NM_000522.5(HOXA13):c.366_386del (p.Ala127_Ala133del) deletion not provided [RCV002667469] Chr7:27199692..27199712 [GRCh38]
Chr7:27239311..27239331 [GRCh37]
Chr7:7p15.2		 likely benign
NM_000522.5(HOXA13):c.24C>T (p.His8=) single nucleotide variant not provided [RCV002594580] Chr7:27200054 [GRCh38]
Chr7:27239673 [GRCh37]
Chr7:7p15.2		 likely benign
NM_000522.5(HOXA13):c.870C>T (p.Tyr290=) single nucleotide variant not provided [RCV002575418] Chr7:27199208 [GRCh38]
Chr7:27238827 [GRCh37]
Chr7:7p15.2		 likely benign
NM_000522.5(HOXA13):c.631A>T (p.Met211Leu) single nucleotide variant Inborn genetic diseases [RCV002712855] Chr7:27199447 [GRCh38]
Chr7:27239066 [GRCh37]
Chr7:7p15.2		 uncertain significance
NM_000522.5(HOXA13):c.1159A>G (p.Thr387Ala) single nucleotide variant not provided [RCV002894147] Chr7:27198206 [GRCh38]
Chr7:27237825 [GRCh37]
Chr7:7p15.2		 uncertain significance
NM_000522.5(HOXA13):c.424G>C (p.Ala142Pro) single nucleotide variant Inborn genetic diseases [RCV002719944] Chr7:27199654 [GRCh38]
Chr7:27239273 [GRCh37]
Chr7:7p15.2		 uncertain significance
NM_000522.5(HOXA13):c.275C>G (p.Ala92Gly) single nucleotide variant not provided [RCV002632200] Chr7:27199803 [GRCh38]
Chr7:27239422 [GRCh37]
Chr7:7p15.2		 uncertain significance
NM_000522.5(HOXA13):c.381CGC[3] (p.Ala131_Ala133del) microsatellite not provided [RCV002967021] Chr7:27199680..27199688 [GRCh38]
Chr7:27239299..27239307 [GRCh37]
Chr7:7p15.2		 uncertain significance
NM_000522.5(HOXA13):c.431C>G (p.Pro144Arg) single nucleotide variant Inborn genetic diseases [RCV002719945] Chr7:27199647 [GRCh38]
Chr7:27239266 [GRCh37]
Chr7:7p15.2		 uncertain significance
NM_000522.5(HOXA13):c.1082T>C (p.Leu361Pro) single nucleotide variant not provided [RCV003028121] Chr7:27198283 [GRCh38]
Chr7:27237902 [GRCh37]
Chr7:7p15.2		 uncertain significance
NM_000522.5(HOXA13):c.129A>G (p.Ala43=) single nucleotide variant HOXA13-related disorder [RCV004756469]|not provided [RCV002579006] Chr7:27199949 [GRCh38]
Chr7:27239568 [GRCh37]
Chr7:7p15.2		 benign|likely benign
NM_000522.5(HOXA13):c.191C>A (p.Ala64Glu) single nucleotide variant not provided [RCV002653428] Chr7:27199887 [GRCh38]
Chr7:27239506 [GRCh37]
Chr7:7p15.2		 uncertain significance
NM_000522.5(HOXA13):c.448G>A (p.Ala150Thr) single nucleotide variant not provided [RCV002680957] Chr7:27199630 [GRCh38]
Chr7:27239249 [GRCh37]
Chr7:7p15.2		 uncertain significance
NM_000522.5(HOXA13):c.504_505delinsAG (p.Leu169Val) indel not provided [RCV002606355] Chr7:27199573..27199574 [GRCh38]
Chr7:27239192..27239193 [GRCh37]
Chr7:7p15.2		 uncertain significance
NM_000522.5(HOXA13):c.357_383del (p.Ala125_Ala133del) deletion not provided [RCV002635036] Chr7:27199695..27199721 [GRCh38]
Chr7:27239314..27239340 [GRCh37]
Chr7:7p15.2		 likely benign
NM_000522.5(HOXA13):c.784G>A (p.Gly262Ser) single nucleotide variant not provided [RCV002585567] Chr7:27199294 [GRCh38]
Chr7:27238913 [GRCh37]
Chr7:7p15.2		 uncertain significance
NM_000522.5(HOXA13):c.1071C>G (p.Ala357=) single nucleotide variant not provided [RCV002606643] Chr7:27198294 [GRCh38]
Chr7:27237913 [GRCh37]
Chr7:7p15.2		 benign
NM_000522.5(HOXA13):c.234_251del (p.Ala79_Ala84del) deletion not provided [RCV003068926] Chr7:27199827..27199844 [GRCh38]
Chr7:27239446..27239463 [GRCh37]
Chr7:7p15.2		 uncertain significance
NM_000522.5(HOXA13):c.529G>C (p.Gly177Arg) single nucleotide variant not provided [RCV002612566] Chr7:27199549 [GRCh38]
Chr7:27239168 [GRCh37]
Chr7:7p15.2		 likely benign
NM_000522.5(HOXA13):c.644G>A (p.Gly215Asp) single nucleotide variant Inborn genetic diseases [RCV003188286] Chr7:27199434 [GRCh38]
Chr7:27239053 [GRCh37]
Chr7:7p15.2		 uncertain significance
NM_000522.5(HOXA13):c.529G>A (p.Gly177Ser) single nucleotide variant Inborn genetic diseases [RCV003179454] Chr7:27199549 [GRCh38]
Chr7:27239168 [GRCh37]
Chr7:7p15.2		 uncertain significance
NM_000522.5(HOXA13):c.133G>A (p.Ala45Thr) single nucleotide variant not provided [RCV003135613] Chr7:27199945 [GRCh38]
Chr7:27239564 [GRCh37]
Chr7:7p15.2		 uncertain significance
NM_000522.5(HOXA13):c.331G>C (p.Glu111Gln) single nucleotide variant Inborn genetic diseases [RCV003220135] Chr7:27199747 [GRCh38]
Chr7:27239366 [GRCh37]
Chr7:7p15.2		 uncertain significance
NM_000522.5(HOXA13):c.784G>T (p.Gly262Cys) single nucleotide variant Inborn genetic diseases [RCV003196083] Chr7:27199294 [GRCh38]
Chr7:27238913 [GRCh37]
Chr7:7p15.2		 uncertain significance
NM_000522.5(HOXA13):c.245C>A (p.Ala82Asp) single nucleotide variant Inborn genetic diseases [RCV003191496] Chr7:27199833 [GRCh38]
Chr7:27239452 [GRCh37]
Chr7:7p15.2		 uncertain significance
NM_000522.5(HOXA13):c.1085C>A (p.Ser362Tyr) single nucleotide variant not provided [RCV003319884] Chr7:27198280 [GRCh38]
Chr7:27237899 [GRCh37]
Chr7:7p15.2		 uncertain significance
NM_000522.5(HOXA13):c.235_252del (p.Ala79_Ala84del) deletion not provided [RCV003875076] Chr7:27199826..27199843 [GRCh38]
Chr7:27239445..27239462 [GRCh37]
Chr7:7p15.2		 uncertain significance
NM_000522.5(HOXA13):c.36C>A (p.Ile12=) single nucleotide variant not provided [RCV003571353] Chr7:27200042 [GRCh38]
Chr7:27239661 [GRCh37]
Chr7:7p15.2		 likely benign
NM_000522.5(HOXA13):c.652G>A (p.Ala218Thr) single nucleotide variant HOXA13-related disorder [RCV003408811] Chr7:27199426 [GRCh38]
Chr7:27239045 [GRCh37]
Chr7:7p15.2		 uncertain significance
NM_000522.5(HOXA13):c.1115A>G (p.Asn372Ser) single nucleotide variant not provided [RCV003692213] Chr7:27198250 [GRCh38]
Chr7:27237869 [GRCh37]
Chr7:7p15.2		 uncertain significance
NM_000522.5(HOXA13):c.177C>G (p.Pro59=) single nucleotide variant not provided [RCV003848949] Chr7:27199901 [GRCh38]
Chr7:27239520 [GRCh37]
Chr7:7p15.2		 likely benign
NM_000522.5(HOXA13):c.579G>A (p.Ser193=) single nucleotide variant not provided [RCV003664949] Chr7:27199499 [GRCh38]
Chr7:27239118 [GRCh37]
Chr7:7p15.2		 likely benign
NM_000522.5(HOXA13):c.138_140dup (p.Ala51_Gly52insAla) duplication not provided [RCV003815763] Chr7:27199937..27199938 [GRCh38]
Chr7:27239556..27239557 [GRCh37]
Chr7:7p15.2		 uncertain significance
NM_000522.5(HOXA13):c.366G>C (p.Ala122=) single nucleotide variant not provided [RCV003835940] Chr7:27199712 [GRCh38]
Chr7:27239331 [GRCh37]
Chr7:7p15.2		 likely benign
NM_000522.5(HOXA13):c.477G>C (p.Ala159=) single nucleotide variant not provided [RCV003552427] Chr7:27199601 [GRCh38]
Chr7:27239220 [GRCh37]
Chr7:7p15.2		 benign
NM_000522.5(HOXA13):c.366_374del (p.Ala131_Ala133del) deletion not provided [RCV003736170] Chr7:27199704..27199712 [GRCh38]
Chr7:27239323..27239331 [GRCh37]
Chr7:7p15.2		 likely benign
NM_000522.5(HOXA13):c.261C>T (p.Cys87=) single nucleotide variant not provided [RCV003843291] Chr7:27199817 [GRCh38]
Chr7:27239436 [GRCh37]
Chr7:7p15.2		 likely benign
NM_000522.5(HOXA13):c.372C>G (p.Ala124=) single nucleotide variant not provided [RCV003708192] Chr7:27199706 [GRCh38]
Chr7:27239325 [GRCh37]
Chr7:7p15.2		 likely benign
NM_000522.5(HOXA13):c.381CGC[9] (p.Ala133_Ser134insAlaAlaAla) microsatellite not provided [RCV003848082] Chr7:27199679..27199680 [GRCh38]
Chr7:27239298..27239299 [GRCh37]
Chr7:7p15.2		 uncertain significance
NM_000522.5(HOXA13):c.154G>T (p.Gly52Trp) single nucleotide variant not provided [RCV003680779] Chr7:27199924 [GRCh38]
Chr7:27239543 [GRCh37]
Chr7:7p15.2		 uncertain significance
GRCh37/hg19 7p21.3-15.2(chr7:13107394-27514163)x1 copy number loss not specified [RCV003986690] Chr7:13107394..27514163 [GRCh37]
Chr7:7p21.3-15.2		 pathogenic
NM_000522.5(HOXA13):c.133G>T (p.Ala45Ser) single nucleotide variant not provided [RCV003721082] Chr7:27199945 [GRCh38]
Chr7:27239564 [GRCh37]
Chr7:7p15.2		 uncertain significance
NM_000522.5(HOXA13):c.597_599dup (p.Ala205_Phe206insAla) duplication not provided [RCV003868125] Chr7:27199478..27199479 [GRCh38]
Chr7:27239097..27239098 [GRCh37]
Chr7:7p15.2		 uncertain significance
NM_000522.5(HOXA13):c.562C>G (p.Pro188Ala) single nucleotide variant not provided [RCV003552746] Chr7:27199516 [GRCh38]
Chr7:27239135 [GRCh37]
Chr7:7p15.2		 likely benign
NM_000522.5(HOXA13):c.354_374del (p.Ala127_Ala133del) deletion not provided [RCV003734176] Chr7:27199704..27199724 [GRCh38]
Chr7:27239323..27239343 [GRCh37]
Chr7:7p15.2		 likely benign
GRCh37/hg19 7p21.1-14.3(chr7:17736012-30663423)x1 copy number loss not specified [RCV003986712] Chr7:17736012..30663423 [GRCh37]
Chr7:7p21.1-14.3		 pathogenic
NM_000522.5(HOXA13):c.339C>A (p.Pro113=) single nucleotide variant not provided [RCV003681831] Chr7:27199739 [GRCh38]
Chr7:27239358 [GRCh37]
Chr7:7p15.2		 likely benign
NM_000522.5(HOXA13):c.923-3T>C single nucleotide variant not provided [RCV003678192] Chr7:27198445 [GRCh38]
Chr7:27238064 [GRCh37]
Chr7:7p15.2		 uncertain significance
NM_000522.5(HOXA13):c.375_377del (p.Ala133del) deletion not provided [RCV003711799] Chr7:27199701..27199703 [GRCh38]
Chr7:27239320..27239322 [GRCh37]
Chr7:7p15.2		 likely benign
NM_000522.5(HOXA13):c.922+13C>T single nucleotide variant not provided [RCV003819506] Chr7:27199143 [GRCh38]
Chr7:27238762 [GRCh37]
Chr7:7p15.2		 benign
NM_000522.5(HOXA13):c.372C>A (p.Ala124=) single nucleotide variant HOXA13-related disorder [RCV003919394] Chr7:27199706 [GRCh38]
Chr7:27239325 [GRCh37]
Chr7:7p15.2		 likely benign
NM_000522.5(HOXA13):c.135T>G (p.Ala45=) single nucleotide variant HOXA13-related disorder [RCV003942140] Chr7:27199943 [GRCh38]
Chr7:27239562 [GRCh37]
Chr7:7p15.2		 likely benign
NM_000522.5(HOXA13):c.384C>G (p.Ala128=) single nucleotide variant HOXA13-related disorder [RCV003921475] Chr7:27199694 [GRCh38]
Chr7:27239313 [GRCh37]
Chr7:7p15.2		 likely benign
NM_000522.5(HOXA13):c.390C>G (p.Ala130=) single nucleotide variant HOXA13-related disorder [RCV003894001] Chr7:27199688 [GRCh38]
Chr7:27239307 [GRCh37]
Chr7:7p15.2		 likely benign
NM_000522.5(HOXA13):c.566A>G (p.Asn189Ser) single nucleotide variant HOXA13-related disorder [RCV003949625] Chr7:27199512 [GRCh38]
Chr7:27239131 [GRCh37]
Chr7:7p15.2		 uncertain significance
NM_000522.5(HOXA13):c.849C>T (p.Asn283=) single nucleotide variant HOXA13-related disorder [RCV003909319] Chr7:27199229 [GRCh38]
Chr7:27238848 [GRCh37]
Chr7:7p15.2		 likely benign
NM_000522.5(HOXA13):c.390C>A (p.Ala130=) single nucleotide variant HOXA13-related disorder [RCV003921795] Chr7:27199688 [GRCh38]
Chr7:27239307 [GRCh37]
Chr7:7p15.2		 likely benign
NM_000522.5(HOXA13):c.363C>G (p.Ala121=) single nucleotide variant HOXA13-related disorder [RCV003904741] Chr7:27199715 [GRCh38]
Chr7:27239334 [GRCh37]
Chr7:7p15.2		 likely benign
NM_000522.5(HOXA13):c.375T>G (p.Ala125=) single nucleotide variant HOXA13-related disorder [RCV003924262] Chr7:27199703 [GRCh38]
Chr7:27239322 [GRCh37]
Chr7:7p15.2		 likely benign
NM_000522.5(HOXA13):c.461G>A (p.Ser154Asn) single nucleotide variant HOXA13-related disorder [RCV003966927] Chr7:27199617 [GRCh38]
Chr7:27239236 [GRCh37]
Chr7:7p15.2		 uncertain significance
NM_000522.5(HOXA13):c.228C>A (p.Ala76=) single nucleotide variant HOXA13-related disorder [RCV003902142] Chr7:27199850 [GRCh38]
Chr7:27239469 [GRCh37]
Chr7:7p15.2		 likely benign
NM_000522.5(HOXA13):c.884A>C (p.Gln295Pro) single nucleotide variant Hand-foot-genital syndrome [RCV004547275] Chr7:27199194 [GRCh38]
Chr7:27238813 [GRCh37]
Chr7:7p15.2		 uncertain significance
NM_000522.5(HOXA13):c.131C>T (p.Ala44Val) single nucleotide variant Inborn genetic diseases [RCV004401929] Chr7:27199947 [GRCh38]
Chr7:27239566 [GRCh37]
Chr7:7p15.2		 uncertain significance
NM_000522.5(HOXA13):c.871T>C (p.Cys291Arg) single nucleotide variant Inborn genetic diseases [RCV004401930] Chr7:27199207 [GRCh38]
Chr7:27238826 [GRCh37]
Chr7:7p15.2		 uncertain significance
NC_000007.13:g.(?_26232136)_(28172587_?)del deletion not provided [RCV004583626] Chr7:26232136..28172587 [GRCh37]
Chr7:7p15.2-15.1		 pathogenic
NM_000522.5(HOXA13):c.203G>C (p.Gly68Ala) single nucleotide variant Inborn genetic diseases [RCV004632989] Chr7:27199875 [GRCh38]
Chr7:27239494 [GRCh37]
Chr7:7p15.2		 uncertain significance
NM_000522.5(HOXA13):c.401C>T (p.Ser134Leu) single nucleotide variant Inborn genetic diseases [RCV004632990] Chr7:27199677 [GRCh38]
Chr7:27239296 [GRCh37]
Chr7:7p15.2		 uncertain significance
NM_000522.5(HOXA13):c.551T>A (p.Met184Lys) single nucleotide variant Inborn genetic diseases [RCV004632988]|not provided [RCV004759432] Chr7:27199527 [GRCh38]
Chr7:27239146 [GRCh37]
Chr7:7p15.2		 uncertain significance
NM_000522.5(HOXA13):c.67G>A (p.Gly23Ser) single nucleotide variant HOXA13-related disorder [RCV004757088] Chr7:27200011 [GRCh38]
Chr7:27239630 [GRCh37]
Chr7:7p15.2		 uncertain significance
NM_000522.5(HOXA13):c.123T>G (p.Ala41=) single nucleotide variant HOXA13-related disorder [RCV004756952] Chr7:27199955 [GRCh38]
Chr7:27239574 [GRCh37]
Chr7:7p15.2		 likely benign
NM_000522.5(HOXA13):c.622G>C (p.Asp208His) single nucleotide variant not provided [RCV004764219]   uncertain significance
NM_000522.5(HOXA13):c.258G>A (p.Gln86=) single nucleotide variant HOXA13-related disorder [RCV004732134] Chr7:27199820 [GRCh38]
Chr7:27239439 [GRCh37]
Chr7:7p15.2		 likely benign
NM_000522.5(HOXA13):c.352G>A (p.Ala118Thr) single nucleotide variant not provided [RCV004726039] Chr7:27199726 [GRCh38]
Chr7:27239345 [GRCh37]
Chr7:7p15.2		 uncertain significance
NM_000522.5(HOXA13):c.126A>G (p.Ala42=) single nucleotide variant HOXA13-related disorder [RCV004757032] Chr7:27199952 [GRCh38]
Chr7:27239571 [GRCh37]
Chr7:7p15.2		 likely benign
NM_000522.5(HOXA13):c.406T>C (p.Ser136Pro) single nucleotide variant HOXA13-related disorder [RCV004756774] Chr7:27199672 [GRCh38]
Chr7:27239291 [GRCh37]
Chr7:7p15.2		 uncertain significance
NM_000522.5(HOXA13):c.378A>C (p.Ala126=) single nucleotide variant HOXA13-related disorder [RCV004756960] Chr7:27199700 [GRCh38]
Chr7:27239319 [GRCh37]
Chr7:7p15.2		 likely benign
NM_000522.5(HOXA13):c.1089G>A (p.Glu363=) single nucleotide variant not provided [RCV004769128] Chr7:27198276 [GRCh38]
Chr7:27237895 [GRCh37]
Chr7:7p15.2		 uncertain significance
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:1507
Count of miRNA genes:833
Interacting mature miRNAs:1005
Transcripts:ENST00000222753, ENST00000518136
Prediction methods:Microtar, 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
407235749GWAS884725_Hbone density QTL GWAS884725 (human)4e-65bone mineral mass (VT:0005007)bone mineral density (CMO:0001226)72719442727194428Human
407285510GWAS934486_Hbody height QTL GWAS934486 (human)8e-30body height (VT:0001253)body height (CMO:0000106)72719783427197835Human
407287798GWAS936774_Hblood urea nitrogen measurement QTL GWAS936774 (human)0.000005blood urea nitrogen measurementblood urea nitrogen level (CMO:0000049)72719866827198669Human
407289239GWAS938215_Hdiastolic blood pressure QTL GWAS938215 (human)2e-30diastolic blood pressurediastolic blood pressure (CMO:0000005)72719694027196941Human
407265715GWAS914691_Hsystolic blood pressure QTL GWAS914691 (human)1e-22systolic blood pressuresystolic blood pressure (CMO:0000004)72719907227199073Human
407294833GWAS943809_Hglomerular filtration rate QTL GWAS943809 (human)4e-14glomerular filtration rateglomerular filtration rate (CMO:0000490)72719866827198669Human
407416865GWAS1065841_Hcreatinine measurement QTL GWAS1065841 (human)7e-12creatinine measurementblood creatinine measurement (CMO:0000767)72719993127199932Human
407256317GWAS905293_Hglomerular filtration rate QTL GWAS905293 (human)1e-10glomerular filtration rateglomerular filtration rate (CMO:0000490)72719866827198669Human
2289453BW297_HBody weight QTL 297 (human)3.83Body weightbody mass index72334946449349464Human

Markers in Region
RH66791  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,237,869 - 27,238,015UniSTSGRCh37
Build 36727,204,394 - 27,204,540RGDNCBI36
Celera727,226,806 - 27,226,952RGD
Cytogenetic Map7p15.2UniSTS
HuRef727,118,433 - 27,118,579UniSTS
CRA_TCAGchr7v2727,289,053 - 27,289,199UniSTS
GeneMap99-GB4 RH Map7117.16UniSTS
RH93295  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,236,609 - 27,236,690UniSTSGRCh37
Build 36727,203,134 - 27,203,215RGDNCBI36
Celera727,225,546 - 27,225,627RGD
Cytogenetic Map7p15.2UniSTS
HuRef727,117,173 - 27,117,254UniSTS
CRA_TCAGchr7v2727,287,793 - 27,287,874UniSTS
GeneMap99-GB4 RH Map7117.3UniSTS
SHGC-107406  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,245,336 - 27,245,618UniSTSGRCh37
Build 36727,211,861 - 27,212,143RGDNCBI36
Celera727,234,286 - 27,234,568RGD
Cytogenetic Map7p15.2UniSTS
HuRef727,125,915 - 27,126,197UniSTS
CRA_TCAGchr7v2727,296,516 - 27,296,798UniSTS
TNG Radiation Hybrid Map712732.0UniSTS
ECD01435  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,242,497 - 27,243,362UniSTSGRCh37
Build 36727,209,022 - 27,209,887RGDNCBI36
Celera727,231,452 - 27,232,317RGD
Cytogenetic Map7p15.2UniSTS
HuRef727,123,081 - 27,123,946UniSTS
CRA_TCAGchr7v2727,293,682 - 27,294,547UniSTS
ECD01531  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,245,265 - 27,246,127UniSTSGRCh37
Build 36727,211,790 - 27,212,652RGDNCBI36
Celera727,234,215 - 27,235,077RGD
Cytogenetic Map7p15.2UniSTS
HuRef727,125,844 - 27,126,706UniSTS
CRA_TCAGchr7v2727,296,445 - 27,297,307UniSTS
ECD01736  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,243,425 - 27,244,280UniSTSGRCh37
Build 36727,209,950 - 27,210,805RGDNCBI36
Celera727,232,380 - 27,233,235RGD
Cytogenetic Map7p15.2UniSTS
HuRef727,124,009 - 27,124,864UniSTS
CRA_TCAGchr7v2727,294,610 - 27,295,465UniSTS
ECD01737  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,244,358 - 27,245,213UniSTSGRCh37
Build 36727,210,883 - 27,211,738RGDNCBI36
Celera727,233,308 - 27,234,163RGD
Cytogenetic Map7p15.2UniSTS
HuRef727,124,937 - 27,125,792UniSTS
CRA_TCAGchr7v2727,295,538 - 27,296,393UniSTS
ECD02701  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,240,791 - 27,241,611UniSTSGRCh37
Build 36727,207,316 - 27,208,136RGDNCBI36
Celera727,229,729 - 27,230,549RGD
Cytogenetic Map7p15.2UniSTS
HuRef727,121,358 - 27,122,178UniSTS
CRA_TCAGchr7v2727,291,976 - 27,292,796UniSTS
ECD03125  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,254,690 - 27,255,495UniSTSGRCh37
Build 36727,221,215 - 27,222,020RGDNCBI36
Celera727,243,638 - 27,244,443RGD
Cytogenetic Map7p15.2UniSTS
HuRef727,135,267 - 27,136,072UniSTS
CRA_TCAGchr7v2727,305,868 - 27,306,673UniSTS
ECD03380  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,252,044 - 27,252,841UniSTSGRCh37
Build 36727,218,569 - 27,219,366RGDNCBI36
Celera727,240,992 - 27,241,789RGD
Cytogenetic Map7p15.2UniSTS
HuRef727,132,621 - 27,133,418UniSTS
CRA_TCAGchr7v2727,303,222 - 27,304,019UniSTS
ECD03381  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,253,821 - 27,254,618UniSTSGRCh37
Build 36727,220,346 - 27,221,143RGDNCBI36
Celera727,242,769 - 27,243,566RGD
Cytogenetic Map7p15.2UniSTS
HuRef727,134,398 - 27,135,195UniSTS
CRA_TCAGchr7v2727,304,999 - 27,305,796UniSTS
ECD03499  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,255,573 - 27,256,366UniSTSGRCh37
Build 36727,222,098 - 27,222,891RGDNCBI36
Celera727,244,521 - 27,245,314RGD
Cytogenetic Map7p15.2UniSTS
HuRef727,136,150 - 27,136,943UniSTS
CRA_TCAGchr7v2727,306,751 - 27,307,544UniSTS
ECD03884  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,250,125 - 27,250,906UniSTSGRCh37
Build 36727,216,650 - 27,217,431RGDNCBI36
Celera727,239,073 - 27,239,854RGD
Cytogenetic Map7p15.2UniSTS
HuRef727,130,702 - 27,131,483UniSTS
CRA_TCAGchr7v2727,301,303 - 27,302,084UniSTS
ECD04307  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,241,669 - 27,242,437UniSTSGRCh37
Build 36727,208,194 - 27,208,962RGDNCBI36
Celera727,230,607 - 27,231,375RGD
Cytogenetic Map7p15.2UniSTS
HuRef727,122,236 - 27,123,004UniSTS
CRA_TCAGchr7v2727,292,854 - 27,293,622UniSTS
ECD04374  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,249,316 - 27,250,082UniSTSGRCh37
Build 36727,215,841 - 27,216,607RGDNCBI36
Celera727,238,264 - 27,239,030RGD
Cytogenetic Map7p15.2UniSTS
HuRef727,129,893 - 27,130,659UniSTS
CRA_TCAGchr7v2727,300,494 - 27,301,260UniSTS
ECD04443  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,238,315 - 27,239,079UniSTSGRCh37
Build 36727,204,840 - 27,205,604RGDNCBI36
Celera727,227,252 - 27,228,016RGD
Cytogenetic Map7p15.2UniSTS
HuRef727,118,879 - 27,119,643UniSTS
CRA_TCAGchr7v2727,289,499 - 27,290,263UniSTS
ECD04965  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,248,278 - 27,249,027UniSTSGRCh37
Build 36727,214,803 - 27,215,552RGDNCBI36
Celera727,237,228 - 27,237,977RGD
Cytogenetic Map7p15.2UniSTS
HuRef727,128,857 - 27,129,606UniSTS
CRA_TCAGchr7v2727,299,458 - 27,300,207UniSTS
ECD05107  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,240,034 - 27,240,779UniSTSGRCh37
Build 36727,206,559 - 27,207,304RGDNCBI36
Celera727,228,972 - 27,229,717RGD
Cytogenetic Map7p15.2UniSTS
HuRef727,120,601 - 27,121,346UniSTS
CRA_TCAGchr7v2727,291,219 - 27,291,964UniSTS
ECD05144  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,250,950 - 27,251,694UniSTSGRCh37
Build 36727,217,475 - 27,218,219RGDNCBI36
Celera727,239,898 - 27,240,642RGD
Cytogenetic Map7p15.2UniSTS
HuRef727,131,527 - 27,132,271UniSTS
CRA_TCAGchr7v2727,302,128 - 27,302,872UniSTS
ECD05314  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,236,710 - 27,237,449UniSTSGRCh37
Build 36727,203,235 - 27,203,974RGDNCBI36
Celera727,225,647 - 27,226,386RGD
Cytogenetic Map7p15.2UniSTS
HuRef727,117,274 - 27,118,013UniSTS
CRA_TCAGchr7v2727,287,894 - 27,288,633UniSTS
ECD05913  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,237,555 - 27,238,278UniSTSGRCh37
Build 36727,204,080 - 27,204,803RGDNCBI36
Celera727,226,492 - 27,227,215RGD
Cytogenetic Map7p15.2UniSTS
HuRef727,118,119 - 27,118,842UniSTS
CRA_TCAGchr7v2727,288,739 - 27,289,462UniSTS
ECD07055  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,266,963 - 27,267,655UniSTSGRCh37
Build 36727,233,488 - 27,234,180RGDNCBI36
Celera727,255,911 - 27,256,603RGD
Cytogenetic Map7p15.2UniSTS
HuRef727,147,542 - 27,148,234UniSTS
CRA_TCAGchr7v2727,318,141 - 27,318,833UniSTS
ECD08102  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,266,235 - 27,266,899UniSTSGRCh37
Build 36727,232,760 - 27,233,424RGDNCBI36
Celera727,255,183 - 27,255,847RGD
Cytogenetic Map7p15.2UniSTS
HuRef727,146,814 - 27,147,478UniSTS
CRA_TCAGchr7v2727,317,413 - 27,318,077UniSTS
ECD09062  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,256,634 - 27,257,272UniSTSGRCh37
Build 36727,223,159 - 27,223,797RGDNCBI36
Celera727,245,582 - 27,246,220RGD
Cytogenetic Map7p15.2UniSTS
HuRef727,137,211 - 27,137,849UniSTS
CRA_TCAGchr7v2727,307,812 - 27,308,450UniSTS
ECD09955  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,253,093 - 27,253,708UniSTSGRCh37
Build 36727,219,618 - 27,220,233RGDNCBI36
Celera727,242,041 - 27,242,656RGD
Cytogenetic Map7p15.2UniSTS
HuRef727,133,670 - 27,134,285UniSTS
CRA_TCAGchr7v2727,304,271 - 27,304,886UniSTS
ECD11436  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,247,597 - 27,248,169UniSTSGRCh37
Build 36727,214,122 - 27,214,694RGDNCBI36
Celera727,236,547 - 27,237,119RGD
Cytogenetic Map7p15.2UniSTS
HuRef727,128,176 - 27,128,748UniSTS
CRA_TCAGchr7v2727,298,777 - 27,299,349UniSTS
ECD12682  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,263,785 - 27,264,322UniSTSGRCh37
Build 36727,230,310 - 27,230,847RGDNCBI36
Celera727,252,733 - 27,253,270RGD
Cytogenetic Map7p15.2UniSTS
HuRef727,144,364 - 27,144,901UniSTS
CRA_TCAGchr7v2727,314,963 - 27,315,500UniSTS
ECD12718  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,261,437 - 27,261,973UniSTSGRCh37
Build 36727,227,962 - 27,228,498RGDNCBI36
Celera727,250,385 - 27,250,921RGD
Cytogenetic Map7p15.2UniSTS
HuRef727,142,016 - 27,142,552UniSTS
CRA_TCAGchr7v2727,312,615 - 27,313,151UniSTS
ECD12925  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,263,180 - 27,263,711UniSTSGRCh37
Build 36727,229,705 - 27,230,236RGDNCBI36
Celera727,252,128 - 27,252,659RGD
Cytogenetic Map7p15.2UniSTS
HuRef727,143,759 - 27,144,290UniSTS
CRA_TCAGchr7v2727,314,358 - 27,314,889UniSTS
ECD13229  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,246,898 - 27,247,421UniSTSGRCh37
Build 36727,213,423 - 27,213,946RGDNCBI36
Celera727,235,848 - 27,236,371RGD
Cytogenetic Map7p15.2UniSTS
HuRef727,127,477 - 27,128,000UniSTS
CRA_TCAGchr7v2727,298,078 - 27,298,601UniSTS
ECD14412  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,259,835 - 27,260,329UniSTSGRCh37
Build 36727,226,360 - 27,226,854RGDNCBI36
Celera727,248,783 - 27,249,277RGD
Cytogenetic Map7p15.2UniSTS
HuRef727,140,414 - 27,140,908UniSTS
CRA_TCAGchr7v2727,311,013 - 27,311,507UniSTS
ECD15160  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,268,665 - 27,269,142UniSTSGRCh37
Build 36727,235,190 - 27,235,667RGDNCBI36
Celera727,257,613 - 27,258,090RGD
Cytogenetic Map7p15.2UniSTS
HuRef727,149,244 - 27,149,721UniSTS
CRA_TCAGchr7v2727,319,843 - 27,320,320UniSTS
ECD15248  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,265,576 - 27,266,051UniSTSGRCh37
Build 36727,232,101 - 27,232,576RGDNCBI36
Celera727,254,524 - 27,254,999RGD
Cytogenetic Map7p15.2UniSTS
HuRef727,146,155 - 27,146,630UniSTS
CRA_TCAGchr7v2727,316,754 - 27,317,229UniSTS
ECD15520  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,265,056 - 27,265,524UniSTSGRCh37
Build 36727,231,581 - 27,232,049RGDNCBI36
Celera727,254,004 - 27,254,472RGD
Cytogenetic Map7p15.2UniSTS
HuRef727,145,635 - 27,146,103UniSTS
CRA_TCAGchr7v2727,316,234 - 27,316,702UniSTS
ECD15569  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,246,361 - 27,246,828UniSTSGRCh37
Build 36727,212,886 - 27,213,353RGDNCBI36
Celera727,235,311 - 27,235,778RGD
Cytogenetic Map7p15.2UniSTS
HuRef727,126,940 - 27,127,407UniSTS
CRA_TCAGchr7v2727,297,541 - 27,298,008UniSTS
ECD16773  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,259,222 - 27,259,648UniSTSGRCh37
Build 36727,225,747 - 27,226,173RGDNCBI36
Celera727,248,170 - 27,248,596RGD
Cytogenetic Map7p15.2UniSTS
HuRef727,139,801 - 27,140,227UniSTS
CRA_TCAGchr7v2727,310,400 - 27,310,826UniSTS
ECD17289  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,258,698 - 27,259,103UniSTSGRCh37
Build 36727,225,223 - 27,225,628RGDNCBI36
Celera727,247,646 - 27,248,051RGD
Cytogenetic Map7p15.2UniSTS
HuRef727,139,277 - 27,139,682UniSTS
CRA_TCAGchr7v2727,309,876 - 27,310,281UniSTS
ECD18837  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,273,837 - 27,274,182UniSTSGRCh37
Build 36727,240,362 - 27,240,707RGDNCBI36
Celera727,262,766 - 27,263,111RGD
Cytogenetic Map7p15.2UniSTS
HuRef727,154,060 - 27,154,405UniSTS
CRA_TCAGchr7v2727,325,016 - 27,325,361UniSTS
ECD20412  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,261,032 - 27,261,317UniSTSGRCh37
Build 36727,227,557 - 27,227,842RGDNCBI36
Celera727,249,980 - 27,250,265RGD
Cytogenetic Map7p15.2UniSTS
HuRef727,141,611 - 27,141,896UniSTS
CRA_TCAGchr7v2727,312,210 - 27,312,495UniSTS
ECD21522  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,257,895 - 27,258,142UniSTSGRCh37
Build 36727,224,420 - 27,224,667RGDNCBI36
Celera727,246,843 - 27,247,090RGD
Cytogenetic Map7p15.2UniSTS
HuRef727,138,474 - 27,138,721UniSTS
CRA_TCAGchr7v2727,309,073 - 27,309,320UniSTS
ECD22264  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,262,687 - 27,262,911UniSTSGRCh37
Build 36727,229,212 - 27,229,436RGDNCBI36
Celera727,251,635 - 27,251,859RGD
Cytogenetic Map7p15.2UniSTS
HuRef727,143,266 - 27,143,490UniSTS
CRA_TCAGchr7v2727,313,865 - 27,314,089UniSTS
ECD22571  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,260,659 - 27,260,874UniSTSGRCh37
Build 36727,227,184 - 27,227,399RGDNCBI36
Celera727,249,607 - 27,249,822RGD
Cytogenetic Map7p15.2UniSTS
HuRef727,141,238 - 27,141,453UniSTS
CRA_TCAGchr7v2727,311,837 - 27,312,052UniSTS
ECD22731  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,269,763 - 27,269,973UniSTSGRCh37
Build 36727,236,288 - 27,236,498RGDNCBI36
Celera727,258,711 - 27,258,921RGD
Cytogenetic Map7p15.2UniSTS
HuRef727,150,342 - 27,150,552UniSTS
CRA_TCAGchr7v2727,320,941 - 27,321,151UniSTS
ECD23379  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,264,739 - 27,264,930UniSTSGRCh37
Build 36727,231,264 - 27,231,455RGDNCBI36
Celera727,253,687 - 27,253,878RGD
Cytogenetic Map7p15.2UniSTS
HuRef727,145,318 - 27,145,509UniSTS
CRA_TCAGchr7v2727,315,917 - 27,316,108UniSTS
ECD23618  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,269,378 - 27,269,561UniSTSGRCh37
Build 36727,235,903 - 27,236,086RGDNCBI36
Celera727,258,326 - 27,258,509RGD
Cytogenetic Map7p15.2UniSTS
HuRef727,149,957 - 27,150,140UniSTS
CRA_TCAGchr7v2727,320,556 - 27,320,739UniSTS
REN100758  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,236,204 - 27,236,447UniSTSGRCh37
Build 36727,202,729 - 27,202,972RGDNCBI36
Celera727,225,142 - 27,225,385RGD
HuRef727,116,769 - 27,117,012UniSTS
CRA_TCAGchr7v2727,287,389 - 27,287,632UniSTS
REN100759  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,236,420 - 27,236,644UniSTSGRCh37
Build 36727,202,945 - 27,203,169RGDNCBI36
Celera727,225,358 - 27,225,581RGD
Cytogenetic Map7p15.2UniSTS
HuRef727,116,985 - 27,117,208UniSTS
CRA_TCAGchr7v2727,287,605 - 27,287,828UniSTS
REN100760  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,236,531 - 27,236,769UniSTSGRCh37
Build 36727,203,056 - 27,203,294RGDNCBI36
Celera727,225,469 - 27,225,706RGD
Cytogenetic Map7p15.2UniSTS
HuRef727,117,096 - 27,117,333UniSTS
CRA_TCAGchr7v2727,287,716 - 27,287,953UniSTS
REN100761  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,236,744 - 27,236,988UniSTSGRCh37
Build 36727,203,269 - 27,203,513RGDNCBI36
Celera727,225,681 - 27,225,925RGD
Cytogenetic Map7p15.2UniSTS
HuRef727,117,308 - 27,117,552UniSTS
CRA_TCAGchr7v2727,287,928 - 27,288,172UniSTS
REN100762  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,236,974 - 27,237,227UniSTSGRCh37
Build 36727,203,499 - 27,203,752RGDNCBI36
Celera727,225,911 - 27,226,164RGD
Cytogenetic Map7p15.2UniSTS
HuRef727,117,538 - 27,117,791UniSTS
CRA_TCAGchr7v2727,288,158 - 27,288,411UniSTS
REN100763  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,237,203 - 27,237,435UniSTSGRCh37
Build 36727,203,728 - 27,203,960RGDNCBI36
Celera727,226,140 - 27,226,372RGD
Cytogenetic Map7p15.2UniSTS
HuRef727,117,767 - 27,117,999UniSTS
CRA_TCAGchr7v2727,288,387 - 27,288,619UniSTS
REN100764  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,237,412 - 27,237,674UniSTSGRCh37
Build 36727,203,937 - 27,204,199RGDNCBI36
Celera727,226,349 - 27,226,611RGD
Cytogenetic Map7p15.2UniSTS
HuRef727,117,976 - 27,118,238UniSTS
CRA_TCAGchr7v2727,288,596 - 27,288,858UniSTS
REN100765  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,237,640 - 27,237,877UniSTSGRCh37
Build 36727,204,165 - 27,204,402RGDNCBI36
Celera727,226,577 - 27,226,814RGD
Cytogenetic Map7p15.2UniSTS
HuRef727,118,204 - 27,118,441UniSTS
CRA_TCAGchr7v2727,288,824 - 27,289,061UniSTS
REN100766  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,237,851 - 27,238,098UniSTSGRCh37
Build 36727,204,376 - 27,204,623RGDNCBI36
Celera727,226,788 - 27,227,035RGD
HuRef727,118,415 - 27,118,662UniSTS
CRA_TCAGchr7v2727,289,035 - 27,289,282UniSTS
REN100767  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,238,062 - 27,238,333UniSTSGRCh37
Build 36727,204,587 - 27,204,858RGDNCBI36
Celera727,226,999 - 27,227,270RGD
HuRef727,118,626 - 27,118,897UniSTS
CRA_TCAGchr7v2727,289,246 - 27,289,517UniSTS
REN100768  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,238,313 - 27,238,551UniSTSGRCh37
Build 36727,204,838 - 27,205,076RGDNCBI36
Celera727,227,250 - 27,227,488RGD
HuRef727,118,877 - 27,119,115UniSTS
CRA_TCAGchr7v2727,289,497 - 27,289,735UniSTS
REN100769  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,238,542 - 27,238,778UniSTSGRCh37
Build 36727,205,067 - 27,205,303RGDNCBI36
Celera727,227,479 - 27,227,715RGD
HuRef727,119,106 - 27,119,342UniSTS
CRA_TCAGchr7v2727,289,726 - 27,289,962UniSTS
REN100770  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,238,752 - 27,239,024UniSTSGRCh37
Build 36727,205,277 - 27,205,549RGDNCBI36
Celera727,227,689 - 27,227,961RGD
HuRef727,119,316 - 27,119,588UniSTS
CRA_TCAGchr7v2727,289,936 - 27,290,208UniSTS
REN100771  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,238,962 - 27,239,194UniSTSGRCh37
Build 36727,205,487 - 27,205,719RGDNCBI36
Celera727,227,899 - 27,228,131RGD
Cytogenetic Map7p15.2UniSTS
HuRef727,119,526 - 27,119,758UniSTS
CRA_TCAGchr7v2727,290,146 - 27,290,378UniSTS
REN100772  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,239,679 - 27,239,904UniSTSGRCh37
Build 36727,206,204 - 27,206,429RGDNCBI36
Celera727,228,616 - 27,228,841RGD
CRA_TCAGchr7v2727,290,863 - 27,291,088UniSTS
REN100773  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,240,036 - 27,240,260UniSTSGRCh37
Build 36727,206,561 - 27,206,785RGDNCBI36
Celera727,228,974 - 27,229,198RGD
Cytogenetic Map7p15.2UniSTS
HuRef727,120,603 - 27,120,827UniSTS
CRA_TCAGchr7v2727,291,221 - 27,291,445UniSTS
REN100776  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,240,712 - 27,240,944UniSTSGRCh37
Build 36727,207,237 - 27,207,469RGDNCBI36
Celera727,229,650 - 27,229,882RGD
Cytogenetic Map7p15.2UniSTS
HuRef727,121,279 - 27,121,511UniSTS
CRA_TCAGchr7v2727,291,897 - 27,292,129UniSTS
REN100779  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,241,366 - 27,241,608UniSTSGRCh37
Build 36727,207,891 - 27,208,133RGDNCBI36
Celera727,230,304 - 27,230,546RGD
Cytogenetic Map7p15.2UniSTS
HuRef727,121,933 - 27,122,175UniSTS
CRA_TCAGchr7v2727,292,551 - 27,292,793UniSTS
REN100783  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,242,319 - 27,242,567UniSTSGRCh37
Build 36727,208,844 - 27,209,092RGDNCBI36
Celera727,231,257 - 27,231,522RGD
HuRef727,122,886 - 27,123,151UniSTS
CRA_TCAGchr7v2727,293,504 - 27,293,752UniSTS
REN100784  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,242,554 - 27,242,799UniSTSGRCh37
Build 36727,209,079 - 27,209,324RGDNCBI36
Celera727,231,509 - 27,231,754RGD
HuRef727,123,138 - 27,123,383UniSTS
CRA_TCAGchr7v2727,293,739 - 27,293,984UniSTS
REN100785  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,242,769 - 27,243,031UniSTSGRCh37
Build 36727,209,294 - 27,209,556RGDNCBI36
Celera727,231,724 - 27,231,986RGD
HuRef727,123,353 - 27,123,615UniSTS
CRA_TCAGchr7v2727,293,954 - 27,294,216UniSTS
REN100786  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,243,021 - 27,243,270UniSTSGRCh37
Build 36727,209,546 - 27,209,795RGDNCBI36
Celera727,231,976 - 27,232,225RGD
HuRef727,123,605 - 27,123,854UniSTS
CRA_TCAGchr7v2727,294,206 - 27,294,455UniSTS
REN100787  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,243,184 - 27,243,448UniSTSGRCh37
Build 36727,209,709 - 27,209,973RGDNCBI36
Celera727,232,139 - 27,232,403RGD
HuRef727,123,768 - 27,124,032UniSTS
CRA_TCAGchr7v2727,294,369 - 27,294,633UniSTS
REN100788  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,243,430 - 27,243,666UniSTSGRCh37
Build 36727,209,955 - 27,210,191RGDNCBI36
Celera727,232,385 - 27,232,621RGD
HuRef727,124,014 - 27,124,250UniSTS
CRA_TCAGchr7v2727,294,615 - 27,294,851UniSTS
REN100789  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,243,637 - 27,243,872UniSTSGRCh37
Build 36727,210,162 - 27,210,397RGDNCBI36
Celera727,232,592 - 27,232,827RGD
HuRef727,124,221 - 27,124,456UniSTS
CRA_TCAGchr7v2727,294,822 - 27,295,057UniSTS
REN100790  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,243,837 - 27,244,079UniSTSGRCh37
Build 36727,210,362 - 27,210,604RGDNCBI36
Celera727,232,792 - 27,233,034RGD
HuRef727,124,421 - 27,124,663UniSTS
CRA_TCAGchr7v2727,295,022 - 27,295,264UniSTS
REN100791  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,244,056 - 27,244,308UniSTSGRCh37
Build 36727,210,581 - 27,210,833RGDNCBI36
Celera727,233,011 - 27,233,263RGD
HuRef727,124,640 - 27,124,892UniSTS
CRA_TCAGchr7v2727,295,241 - 27,295,493UniSTS
REN100792  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,244,285 - 27,244,522UniSTSGRCh37
Build 36727,210,810 - 27,211,047RGDNCBI36
Celera727,233,240 - 27,233,472RGD
Cytogenetic Map7p15.2UniSTS
HuRef727,124,869 - 27,125,101UniSTS
CRA_TCAGchr7v2727,295,470 - 27,295,702UniSTS
REN100793  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,244,486 - 27,244,746UniSTSGRCh37
Build 36727,211,011 - 27,211,271RGDNCBI36
Celera727,233,436 - 27,233,696RGD
HuRef727,125,065 - 27,125,325UniSTS
CRA_TCAGchr7v2727,295,666 - 27,295,926UniSTS
REN100794  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,244,724 - 27,244,978UniSTSGRCh37
Build 36727,211,249 - 27,211,503RGDNCBI36
Celera727,233,674 - 27,233,928RGD
HuRef727,125,303 - 27,125,557UniSTS
CRA_TCAGchr7v2727,295,904 - 27,296,158UniSTS
REN100795  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,244,957 - 27,245,218UniSTSGRCh37
Build 36727,211,482 - 27,211,743RGDNCBI36
Celera727,233,907 - 27,234,168RGD
Cytogenetic Map7p15.2UniSTS
HuRef727,125,536 - 27,125,797UniSTS
CRA_TCAGchr7v2727,296,137 - 27,296,398UniSTS
REN100796  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,245,195 - 27,245,443UniSTSGRCh37
Build 36727,211,720 - 27,211,968RGDNCBI36
Celera727,234,145 - 27,234,393RGD
HuRef727,125,774 - 27,126,022UniSTS
CRA_TCAGchr7v2727,296,375 - 27,296,623UniSTS
REN100797  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,245,421 - 27,245,669UniSTSGRCh37
Build 36727,211,946 - 27,212,194RGDNCBI36
Celera727,234,371 - 27,234,619RGD
HuRef727,126,000 - 27,126,248UniSTS
CRA_TCAGchr7v2727,296,601 - 27,296,849UniSTS
REN100798  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,245,664 - 27,245,903UniSTSGRCh37
Build 36727,212,189 - 27,212,428RGDNCBI36
Celera727,234,614 - 27,234,853RGD
HuRef727,126,243 - 27,126,482UniSTS
CRA_TCAGchr7v2727,296,844 - 27,297,083UniSTS
REN100799  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,245,893 - 27,246,132UniSTSGRCh37
Build 36727,212,418 - 27,212,657RGDNCBI36
Celera727,234,843 - 27,235,082RGD
HuRef727,126,472 - 27,126,711UniSTS
CRA_TCAGchr7v2727,297,073 - 27,297,312UniSTS
REN100800  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,246,108 - 27,246,369UniSTSGRCh37
Build 36727,212,633 - 27,212,894RGDNCBI36
Celera727,235,058 - 27,235,319RGD
HuRef727,126,687 - 27,126,948UniSTS
CRA_TCAGchr7v2727,297,288 - 27,297,549UniSTS
REN100801  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,246,347 - 27,246,595UniSTSGRCh37
Build 36727,212,872 - 27,213,120RGDNCBI36
Celera727,235,297 - 27,235,545RGD
HuRef727,126,926 - 27,127,174UniSTS
CRA_TCAGchr7v2727,297,527 - 27,297,775UniSTS
REN100802  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,246,571 - 27,246,795UniSTSGRCh37
Build 36727,213,096 - 27,213,320RGDNCBI36
Celera727,235,521 - 27,235,745RGD
HuRef727,127,150 - 27,127,374UniSTS
CRA_TCAGchr7v2727,297,751 - 27,297,975UniSTS
REN100803  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,246,789 - 27,247,038UniSTSGRCh37
Build 36727,213,314 - 27,213,563RGDNCBI36
Celera727,235,739 - 27,235,988RGD
HuRef727,127,368 - 27,127,617UniSTS
CRA_TCAGchr7v2727,297,969 - 27,298,218UniSTS
REN100804  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,247,010 - 27,247,234UniSTSGRCh37
Build 36727,213,535 - 27,213,759RGDNCBI36
Celera727,235,960 - 27,236,184RGD
HuRef727,127,589 - 27,127,813UniSTS
CRA_TCAGchr7v2727,298,190 - 27,298,414UniSTS
REN100805  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,247,201 - 27,247,463UniSTSGRCh37
Build 36727,213,726 - 27,213,988RGDNCBI36
Celera727,236,151 - 27,236,413RGD
HuRef727,127,780 - 27,128,042UniSTS
CRA_TCAGchr7v2727,298,381 - 27,298,643UniSTS
REN100806  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,247,453 - 27,247,680UniSTSGRCh37
Build 36727,213,978 - 27,214,205RGDNCBI36
Celera727,236,403 - 27,236,630RGD
HuRef727,128,032 - 27,128,259UniSTS
CRA_TCAGchr7v2727,298,633 - 27,298,860UniSTS
REN100807  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,247,653 - 27,247,923UniSTSGRCh37
Build 36727,214,178 - 27,214,448RGDNCBI36
Celera727,236,603 - 27,236,873RGD
HuRef727,128,232 - 27,128,502UniSTS
CRA_TCAGchr7v2727,298,833 - 27,299,103UniSTS
REN100808  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,247,909 - 27,248,153UniSTSGRCh37
Build 36727,214,434 - 27,214,678RGDNCBI36
Celera727,236,859 - 27,237,103RGD
Cytogenetic Map7p15.2UniSTS
HuRef727,128,488 - 27,128,732UniSTS
CRA_TCAGchr7v2727,299,089 - 27,299,333UniSTS
REN100809  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,248,133 - 27,248,385UniSTSGRCh37
Build 36727,214,658 - 27,214,910RGDNCBI36
Celera727,237,083 - 27,237,335RGD
HuRef727,128,712 - 27,128,964UniSTS
CRA_TCAGchr7v2727,299,313 - 27,299,565UniSTS
REN100810  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,248,362 - 27,248,612UniSTSGRCh37
Build 36727,214,887 - 27,215,137RGDNCBI36
Celera727,237,312 - 27,237,562RGD
HuRef727,128,941 - 27,129,191UniSTS
CRA_TCAGchr7v2727,299,542 - 27,299,792UniSTS
REN100811  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,248,590 - 27,248,814UniSTSGRCh37
Build 36727,215,115 - 27,215,339RGDNCBI36
Celera727,237,540 - 27,237,764RGD
Cytogenetic Map7p15.2UniSTS
HuRef727,129,169 - 27,129,393UniSTS
CRA_TCAGchr7v2727,299,770 - 27,299,994UniSTS
REN100812  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,248,787 - 27,249,037UniSTSGRCh37
Build 36727,215,312 - 27,215,562RGDNCBI36
Celera727,237,737 - 27,237,987RGD
HuRef727,129,366 - 27,129,616UniSTS
CRA_TCAGchr7v2727,299,967 - 27,300,217UniSTS
REN100813  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,249,021 - 27,249,245UniSTSGRCh37
Build 36727,215,546 - 27,215,770RGDNCBI36
Celera727,237,971 - 27,238,195RGD
HuRef727,129,600 - 27,129,824UniSTS
CRA_TCAGchr7v2727,300,201 - 27,300,425UniSTS
REN100814  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,249,212 - 27,249,482UniSTSGRCh37
Build 36727,215,737 - 27,216,007RGDNCBI36
Celera727,238,162 - 27,238,430RGD
HuRef727,129,791 - 27,130,059UniSTS
CRA_TCAGchr7v2727,300,392 - 27,300,660UniSTS
REN100815  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,249,429 - 27,249,681UniSTSGRCh37
Build 36727,215,954 - 27,216,206RGDNCBI36
Celera727,238,377 - 27,238,629RGD
HuRef727,130,006 - 27,130,258UniSTS
CRA_TCAGchr7v2727,300,607 - 27,300,859UniSTS
REN100816  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,249,656 - 27,249,917UniSTSGRCh37
Build 36727,216,181 - 27,216,442RGDNCBI36
Celera727,238,604 - 27,238,865RGD
HuRef727,130,233 - 27,130,494UniSTS
CRA_TCAGchr7v2727,300,834 - 27,301,095UniSTS
REN100817  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,249,894 - 27,250,158UniSTSGRCh37
Build 36727,216,419 - 27,216,683RGDNCBI36
Celera727,238,842 - 27,239,106RGD
HuRef727,130,471 - 27,130,735UniSTS
CRA_TCAGchr7v2727,301,072 - 27,301,336UniSTS
REN100818  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,250,151 - 27,250,425UniSTSGRCh37
Build 36727,216,676 - 27,216,950RGDNCBI36
Celera727,239,099 - 27,239,373RGD
HuRef727,130,728 - 27,131,002UniSTS
CRA_TCAGchr7v2727,301,329 - 27,301,603UniSTS
REN100819  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,250,421 - 27,250,666UniSTSGRCh37
Build 36727,216,946 - 27,217,191RGDNCBI36
Celera727,239,369 - 27,239,614RGD
HuRef727,130,998 - 27,131,243UniSTS
CRA_TCAGchr7v2727,301,599 - 27,301,844UniSTS
REN100820  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,250,659 - 27,250,904UniSTSGRCh37
Build 36727,217,184 - 27,217,429RGDNCBI36
Celera727,239,607 - 27,239,852RGD
HuRef727,131,236 - 27,131,481UniSTS
CRA_TCAGchr7v2727,301,837 - 27,302,082UniSTS
REN100821  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,250,897 - 27,251,148UniSTSGRCh37
Build 36727,217,422 - 27,217,673RGDNCBI36
Celera727,239,845 - 27,240,096RGD
HuRef727,131,474 - 27,131,725UniSTS
CRA_TCAGchr7v2727,302,075 - 27,302,326UniSTS
REN100822  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,251,123 - 27,251,379UniSTSGRCh37
Build 36727,217,648 - 27,217,904RGDNCBI36
Celera727,240,071 - 27,240,327RGD
HuRef727,131,700 - 27,131,956UniSTS
CRA_TCAGchr7v2727,302,301 - 27,302,557UniSTS
REN100823  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,251,369 - 27,251,615UniSTSGRCh37
Build 36727,217,894 - 27,218,140RGDNCBI36
Celera727,240,317 - 27,240,563RGD
HuRef727,131,946 - 27,132,192UniSTS
CRA_TCAGchr7v2727,302,547 - 27,302,793UniSTS
REN100824  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,251,561 - 27,251,785UniSTSGRCh37
Build 36727,218,086 - 27,218,310RGDNCBI36
Celera727,240,509 - 27,240,733RGD
Cytogenetic Map7p15.2UniSTS
HuRef727,132,138 - 27,132,362UniSTS
CRA_TCAGchr7v2727,302,739 - 27,302,963UniSTS
REN100825  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,251,783 - 27,252,048UniSTSGRCh37
Build 36727,218,308 - 27,218,573RGDNCBI36
Celera727,240,731 - 27,240,996RGD
HuRef727,132,360 - 27,132,625UniSTS
CRA_TCAGchr7v2727,302,961 - 27,303,226UniSTS
REN100826  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,252,021 - 27,252,265UniSTSGRCh37
Build 36727,218,546 - 27,218,790RGDNCBI36
Celera727,240,969 - 27,241,213RGD
HuRef727,132,598 - 27,132,842UniSTS
CRA_TCAGchr7v2727,303,199 - 27,303,443UniSTS
REN100827  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,252,208 - 27,252,467UniSTSGRCh37
Build 36727,218,733 - 27,218,992RGDNCBI36
Celera727,241,156 - 27,241,415RGD
HuRef727,132,785 - 27,133,044UniSTS
CRA_TCAGchr7v2727,303,386 - 27,303,645UniSTS
REN100828  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,252,465 - 27,252,710UniSTSGRCh37
Build 36727,218,990 - 27,219,235RGDNCBI36
Celera727,241,413 - 27,241,658RGD
HuRef727,133,042 - 27,133,287UniSTS
CRA_TCAGchr7v2727,303,643 - 27,303,888UniSTS
REN100829  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,252,652 - 27,252,915UniSTSGRCh37
Build 36727,219,177 - 27,219,440RGDNCBI36
Celera727,241,600 - 27,241,863RGD
HuRef727,133,229 - 27,133,492UniSTS
CRA_TCAGchr7v2727,303,830 - 27,304,093UniSTS
REN100830  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,252,841 - 27,253,089UniSTSGRCh37
Build 36727,219,366 - 27,219,614RGDNCBI36
Celera727,241,789 - 27,242,037RGD
HuRef727,133,418 - 27,133,666UniSTS
CRA_TCAGchr7v2727,304,019 - 27,304,267UniSTS
REN100831  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,253,064 - 27,253,300UniSTSGRCh37
Build 36727,219,589 - 27,219,825RGDNCBI36
Celera727,242,012 - 27,242,248RGD
HuRef727,133,641 - 27,133,877UniSTS
CRA_TCAGchr7v2727,304,242 - 27,304,478UniSTS
REN100832  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,253,281 - 27,253,555UniSTSGRCh37
Build 36727,219,806 - 27,220,080RGDNCBI36
Celera727,242,229 - 27,242,503RGD
HuRef727,133,858 - 27,134,132UniSTS
CRA_TCAGchr7v2727,304,459 - 27,304,733UniSTS
REN100833  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,253,500 - 27,253,733UniSTSGRCh37
Build 36727,220,025 - 27,220,258RGDNCBI36
Celera727,242,448 - 27,242,681RGD
HuRef727,134,077 - 27,134,310UniSTS
CRA_TCAGchr7v2727,304,678 - 27,304,911UniSTS
REN100834  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,253,715 - 27,253,946UniSTSGRCh37
Build 36727,220,240 - 27,220,471RGDNCBI36
Celera727,242,663 - 27,242,894RGD
HuRef727,134,292 - 27,134,523UniSTS
CRA_TCAGchr7v2727,304,893 - 27,305,124UniSTS
REN100835  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,253,917 - 27,254,167UniSTSGRCh37
Build 36727,220,442 - 27,220,692RGDNCBI36
Celera727,242,865 - 27,243,115RGD
HuRef727,134,494 - 27,134,744UniSTS
CRA_TCAGchr7v2727,305,095 - 27,305,345UniSTS
REN100836  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,254,157 - 27,254,425UniSTSGRCh37
Build 36727,220,682 - 27,220,950RGDNCBI36
Celera727,243,105 - 27,243,373RGD
HuRef727,134,734 - 27,135,002UniSTS
CRA_TCAGchr7v2727,305,335 - 27,305,603UniSTS
REN100837  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,254,406 - 27,254,642UniSTSGRCh37
Build 36727,220,931 - 27,221,167RGDNCBI36
Celera727,243,354 - 27,243,590RGD
HuRef727,134,983 - 27,135,219UniSTS
CRA_TCAGchr7v2727,305,584 - 27,305,820UniSTS
REN100838  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,254,603 - 27,254,854UniSTSGRCh37
Build 36727,221,128 - 27,221,379RGDNCBI36
Celera727,243,551 - 27,243,802RGD
HuRef727,135,180 - 27,135,431UniSTS
CRA_TCAGchr7v2727,305,781 - 27,306,032UniSTS
REN100839  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,254,849 - 27,255,078UniSTSGRCh37
Build 36727,221,374 - 27,221,603RGDNCBI36
Celera727,243,797 - 27,244,026RGD
HuRef727,135,426 - 27,135,655UniSTS
CRA_TCAGchr7v2727,306,027 - 27,306,256UniSTS
REN100840  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,255,056 - 27,255,315UniSTSGRCh37
Build 36727,221,581 - 27,221,840RGDNCBI36
Celera727,244,004 - 27,244,263RGD
Cytogenetic Map7p15.2UniSTS
HuRef727,135,633 - 27,135,892UniSTS
CRA_TCAGchr7v2727,306,234 - 27,306,493UniSTS
REN100841  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,255,301 - 27,255,549UniSTSGRCh37
Build 36727,221,826 - 27,222,074RGDNCBI36
Celera727,244,249 - 27,244,497RGD
HuRef727,135,878 - 27,136,126UniSTS
CRA_TCAGchr7v2727,306,479 - 27,306,727UniSTS
REN100842  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,255,542 - 27,255,794UniSTSGRCh37
Build 36727,222,067 - 27,222,319RGDNCBI36
Celera727,244,490 - 27,244,742RGD
HuRef727,136,119 - 27,136,371UniSTS
CRA_TCAGchr7v2727,306,720 - 27,306,972UniSTS
REN100843  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,255,792 - 27,256,042UniSTSGRCh37
Build 36727,222,317 - 27,222,567RGDNCBI36
Celera727,244,740 - 27,244,990RGD
HuRef727,136,369 - 27,136,619UniSTS
CRA_TCAGchr7v2727,306,970 - 27,307,220UniSTS
REN100844  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,256,020 - 27,256,262UniSTSGRCh37
Build 36727,222,545 - 27,222,787RGDNCBI36
Celera727,244,968 - 27,245,210RGD
HuRef727,136,597 - 27,136,839UniSTS
CRA_TCAGchr7v2727,307,198 - 27,307,440UniSTS
REN100845  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,256,258 - 27,256,500UniSTSGRCh37
Build 36727,222,783 - 27,223,025RGDNCBI36
Celera727,245,206 - 27,245,448RGD
HuRef727,136,835 - 27,137,077UniSTS
CRA_TCAGchr7v2727,307,436 - 27,307,678UniSTS
REN100846  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,256,493 - 27,256,748UniSTSGRCh37
Build 36727,223,018 - 27,223,273RGDNCBI36
Celera727,245,441 - 27,245,696RGD
HuRef727,137,070 - 27,137,325UniSTS
CRA_TCAGchr7v2727,307,671 - 27,307,926UniSTS
REN100847  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,256,734 - 27,256,982UniSTSGRCh37
Build 36727,223,259 - 27,223,507RGDNCBI36
Celera727,245,682 - 27,245,930RGD
HuRef727,137,311 - 27,137,559UniSTS
CRA_TCAGchr7v2727,307,912 - 27,308,160UniSTS
REN100848  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,256,959 - 27,257,203UniSTSGRCh37
Build 36727,223,484 - 27,223,728RGDNCBI36
Celera727,245,907 - 27,246,151RGD
HuRef727,137,536 - 27,137,780UniSTS
CRA_TCAGchr7v2727,308,137 - 27,308,381UniSTS
REN100849  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,257,158 - 27,257,411UniSTSGRCh37
Build 36727,223,683 - 27,223,936RGDNCBI36
Celera727,246,106 - 27,246,359RGD
HuRef727,137,735 - 27,137,988UniSTS
CRA_TCAGchr7v2727,308,336 - 27,308,589UniSTS
REN100850  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,257,641 - 27,257,873UniSTSGRCh37
Build 36727,224,166 - 27,224,398RGDNCBI36
Celera727,246,589 - 27,246,821RGD
HuRef727,138,220 - 27,138,452UniSTS
CRA_TCAGchr7v2727,308,819 - 27,309,051UniSTS
REN100851  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,257,853 - 27,258,099UniSTSGRCh37
Build 36727,224,378 - 27,224,624RGDNCBI36
Celera727,246,801 - 27,247,047RGD
HuRef727,138,432 - 27,138,678UniSTS
CRA_TCAGchr7v2727,309,031 - 27,309,277UniSTS
REN100852  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,258,076 - 27,258,330UniSTSGRCh37
Build 36727,224,601 - 27,224,855RGDNCBI36
Celera727,247,024 - 27,247,278RGD
HuRef727,138,655 - 27,138,909UniSTS
CRA_TCAGchr7v2727,309,254 - 27,309,508UniSTS
REN100853  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,258,126 - 27,258,393UniSTSGRCh37
Build 36727,224,651 - 27,224,918RGDNCBI36
Celera727,247,074 - 27,247,341RGD
HuRef727,138,705 - 27,138,972UniSTS
CRA_TCAGchr7v2727,309,304 - 27,309,571UniSTS
REN100854  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,258,654 - 27,258,908UniSTSGRCh37
Build 36727,225,179 - 27,225,433RGDNCBI36
Celera727,247,602 - 27,247,856RGD
HuRef727,139,233 - 27,139,487UniSTS
CRA_TCAGchr7v2727,309,832 - 27,310,086UniSTS
REN100855  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,258,903 - 27,259,169UniSTSGRCh37
Build 36727,225,428 - 27,225,694RGDNCBI36
Celera727,247,851 - 27,248,117RGD
HuRef727,139,482 - 27,139,748UniSTS
CRA_TCAGchr7v2727,310,081 - 27,310,347UniSTS
REN100856  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,259,140 - 27,259,372UniSTSGRCh37
Build 36727,225,665 - 27,225,897RGDNCBI36
Celera727,248,088 - 27,248,320RGD
HuRef727,139,719 - 27,139,951UniSTS
CRA_TCAGchr7v2727,310,318 - 27,310,550UniSTS
REN100857  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,259,352 - 27,259,617UniSTSGRCh37
Build 36727,225,877 - 27,226,142RGDNCBI36
Celera727,248,300 - 27,248,565RGD
HuRef727,139,931 - 27,140,196UniSTS
CRA_TCAGchr7v2727,310,530 - 27,310,795UniSTS
REN100858  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,259,603 - 27,259,843UniSTSGRCh37
Build 36727,226,128 - 27,226,368RGDNCBI36
Celera727,248,551 - 27,248,791RGD
HuRef727,140,182 - 27,140,422UniSTS
CRA_TCAGchr7v2727,310,781 - 27,311,021UniSTS
REN100859  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,259,821 - 27,260,079UniSTSGRCh37
Build 36727,226,346 - 27,226,604RGDNCBI36
Celera727,248,769 - 27,249,027RGD
HuRef727,140,400 - 27,140,658UniSTS
CRA_TCAGchr7v2727,310,999 - 27,311,257UniSTS
REN100860  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,260,060 - 27,260,325UniSTSGRCh37
Build 36727,226,585 - 27,226,850RGDNCBI36
Celera727,249,008 - 27,249,273RGD
HuRef727,140,639 - 27,140,904UniSTS
CRA_TCAGchr7v2727,311,238 - 27,311,503UniSTS
REN100861  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,260,306 - 27,260,567UniSTSGRCh37
Build 36727,226,831 - 27,227,092RGDNCBI36
Celera727,249,254 - 27,249,515RGD
HuRef727,140,885 - 27,141,146UniSTS
CRA_TCAGchr7v2727,311,484 - 27,311,745UniSTS
REN100862  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,260,544 - 27,260,792UniSTSGRCh37
Build 36727,227,069 - 27,227,317RGDNCBI36
Celera727,249,492 - 27,249,740RGD
HuRef727,141,123 - 27,141,371UniSTS
CRA_TCAGchr7v2727,311,722 - 27,311,970UniSTS
REN100863  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,260,790 - 27,261,037UniSTSGRCh37
Build 36727,227,315 - 27,227,562RGDNCBI36
Celera727,249,738 - 27,249,985RGD
HuRef727,141,369 - 27,141,616UniSTS
CRA_TCAGchr7v2727,311,968 - 27,312,215UniSTS
REN100864  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,261,034 - 27,261,286UniSTSGRCh37
Build 36727,227,559 - 27,227,811RGDNCBI36
Celera727,249,982 - 27,250,234RGD
HuRef727,141,613 - 27,141,865UniSTS
CRA_TCAGchr7v2727,312,212 - 27,312,464UniSTS
REN100865  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,261,262 - 27,261,511UniSTSGRCh37
Build 36727,227,787 - 27,228,036RGDNCBI36
Celera727,250,210 - 27,250,459RGD
HuRef727,141,841 - 27,142,090UniSTS
CRA_TCAGchr7v2727,312,440 - 27,312,689UniSTS
REN100866  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,261,501 - 27,261,747UniSTSGRCh37
Build 36727,228,026 - 27,228,272RGDNCBI36
Celera727,250,449 - 27,250,695RGD
HuRef727,142,080 - 27,142,326UniSTS
CRA_TCAGchr7v2727,312,679 - 27,312,925UniSTS
REN100867  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,261,706 - 27,261,956UniSTSGRCh37
Build 36727,228,231 - 27,228,481RGDNCBI36
Celera727,250,654 - 27,250,904RGD
HuRef727,142,285 - 27,142,535UniSTS
CRA_TCAGchr7v2727,312,884 - 27,313,134UniSTS
REN100868  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,261,933 - 27,262,157UniSTSGRCh37
Build 36727,228,458 - 27,228,682RGDNCBI36
Celera727,250,881 - 27,251,105RGD
HuRef727,142,512 - 27,142,736UniSTS
CRA_TCAGchr7v2727,313,111 - 27,313,335UniSTS
REN100869  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,262,146 - 27,262,406UniSTSGRCh37
Build 36727,228,671 - 27,228,931RGDNCBI36
Celera727,251,094 - 27,251,354RGD
HuRef727,142,725 - 27,142,985UniSTS
CRA_TCAGchr7v2727,313,324 - 27,313,584UniSTS
REN100870  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,262,376 - 27,262,629UniSTSGRCh37
Build 36727,228,901 - 27,229,154RGDNCBI36
Celera727,251,324 - 27,251,577RGD
HuRef727,142,955 - 27,143,208UniSTS
CRA_TCAGchr7v2727,313,554 - 27,313,807UniSTS
REN100871  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,262,607 - 27,262,863UniSTSGRCh37
Build 36727,229,132 - 27,229,388RGDNCBI36
Celera727,251,555 - 27,251,811RGD
HuRef727,143,186 - 27,143,442UniSTS
CRA_TCAGchr7v2727,313,785 - 27,314,041UniSTS
REN100872  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,262,840 - 27,263,100UniSTSGRCh37
Build 36727,229,365 - 27,229,625RGDNCBI36
Celera727,251,788 - 27,252,048RGD
HuRef727,143,419 - 27,143,679UniSTS
CRA_TCAGchr7v2727,314,018 - 27,314,278UniSTS
REN100873  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,263,077 - 27,263,309UniSTSGRCh37
Build 36727,229,602 - 27,229,834RGDNCBI36
Celera727,252,025 - 27,252,257RGD
HuRef727,143,656 - 27,143,888UniSTS
CRA_TCAGchr7v2727,314,255 - 27,314,487UniSTS
REN100874  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,263,233 - 27,263,487UniSTSGRCh37
Build 36727,229,758 - 27,230,012RGDNCBI36
Celera727,252,181 - 27,252,435RGD
HuRef727,143,812 - 27,144,066UniSTS
CRA_TCAGchr7v2727,314,411 - 27,314,665UniSTS
REN100875  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,263,462 - 27,263,715UniSTSGRCh37
Build 36727,229,987 - 27,230,240RGDNCBI36
Celera727,252,410 - 27,252,663RGD
HuRef727,144,041 - 27,144,294UniSTS
CRA_TCAGchr7v2727,314,640 - 27,314,893UniSTS
REN100876  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,263,702 - 27,263,966UniSTSGRCh37
Build 36727,230,227 - 27,230,491RGDNCBI36
Celera727,252,650 - 27,252,914RGD
HuRef727,144,281 - 27,144,545UniSTS
CRA_TCAGchr7v2727,314,880 - 27,315,144UniSTS
REN100877  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,263,943 - 27,264,179UniSTSGRCh37
Build 36727,230,468 - 27,230,704RGDNCBI36
Celera727,252,891 - 27,253,127RGD
HuRef727,144,522 - 27,144,758UniSTS
CRA_TCAGchr7v2727,315,121 - 27,315,357UniSTS
REN100878  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,264,085 - 27,264,328UniSTSGRCh37
Build 36727,230,610 - 27,230,853RGDNCBI36
Celera727,253,033 - 27,253,276RGD
HuRef727,144,664 - 27,144,907UniSTS
CRA_TCAGchr7v2727,315,263 - 27,315,506UniSTS
REN100879  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,264,210 - 27,264,452UniSTSGRCh37
Build 36727,230,735 - 27,230,977RGDNCBI36
Celera727,253,158 - 27,253,400RGD
HuRef727,144,789 - 27,145,031UniSTS
CRA_TCAGchr7v2727,315,388 - 27,315,630UniSTS
REN100880  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,264,429 - 27,264,670UniSTSGRCh37
Build 36727,230,954 - 27,231,195RGDNCBI36
Celera727,253,377 - 27,253,618RGD
HuRef727,145,008 - 27,145,249UniSTS
CRA_TCAGchr7v2727,315,607 - 27,315,848UniSTS
REN100881  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,264,638 - 27,264,883UniSTSGRCh37
Build 36727,231,163 - 27,231,408RGDNCBI36
Celera727,253,586 - 27,253,831RGD
HuRef727,145,217 - 27,145,462UniSTS
CRA_TCAGchr7v2727,315,816 - 27,316,061UniSTS
REN100882  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,264,862 - 27,265,121UniSTSGRCh37
Build 36727,231,387 - 27,231,646RGDNCBI36
Celera727,253,810 - 27,254,069RGD
HuRef727,145,441 - 27,145,700UniSTS
CRA_TCAGchr7v2727,316,040 - 27,316,299UniSTS
REN100883  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,265,113 - 27,265,352UniSTSGRCh37
Build 36727,231,638 - 27,231,877RGDNCBI36
Celera727,254,061 - 27,254,300RGD
HuRef727,145,692 - 27,145,931UniSTS
CRA_TCAGchr7v2727,316,291 - 27,316,530UniSTS
REN100884  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,265,328 - 27,265,552UniSTSGRCh37
Build 36727,231,853 - 27,232,077RGDNCBI36
Celera727,254,276 - 27,254,500RGD
HuRef727,145,907 - 27,146,131UniSTS
CRA_TCAGchr7v2727,316,506 - 27,316,730UniSTS
REN100885  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,265,493 - 27,265,747UniSTSGRCh37
Build 36727,232,018 - 27,232,272RGDNCBI36
Celera727,254,441 - 27,254,695RGD
HuRef727,146,072 - 27,146,326UniSTS
CRA_TCAGchr7v2727,316,671 - 27,316,925UniSTS
REN100886  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,265,729 - 27,265,978UniSTSGRCh37
Build 36727,232,254 - 27,232,503RGDNCBI36
Celera727,254,677 - 27,254,926RGD
HuRef727,146,308 - 27,146,557UniSTS
CRA_TCAGchr7v2727,316,907 - 27,317,156UniSTS
REN100887  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,265,958 - 27,266,221UniSTSGRCh37
Build 36727,232,483 - 27,232,746RGDNCBI36
Celera727,254,906 - 27,255,169RGD
HuRef727,146,537 - 27,146,800UniSTS
CRA_TCAGchr7v2727,317,136 - 27,317,399UniSTS
REN100888  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,266,199 - 27,266,446UniSTSGRCh37
Build 36727,232,724 - 27,232,971RGDNCBI36
Celera727,255,147 - 27,255,394RGD
HuRef727,146,778 - 27,147,025UniSTS
CRA_TCAGchr7v2727,317,377 - 27,317,624UniSTS
REN100889  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,266,445 - 27,266,699UniSTSGRCh37
Build 36727,232,970 - 27,233,224RGDNCBI36
Celera727,255,393 - 27,255,647RGD
HuRef727,147,024 - 27,147,278UniSTS
CRA_TCAGchr7v2727,317,623 - 27,317,877UniSTS
REN100890  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,266,685 - 27,266,935UniSTSGRCh37
Build 36727,233,210 - 27,233,460RGDNCBI36
Celera727,255,633 - 27,255,883RGD
HuRef727,147,264 - 27,147,514UniSTS
CRA_TCAGchr7v2727,317,863 - 27,318,113UniSTS
REN100891  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,266,912 - 27,267,183UniSTSGRCh37
Build 36727,233,437 - 27,233,708RGDNCBI36
Celera727,255,860 - 27,256,131RGD
HuRef727,147,491 - 27,147,762UniSTS
CRA_TCAGchr7v2727,318,090 - 27,318,361UniSTS
REN100892  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,267,160 - 27,267,400UniSTSGRCh37
Build 36727,233,685 - 27,233,925RGDNCBI36
Celera727,256,108 - 27,256,348RGD
HuRef727,147,739 - 27,147,979UniSTS
CRA_TCAGchr7v2727,318,338 - 27,318,578UniSTS
REN100893  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,267,329 - 27,267,580UniSTSGRCh37
Build 36727,233,854 - 27,234,105RGDNCBI36
Celera727,256,277 - 27,256,528RGD
HuRef727,147,908 - 27,148,159UniSTS
CRA_TCAGchr7v2727,318,507 - 27,318,758UniSTS
REN100894  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,267,557 - 27,267,800UniSTSGRCh37
Build 36727,234,082 - 27,234,325RGDNCBI36
Celera727,256,505 - 27,256,748RGD
HuRef727,148,136 - 27,148,379UniSTS
CRA_TCAGchr7v2727,318,735 - 27,318,978UniSTS
REN100895  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,267,740 - 27,267,965UniSTSGRCh37
Build 36727,234,265 - 27,234,490RGDNCBI36
Celera727,256,688 - 27,256,913RGD
HuRef727,148,319 - 27,148,544UniSTS
CRA_TCAGchr7v2727,318,918 - 27,319,143UniSTS
REN100896  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,268,253 - 27,268,479UniSTSGRCh37
Build 36727,234,778 - 27,235,004RGDNCBI36
Celera727,257,201 - 27,257,427RGD
HuRef727,148,832 - 27,149,058UniSTS
CRA_TCAGchr7v2727,319,431 - 27,319,657UniSTS
REN100897  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,268,462 - 27,268,718UniSTSGRCh37
Build 36727,234,987 - 27,235,243RGDNCBI36
Celera727,257,410 - 27,257,666RGD
HuRef727,149,041 - 27,149,297UniSTS
CRA_TCAGchr7v2727,319,640 - 27,319,896UniSTS
REN100898  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,268,717 - 27,268,942UniSTSGRCh37
Build 36727,235,242 - 27,235,467RGDNCBI36
Celera727,257,665 - 27,257,890RGD
HuRef727,149,296 - 27,149,521UniSTS
CRA_TCAGchr7v2727,319,895 - 27,320,120UniSTS
REN100899  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,268,917 - 27,269,160UniSTSGRCh37
Build 36727,235,442 - 27,235,685RGDNCBI36
Celera727,257,865 - 27,258,108RGD
HuRef727,149,496 - 27,149,739UniSTS
CRA_TCAGchr7v2727,320,095 - 27,320,338UniSTS
REN100900  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,269,118 - 27,269,380UniSTSGRCh37
Build 36727,235,643 - 27,235,905RGDNCBI36
Celera727,258,066 - 27,258,328RGD
HuRef727,149,697 - 27,149,959UniSTS
CRA_TCAGchr7v2727,320,296 - 27,320,558UniSTS
REN100901  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,269,379 - 27,269,604UniSTSGRCh37
Build 36727,235,904 - 27,236,129RGDNCBI36
Celera727,258,327 - 27,258,552RGD
HuRef727,149,958 - 27,150,183UniSTS
CRA_TCAGchr7v2727,320,557 - 27,320,782UniSTS
REN100902  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,269,581 - 27,269,822UniSTSGRCh37
Build 36727,236,106 - 27,236,347RGDNCBI36
Celera727,258,529 - 27,258,770RGD
HuRef727,150,160 - 27,150,401UniSTS
CRA_TCAGchr7v2727,320,759 - 27,321,000UniSTS
REN100903  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,269,758 - 27,270,014UniSTSGRCh37
Build 36727,236,283 - 27,236,539RGDNCBI36
Celera727,258,706 - 27,258,962RGD
HuRef727,150,337 - 27,150,593UniSTS
CRA_TCAGchr7v2727,320,936 - 27,321,192UniSTS
REN100904  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,269,981 - 27,270,220UniSTSGRCh37
Build 36727,236,506 - 27,236,745RGDNCBI36
Celera727,258,929 - 27,259,168RGD
HuRef727,150,560 - 27,150,799UniSTS
CRA_TCAGchr7v2727,321,159 - 27,321,398UniSTS
REN100905  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,270,191 - 27,270,426UniSTSGRCh37
Build 36727,236,716 - 27,236,951RGDNCBI36
Celera727,259,139 - 27,259,354RGD
HuRef727,150,770 - 27,150,985UniSTS
CRA_TCAGchr7v2727,321,369 - 27,321,604UniSTS
REN100906  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,271,686 - 27,271,931UniSTSGRCh37
Build 36727,238,211 - 27,238,456RGDNCBI36
Celera727,260,615 - 27,260,860RGD
HuRef727,151,909 - 27,152,154UniSTS
CRA_TCAGchr7v2727,322,865 - 27,323,110UniSTS
REN100907  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,271,904 - 27,272,153UniSTSGRCh37
Build 36727,238,429 - 27,238,678RGDNCBI36
Celera727,260,833 - 27,261,082RGD
HuRef727,152,127 - 27,152,376UniSTS
CRA_TCAGchr7v2727,323,083 - 27,323,332UniSTS
REN100908  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,272,524 - 27,272,748UniSTSGRCh37
Build 36727,239,049 - 27,239,273RGDNCBI36
Celera727,261,453 - 27,261,677RGD
HuRef727,152,747 - 27,152,971UniSTS
CRA_TCAGchr7v2727,323,703 - 27,323,927UniSTS
REN100909  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,272,727 - 27,272,953UniSTSGRCh37
Build 36727,239,252 - 27,239,478RGDNCBI36
Celera727,261,656 - 27,261,882RGD
HuRef727,152,950 - 27,153,176UniSTS
CRA_TCAGchr7v2727,323,906 - 27,324,132UniSTS
REN100910  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,272,937 - 27,273,200UniSTSGRCh37
Build 36727,239,462 - 27,239,725RGDNCBI36
Celera727,261,866 - 27,262,129RGD
HuRef727,153,160 - 27,153,423UniSTS
CRA_TCAGchr7v2727,324,116 - 27,324,379UniSTS
REN100911  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,273,177 - 27,273,420UniSTSGRCh37
Build 36727,239,702 - 27,239,945RGDNCBI36
Celera727,262,106 - 27,262,349RGD
HuRef727,153,400 - 27,153,643UniSTS
CRA_TCAGchr7v2727,324,356 - 27,324,599UniSTS
REN100912  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,273,389 - 27,273,647UniSTSGRCh37
Build 36727,239,914 - 27,240,172RGDNCBI36
Celera727,262,318 - 27,262,576RGD
HuRef727,153,612 - 27,153,870UniSTS
CRA_TCAGchr7v2727,324,568 - 27,324,826UniSTS
REN100913  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,273,835 - 27,274,073UniSTSGRCh37
Build 36727,240,360 - 27,240,598RGDNCBI36
Celera727,262,764 - 27,263,002RGD
HuRef727,154,058 - 27,154,296UniSTS
CRA_TCAGchr7v2727,325,014 - 27,325,252UniSTS
REN100914  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,273,881 - 27,274,106UniSTSGRCh37
Build 36727,240,406 - 27,240,631RGDNCBI36
Celera727,262,810 - 27,263,035RGD
HuRef727,154,104 - 27,154,329UniSTS
CRA_TCAGchr7v2727,325,060 - 27,325,285UniSTS
GDB:1318328  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,265,535 - 27,265,765UniSTSGRCh37
Build 36727,232,060 - 27,232,290RGDNCBI36
Celera727,254,483 - 27,254,713RGD
Cytogenetic Map7p15.2UniSTS
HuRef727,146,114 - 27,146,344UniSTS
CRA_TCAGchr7v2727,316,713 - 27,316,943UniSTS
stSG609399  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,237,365 - 27,237,557UniSTSGRCh37
Build 36727,203,890 - 27,204,082RGDNCBI36
Celera727,226,302 - 27,226,494RGD
Cytogenetic Map7p15.2UniSTS
HuRef727,117,929 - 27,118,121UniSTS
CRA_TCAGchr7v2727,288,549 - 27,288,741UniSTS
stSG609400  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,237,563 - 27,238,845UniSTSGRCh37
Build 36727,204,088 - 27,205,370RGDNCBI36
Celera727,226,500 - 27,227,782RGD
Cytogenetic Map7p15.2UniSTS
HuRef727,118,127 - 27,119,409UniSTS
CRA_TCAGchr7v2727,288,747 - 27,290,029UniSTS
stSG609403  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,241,412 - 27,242,516UniSTSGRCh37
Build 36727,207,937 - 27,209,041RGDNCBI36
Celera727,230,350 - 27,231,471RGD
HuRef727,121,979 - 27,123,100UniSTS
CRA_TCAGchr7v2727,292,597 - 27,293,701UniSTS
stSG609404  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,242,497 - 27,243,907UniSTSGRCh37
Build 36727,209,022 - 27,210,432RGDNCBI36
Celera727,231,452 - 27,232,862RGD
HuRef727,123,081 - 27,124,491UniSTS
CRA_TCAGchr7v2727,293,682 - 27,295,092UniSTS
stSG609405  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,243,891 - 27,245,016UniSTSGRCh37
Build 36727,210,416 - 27,211,541RGDNCBI36
Celera727,232,846 - 27,233,966RGD
HuRef727,124,475 - 27,125,595UniSTS
CRA_TCAGchr7v2727,295,076 - 27,296,196UniSTS
stSG609406  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,244,999 - 27,246,471UniSTSGRCh37
Build 36727,211,524 - 27,212,996RGDNCBI36
Celera727,233,949 - 27,235,421RGD
HuRef727,125,578 - 27,127,050UniSTS
CRA_TCAGchr7v2727,296,179 - 27,297,651UniSTS
stSG609407  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,246,452 - 27,247,923UniSTSGRCh37
Build 36727,212,977 - 27,214,448RGDNCBI36
Celera727,235,402 - 27,236,873RGD
HuRef727,127,031 - 27,128,502UniSTS
CRA_TCAGchr7v2727,297,632 - 27,299,103UniSTS
stSG609408  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,247,923 - 27,249,397UniSTSGRCh37
Build 36727,214,448 - 27,215,922RGDNCBI36
Celera727,236,873 - 27,238,345RGD
HuRef727,128,502 - 27,129,974UniSTS
CRA_TCAGchr7v2727,299,103 - 27,300,575UniSTS
stSG609409  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,249,378 - 27,249,654UniSTSGRCh37
Build 36727,215,903 - 27,216,179RGDNCBI36
Celera727,238,326 - 27,238,602RGD
HuRef727,129,955 - 27,130,231UniSTS
CRA_TCAGchr7v2727,300,556 - 27,300,832UniSTS
stSG609410  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,249,705 - 27,250,786UniSTSGRCh37
Build 36727,216,230 - 27,217,311RGDNCBI36
Celera727,238,653 - 27,239,734RGD
HuRef727,130,282 - 27,131,363UniSTS
CRA_TCAGchr7v2727,300,883 - 27,301,964UniSTS
stSG609411  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,250,767 - 27,252,062UniSTSGRCh37
Build 36727,217,292 - 27,218,587RGDNCBI36
Celera727,239,715 - 27,241,010RGD
HuRef727,131,344 - 27,132,639UniSTS
CRA_TCAGchr7v2727,301,945 - 27,303,240UniSTS
stSG609413  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,253,093 - 27,254,499UniSTSGRCh37
Build 36727,219,618 - 27,221,024RGDNCBI36
Celera727,242,041 - 27,243,447RGD
HuRef727,133,670 - 27,135,076UniSTS
CRA_TCAGchr7v2727,304,271 - 27,305,677UniSTS
stSG609414  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,254,480 - 27,255,592UniSTSGRCh37
Build 36727,221,005 - 27,222,117RGDNCBI36
Celera727,243,428 - 27,244,540RGD
HuRef727,135,057 - 27,136,169UniSTS
CRA_TCAGchr7v2727,305,658 - 27,306,770UniSTS
stSG609415  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,255,654 - 27,257,005UniSTSGRCh37
Build 36727,222,179 - 27,223,530RGDNCBI36
Celera727,244,602 - 27,245,953RGD
HuRef727,136,231 - 27,137,582UniSTS
CRA_TCAGchr7v2727,306,832 - 27,308,183UniSTS
stSG609416  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,257,015 - 27,258,088UniSTSGRCh37
Build 36727,223,540 - 27,224,613RGDNCBI36
Celera727,245,963 - 27,247,036RGD
HuRef727,137,592 - 27,138,667UniSTS
CRA_TCAGchr7v2727,308,193 - 27,309,266UniSTS
stSG609417  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,258,071 - 27,259,103UniSTSGRCh37
Build 36727,224,596 - 27,225,628RGDNCBI36
Celera727,247,019 - 27,248,051RGD
HuRef727,138,650 - 27,139,682UniSTS
CRA_TCAGchr7v2727,309,249 - 27,310,281UniSTS
stSG609419  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,260,542 - 27,261,806UniSTSGRCh37
Build 36727,227,067 - 27,228,331RGDNCBI36
Celera727,249,490 - 27,250,754RGD
HuRef727,141,121 - 27,142,385UniSTS
CRA_TCAGchr7v2727,311,720 - 27,312,984UniSTS
stSG609420  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,261,787 - 27,262,795UniSTSGRCh37
Build 36727,228,312 - 27,229,320RGDNCBI36
Celera727,250,735 - 27,251,743RGD
HuRef727,142,366 - 27,143,374UniSTS
CRA_TCAGchr7v2727,312,965 - 27,313,973UniSTS
stSG609421  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,262,781 - 27,264,179UniSTSGRCh37
Build 36727,229,306 - 27,230,704RGDNCBI36
Celera727,251,729 - 27,253,127RGD
HuRef727,143,360 - 27,144,758UniSTS
CRA_TCAGchr7v2727,313,959 - 27,315,357UniSTS
stSG609422  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,264,160 - 27,265,598UniSTSGRCh37
Build 36727,230,685 - 27,232,123RGDNCBI36
Celera727,253,108 - 27,254,546RGD
HuRef727,144,739 - 27,146,177UniSTS
CRA_TCAGchr7v2727,315,338 - 27,316,776UniSTS
stSG609423  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,265,615 - 27,266,809UniSTSGRCh37
Build 36727,232,140 - 27,233,334RGDNCBI36
Celera727,254,563 - 27,255,757RGD
HuRef727,146,194 - 27,147,388UniSTS
CRA_TCAGchr7v2727,316,793 - 27,317,987UniSTS
stSG609424  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,266,638 - 27,267,655UniSTSGRCh37
Build 36727,233,163 - 27,234,180RGDNCBI36
Celera727,255,586 - 27,256,603RGD
HuRef727,147,217 - 27,148,234UniSTS
CRA_TCAGchr7v2727,317,816 - 27,318,833UniSTS
stSG609425  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,267,636 - 27,268,911UniSTSGRCh37
Build 36727,234,161 - 27,235,436RGDNCBI36
Celera727,256,584 - 27,257,859RGD
HuRef727,148,215 - 27,149,490UniSTS
CRA_TCAGchr7v2727,318,814 - 27,320,089UniSTS
stSG609426  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,268,892 - 27,269,983UniSTSGRCh37
Build 36727,235,417 - 27,236,508RGDNCBI36
Celera727,257,840 - 27,258,931RGD
HuRef727,149,471 - 27,150,562UniSTS
CRA_TCAGchr7v2727,320,070 - 27,321,161UniSTS
stSG609427  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,269,964 - 27,270,274UniSTSGRCh37
GRCh37727,269,964 - 27,270,270UniSTSGRCh37
Build 36727,236,489 - 27,236,799RGDNCBI36
Celera727,258,912 - 27,259,218UniSTS
Celera727,258,912 - 27,259,222RGD
HuRef727,150,543 - 27,150,853UniSTS
HuRef727,150,543 - 27,150,849UniSTS
CRA_TCAGchr7v2727,321,142 - 27,321,452UniSTS
CRA_TCAGchr7v2727,321,142 - 27,321,448UniSTS
stSG609430  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,273,017 - 27,274,121UniSTSGRCh37
Build 36727,239,542 - 27,240,646RGDNCBI36
Celera727,261,946 - 27,263,050RGD
HuRef727,153,240 - 27,154,344UniSTS
CRA_TCAGchr7v2727,324,196 - 27,325,300UniSTS
Hoxa13  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37727,238,004 - 27,239,181UniSTSGRCh37
Celera727,226,941 - 27,228,118UniSTS
HuRef727,118,568 - 27,119,745UniSTS
CRA_TCAGchr7v2727,289,188 - 27,290,365UniSTS


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
renal system
reproductive system
respiratory system
sensory system
1027 1608 2787 1380 2680 945 1297 5 363 610 216 2104 4817 3857 39 1601 763 1389 809 158

Sequence


Ensembl Acc Id: ENST00000518136
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl727,193,503 - 27,195,600 (-)Ensembl
Ensembl Acc Id: ENST00000649031   ⟹   ENSP00000497112
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl727,194,364 - 27,200,091 (-)Ensembl
RefSeq Acc Id: NM_000522   ⟹   NP_000513
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38727,194,364 - 27,200,091 (-)NCBI
GRCh37727,236,499 - 27,239,725 (-)ENTREZGENE
Build 36727,203,024 - 27,206,250 (-)NCBI Archive
HuRef727,117,064 - 27,119,882 (-)ENTREZGENE
CHM1_1727,236,223 - 27,239,448 (-)NCBI
T2T-CHM13v2.0727,330,371 - 27,336,079 (-)NCBI
CRA_TCAGchr7v2727,287,684 - 27,290,909 (-)ENTREZGENE
Sequence:
Protein Sequences
Protein RefSeqs NP_000513 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAC50993 (Get FASTA)   NCBI Sequence Viewer  
  AAH75791 (Get FASTA)   NCBI Sequence Viewer  
  AEQ29847 (Get FASTA)   NCBI Sequence Viewer  
  EAL24218 (Get FASTA)   NCBI Sequence Viewer  
  EAW93890 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000497112
  ENSP00000497112.1
GenBank Protein P31271 (Get FASTA)   NCBI Sequence Viewer  
RefSeq Acc Id: NP_000513   ⟸   NM_000522
- UniProtKB: A4D188 (UniProtKB/Swiss-Prot),   O43371 (UniProtKB/Swiss-Prot),   P31271 (UniProtKB/Swiss-Prot),   Q6DI00 (UniProtKB/TrEMBL)
- Sequence:
Ensembl Acc Id: ENSP00000497112   ⟸   ENST00000649031
Protein Domains
Homeobox   Homeobox protein Hox1A3 N-terminal

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-P31271-F1-model_v2 AlphaFold P31271 1-388 view protein structure

Promoters
RGD ID:7210213
Promoter ID:EPDNEW_H10852
Type:initiation region
Name:HOXA13_1
Description:homeobox A13
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
GRCh38727,200,091 - 27,200,151EPDNEW
RGD ID:6805088
Promoter ID:HG_KWN:56696
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell_12Hour,   HeLa_S3,   NB4
Transcripts:OTTHUMT00000059759,   OTTHUMT00000137902
Position:
Human AssemblyChrPosition (strand)Source
Build 36727,205,296 - 27,206,497 (+)MPROMDB

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:5102 AgrOrtholog
COSMIC HOXA13 COSMIC
Ensembl Genes ENSG00000106031 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript ENST00000649031 ENTREZGENE
  ENST00000649031.1 UniProtKB/Swiss-Prot
Gene3D-CATH Homeodomain-like UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000106031 GTEx
HGNC ID HGNC:5102 ENTREZGENE
Human Proteome Map HOXA13 Human Proteome Map
InterPro AP_axis_regulatory_Homeobox UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Homeobox-like_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Homeobox_CS UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Homeobox_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  HoxA13_N UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:3209 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
NCBI Gene 3209 ENTREZGENE
OMIM 142959 OMIM
PANTHER HOMEOBOX PROTEIN HOX-A13 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SEGMENTATION PROTEIN FUSHI TARAZU-LIKE PROTEIN UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam Homeodomain UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  HoxA13_N UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA29379 PharmGKB
PROSITE HOMEOBOX_1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  HOMEOBOX_2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART HOX UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP SSF46689 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A4D188 ENTREZGENE
  HXA13_HUMAN UniProtKB/Swiss-Prot
  I6N936_HUMAN UniProtKB/TrEMBL
  O43371 ENTREZGENE
  P31271 ENTREZGENE
  Q6DI00 ENTREZGENE, UniProtKB/TrEMBL
UniProt Secondary A4D188 UniProtKB/Swiss-Prot
  O43371 UniProtKB/Swiss-Prot