ITSN1 (intersectin 1) - Rat Genome Database

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Gene: ITSN1 (intersectin 1) Homo sapiens
Analyze
Symbol: ITSN1
Name: intersectin 1
RGD ID: 737072
HGNC Page HGNC:6183
Description: Enables molecular adaptor activity and proline-rich region binding activity. Involved in protein localization. Located in several cellular components, including clathrin-coated pit; nuclear envelope; and plasma membrane.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: human intersectin-SH3 domain-containing protein SH3P17; intersectin 1 (SH3 domain protein); intersectin 1 short form variant 3; intersectin 1 short form variant, 11; intersectin short variant 12; intersectin-1; ITSN; MGC134948; MGC134949; SH3 domain protein-1A; SH3 domain-containing protein 1A; SH3D1A; SH3P17; Src homology 3 domain-containing protein
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Orthologs
More Info more info ...
Related Pseudogenes: LOC645763  
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh382133,642,501 - 33,899,861 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl2133,642,400 - 33,899,861 (+)EnsemblGRCh38hg38GRCh38
GRCh372135,014,807 - 35,272,165 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 362133,936,654 - 34,183,479 (+)NCBINCBI36Build 36hg18NCBI36
Build 342133,936,653 - 34,183,479NCBI
Celera2120,214,405 - 20,461,193 (+)NCBICelera
Cytogenetic Map21q22.11NCBI
HuRef2120,493,109 - 20,739,668 (+)NCBIHuRef
CHM1_12134,577,248 - 34,824,084 (+)NCBICHM1_1
T2T-CHM13v2.02132,024,315 - 32,281,564 (+)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
(-)-epigallocatechin 3-gallate  (EXP)
(1->4)-beta-D-glucan  (ISO)
1,2-dichloroethane  (ISO)
2,2',4,4',5,5'-hexachlorobiphenyl  (ISO)
2,2',4,4'-Tetrabromodiphenyl ether  (EXP)
2,2',5,5'-tetrachlorobiphenyl  (ISO)
2,3,7,8-tetrachlorodibenzodioxine  (EXP,ISO)
2,6-dinitrotoluene  (ISO)
2-butoxyethanol  (ISO)
2-methylcholine  (EXP)
3,3',4,4',5-pentachlorobiphenyl  (EXP,ISO)
3,4-methylenedioxymethamphetamine  (ISO)
4,4'-sulfonyldiphenol  (EXP)
4-hydroxynon-2-enal  (EXP)
5-fluorouracil  (EXP)
acrylamide  (ISO)
aflatoxin B1  (EXP)
Aflatoxin B2 alpha  (EXP)
all-trans-retinoic acid  (EXP)
allethrin  (ISO)
ammonium chloride  (ISO)
Aroclor 1254  (ISO)
arsenite(3-)  (EXP)
benzo[a]pyrene  (EXP,ISO)
benzo[a]pyrene diol epoxide I  (EXP)
benzo[e]pyrene  (EXP)
bisphenol A  (ISO)
Bisphenol B  (EXP)
butanal  (EXP)
C60 fullerene  (ISO)
cadmium atom  (EXP)
cadmium dichloride  (EXP)
caffeine  (EXP)
carbon nanotube  (ISO)
chlorpyrifos  (ISO)
cisplatin  (EXP)
clobetasol  (ISO)
clothianidin  (EXP)
cobalt dichloride  (EXP)
copper atom  (ISO)
copper(0)  (ISO)
crocidolite asbestos  (EXP,ISO)
cyclosporin A  (EXP,ISO)
cyhalothrin  (ISO)
cypermethrin  (ISO)
decabromodiphenyl ether  (ISO)
dexamethasone  (ISO)
Diacetoxyscirpenol  (ISO)
dibutyl phthalate  (ISO)
ethanol  (ISO)
fenvalerate  (ISO)
fipronil  (ISO)
formaldehyde  (EXP)
gentamycin  (ISO)
glyphosate  (ISO)
hexadecanoic acid  (EXP)
hydralazine  (EXP)
ivermectin  (EXP)
lidocaine  (ISO)
methapyrilene  (EXP)
methoxychlor  (ISO)
nickel atom  (ISO)
oxaliplatin  (ISO)
ozone  (ISO)
paracetamol  (ISO)
PCB138  (ISO)
perfluorooctane-1-sulfonic acid  (ISO)
perfluorooctanoic acid  (ISO)
phenobarbital  (ISO)
pirinixic acid  (ISO)
potassium chromate  (EXP)
pyrethrins  (ISO)
quercetin  (EXP)
sodium fluoride  (ISO)
sunitinib  (EXP)
tert-butyl hydroperoxide  (EXP)
testosterone  (EXP,ISO)
tetrachloromethane  (ISO)
tetraphene  (ISO)
thioacetamide  (ISO)
topotecan  (ISO)
trichloroethene  (ISO)
triptonide  (ISO)
valproic acid  (EXP,ISO)

Gene Ontology Annotations     Click to see Annotation Detail View

Molecular Function

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

Human Phenotype
References

References - curated
# Reference Title Reference Citation
1. GOAs Human GO annotations GOA_HUMAN data from the GO Consortium
2. PID Annotation Import Pipeline Pipeline to import Pathway Interaction Database annotations from NCI into RGD
3. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
4. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
5. Synaptic vesicle endocytosis. Saheki Y and De Camilli P, Cold Spring Harb Perspect Biol. 2012 Sep 1;4(9):a005645. doi: 10.1101/cshperspect.a005645.
6. Transcriptomic characteristics of bronchoalveolar lavage fluid and peripheral blood mononuclear cells in COVID-19 patients. Xiong Y, etal., Emerg Microbes Infect. 2020 Dec;9(1):761-770. doi: 10.1080/22221751.2020.1747363.
Additional References at PubMed
PMID:9465890   PMID:9630982   PMID:9799604   PMID:9813051   PMID:10064583   PMID:10072581   PMID:10373452   PMID:10482960   PMID:10716926   PMID:10777571   PMID:10830953   PMID:10922467  
PMID:11381094   PMID:11584276   PMID:11690630   PMID:11744688   PMID:11756498   PMID:12006984   PMID:12376548   PMID:12389031   PMID:12477932   PMID:12787561   PMID:12812986   PMID:12960435  
PMID:12970366   PMID:14702039   PMID:15203208   PMID:15231748   PMID:15256501   PMID:15302935   PMID:15719014   PMID:15824104   PMID:15834155   PMID:16169070   PMID:16442855   PMID:16696976  
PMID:16874303   PMID:16903783   PMID:16914641   PMID:17081983   PMID:17140284   PMID:17405881   PMID:18029348   PMID:18067320   PMID:18539136   PMID:18654987   PMID:18692052   PMID:19166927  
PMID:19356586   PMID:19777371   PMID:20448150   PMID:20493827   PMID:20659428   PMID:20842712   PMID:20936779   PMID:20946875   PMID:21129155   PMID:21503949   PMID:21653829   PMID:21712076  
PMID:21873635   PMID:21876463   PMID:21900206   PMID:22266851   PMID:22558309   PMID:22648170   PMID:22745667   PMID:22750298   PMID:22939629   PMID:23873930   PMID:23936226   PMID:24284073  
PMID:24458657   PMID:24463507   PMID:25036637   PMID:25201988   PMID:25496667   PMID:25621899   PMID:25783631   PMID:25832561   PMID:26037503   PMID:26186194   PMID:26344197   PMID:26496610  
PMID:26613292   PMID:27237791   PMID:27670116   PMID:28161632   PMID:28484035   PMID:28514442   PMID:28718761   PMID:28787396   PMID:28986522   PMID:29030480   PMID:29117863   PMID:29395067  
PMID:29467281   PMID:29507755   PMID:29568061   PMID:29676528   PMID:29851086   PMID:29887380   PMID:29958948   PMID:30540523   PMID:31160551   PMID:31413325   PMID:31452512   PMID:31462741  
PMID:31732153   PMID:31871319   PMID:32203420   PMID:32315611   PMID:32780150   PMID:33277362   PMID:33417976   PMID:33644029   PMID:33957083   PMID:33961781   PMID:34079125   PMID:34299191  
PMID:34369648   PMID:34625530   PMID:34672954   PMID:34702444   PMID:34707297   PMID:34761192   PMID:35044719   PMID:35271311   PMID:35384245   PMID:35439318   PMID:35914814   PMID:35944360  
PMID:36171198   PMID:36215168   PMID:37219487  


Genomics

Comparative Map Data
ITSN1
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh382133,642,501 - 33,899,861 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl2133,642,400 - 33,899,861 (+)EnsemblGRCh38hg38GRCh38
GRCh372135,014,807 - 35,272,165 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 362133,936,654 - 34,183,479 (+)NCBINCBI36Build 36hg18NCBI36
Build 342133,936,653 - 34,183,479NCBI
Celera2120,214,405 - 20,461,193 (+)NCBICelera
Cytogenetic Map21q22.11NCBI
HuRef2120,493,109 - 20,739,668 (+)NCBIHuRef
CHM1_12134,577,248 - 34,824,084 (+)NCBICHM1_1
T2T-CHM13v2.02132,024,315 - 32,281,564 (+)NCBIT2T-CHM13v2.0
Itsn1
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391691,526,198 - 91,717,479 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl1691,526,169 - 91,717,485 (+)EnsemblGRCm39 Ensembl
GRCm381691,729,310 - 91,920,591 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1691,729,281 - 91,920,597 (+)EnsemblGRCm38mm10GRCm38
MGSCv371691,729,616 - 91,920,824 (+)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv361691,671,052 - 91,800,868 (+)NCBIMGSCv36mm8
Celera1692,808,009 - 93,004,876 (+)NCBICelera
Cytogenetic Map16C4NCBI
cM Map1653.28NCBI
Itsn1
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr81144,464,515 - 44,646,598 (+)NCBIGRCr8
mRatBN7.21130,978,590 - 31,160,645 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl1130,978,590 - 31,160,645 (+)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx1139,672,533 - 39,854,583 (+)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.01132,343,963 - 32,526,016 (+)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.01131,506,203 - 31,688,572 (+)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.01131,943,119 - 32,069,249 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl1131,893,489 - 32,069,249 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.01135,547,331 - 35,672,959 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41131,721,528 - 31,901,963 (+)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.11131,815,217 - 31,903,071 (+)NCBI
Celera1130,687,099 - 30,812,424 (+)NCBICelera
Cytogenetic Map11q11NCBI
Itsn1
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_00495540733,113,319 - 33,275,675 (+)EnsemblChiLan1.0
ChiLan1.0NW_00495540733,056,004 - 33,275,681 (+)NCBIChiLan1.0ChiLan1.0
ITSN1
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v22229,759,728 - 30,017,340 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan12124,617,929 - 24,875,764 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v02120,009,385 - 20,266,835 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.12133,381,640 - 33,625,603 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl2133,457,081 - 33,625,248 (+)Ensemblpanpan1.1panPan2
ITSN1
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.13129,144,754 - 29,360,134 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha3128,243,620 - 28,459,926 (+)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.03128,451,006 - 28,667,391 (+)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl3128,451,116 - 28,661,479 (+)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.13128,317,804 - 28,534,014 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.03128,331,715 - 28,548,460 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.03128,831,446 - 29,047,794 (+)NCBIUU_Cfam_GSD_1.0
Itsn1
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440497128,789,742 - 28,977,174 (+)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_0049365008,468,940 - 8,612,942 (-)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_0049365008,490,514 - 8,678,127 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
ITSN1
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl13197,249,061 - 197,481,245 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.113197,301,515 - 197,492,537 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.213207,205,545 - 207,267,672 (-)NCBISscrofa10.2Sscrofa10.2susScr3
ITSN1
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.1258,298,529 - 58,543,297 (-)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl258,301,399 - 58,543,281 (-)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_023666071805,376 - 1,047,516 (-)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Itsn1
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_00462474521,906,187 - 22,050,822 (+)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_00462474521,847,593 - 22,055,141 (+)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in ITSN1
168 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 21p11.2-q22.3(chr21:7749532-46670405)x3 copy number gain See cases [RCV000050445] Chr21:7749532..46670405 [GRCh38]
Chr21:15499847..48090317 [GRCh37]
Chr21:14421718..46914745 [NCBI36]
Chr21:21p11.2-q22.3		 pathogenic|conflicting interpretations of pathogenicity|conflicting data from submitters
GRCh38/hg38 21q22.11(chr21:33437186-33767838)x3 copy number gain See cases [RCV000052797] Chr21:33437186..33767838 [GRCh38]
Chr21:34809493..35140142 [GRCh37]
Chr21:33731363..34062012 [NCBI36]
Chr21:21q22.11		 uncertain significance
GRCh38/hg38 21q22.11(chr21:33465408-33806416)x1 copy number loss See cases [RCV000052806] Chr21:33465408..33806416 [GRCh38]
Chr21:34837715..35178720 [GRCh37]
Chr21:33759585..34100590 [NCBI36]
Chr21:21q22.11		 pathogenic
GRCh38/hg38 21p11.2-q22.3(chr21:7749532-46623792)x3 copy number gain See cases [RCV000053042] Chr21:7749532..46623792 [GRCh38]
Chr21:14595524..48043704 [GRCh37]
Chr21:13517395..46868132 [NCBI36]
Chr21:21p11.2-q22.3		 pathogenic
GRCh38/hg38 21p11.2-q22.3(chr21:7749532-46623792)x3 copy number gain See cases [RCV000053043] Chr21:7749532..46623792 [GRCh38]
Chr21:14629063..48043704 [GRCh37]
Chr21:13550934..46868132 [NCBI36]
Chr21:21p11.2-q22.3		 pathogenic
GRCh38/hg38 21p11.2-q22.3(chr21:7749532-46670546)x3 copy number gain See cases [RCV000053045] Chr21:7749532..46670546 [GRCh38]
Chr21:15499647..48090458 [GRCh37]
Chr21:14421518..46914886 [NCBI36]
Chr21:21p11.2-q22.3		 pathogenic
GRCh38/hg38 21p11.2-q22.3(chr21:7749532-46661140)x3 copy number gain See cases [RCV000053065] Chr21:7749532..46661140 [GRCh38]
Chr21:15499647..48081052 [GRCh37]
Chr21:14421518..46905480 [NCBI36]
Chr21:21p11.2-q22.3		 pathogenic
GRCh38/hg38 21p11.2-q22.3(chr21:7749532-46661140)x3 copy number gain See cases [RCV000053067] Chr21:7749532..46661140 [GRCh38]
Chr21:15499847..48081052 [GRCh37]
Chr21:14421718..46905480 [NCBI36]
Chr21:21p11.2-q22.3		 pathogenic
GRCh38/hg38 21p11.2-q22.3(chr21:7749532-46670405)x3 copy number gain See cases [RCV000053068] Chr21:7749532..46670405 [GRCh38]
Chr21:20655360..48090317 [GRCh37]
Chr21:19577231..46914745 [NCBI36]
Chr21:21p11.2-q22.3		 pathogenic
GRCh38/hg38 21p11.2-q22.3(chr21:7749532-46670405)x3 copy number gain See cases [RCV000053069] Chr21:7749532..46670405 [GRCh38]
Chr21:34423268..48090317 [GRCh37]
Chr21:33345138..46914745 [NCBI36]
Chr21:21p11.2-q22.3		 pathogenic
GRCh38/hg38 21p11.2-q22.3(chr21:7749532-46623792)x3 copy number gain See cases [RCV000053039] Chr21:7749532..46623792 [GRCh38]
Chr21:14524963..48043704 [GRCh37]
Chr21:13446834..46868132 [NCBI36]
Chr21:21p11.2-q22.3		 pathogenic
GRCh38/hg38 21p11.2-q22.3(chr21:7749532-46653090)x3 copy number gain See cases [RCV000053040] Chr21:7749532..46653090 [GRCh38]
Chr21:14539679..48073002 [GRCh37]
Chr21:13461550..46897430 [NCBI36]
Chr21:21p11.2-q22.3		 pathogenic
NM_003024.2(ITSN1):c.2175C>T (p.Ser725=) single nucleotide variant Malignant melanoma [RCV000072822] Chr21:33797601 [GRCh38]
Chr21:35169905 [GRCh37]
Chr21:34091775 [NCBI36]
Chr21:21q22.11		 not provided
NM_003024.2(ITSN1):c.2398T>A (p.Tyr800Asn) single nucleotide variant Malignant melanoma [RCV000072823] Chr21:33811053 [GRCh38]
Chr21:35183357 [GRCh37]
Chr21:34105227 [NCBI36]
Chr21:21q22.11		 not provided
NM_003024.2(ITSN1):c.3484G>C (p.Gly1162Arg) single nucleotide variant Malignant melanoma [RCV000072824] Chr21:33836455 [GRCh38]
Chr21:35208759 [GRCh37]
Chr21:34130629 [NCBI36]
Chr21:21q22.11		 not provided
NM_003024.2(ITSN1):c.5088G>A (p.Thr1696=) single nucleotide variant Malignant melanoma [RCV000072825] Chr21:33888222 [GRCh38]
Chr21:35260526 [GRCh37]
Chr21:34182396 [NCBI36]
Chr21:21q22.11		 not provided
NM_003024.2(ITSN1):c.4026G>A (p.Leu1342=) single nucleotide variant Malignant melanoma [RCV000063823] Chr21:33865286 [GRCh38]
Chr21:35237590 [GRCh37]
Chr21:34159460 [NCBI36]
Chr21:21q22.11		 not provided
GRCh38/hg38 21p11.2-q22.3(chr21:7749532-42971047)x3 copy number gain See cases [RCV000133676] Chr21:7749532..42971047 [GRCh38]
Chr21:15499847..44391157 [GRCh37]
Chr21:14421718..43264226 [NCBI36]
Chr21:21p11.2-q22.3		 pathogenic
GRCh38/hg38 21p11.2-q22.3(chr21:7749532-46653084)x3 copy number gain See cases [RCV000134727] Chr21:7749532..46653084 [GRCh38]
Chr21:15485038..48072996 [GRCh37]
Chr21:14406909..46897424 [NCBI36]
Chr21:21p11.2-q22.3		 pathogenic
GRCh38/hg38 21q11.2-22.3(chr21:7749532-46649831)x3 copy number gain See cases [RCV000134509] Chr21:7749532..46649831 [GRCh38]
Chr21:14577835..48069743 [GRCh37]
Chr21:13499706..46894171 [NCBI36]
Chr21:21q11.2-22.3		 pathogenic
GRCh38/hg38 21p11.2-q22.3(chr21:7749532-46670440)x3 copy number gain See cases [RCV000134119] Chr21:7749532..46670440 [GRCh38]
Chr21:15485038..48090352 [GRCh37]
Chr21:14406909..46914780 [NCBI36]
Chr21:21p11.2-q22.3		 pathogenic
GRCh38/hg38 21q22.11-22.3(chr21:7749532-46670346)x3 copy number gain See cases [RCV000135310] Chr21:7749532..46670346 [GRCh38]
Chr21:34111831..48090258 [GRCh37]
Chr21:33033702..46914686 [NCBI36]
Chr21:21q22.11-22.3		 pathogenic
GRCh38/hg38 21p11.2-q22.3(chr21:7749532-46664250)x3 copy number gain See cases [RCV000134836] Chr21:7749532..46664250 [GRCh38]
Chr21:15485038..48084162 [GRCh37]
Chr21:14406909..46908590 [NCBI36]
Chr21:21p11.2-q22.3		 pathogenic
GRCh38/hg38 21p11.2-q22.3(chr21:7749532-46670440)x3 copy number gain See cases [RCV000134842] Chr21:7749532..46670440 [GRCh38]
Chr21:15513244..48090352 [GRCh37]
Chr21:14435115..46914780 [NCBI36]
Chr21:21p11.2-q22.3		 pathogenic
GRCh38/hg38 21p11.2-q22.3(chr21:7749532-46660999)x3 copy number gain See cases [RCV000135448] Chr21:7749532..46660999 [GRCh38]
Chr21:15499847..48080911 [GRCh37]
Chr21:14421718..46905339 [NCBI36]
Chr21:21p11.2-q22.3		 pathogenic
GRCh37/hg19 21q22.11-22.12(chr21:34997018-36118212)x3 copy number gain See cases [RCV000136827] Chr21:34997018..36118212 [GRCh37]
Chr21:33918888..35040082 [NCBI36]
Chr21:21q22.11-22.12		 pathogenic
GRCh38/hg38 21p11.2-q22.3(chr21:7749532-46671060)x3 copy number gain See cases [RCV000137255] Chr21:7749532..46671060 [GRCh38]
Chr21:35319225..48090972 [GRCh37]
Chr21:34241095..46915400 [NCBI36]
Chr21:21p11.2-q22.3		 pathogenic
GRCh38/hg38 21p11.2-q22.3(chr21:7749532-46671060)x3 copy number gain See cases [RCV000137337] Chr21:7749532..46671060 [GRCh38]
Chr21:10697897..48090972 [GRCh37]
Chr21:1..46915400 [NCBI36]
Chr21:21p11.2-q22.3		 pathogenic
GRCh38/hg38 21p11.2-q22.13(chr21:7749532-37653653)x1 copy number loss See cases [RCV000138095] Chr21:7749532..37653653 [GRCh38]
Chr21:15451032..39025955 [GRCh37]
Chr21:14372903..37947825 [NCBI36]
Chr21:21p11.2-q22.13		 pathogenic
GRCh38/hg38 21p11.2-q22.3(chr21:7749532-46671060)x3 copy number gain See cases [RCV000138216] Chr21:7749532..46671060 [GRCh38]
Chr21:10944001..48090972 [GRCh37]
Chr21:9965872..46915400 [NCBI36]
Chr21:21p11.2-q22.3		 pathogenic
GRCh38/hg38 21p11.2-q22.3(chr21:7749532-46671060)x3 copy number gain See cases [RCV000138436] Chr21:7749532..46671060 [GRCh38]
Chr21:15451032..48090972 [GRCh37]
Chr21:14372903..46915400 [NCBI36]
Chr21:21p11.2-q22.3		 pathogenic|conflicting data from submitters
GRCh38/hg38 21q22.11(chr21:33361172-34048047)x1 copy number loss See cases [RCV000140099] Chr21:33361172..34048047 [GRCh38]
Chr21:34733478..35420347 [GRCh37]
Chr21:33655348..34342217 [NCBI36]
Chr21:21q22.11		 likely pathogenic
GRCh38/hg38 21q11.2-22.3(chr21:7749532-46670346)x3 copy number gain See cases [RCV000140103] Chr21:7749532..46670346 [GRCh38]
Chr21:14577894..48090258 [GRCh37]
Chr21:13499765..46914686 [NCBI36]
Chr21:21q11.2-22.3		 pathogenic
GRCh38/hg38 21q11.2-22.3(chr21:7749532-46698247)x3 copy number gain See cases [RCV000141346] Chr21:7749532..46698247 [GRCh38]
Chr21:14577835..48118159 [GRCh37]
Chr21:13499706..46942587 [NCBI36]
Chr21:21q11.2-22.3		 pathogenic
GRCh38/hg38 21q21.3-22.3(chr21:7749532-46677460)x3 copy number gain See cases [RCV000141827] Chr21:7749532..46677460 [GRCh38]
Chr21:28285299..48097372 [GRCh37]
Chr21:27207170..46921800 [NCBI36]
Chr21:21q21.3-22.3		 uncertain significance
GRCh37/hg19 21q21.3-22.12(chr21:29880468-36062331)x1 copy number loss See cases [RCV000141575] Chr21:29880468..36062331 [GRCh37]
Chr21:28802339..34984201 [NCBI36]
Chr21:21q21.3-22.12		 pathogenic
GRCh38/hg38 21p11.2-q22.3(chr21:7817158-46670440)x1 copy number loss See cases [RCV000142427] Chr21:7817158..46670440 [GRCh38]
Chr21:15485038..48090352 [GRCh37]
Chr21:14406909..46914780 [NCBI36]
Chr21:21p11.2-q22.3		 pathogenic
GRCh38/hg38 21q11.2-22.3(chr21:7749532-46677460)x3 copy number gain See cases [RCV000143120] Chr21:7749532..46677460 [GRCh38]
Chr21:15006457..48097372 [GRCh37]
Chr21:13928328..46921800 [NCBI36]
Chr21:21q11.2-22.3		 pathogenic
GRCh38/hg38 21q11.2-22.3(chr21:7749532-46677460)x3 copy number gain See cases [RCV000143376] Chr21:7749532..46677460 [GRCh38]
Chr21:15006458..48097372 [GRCh37]
Chr21:13928329..46921800 [NCBI36]
Chr21:21q11.2-22.3		 pathogenic
GRCh38/hg38 21q11.2-22.3(chr21:7749532-46677460) copy number gain See cases [RCV000143160] Chr21:7749532..46677460 [GRCh38]
Chr21:14386013..48097372 [GRCh37]
Chr21:13307884..46921800 [NCBI36]
Chr21:21q11.2-22.3		 pathogenic
GRCh38/hg38 21p11.2-q22.3(chr21:7749532-46670405)x3 copy number gain See cases [RCV000148131] Chr21:7749532..46670405 [GRCh38]
Chr21:15499847..48090317 [GRCh37]
Chr21:14421718..46914745 [NCBI36]
Chr21:21p11.2-q22.3		 pathogenic
NC_000021.8:g.35027142_35056247del deletion Preeclampsia [RCV000161896] Chr21:35027142..35056247 [GRCh37]
Chr21:21q22.11		 not provided
NM_003024.3(ITSN1):c.2227G>T (p.Val743Leu) single nucleotide variant Inborn genetic diseases [RCV000210640] Chr21:33799852 [GRCh38]
Chr21:35172156 [GRCh37]
Chr21:21q22.11		 pathogenic|likely pathogenic
GRCh37/hg19 21q11.2-22.3(chr21:15538655-48080926)x1 copy number loss See cases [RCV000239948] Chr21:15538655..48080926 [GRCh37]
Chr21:21q11.2-22.3		 pathogenic
GRCh37/hg19 21q11.2-22.3(chr21:15410701-48090317)x3 copy number gain See cases [RCV000240397] Chr21:15410701..48090317 [GRCh37]
Chr21:21q11.2-22.3		 pathogenic
GRCh37/hg19 21q22.11(chr21:32578640-35060092)x1 copy number loss See cases [RCV000240540] Chr21:32578640..35060092 [GRCh37]
Chr21:21q22.11		 pathogenic
NM_003024.3(ITSN1):c.1726G>T (p.Glu576Ter) single nucleotide variant Autistic behavior [RCV001579320] Chr21:33782035 [GRCh38]
Chr21:35154339 [GRCh37]
Chr21:21q22.11		 uncertain significance
GRCh37/hg19 21q22.11(chr21:35235463-35289266)x3 copy number gain See cases [RCV000449329] Chr21:35235463..35289266 [GRCh37]
Chr21:21q22.11		 uncertain significance
GRCh37/hg19 21q11.2-22.3(chr21:15006457-43598570)x3 copy number gain See cases [RCV000446716] Chr21:15006457..43598570 [GRCh37]
Chr21:21q11.2-22.3		 pathogenic
GRCh37/hg19 21q21.3-22.13(chr21:29812033-39282854)x3 copy number gain See cases [RCV000448874] Chr21:29812033..39282854 [GRCh37]
Chr21:21q21.3-22.13		 pathogenic
GRCh37/hg19 21q11.2-22.3(chr21:14771770-48080867)x3 copy number gain See cases [RCV000447884] Chr21:14771770..48080867 [GRCh37]
Chr21:21q11.2-22.3		 pathogenic
GRCh37/hg19 21q11.2-22.3(chr21:15006457-44827632)x3 copy number gain See cases [RCV000448199] Chr21:15006457..44827632 [GRCh37]
Chr21:21q11.2-22.3		 pathogenic
GRCh37/hg19 21q11.2-22.3(chr21:15285841-48097372)x3 copy number gain See cases [RCV000447729] Chr21:15285841..48097372 [GRCh37]
Chr21:21q11.2-22.3		 pathogenic
GRCh37/hg19 21q11.2-22.3(chr21:15006457-48097372)x3 copy number gain See cases [RCV000447749] Chr21:15006457..48097372 [GRCh37]
Chr21:21q11.2-22.3		 pathogenic
GRCh37/hg19 21q11.2-22.3(chr21:15006458-48097372) copy number gain See cases [RCV000511589] Chr21:15006458..48097372 [GRCh37]
Chr21:21q11.2-22.3		 pathogenic
NM_003024.3(ITSN1):c.1742A>C (p.His581Pro) single nucleotide variant Inborn genetic diseases [RCV003282261] Chr21:33782051 [GRCh38]
Chr21:35154355 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_003024.3(ITSN1):c.2482G>A (p.Ala828Thr) single nucleotide variant Inborn genetic diseases [RCV003242339] Chr21:33811137 [GRCh38]
Chr21:35183441 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_003024.3(ITSN1):c.3452C>T (p.Ser1151Leu) single nucleotide variant Inborn genetic diseases [RCV003290465] Chr21:33834407 [GRCh38]
Chr21:35206711 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_003024.3(ITSN1):c.4436A>G (p.Tyr1479Cys) single nucleotide variant Inborn genetic diseases [RCV003285446] Chr21:33882337 [GRCh38]
Chr21:35254641 [GRCh37]
Chr21:21q22.11		 uncertain significance
GRCh37/hg19 21q22.11(chr21:35210724-35346920)x3 copy number gain not provided [RCV000585572] Chr21:35210724..35346920 [GRCh37]
Chr21:21q22.11		 likely benign
GRCh37/hg19 21q22.11-22.2(chr21:33980213-42542987)x3 copy number gain not provided [RCV000684166] Chr21:33980213..42542987 [GRCh37]
Chr21:21q22.11-22.2		 pathogenic
NM_003024.3(ITSN1):c.1222G>T (p.Glu408Ter) single nucleotide variant not provided [RCV000678374] Chr21:33772240 [GRCh38]
Chr21:35144544 [GRCh37]
Chr21:21q22.11		 uncertain significance
GRCh37/hg19 21q22.11(chr21:34281910-35748170)x1 copy number loss not provided [RCV000709834] Chr21:34281910..35748170 [GRCh37]
Chr21:21q22.11		 not provided
GRCh37/hg19 21p11.2-q22.3(chr21:10827533-48100155)x3 copy number gain not provided [RCV000741419] Chr21:10827533..48100155 [GRCh37]
Chr21:21p11.2-q22.3		 pathogenic
GRCh37/hg19 21q22.11(chr21:34925753-35020161)x3 copy number gain not provided [RCV000741540] Chr21:34925753..35020161 [GRCh37]
Chr21:21q22.11		 benign
GRCh37/hg19 21p11.2-q22.3(chr21:10699330-48117896)x3 copy number gain not provided [RCV000741413] Chr21:10699330..48117896 [GRCh37]
Chr21:21p11.2-q22.3		 pathogenic
GRCh37/hg19 21p11.2-q22.3(chr21:10704198-48117896)x3 copy number gain not provided [RCV000741415] Chr21:10704198..48117896 [GRCh37]
Chr21:21p11.2-q22.3		 pathogenic
GRCh37/hg19 21p11.2-q22.3(chr21:10824040-48090629)x3 copy number gain not provided [RCV000741418] Chr21:10824040..48090629 [GRCh37]
Chr21:21p11.2-q22.3		 pathogenic
NM_003024.3(ITSN1):c.3890+192A>G single nucleotide variant not provided [RCV001680053] Chr21:33858984 [GRCh38]
Chr21:35231288 [GRCh37]
Chr21:21q22.11		 benign
NM_003024.3(ITSN1):c.623+42A>G single nucleotide variant not provided [RCV001679481] Chr21:33751948 [GRCh38]
Chr21:35124253 [GRCh37]
Chr21:21q22.11		 benign
NM_003024.3(ITSN1):c.3256A>G (p.Thr1086Ala) single nucleotide variant not provided [RCV003314852] Chr21:33829650 [GRCh38]
Chr21:35201954 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_003024.3(ITSN1):c.3469+152A>G single nucleotide variant not provided [RCV001647842] Chr21:33834576 [GRCh38]
Chr21:35206880 [GRCh37]
Chr21:21q22.11		 benign
NM_003024.3(ITSN1):c.789-5A>G single nucleotide variant ITSN1-related condition [RCV003935999]|not provided [RCV000965488] Chr21:33765870 [GRCh38]
Chr21:35138174 [GRCh37]
Chr21:21q22.11		 benign
NM_003024.3(ITSN1):c.450T>C (p.Val150=) single nucleotide variant ITSN1-related condition [RCV003962848]|not provided [RCV000968410] Chr21:33750246 [GRCh38]
Chr21:35122551 [GRCh37]
Chr21:21q22.11		 benign
GRCh37/hg19 21q22.11(chr21:32589903-35359935) copy number loss not provided [RCV000767744] Chr21:32589903..35359935 [GRCh37]
Chr21:21q22.11		 pathogenic
NM_003024.3(ITSN1):c.3321C>T (p.Asn1107=) single nucleotide variant not provided [RCV000919798] Chr21:33829715 [GRCh38]
Chr21:35202019 [GRCh37]
Chr21:21q22.11		 likely benign
NM_003024.3(ITSN1):c.3469+7A>C single nucleotide variant ITSN1-related condition [RCV003936075]|not provided [RCV000969126] Chr21:33834431 [GRCh38]
Chr21:35206735 [GRCh37]
Chr21:21q22.11		 benign
NM_003024.3(ITSN1):c.927-10G>A single nucleotide variant ITSN1-related condition [RCV003928457]|not provided [RCV000969125] Chr21:33767703 [GRCh38]
Chr21:35140007 [GRCh37]
Chr21:21q22.11		 benign
NM_003024.3(ITSN1):c.5162C>T (p.Pro1721Leu) single nucleotide variant not provided [RCV000997827] Chr21:33888296 [GRCh38]
Chr21:35260600 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_003024.3(ITSN1):c.298C>T (p.Pro100Ser) single nucleotide variant Inborn genetic diseases [RCV003245152] Chr21:33735156 [GRCh38]
Chr21:35107461 [GRCh37]
Chr21:21q22.11		 uncertain significance
GRCh37/hg19 21q11.2-22.3(chr21:15006457-48097372)x3 copy number gain not provided [RCV000846937] Chr21:15006457..48097372 [GRCh37]
Chr21:21q11.2-22.3		 pathogenic
GRCh37/hg19 21q22.11-22.12(chr21:33205064-36039022) copy number loss 21q22.11q22.12 microdeletion syndrome [RCV001093501] Chr21:33205064..36039022 [GRCh37]
Chr21:21q22.11-22.12		 pathogenic
NC_000021.8:g.(?_35183279)_(35191627_?)del deletion not provided [RCV003105385] Chr21:35183279..35191627 [GRCh37]
Chr21:21q22.11		 pathogenic
NM_003024.3(ITSN1):c.3660A>C (p.Gln1220His) single nucleotide variant not provided [RCV003233417] Chr21:33836631 [GRCh38]
Chr21:35208935 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_003024.3(ITSN1):c.4414G>A (p.Ala1472Thr) single nucleotide variant Inborn genetic diseases [RCV003291070] Chr21:33882315 [GRCh38]
Chr21:35254619 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_003024.3(ITSN1):c.2933+26T>C single nucleotide variant not provided [RCV001643727] Chr21:33818498 [GRCh38]
Chr21:35190802 [GRCh37]
Chr21:21q22.11		 benign
NM_003024.3(ITSN1):c.2894dup (p.Tyr965Ter) duplication Autistic behavior [RCV001579318] Chr21:33818432..33818433 [GRCh38]
Chr21:35190736..35190737 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_003024.3(ITSN1):c.3116G>A (p.Trp1039Ter) single nucleotide variant Autistic behavior [RCV001579324] Chr21:33823586 [GRCh38]
Chr21:35195890 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_003024.3(ITSN1):c.1952+31G>T single nucleotide variant not provided [RCV001643841] Chr21:33794499 [GRCh38]
Chr21:35166803 [GRCh37]
Chr21:21q22.11		 benign
NM_003024.3(ITSN1):c.788+131T>C single nucleotide variant not provided [RCV001684123] Chr21:33762117 [GRCh38]
Chr21:35134421 [GRCh37]
Chr21:21q22.11		 benign
NM_003024.3(ITSN1):c.724+33C>A single nucleotide variant not provided [RCV001635975] Chr21:33755430 [GRCh38]
Chr21:35127735 [GRCh37]
Chr21:21q22.11		 benign
NM_003024.3(ITSN1):c.926+10A>G single nucleotide variant not provided [RCV001688385] Chr21:33766022 [GRCh38]
Chr21:35138326 [GRCh37]
Chr21:21q22.11		 benign
NM_003024.3(ITSN1):c.5018-198del deletion not provided [RCV001608527] Chr21:33887944 [GRCh38]
Chr21:35260248 [GRCh37]
Chr21:21q22.11		 benign
NM_003024.3(ITSN1):c.4174-189G>C single nucleotide variant not provided [RCV001721568] Chr21:33875165 [GRCh38]
Chr21:35247469 [GRCh37]
Chr21:21q22.11		 benign
NM_003024.3(ITSN1):c.4174-198C>T single nucleotide variant not provided [RCV001619699] Chr21:33875156 [GRCh38]
Chr21:35247460 [GRCh37]
Chr21:21q22.11		 benign
NM_003024.3(ITSN1):c.3784-3T>C single nucleotide variant not provided [RCV001656996] Chr21:33858683 [GRCh38]
Chr21:35230987 [GRCh37]
Chr21:21q22.11		 benign
NM_003024.3(ITSN1):c.1566C>T (p.Ala522=) single nucleotide variant ITSN1-related condition [RCV003936182]|not provided [RCV000974153] Chr21:33775078 [GRCh38]
Chr21:35147382 [GRCh37]
Chr21:21q22.11		 benign
NM_003024.3(ITSN1):c.789-2A>G single nucleotide variant Autistic behavior [RCV001579319] Chr21:33765873 [GRCh38]
Chr21:35138177 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_003024.3(ITSN1):c.4354A>T (p.Asn1452Tyr) single nucleotide variant Autistic behavior [RCV001579321] Chr21:33882255 [GRCh38]
Chr21:35254559 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_003024.3(ITSN1):c.-32-237G>C single nucleotide variant not provided [RCV001669563] Chr21:33718560 [GRCh38]
Chr21:35090865 [GRCh37]
Chr21:21q22.11		 benign
NM_003024.3(ITSN1):c.398C>A (p.Pro133Gln) single nucleotide variant not provided [RCV002464704] Chr21:33750194 [GRCh38]
Chr21:35122499 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_003024.3(ITSN1):c.725-140dup duplication not provided [RCV001595895] Chr21:33761779..33761780 [GRCh38]
Chr21:35134084..35134085 [GRCh37]
Chr21:21q22.11		 benign
NM_003024.3(ITSN1):c.2934-158dup duplication not provided [RCV001678055] Chr21:33819082..33819083 [GRCh38]
Chr21:35191386..35191387 [GRCh37]
Chr21:21q22.11		 benign
NM_003024.3(ITSN1):c.2567+5G>A single nucleotide variant not provided [RCV002464703] Chr21:33811227 [GRCh38]
Chr21:35183531 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_003024.3(ITSN1):c.2122C>G (p.Leu708Val) single nucleotide variant Nephrotic syndrome [RCV002472299] Chr21:33797548 [GRCh38]
Chr21:35169852 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_003024.3(ITSN1):c.2934-18C>G single nucleotide variant not provided [RCV001676248] Chr21:33819223 [GRCh38]
Chr21:35191527 [GRCh37]
Chr21:21q22.11		 benign
NM_003024.3(ITSN1):c.526+98A>G single nucleotide variant not provided [RCV001596002] Chr21:33750420 [GRCh38]
Chr21:35122725 [GRCh37]
Chr21:21q22.11		 benign
NM_003024.3(ITSN1):c.3352-212A>G single nucleotide variant not provided [RCV001641510] Chr21:33834095 [GRCh38]
Chr21:35206399 [GRCh37]
Chr21:21q22.11		 benign
NM_003024.3(ITSN1):c.1960C>T (p.Gln654Ter) single nucleotide variant Autistic behavior [RCV001579317] Chr21:33797386 [GRCh38]
Chr21:35169690 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_003024.3(ITSN1):c.1258G>T (p.Glu420Ter) single nucleotide variant Autistic behavior [RCV001579322] Chr21:33772276 [GRCh38]
Chr21:35144580 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_003024.3(ITSN1):c.4676+245_4676+246dup duplication not provided [RCV001598258] Chr21:33883894..33883895 [GRCh38]
Chr21:35256198..35256199 [GRCh37]
Chr21:21q22.11		 benign
NM_003024.3(ITSN1):c.4676+246dup duplication not provided [RCV001595848] Chr21:33883894..33883895 [GRCh38]
Chr21:35256198..35256199 [GRCh37]
Chr21:21q22.11		 benign
NM_003024.3(ITSN1):c.3890+168G>A single nucleotide variant not provided [RCV001598929] Chr21:33858960 [GRCh38]
Chr21:35231264 [GRCh37]
Chr21:21q22.11		 benign
NM_003024.3(ITSN1):c.3784-210G>A single nucleotide variant not provided [RCV001716501] Chr21:33858476 [GRCh38]
Chr21:35230780 [GRCh37]
Chr21:21q22.11		 benign
NM_003024.3(ITSN1):c.723A>G (p.Thr241=) single nucleotide variant not provided [RCV001093467] Chr21:33755396 [GRCh38]
Chr21:35127701 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_003024.3(ITSN1):c.1389_1392del (p.Lys463fs) deletion Autistic behavior [RCV001579323] Chr21:33774810..33774813 [GRCh38]
Chr21:35147114..35147117 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_003024.3(ITSN1):c.1952+173A>G single nucleotide variant not provided [RCV001693075] Chr21:33794641 [GRCh38]
Chr21:35166945 [GRCh37]
Chr21:21q22.11		 benign
NM_003024.3(ITSN1):c.122-29dup duplication not provided [RCV001695451] Chr21:33722544..33722545 [GRCh38]
Chr21:35094849..35094850 [GRCh37]
Chr21:21q22.11		 benign
NM_003024.3(ITSN1):c.4676+25T>A single nucleotide variant not provided [RCV001686054] Chr21:33883696 [GRCh38]
Chr21:35256000 [GRCh37]
Chr21:21q22.11		 benign
NM_003024.3(ITSN1):c.2568-158TTTA[5] microsatellite not provided [RCV001609885] Chr21:33813754..33813755 [GRCh38]
Chr21:35186058..35186059 [GRCh37]
Chr21:21q22.11		 benign
NM_003024.3(ITSN1):c.2568-76dup duplication not provided [RCV001667276] Chr21:33813823..33813824 [GRCh38]
Chr21:35186127..35186128 [GRCh37]
Chr21:21q22.11		 benign
NM_003024.3(ITSN1):c.3891-106A>G single nucleotide variant not provided [RCV001679063] Chr21:33865045 [GRCh38]
Chr21:35237349 [GRCh37]
Chr21:21q22.11		 benign
NM_003024.3(ITSN1):c.4174-47G>A single nucleotide variant not provided [RCV001708864] Chr21:33875307 [GRCh38]
Chr21:35247611 [GRCh37]
Chr21:21q22.11		 benign
NM_003024.3(ITSN1):c.4100A>G (p.Lys1367Arg) single nucleotide variant not provided [RCV001693616] Chr21:33867258 [GRCh38]
Chr21:35239562 [GRCh37]
Chr21:21q22.11		 benign
NM_003024.3(ITSN1):c.4342-94T>G single nucleotide variant not provided [RCV001536572] Chr21:33882149 [GRCh38]
Chr21:35254453 [GRCh37]
Chr21:21q22.11		 benign
NM_003024.3(ITSN1):c.624-242A>G single nucleotide variant not provided [RCV001648593] Chr21:33755055 [GRCh38]
Chr21:35127360 [GRCh37]
Chr21:21q22.11		 benign
NM_003024.3(ITSN1):c.3662-87A>G single nucleotide variant not provided [RCV001539039] Chr21:33856649 [GRCh38]
Chr21:35228953 [GRCh37]
Chr21:21q22.11		 benign
NM_003024.3(ITSN1):c.3784-69G>C single nucleotide variant not provided [RCV001642193] Chr21:33858617 [GRCh38]
Chr21:35230921 [GRCh37]
Chr21:21q22.11		 benign
NM_003024.3(ITSN1):c.4341+48C>G single nucleotide variant not provided [RCV001690552] Chr21:33875569 [GRCh38]
Chr21:35247873 [GRCh37]
Chr21:21q22.11		 benign
NM_003024.3(ITSN1):c.5043T>C (p.Arg1681=) single nucleotide variant not provided [RCV001613626] Chr21:33888177 [GRCh38]
Chr21:35260481 [GRCh37]
Chr21:21q22.11		 benign
NM_003024.3(ITSN1):c.4676+244_4676+246dup duplication not provided [RCV001693054] Chr21:33883894..33883895 [GRCh38]
Chr21:35256198..35256199 [GRCh37]
Chr21:21q22.11		 benign
NM_003024.3(ITSN1):c.4381C>T (p.Arg1461Cys) single nucleotide variant Tracheoesophageal fistula [RCV001172294]|not provided [RCV002462339] Chr21:33882282 [GRCh38]
Chr21:35254586 [GRCh37]
Chr21:21q22.11		 likely pathogenic|uncertain significance
GRCh37/hg19 21q22.11(chr21:34379096-35572731)x1 copy number loss not provided [RCV001259407] Chr21:34379096..35572731 [GRCh37]
Chr21:21q22.11		 pathogenic
GRCh37/hg19 21q22.11(chr21:34999977-35131913)x1 copy number loss not provided [RCV001259410] Chr21:34999977..35131913 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_003024.3(ITSN1):c.2191C>T (p.Pro731Ser) single nucleotide variant Inborn genetic diseases [RCV001266623] Chr21:33799816 [GRCh38]
Chr21:35172120 [GRCh37]
Chr21:21q22.11		 uncertain significance
GRCh37/hg19 21q11.2-22.3(chr21:14629063-48090317)x3 copy number gain See cases [RCV001263025] Chr21:14629063..48090317 [GRCh37]
Chr21:21q11.2-22.3		 pathogenic
NC_000021.8:g.(?_32439271)_(37133458_?)dup duplication Early-onset Parkinson disease 20 [RCV001338842] Chr21:32439271..37133458 [GRCh37]
Chr21:21q22.11-22.12		 uncertain significance
GRCh37/hg19 21q11.2-22.3(chr21:14420615-48080926)x3 copy number gain Complete trisomy 21 syndrome [RCV002284306] Chr21:14420615..48080926 [GRCh37]
Chr21:21q11.2-22.3		 pathogenic
NM_003024.3(ITSN1):c.5106C>T (p.His1702=) single nucleotide variant not provided [RCV001536656] Chr21:33888240 [GRCh38]
Chr21:35260544 [GRCh37]
Chr21:21q22.11		 benign
NM_003024.3(ITSN1):c.4075-132A>T single nucleotide variant not provided [RCV001536858] Chr21:33867101 [GRCh38]
Chr21:35239405 [GRCh37]
Chr21:21q22.11		 benign
NM_003024.3(ITSN1):c.4173+99C>T single nucleotide variant not provided [RCV001725440] Chr21:33867430 [GRCh38]
Chr21:35239734 [GRCh37]
Chr21:21q22.11		 benign
NM_003024.3(ITSN1):c.4044T>C (p.Asp1348=) single nucleotide variant not provided [RCV001691398] Chr21:33865304 [GRCh38]
Chr21:35237608 [GRCh37]
Chr21:21q22.11		 benign
NM_003024.3(ITSN1):c.5018-37_5018-30del deletion not provided [RCV001615931] Chr21:33888115..33888122 [GRCh38]
Chr21:35260419..35260426 [GRCh37]
Chr21:21q22.11		 benign
NM_003024.3(ITSN1):c.3249C>T (p.Ala1083=) single nucleotide variant not provided [RCV001665810] Chr21:33829643 [GRCh38]
Chr21:35201947 [GRCh37]
Chr21:21q22.11		 benign
NM_003024.3(ITSN1):c.122-29del deletion not provided [RCV001674453] Chr21:33722545 [GRCh38]
Chr21:35094850 [GRCh37]
Chr21:21q22.11		 benign
NM_003024.3(ITSN1):c.1952+43G>T single nucleotide variant not provided [RCV001675192] Chr21:33794511 [GRCh38]
Chr21:35166815 [GRCh37]
Chr21:21q22.11		 benign
NM_003024.3(ITSN1):c.4554+189T>G single nucleotide variant not provided [RCV001655258] Chr21:33882644 [GRCh38]
Chr21:35254948 [GRCh37]
Chr21:21q22.11		 benign
GRCh37/hg19 21p13-q22.3(chr21:1-48129895)x3 copy number gain See cases [RCV001780078] Chr21:1..48129895 [GRCh37]
Chr21:21p13-q22.3		 pathogenic
GRCh37/hg19 21q11.2-22.3(chr21:15006457-48097372)x3 copy number gain not provided [RCV001829203] Chr21:15006457..48097372 [GRCh37]
Chr21:21q11.2-22.3		 pathogenic
GRCh37/hg19 21q11.2-22.3(chr21:15006457-48097372) copy number gain not specified [RCV002052723] Chr21:15006457..48097372 [GRCh37]
Chr21:21q11.2-22.3		 pathogenic
GRCh37/hg19 21q11.2-22.3(chr21:15285841-48097372) copy number gain not specified [RCV002052725] Chr21:15285841..48097372 [GRCh37]
Chr21:21q11.2-22.3		 pathogenic
GRCh37/hg19 21q11.2-22.3(chr21:15041209-48097372) copy number gain not specified [RCV002052724] Chr21:15041209..48097372 [GRCh37]
Chr21:21q11.2-22.3		 pathogenic
GRCh37/hg19 21q21.3-22.13(chr21:29812033-39282854) copy number gain not specified [RCV002052729] Chr21:29812033..39282854 [GRCh37]
Chr21:21q21.3-22.13		 pathogenic
GRCh37/hg19 21q22.11(chr21:34944264-35151870) copy number loss not specified [RCV002052734] Chr21:34944264..35151870 [GRCh37]
Chr21:21q22.11		 uncertain significance
GRCh37/hg19 21q22.11(chr21:32676376-35131913)x3 copy number gain not provided [RCV001832874] Chr21:32676376..35131913 [GRCh37]
Chr21:21q22.11		 uncertain significance
GRCh37/hg19 21q21.3-22.12(chr21:27185913-35853445) copy number loss not specified [RCV002052728] Chr21:27185913..35853445 [GRCh37]
Chr21:21q21.3-22.12		 uncertain significance
NM_003024.3(ITSN1):c.356G>A (p.Gly119Asp) single nucleotide variant Nephrotic syndrome [RCV001823688] Chr21:33750152 [GRCh38]
Chr21:35122457 [GRCh37]
Chr21:21q22.11		 uncertain significance
NC_000021.8:g.(?_32439271)_(39212984_?)dup duplication Amyotrophic lateral sclerosis type 1 [RCV001939883]|DYRK1A-related intellectual disability syndrome [RCV003107882] Chr21:32439271..39212984 [GRCh37]
Chr21:21q22.11-22.13		 uncertain significance
Single allele deletion ZTTK syndrome [RCV002247722] Chr21:32213458..34373118 [GRCh38]
Chr21:21q22.11		 pathogenic
NM_003024.3(ITSN1):c.2772G>A (p.Trp924Ter) single nucleotide variant Neurodevelopmental disorder [RCV003123315] Chr21:33818311 [GRCh38]
Chr21:35190615 [GRCh37]
Chr21:21q22.11		 likely pathogenic
NM_003024.3(ITSN1):c.3017-2A>G single nucleotide variant Generalized-onset seizure [RCV002286485] Chr21:33823485 [GRCh38]
Chr21:35195789 [GRCh37]
Chr21:21q22.11		 likely pathogenic
NM_003024.3(ITSN1):c.473del (p.Leu158fs) deletion Autistic behavior [RCV002287213] Chr21:33750269 [GRCh38]
Chr21:35122574 [GRCh37]
Chr21:21q22.11		 pathogenic
NM_003024.3(ITSN1):c.3893C>T (p.Ala1298Val) single nucleotide variant not provided [RCV002267343] Chr21:33865153 [GRCh38]
Chr21:35237457 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_003024.3(ITSN1):c.147dup (p.Gln50fs) duplication not provided [RCV002293656] Chr21:33722604..33722605 [GRCh38]
Chr21:35094909..35094910 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_003024.3(ITSN1):c.1254G>T (p.Glu418Asp) single nucleotide variant not provided [RCV002469593] Chr21:33772272 [GRCh38]
Chr21:35144576 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_003024.3(ITSN1):c.10T>C (p.Phe4Leu) single nucleotide variant not provided [RCV003152169] Chr21:33718838 [GRCh38]
Chr21:35091143 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_003024.3(ITSN1):c.382G>T (p.Ala128Ser) single nucleotide variant Inborn genetic diseases [RCV003285285] Chr21:33750178 [GRCh38]
Chr21:35122483 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_003024.3(ITSN1):c.2287C>G (p.Pro763Ala) single nucleotide variant not provided [RCV002467074] Chr21:33799912 [GRCh38]
Chr21:35172216 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_003024.3(ITSN1):c.4316A>G (p.His1439Arg) single nucleotide variant not provided [RCV002511229] Chr21:33875496 [GRCh38]
Chr21:35247800 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_003024.3(ITSN1):c.2600C>T (p.Thr867Met) single nucleotide variant Inborn genetic diseases [RCV002906749] Chr21:33813945 [GRCh38]
Chr21:35186249 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_003024.3(ITSN1):c.2120G>A (p.Arg707Gln) single nucleotide variant Inborn genetic diseases [RCV002734415] Chr21:33797546 [GRCh38]
Chr21:35169850 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_003024.3(ITSN1):c.1496T>C (p.Ile499Thr) single nucleotide variant not provided [RCV002880766] Chr21:33775008 [GRCh38]
Chr21:35147312 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_003024.3(ITSN1):c.4160T>C (p.Leu1387Pro) single nucleotide variant Inborn genetic diseases [RCV002883782] Chr21:33867318 [GRCh38]
Chr21:35239622 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_003024.3(ITSN1):c.3028A>G (p.Met1010Val) single nucleotide variant Inborn genetic diseases [RCV002732124] Chr21:33823498 [GRCh38]
Chr21:35195802 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_003024.3(ITSN1):c.1988A>G (p.His663Arg) single nucleotide variant Inborn genetic diseases [RCV002685239] Chr21:33797414 [GRCh38]
Chr21:35169718 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_003024.3(ITSN1):c.1693C>T (p.Leu565Phe) single nucleotide variant Inborn genetic diseases [RCV002945551] Chr21:33782002 [GRCh38]
Chr21:35154306 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_003024.3(ITSN1):c.3541A>G (p.Ile1181Val) single nucleotide variant Inborn genetic diseases [RCV002732898] Chr21:33836512 [GRCh38]
Chr21:35208816 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_003024.3(ITSN1):c.809A>G (p.Gln270Arg) single nucleotide variant not provided [RCV003097618] Chr21:33765895 [GRCh38]
Chr21:35138199 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_003024.3(ITSN1):c.2210A>C (p.Gln737Pro) single nucleotide variant Inborn genetic diseases [RCV002907348] Chr21:33799835 [GRCh38]
Chr21:35172139 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_003024.3(ITSN1):c.3318G>C (p.Lys1106Asn) single nucleotide variant Inborn genetic diseases [RCV002778607] Chr21:33829712 [GRCh38]
Chr21:35202016 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_003024.3(ITSN1):c.4901C>T (p.Thr1634Met) single nucleotide variant Inborn genetic diseases [RCV002845153] Chr21:33886344 [GRCh38]
Chr21:35258648 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_003024.3(ITSN1):c.3125C>G (p.Thr1042Arg) single nucleotide variant Inborn genetic diseases [RCV002738735] Chr21:33823595 [GRCh38]
Chr21:35195899 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_003024.3(ITSN1):c.2489G>A (p.Arg830His) single nucleotide variant Inborn genetic diseases [RCV002707087] Chr21:33811144 [GRCh38]
Chr21:35183448 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_003024.3(ITSN1):c.3657G>T (p.Gln1219His) single nucleotide variant Inborn genetic diseases [RCV002661887] Chr21:33836628 [GRCh38]
Chr21:35208932 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_003024.3(ITSN1):c.1102C>G (p.Arg368Gly) single nucleotide variant not provided [RCV002510009] Chr21:33772120 [GRCh38]
Chr21:35144424 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_003024.3(ITSN1):c.199A>G (p.Met67Val) single nucleotide variant Inborn genetic diseases [RCV002713337] Chr21:33735057 [GRCh38]
Chr21:35107362 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_003024.3(ITSN1):c.1621C>A (p.Leu541Ile) single nucleotide variant Inborn genetic diseases [RCV002853990] Chr21:33781485 [GRCh38]
Chr21:35153789 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_003024.3(ITSN1):c.3205A>G (p.Thr1069Ala) single nucleotide variant Inborn genetic diseases [RCV002930142] Chr21:33826839 [GRCh38]
Chr21:35199143 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_003024.3(ITSN1):c.3178T>G (p.Ser1060Ala) single nucleotide variant Inborn genetic diseases [RCV002788910] Chr21:33823648 [GRCh38]
Chr21:35195952 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_003024.3(ITSN1):c.4294C>T (p.Arg1432Trp) single nucleotide variant Inborn genetic diseases [RCV002874881] Chr21:33875474 [GRCh38]
Chr21:35247778 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_003024.3(ITSN1):c.4069G>A (p.Val1357Ile) single nucleotide variant Inborn genetic diseases [RCV002825878] Chr21:33865329 [GRCh38]
Chr21:35237633 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_003024.3(ITSN1):c.3293G>C (p.Gly1098Ala) single nucleotide variant Inborn genetic diseases [RCV002645046] Chr21:33829687 [GRCh38]
Chr21:35201991 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_003024.3(ITSN1):c.2399A>G (p.Tyr800Cys) single nucleotide variant Inborn genetic diseases [RCV002934424] Chr21:33811054 [GRCh38]
Chr21:35183358 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_003024.3(ITSN1):c.2534C>T (p.Thr845Met) single nucleotide variant ITSN1-related condition [RCV003395629]|Inborn genetic diseases [RCV002672655] Chr21:33811189 [GRCh38]
Chr21:35183493 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_003024.3(ITSN1):c.2623G>A (p.Ala875Thr) single nucleotide variant Inborn genetic diseases [RCV002714333] Chr21:33813968 [GRCh38]
Chr21:35186272 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_003024.3(ITSN1):c.725-1G>A single nucleotide variant not provided [RCV002715404] Chr21:33761922 [GRCh38]
Chr21:35134226 [GRCh37]
Chr21:21q22.11		 likely pathogenic
NM_003024.3(ITSN1):c.1813A>G (p.Asn605Asp) single nucleotide variant Inborn genetic diseases [RCV002747484] Chr21:33782122 [GRCh38]
Chr21:35154426 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_003024.3(ITSN1):c.1202A>G (p.Gln401Arg) single nucleotide variant not provided [RCV002814281] Chr21:33772220 [GRCh38]
Chr21:35144524 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_003024.3(ITSN1):c.3458C>T (p.Ala1153Val) single nucleotide variant Inborn genetic diseases [RCV002656270] Chr21:33834413 [GRCh38]
Chr21:35206717 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_003024.3(ITSN1):c.1355A>G (p.Asn452Ser) single nucleotide variant not provided [RCV003154409] Chr21:33774778 [GRCh38]
Chr21:35147082 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_003024.3(ITSN1):c.439G>T (p.Val147Leu) single nucleotide variant Inborn genetic diseases [RCV003256215] Chr21:33750235 [GRCh38]
Chr21:35122540 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_003024.3(ITSN1):c.2071A>G (p.Lys691Glu) single nucleotide variant Inborn genetic diseases [RCV003173650] Chr21:33797497 [GRCh38]
Chr21:35169801 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_003024.3(ITSN1):c.1274A>C (p.Glu425Ala) single nucleotide variant Inborn genetic diseases [RCV003192556] Chr21:33772292 [GRCh38]
Chr21:35144596 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_003024.3(ITSN1):c.5122G>A (p.Glu1708Lys) single nucleotide variant not provided [RCV003159361] Chr21:33888256 [GRCh38]
Chr21:35260560 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_003024.3(ITSN1):c.1930A>G (p.Lys644Glu) single nucleotide variant not provided [RCV003221633] Chr21:33794446 [GRCh38]
Chr21:35166750 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_003024.3(ITSN1):c.4040C>T (p.Thr1347Met) single nucleotide variant Inborn genetic diseases [RCV003181453] Chr21:33865300 [GRCh38]
Chr21:35237604 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_003024.3(ITSN1):c.3409A>G (p.Ser1137Gly) single nucleotide variant Inborn genetic diseases [RCV003198370] Chr21:33834364 [GRCh38]
Chr21:35206668 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_003024.3(ITSN1):c.5044G>A (p.Val1682Met) single nucleotide variant Inborn genetic diseases [RCV003220206] Chr21:33888178 [GRCh38]
Chr21:35260482 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_003024.3(ITSN1):c.466C>T (p.Pro156Ser) single nucleotide variant Inborn genetic diseases [RCV003205715] Chr21:33750262 [GRCh38]
Chr21:35122567 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_003024.3(ITSN1):c.3265G>A (p.Gly1089Ser) single nucleotide variant Inborn genetic diseases [RCV003175821] Chr21:33829659 [GRCh38]
Chr21:35201963 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_003024.3(ITSN1):c.2431G>A (p.Ala811Thr) single nucleotide variant Inborn genetic diseases [RCV003190833] Chr21:33811086 [GRCh38]
Chr21:35183390 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_003024.3(ITSN1):c.1666C>G (p.Gln556Glu) single nucleotide variant not provided [RCV003225376] Chr21:33781530 [GRCh38]
Chr21:35153834 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_003024.3(ITSN1):c.2192C>T (p.Pro731Leu) single nucleotide variant not provided [RCV003319110] Chr21:33799817 [GRCh38]
Chr21:35172121 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_003024.3(ITSN1):c.4044T>G (p.Asp1348Glu) single nucleotide variant not provided [RCV003322041] Chr21:33865304 [GRCh38]
Chr21:35237608 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_003024.3(ITSN1):c.3937_3941dup (p.Met1314fs) duplication not provided [RCV003322187] Chr21:33865196..33865197 [GRCh38]
Chr21:35237500..35237501 [GRCh37]
Chr21:21q22.11		 likely pathogenic
NM_003024.3(ITSN1):c.2789A>G (p.Asn930Ser) single nucleotide variant not provided [RCV003325722] Chr21:33818328 [GRCh38]
Chr21:35190632 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_003024.3(ITSN1):c.2314G>A (p.Glu772Lys) single nucleotide variant not provided [RCV003329666] Chr21:33802439 [GRCh38]
Chr21:35174743 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_003024.3(ITSN1):c.1880C>T (p.Ala627Val) single nucleotide variant not provided [RCV003387565] Chr21:33794396 [GRCh38]
Chr21:35166700 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_003024.3(ITSN1):c.1909C>T (p.Arg637Ter) single nucleotide variant Inborn genetic diseases [RCV003352098] Chr21:33794425 [GRCh38]
Chr21:35166729 [GRCh37]
Chr21:21q22.11		 pathogenic
NM_003024.3(ITSN1):c.1615G>A (p.Gly539Arg) single nucleotide variant ITSN1-related condition [RCV003418954] Chr21:33781479 [GRCh38]
Chr21:35153783 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_003024.3(ITSN1):c.3104A>G (p.Asp1035Gly) single nucleotide variant not provided [RCV003332910] Chr21:33823574 [GRCh38]
Chr21:35195878 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_003024.3(ITSN1):c.1781G>A (p.Arg594Lys) single nucleotide variant Inborn genetic diseases [RCV003349987] Chr21:33782090 [GRCh38]
Chr21:35154394 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_003024.3(ITSN1):c.2895C>G (p.Tyr965Ter) single nucleotide variant Inborn genetic diseases [RCV003363752] Chr21:33818434 [GRCh38]
Chr21:35190738 [GRCh37]
Chr21:21q22.11		 pathogenic
NM_003024.3(ITSN1):c.908A>G (p.Tyr303Cys) single nucleotide variant not provided [RCV003487941] Chr21:33765994 [GRCh38]
Chr21:35138298 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_003024.3(ITSN1):c.2644C>A (p.Pro882Thr) single nucleotide variant ITSN1-related neurodevelopmental disorders [RCV003458979] Chr21:33813989 [GRCh38]
Chr21:35186293 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_003024.3(ITSN1):c.3779C>T (p.Thr1260Ile) single nucleotide variant ITSN1-related condition [RCV003404529] Chr21:33856853 [GRCh38]
Chr21:35229157 [GRCh37]
Chr21:21q22.11		 uncertain significance
GRCh37/hg19 21q11.2-22.3(chr21:15006458-45674637)x3 copy number gain not provided [RCV003485218] Chr21:15006458..45674637 [GRCh37]
Chr21:21q11.2-22.3		 pathogenic
GRCh37/hg19 21q22.11-22.3(chr21:33015681-48097372)x3 copy number gain not provided [RCV003485222] Chr21:33015681..48097372 [GRCh37]
Chr21:21q22.11-22.3		 pathogenic
NM_003024.3(ITSN1):c.1975C>T (p.Gln659Ter) single nucleotide variant ITSN1-related condition [RCV003399957] Chr21:33797401 [GRCh38]
Chr21:35169705 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_003024.3(ITSN1):c.1954C>T (p.Arg652Ter) single nucleotide variant not provided [RCV003443781] Chr21:33797380 [GRCh38]
Chr21:35169684 [GRCh37]
Chr21:21q22.11		 likely pathogenic
NM_003024.3(ITSN1):c.5114C>T (p.Pro1705Leu) single nucleotide variant ITSN1-related condition [RCV003402506] Chr21:33888248 [GRCh38]
Chr21:35260552 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_003024.3(ITSN1):c.1043-18T>C single nucleotide variant not provided [RCV003431479] Chr21:33772043 [GRCh38]
Chr21:35144347 [GRCh37]
Chr21:21q22.11		 likely benign
NM_003024.3(ITSN1):c.69G>A (p.Ala23=) single nucleotide variant ITSN1-related condition [RCV003984367]|not provided [RCV003431478] Chr21:33721218 [GRCh38]
Chr21:35093523 [GRCh37]
Chr21:21q22.11		 likely benign
NM_003024.3(ITSN1):c.2079C>T (p.Gly693=) single nucleotide variant ITSN1-related condition [RCV003938982]|not provided [RCV003431480] Chr21:33797505 [GRCh38]
Chr21:35169809 [GRCh37]
Chr21:21q22.11		 benign|likely benign
NM_003024.3(ITSN1):c.5048C>T (p.Ala1683Val) single nucleotide variant ITSN1-related condition [RCV003399535] Chr21:33888182 [GRCh38]
Chr21:35260486 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_003024.3(ITSN1):c.2330G>T (p.Ser777Ile) single nucleotide variant not provided [RCV003443565] Chr21:33810985 [GRCh38]
Chr21:35183289 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_003024.3(ITSN1):c.4608C>T (p.Asp1536=) single nucleotide variant not provided [RCV003440551] Chr21:33883603 [GRCh38]
Chr21:35255907 [GRCh37]
Chr21:21q22.11		 likely benign
NM_003024.3(ITSN1):c.2978_2980dup (p.Val993_Ala994insVal) duplication not provided [RCV003443374] Chr21:33819282..33819283 [GRCh38]
Chr21:35191586..35191587 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_003024.3(ITSN1):c.1838T>G (p.Ile613Arg) single nucleotide variant ITSN1-related condition [RCV003397572] Chr21:33794354 [GRCh38]
Chr21:35166658 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_003024.3(ITSN1):c.3419C>T (p.Thr1140Met) single nucleotide variant ITSN1-related condition [RCV003397603] Chr21:33834374 [GRCh38]
Chr21:35206678 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_003024.3(ITSN1):c.973G>A (p.Val325Ile) single nucleotide variant ITSN1-related condition [RCV003414552] Chr21:33767759 [GRCh38]
Chr21:35140063 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_003024.3(ITSN1):c.2792A>G (p.His931Arg) single nucleotide variant ITSN1-related condition [RCV003399621] Chr21:33818331 [GRCh38]
Chr21:35190635 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_003024.3(ITSN1):c.1684+5G>T single nucleotide variant not provided [RCV003579346] Chr21:33781553 [GRCh38]
Chr21:35153857 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_003024.3(ITSN1):c.25G>A (p.Gly9Ser) single nucleotide variant not provided [RCV003487940] Chr21:33718853 [GRCh38]
Chr21:35091158 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_003024.3(ITSN1):c.2348G>A (p.Gly783Asp) single nucleotide variant not provided [RCV003712718] Chr21:33811003 [GRCh38]
Chr21:35183307 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_003024.3(ITSN1):c.4379C>T (p.Pro1460Leu) single nucleotide variant not provided [RCV003551409] Chr21:33882280 [GRCh38]
Chr21:35254584 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_003024.3(ITSN1):c.813T>C (p.Asp271=) single nucleotide variant ITSN1-related condition [RCV003939482] Chr21:33765899 [GRCh38]
Chr21:35138203 [GRCh37]
Chr21:21q22.11		 likely benign
GRCh37/hg19 21q21.3-22.3(chr21:30685776-48097372)x3 copy number gain not specified [RCV003986149] Chr21:30685776..48097372 [GRCh37]
Chr21:21q21.3-22.3		 pathogenic
GRCh37/hg19 21q22.11(chr21:35199880-35364620)x1 copy number loss not specified [RCV003986162] Chr21:35199880..35364620 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_003024.3(ITSN1):c.4555-8C>A single nucleotide variant ITSN1-related condition [RCV003939837] Chr21:33883542 [GRCh38]
Chr21:35255846 [GRCh37]
Chr21:21q22.11		 benign
GRCh37/hg19 21q21.3-22.3(chr21:26929299-48097372)x3 copy number gain not specified [RCV003986152] Chr21:26929299..48097372 [GRCh37]
Chr21:21q21.3-22.3		 pathogenic
GRCh37/hg19 21q11.2-22.3(chr21:15023401-48097372)x3 copy number gain not specified [RCV003986160] Chr21:15023401..48097372 [GRCh37]
Chr21:21q11.2-22.3		 pathogenic
NM_003024.3(ITSN1):c.1701A>G (p.Thr567=) single nucleotide variant ITSN1-related condition [RCV003941649] Chr21:33782010 [GRCh38]
Chr21:35154314 [GRCh37]
Chr21:21q22.11		 likely benign
GRCh37/hg19 21q22.11-22.3(chr21:34092685-48097372)x3 copy number gain not specified [RCV003986158] Chr21:34092685..48097372 [GRCh37]
Chr21:21q22.11-22.3		 pathogenic
NM_003024.3(ITSN1):c.4503C>T (p.Thr1501=) single nucleotide variant ITSN1-related condition [RCV003892299] Chr21:33882404 [GRCh38]
Chr21:35254708 [GRCh37]
Chr21:21q22.11		 likely benign
NM_003024.3(ITSN1):c.4980C>T (p.Cys1660=) single nucleotide variant ITSN1-related condition [RCV003949547] Chr21:33886423 [GRCh38]
Chr21:35258727 [GRCh37]
Chr21:21q22.11		 likely benign
NM_003024.3(ITSN1):c.2405A>C (p.Glu802Ala) single nucleotide variant Autism [RCV003988613] Chr21:33811060 [GRCh38]
Chr21:35183364 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_003024.3(ITSN1):c.2641G>A (p.Val881Ile) single nucleotide variant ITSN1-related condition [RCV003944400] Chr21:33813986 [GRCh38]
Chr21:35186290 [GRCh37]
Chr21:21q22.11		 benign
NM_003024.3(ITSN1):c.1952+10C>T single nucleotide variant ITSN1-related condition [RCV003981821] Chr21:33794478 [GRCh38]
Chr21:35166782 [GRCh37]
Chr21:21q22.11		 likely benign
NM_003024.3(ITSN1):c.4317C>T (p.His1439=) single nucleotide variant ITSN1-related condition [RCV003983549] Chr21:33875497 [GRCh38]
Chr21:35247801 [GRCh37]
Chr21:21q22.11		 likely benign
NM_003024.3(ITSN1):c.*6G>A single nucleotide variant ITSN1-related condition [RCV003921800] Chr21:33888306 [GRCh38]
Chr21:35260610 [GRCh37]
Chr21:21q22.11		 likely benign
NM_003024.3(ITSN1):c.1597-3C>T single nucleotide variant ITSN1-related condition [RCV003983579] Chr21:33781458 [GRCh38]
Chr21:35153762 [GRCh37]
Chr21:21q22.11		 likely benign
NM_003024.3(ITSN1):c.1507T>C (p.Leu503=) single nucleotide variant ITSN1-related condition [RCV003959025] Chr21:33775019 [GRCh38]
Chr21:35147323 [GRCh37]
Chr21:21q22.11		 likely benign
NM_003024.3(ITSN1):c.4224C>T (p.His1408=) single nucleotide variant ITSN1-related condition [RCV003947098] Chr21:33875404 [GRCh38]
Chr21:35247708 [GRCh37]
Chr21:21q22.11		 likely benign
NM_003024.3(ITSN1):c.2582C>T (p.Thr861Met) single nucleotide variant ITSN1-related condition [RCV003969558] Chr21:33813927 [GRCh38]
Chr21:35186231 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_003024.3(ITSN1):c.2568-9dup duplication ITSN1-related condition [RCV003936780] Chr21:33813900..33813901 [GRCh38]
Chr21:35186204..35186205 [GRCh37]
Chr21:21q22.11		 likely benign
NM_003024.3(ITSN1):c.2836C>G (p.Gln946Glu) single nucleotide variant ITSN1-related condition [RCV003969722] Chr21:33818375 [GRCh38]
Chr21:35190679 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_003024.3(ITSN1):c.3700A>G (p.Thr1234Ala) single nucleotide variant ITSN1-related condition [RCV003902017] Chr21:33856774 [GRCh38]
Chr21:35229078 [GRCh37]
Chr21:21q22.11		 likely benign
NM_003024.3(ITSN1):c.4884G>A (p.Gln1628=) single nucleotide variant ITSN1-related condition [RCV003931600] Chr21:33886327 [GRCh38]
Chr21:35258631 [GRCh37]
Chr21:21q22.11		 likely benign
NM_003024.3(ITSN1):c.3606G>A (p.Gly1202=) single nucleotide variant ITSN1-related condition [RCV003896663] Chr21:33836577 [GRCh38]
Chr21:35208881 [GRCh37]
Chr21:21q22.11		 likely benign
NM_003024.3(ITSN1):c.3891-6G>A single nucleotide variant ITSN1-related condition [RCV003913917] Chr21:33865145 [GRCh38]
Chr21:35237449 [GRCh37]
Chr21:21q22.11		 likely benign
NM_003024.3(ITSN1):c.4146A>G (p.Val1382=) single nucleotide variant ITSN1-related condition [RCV003937413] Chr21:33867304 [GRCh38]
Chr21:35239608 [GRCh37]
Chr21:21q22.11		 likely benign
NM_003024.3(ITSN1):c.816A>G (p.Gly272=) single nucleotide variant not provided [RCV003884892] Chr21:33765902 [GRCh38]
Chr21:35138206 [GRCh37]
Chr21:21q22.11		 likely benign
NM_003024.3(ITSN1):c.4314C>A (p.Ala1438=) single nucleotide variant ITSN1-related condition [RCV003951564] Chr21:33875494 [GRCh38]
Chr21:35247798 [GRCh37]
Chr21:21q22.11		 likely benign
NM_003024.3(ITSN1):c.2708C>T (p.Pro903Leu) single nucleotide variant ITSN1-related condition [RCV003952038] Chr21:33814053 [GRCh38]
Chr21:35186357 [GRCh37]
Chr21:21q22.11		 benign
NM_003024.3(ITSN1):c.3109G>A (p.Asp1037Asn) single nucleotide variant ITSN1-related condition [RCV003969674] Chr21:33823579 [GRCh38]
Chr21:35195883 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_003024.3(ITSN1):c.624-7C>G single nucleotide variant ITSN1-related condition [RCV003934196] Chr21:33755290 [GRCh38]
Chr21:35127595 [GRCh37]
Chr21:21q22.11		 likely benign
NM_003024.3(ITSN1):c.189A>G (p.Ala63=) single nucleotide variant ITSN1-related condition [RCV003907198] Chr21:33735047 [GRCh38]
Chr21:35107352 [GRCh37]
Chr21:21q22.11		 likely benign
NM_003024.3(ITSN1):c.3513C>T (p.Asp1171=) single nucleotide variant ITSN1-related condition [RCV003949540] Chr21:33836484 [GRCh38]
Chr21:35208788 [GRCh37]
Chr21:21q22.11		 likely benign
NM_003024.3(ITSN1):c.297C>G (p.Pro99=) single nucleotide variant ITSN1-related condition [RCV003907361] Chr21:33735155 [GRCh38]
Chr21:35107460 [GRCh37]
Chr21:21q22.11		 likely benign
NM_003024.3(ITSN1):c.3744C>T (p.Thr1248=) single nucleotide variant ITSN1-related condition [RCV003904727] Chr21:33856818 [GRCh38]
Chr21:35229122 [GRCh37]
Chr21:21q22.11		 likely benign
NM_003024.3(ITSN1):c.1015CAA[2] (p.Gln341del) microsatellite ITSN1-related condition [RCV003901608] Chr21:33767799..33767801 [GRCh38]
Chr21:35140103..35140105 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_003024.3(ITSN1):c.4078T>C (p.Leu1360=) single nucleotide variant ITSN1-related condition [RCV003911998] Chr21:33867236 [GRCh38]
Chr21:35239540 [GRCh37]
Chr21:21q22.11		 likely benign
NM_003024.3(ITSN1):c.1374A>G (p.Leu458=) single nucleotide variant ITSN1-related condition [RCV003899666] Chr21:33774797 [GRCh38]
Chr21:35147101 [GRCh37]
Chr21:21q22.11		 likely benign
NM_003024.3(ITSN1):c.1455+8A>C single nucleotide variant ITSN1-related condition [RCV003921564] Chr21:33774886 [GRCh38]
Chr21:35147190 [GRCh37]
Chr21:21q22.11		 likely benign
NM_003024.3(ITSN1):c.4676+7C>T single nucleotide variant ITSN1-related condition [RCV003914010] Chr21:33883678 [GRCh38]
Chr21:35255982 [GRCh37]
Chr21:21q22.11		 likely benign
NM_003024.3(ITSN1):c.4510G>A (p.Val1504Ile) single nucleotide variant ITSN1-related condition [RCV003901632] Chr21:33882411 [GRCh38]
Chr21:35254715 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_003024.3(ITSN1):c.963C>T (p.Ser321=) single nucleotide variant ITSN1-related condition [RCV003909330] Chr21:33767749 [GRCh38]
Chr21:35140053 [GRCh37]
Chr21:21q22.11		 likely benign
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:15075
Count of miRNA genes:1615
Interacting mature miRNAs:2321
Transcripts:ENST00000379960, ENST00000381283, ENST00000381284, ENST00000381285, ENST00000381291, ENST00000381318, ENST00000399326, ENST00000399338, ENST00000399349, ENST00000399352, ENST00000399353, ENST00000399355, ENST00000399367, ENST00000415023, ENST00000419241, ENST00000420666, ENST00000428240, ENST00000437126, ENST00000437442, ENST00000440794, ENST00000444491, ENST00000451686, ENST00000456489, ENST00000462212, ENST00000465143, ENST00000470742, ENST00000472548, ENST00000474132, ENST00000475422, ENST00000479424, ENST00000487427, ENST00000488166, ENST00000489261, ENST00000495656
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.

Markers in Region
D21S1254  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,075,367 - 35,075,630UniSTSGRCh37
GRCh372135,075,512 - 35,075,659UniSTSGRCh37
Build 362133,997,237 - 33,997,500RGDNCBI36
Celera2120,274,988 - 20,275,251RGD
Celera2120,275,133 - 20,275,280UniSTS
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,553,764 - 20,553,911UniSTS
HuRef2120,553,617 - 20,553,882UniSTS
Marshfield Genetic Map2131.26RGD
Marshfield Genetic Map2131.26UniSTS
Genethon Genetic Map2134.7UniSTS
TNG Radiation Hybrid Map2111783.0UniSTS
deCODE Assembly Map2138.2UniSTS
Stanford-G3 RH Map21872.0UniSTS
GeneMap99-GB4 RH Map21167.97UniSTS
Whitehead-RH Map21157.4UniSTS
Whitehead-YAC Contig Map21 UniSTS
NCBI RH Map21257.5UniSTS
GeneMap99-G3 RH Map21872.0UniSTS
D21S1976  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,047,895 - 35,048,024UniSTSGRCh37
Build 362133,969,765 - 33,969,894RGDNCBI36
Celera2120,247,516 - 20,247,645RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,526,223 - 20,526,352UniSTS
SHGC-87560  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,210,519 - 35,210,779UniSTSGRCh37
Build 362134,132,389 - 34,132,649RGDNCBI36
Celera2120,410,141 - 20,410,401RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,688,665 - 20,688,925UniSTS
TNG Radiation Hybrid Map2111876.0UniSTS
GeneMap99-GB4 RH Map21156.19UniSTS
NCBI RH Map21246.2UniSTS
SHGC-7353  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,083,920 - 35,084,138UniSTSGRCh37
Build 362134,005,790 - 34,006,008RGDNCBI36
Celera2120,283,542 - 20,283,760RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,561,985 - 20,562,201UniSTS
TNG Radiation Hybrid Map2111799.0UniSTS
SHGC-6846  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,250,932 - 35,251,047UniSTSGRCh37
Build 362134,172,802 - 34,172,917RGDNCBI36
Celera2120,450,516 - 20,450,631RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,728,996 - 20,729,111UniSTS
RH80986  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,169,284 - 35,169,485UniSTSGRCh37
Build 362134,091,154 - 34,091,355RGDNCBI36
Celera2120,368,906 - 20,369,107RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,647,283 - 20,647,484UniSTS
RH104301  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,200,991 - 35,201,174UniSTSGRCh37
Build 362134,122,861 - 34,123,044RGDNCBI36
Celera2120,400,613 - 20,400,796RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,679,011 - 20,679,194UniSTS
GeneMap99-GB4 RH Map21157.95UniSTS
RH122567  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,198,524 - 35,198,794UniSTSGRCh37
Build 362134,120,394 - 34,120,664RGDNCBI36
Celera2120,398,146 - 20,398,416RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,676,544 - 20,676,814UniSTS
TNG Radiation Hybrid Map2111866.0UniSTS
RH119211  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,158,043 - 35,158,316UniSTSGRCh37
Build 362134,079,913 - 34,080,186RGDNCBI36
Celera2120,357,665 - 20,357,938RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,636,085 - 20,636,358UniSTS
TNG Radiation Hybrid Map2111842.0UniSTS
D21S216  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,096,351 - 35,096,467UniSTSGRCh37
Build 362134,018,221 - 34,018,337RGDNCBI36
Celera2120,295,973 - 20,296,089RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,574,381 - 20,574,497UniSTS
D21S219  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,083,921 - 35,084,097UniSTSGRCh37
Build 362134,005,791 - 34,005,967RGDNCBI36
Celera2120,283,543 - 20,283,719RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,561,986 - 20,562,160UniSTS
D21S235  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,250,088 - 35,250,248UniSTSGRCh37
GRCh372135,250,229 - 35,250,405UniSTSGRCh37
GRCh37273,099,467 - 73,099,797UniSTSGRCh37
Build 362134,171,958 - 34,172,118RGDNCBI36
Celera2120,449,813 - 20,449,989UniSTS
Celera272,950,301 - 72,950,631UniSTS
Celera2120,449,672 - 20,449,832RGD
HuRef2120,728,170 - 20,728,318UniSTS
HuRef272,835,054 - 72,835,384UniSTS
HuRef2120,728,299 - 20,728,469UniSTS
D21S324  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,250,859 - 35,251,118UniSTSGRCh37
Build 362134,172,729 - 34,172,988RGDNCBI36
Celera2120,450,443 - 20,450,702RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,728,923 - 20,729,182UniSTS
D21S1697  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,189,686 - 35,189,764UniSTSGRCh37
Build 362134,111,556 - 34,111,634RGDNCBI36
Celera2120,389,308 - 20,389,386RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,667,707 - 20,667,785UniSTS
SHGC-170113  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,179,224 - 35,179,522UniSTSGRCh37
Build 362134,101,094 - 34,101,392RGDNCBI36
Celera2120,378,846 - 20,379,144RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,657,287 - 20,657,585UniSTS
TNG Radiation Hybrid Map2111850.0UniSTS
SHGC-170295  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,045,803 - 35,046,114UniSTSGRCh37
Build 362133,967,673 - 33,967,984RGDNCBI36
Celera2120,245,424 - 20,245,735RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,524,131 - 20,524,442UniSTS
TNG Radiation Hybrid Map2111765.0UniSTS
SHGC-170327  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,082,687 - 35,082,960UniSTSGRCh37
Build 362134,004,557 - 34,004,830RGDNCBI36
Celera2120,282,309 - 20,282,582RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,560,752 - 20,561,025UniSTS
TNG Radiation Hybrid Map2111794.0UniSTS
STS-H50535  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,209,534 - 35,209,726UniSTSGRCh37
Build 362134,131,404 - 34,131,596RGDNCBI36
Celera2120,409,156 - 20,409,348RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,687,680 - 20,687,872UniSTS
TNG Radiation Hybrid Map2111876.0UniSTS
GeneMap99-GB4 RH Map21154.82UniSTS
NCBI RH Map21246.2UniSTS
ECD00010  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,198,437 - 35,199,406UniSTSGRCh37
Build 362134,120,307 - 34,121,276RGDNCBI36
Celera2120,398,059 - 20,399,028RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,676,457 - 20,677,426UniSTS
ECD00329  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,196,466 - 35,197,379UniSTSGRCh37
Build 362134,118,336 - 34,119,249RGDNCBI36
Celera2120,396,088 - 20,397,001RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,674,486 - 20,675,399UniSTS
ECD00472  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,238,861 - 35,239,765UniSTSGRCh37
Build 362134,160,731 - 34,161,635RGDNCBI36
Celera2120,438,484 - 20,439,388RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,717,007 - 20,717,911UniSTS
ECD00597  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,195,523 - 35,196,421UniSTSGRCh37
Build 362134,117,393 - 34,118,291RGDNCBI36
Celera2120,395,145 - 20,396,043RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,673,543 - 20,674,441UniSTS
ECD00613  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,157,836 - 35,158,733UniSTSGRCh37
Build 362134,079,706 - 34,080,603RGDNCBI36
Celera2120,357,458 - 20,358,355RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,635,878 - 20,636,775UniSTS
ECD00697  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,204,399 - 35,205,292UniSTSGRCh37
Build 362134,126,269 - 34,127,162RGDNCBI36
Celera2120,404,021 - 20,404,914RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,682,419 - 20,683,312UniSTS
ECD00698  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,233,072 - 35,233,965UniSTSGRCh37
Build 362134,154,942 - 34,155,835RGDNCBI36
Celera2120,432,695 - 20,433,588RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,711,218 - 20,712,111UniSTS
ECD00840  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,158,829 - 35,159,717UniSTSGRCh37
Build 362134,080,699 - 34,081,587RGDNCBI36
Celera2120,358,451 - 20,359,339RGD
Cytogenetic Map21q22.1-q22.2UniSTS
ECD01060  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,203,450 - 35,204,329UniSTSGRCh37
Build 362134,125,320 - 34,126,199RGDNCBI36
Celera2120,403,072 - 20,403,951RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,681,470 - 20,682,349UniSTS
ECD01061  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,226,426 - 35,227,305UniSTSGRCh37
Build 362134,148,296 - 34,149,175RGDNCBI36
Celera2120,426,049 - 20,426,928RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,704,573 - 20,705,452UniSTS
ECD01062  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,237,945 - 35,238,824UniSTSGRCh37
Build 362134,159,815 - 34,160,694RGDNCBI36
Celera2120,437,568 - 20,438,447RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,716,091 - 20,716,970UniSTS
ECD01134  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,235,951 - 35,236,827UniSTSGRCh37
Build 362134,157,821 - 34,158,697RGDNCBI36
Celera2120,435,574 - 20,436,450RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,714,097 - 20,714,973UniSTS
ECD01164  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,236,919 - 35,237,794UniSTSGRCh37
Build 362134,158,789 - 34,159,664RGDNCBI36
Celera2120,436,542 - 20,437,417RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,715,065 - 20,715,940UniSTS
ECD01165  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,255,242 - 35,256,117UniSTSGRCh37
Build 362134,177,112 - 34,177,987RGDNCBI36
Celera2120,454,826 - 20,455,701RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,733,306 - 20,734,181UniSTS
ECD01288  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,254,304 - 35,255,174UniSTSGRCh37
Build 362134,176,174 - 34,177,044RGDNCBI36
Celera2120,453,888 - 20,454,758RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,732,368 - 20,733,238UniSTS
ECD01917  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,107,106 - 35,107,954UniSTSGRCh37
Build 362134,028,976 - 34,029,824RGDNCBI36
Celera2120,306,728 - 20,307,576RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,585,138 - 20,585,986UniSTS
ECD01971  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,162,662 - 35,163,508UniSTSGRCh37
Build 362134,084,532 - 34,085,378RGDNCBI36
Celera2120,362,284 - 20,363,130RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,640,660 - 20,641,506UniSTS
ECD02128  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,067,568 - 35,068,408UniSTSGRCh37
Build 362133,989,438 - 33,990,278RGDNCBI36
Celera2120,267,189 - 20,268,029RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,545,876 - 20,546,716UniSTS
ECD02152  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,068,494 - 35,069,333UniSTSGRCh37
Build 362133,990,364 - 33,991,203RGDNCBI36
Celera2120,268,115 - 20,268,954RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,546,802 - 20,547,641UniSTS
ECD02248  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,225,425 - 35,226,261UniSTSGRCh37
Build 362134,147,295 - 34,148,131RGDNCBI36
Celera2120,425,048 - 20,425,884RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,703,572 - 20,704,408UniSTS
ECD02452  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,163,607 - 35,164,436UniSTSGRCh37
Build 362134,085,477 - 34,086,306RGDNCBI36
Celera2120,363,229 - 20,364,058RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,641,605 - 20,642,434UniSTS
ECD02522  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,197,564 - 35,198,391UniSTSGRCh37
Build 362134,119,434 - 34,120,261RGDNCBI36
Celera2120,397,186 - 20,398,013RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,675,584 - 20,676,411UniSTS
ECD02552  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,156,872 - 35,157,698UniSTSGRCh37
Build 362134,078,742 - 34,079,568RGDNCBI36
Celera2120,356,494 - 20,357,320RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,634,914 - 20,635,740UniSTS
ECD02846  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,224,549 - 35,225,364UniSTSGRCh37
Build 362134,146,419 - 34,147,234RGDNCBI36
Celera2120,424,172 - 20,424,987RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,702,696 - 20,703,511UniSTS
ECD02923  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,219,348 - 35,220,160UniSTSGRCh37
Build 362134,141,218 - 34,142,030RGDNCBI36
Celera2120,418,970 - 20,419,782RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,697,494 - 20,698,306UniSTS
ECD03120  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,159,795 - 35,160,600UniSTSGRCh37
Build 362134,081,665 - 34,082,470RGDNCBI36
Celera2120,359,417 - 20,360,222RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,637,797 - 20,638,602UniSTS
ECD03142  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,256,548 - 35,257,352UniSTSGRCh37
Build 362134,178,418 - 34,179,222RGDNCBI36
Celera2120,456,132 - 20,456,936RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,734,613 - 20,735,417UniSTS
ECD03377  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,124,107 - 35,124,904UniSTSGRCh37
Build 362134,045,977 - 34,046,774RGDNCBI36
Celera2120,323,729 - 20,324,526RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,602,139 - 20,602,936UniSTS
ECD03465  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,192,361 - 35,193,155UniSTSGRCh37
Build 362134,114,231 - 34,115,025RGDNCBI36
Celera2120,391,983 - 20,392,777RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,670,382 - 20,671,176UniSTS
ECD03530  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,201,778 - 35,202,570UniSTSGRCh37
Build 362134,123,648 - 34,124,440RGDNCBI36
Celera2120,401,400 - 20,402,192RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,679,798 - 20,680,590UniSTS
ECD03562  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,207,137 - 35,207,928UniSTSGRCh37
Build 362134,129,007 - 34,129,798RGDNCBI36
Celera2120,406,759 - 20,407,550RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,685,283 - 20,686,074UniSTS
ECD03678  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,123,193 - 35,123,980UniSTSGRCh37
Build 362134,045,063 - 34,045,850RGDNCBI36
Celera2120,322,815 - 20,323,602RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,601,225 - 20,602,012UniSTS
ECD03679  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,206,291 - 35,207,078UniSTSGRCh37
Build 362134,128,161 - 34,128,948RGDNCBI36
Celera2120,405,913 - 20,406,700RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,684,311 - 20,685,224UniSTS
ECD04337  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,183,211 - 35,183,978UniSTSGRCh37
Build 362134,105,081 - 34,105,848RGDNCBI36
Celera2120,382,833 - 20,383,600RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,661,274 - 20,662,041UniSTS
ECD04400  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,257,397 - 35,258,162UniSTSGRCh37
Build 362134,179,267 - 34,180,032RGDNCBI36
Celera2120,456,981 - 20,457,746RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,735,462 - 20,736,227UniSTS
ECD04685  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,194,630 - 35,195,387UniSTSGRCh37
Build 362134,116,500 - 34,117,257RGDNCBI36
Celera2120,394,252 - 20,395,009RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,672,650 - 20,673,407UniSTS
ECD04817  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,193,828 - 35,194,581UniSTSGRCh37
Build 362134,115,698 - 34,116,451RGDNCBI36
Celera2120,393,450 - 20,394,203RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,671,848 - 20,672,601UniSTS
ECD04848  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,139,798 - 35,140,550UniSTSGRCh37
Build 362134,061,668 - 34,062,420RGDNCBI36
Celera2120,339,420 - 20,340,172RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,617,831 - 20,618,583UniSTS
ECD04882  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,184,021 - 35,184,772UniSTSGRCh37
Build 362134,105,891 - 34,106,642RGDNCBI36
Celera2120,383,643 - 20,384,394RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,662,084 - 20,662,835UniSTS
ECD04953  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,070,843 - 35,071,592UniSTSGRCh37
Build 362133,992,713 - 33,993,462RGDNCBI36
Celera2120,270,464 - 20,271,213RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,549,152 - 20,549,901UniSTS
ECD05143  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,133,689 - 35,134,433UniSTSGRCh37
Build 362134,055,559 - 34,056,303RGDNCBI36
Celera2120,333,311 - 20,334,055RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,611,721 - 20,612,466UniSTS
ECD05168  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,222,126 - 35,222,869UniSTSGRCh37
Build 362134,143,996 - 34,144,739RGDNCBI36
Celera2120,421,748 - 20,422,491RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,700,272 - 20,701,015UniSTS
ECD05201  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,099,151 - 35,099,893UniSTSGRCh37
Build 362134,021,021 - 34,021,763RGDNCBI36
Celera2120,298,773 - 20,299,515RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,577,181 - 20,577,923UniSTS
ECD05234  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,015,602 - 35,016,343UniSTSGRCh37
Build 362133,937,472 - 33,938,213RGDNCBI36
Celera2120,215,223 - 20,215,964RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,493,927 - 20,494,668UniSTS
ECD05235  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,260,277 - 35,261,018UniSTSGRCh37
Build 362134,182,147 - 34,182,888RGDNCBI36
Celera2120,459,861 - 20,460,602RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,738,344 - 20,739,077UniSTS
ECD05283  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,069,968 - 35,070,708UniSTSGRCh37
Build 362133,991,838 - 33,992,578RGDNCBI36
Celera2120,269,589 - 20,270,329RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,548,277 - 20,549,017UniSTS
ECD05420  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,021,234 - 35,021,970UniSTSGRCh37
Build 362133,943,104 - 33,943,840RGDNCBI36
Celera2120,220,855 - 20,221,591RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,499,560 - 20,500,296UniSTS
ECD05524  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,129,434 - 35,130,167UniSTSGRCh37
Build 362134,051,304 - 34,052,037RGDNCBI36
Celera2120,329,056 - 20,329,789RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,607,466 - 20,608,199UniSTS
ECD05525  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,258,596 - 35,259,329UniSTSGRCh37
Build 362134,180,466 - 34,181,199RGDNCBI36
Celera2120,458,180 - 20,458,913RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,736,661 - 20,737,394UniSTS
ECD05607  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,165,248 - 35,165,979UniSTSGRCh37
Build 362134,087,118 - 34,087,849RGDNCBI36
Celera2120,364,870 - 20,365,601RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,643,246 - 20,643,977UniSTS
ECD05608  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,182,416 - 35,183,147UniSTSGRCh37
Build 362134,104,286 - 34,105,017RGDNCBI36
Celera2120,382,038 - 20,382,769RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,660,479 - 20,661,210UniSTS
ECD05687  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,051,223 - 35,051,952UniSTSGRCh37
Build 362133,973,093 - 33,973,822RGDNCBI36
Celera2120,250,844 - 20,251,573RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,529,552 - 20,530,281UniSTS
ECD05804  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,200,980 - 35,201,706UniSTSGRCh37
Build 362134,122,850 - 34,123,576RGDNCBI36
Celera2120,400,602 - 20,401,328RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,679,000 - 20,679,726UniSTS
ECD05805  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,261,037 - 35,261,763UniSTSGRCh37
Build 362134,182,907 - 34,183,633RGDNCBI36
Celera2120,460,621 - 20,461,347RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,739,096 - 20,739,822UniSTS
ECD06002  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,222,937 - 35,223,657UniSTSGRCh37
Build 362134,144,807 - 34,145,527RGDNCBI36
Celera2120,422,559 - 20,423,279RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,701,083 - 20,701,803UniSTS
ECD06048  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,016,405 - 35,017,124UniSTSGRCh37
Build 362133,938,275 - 33,938,994RGDNCBI36
Celera2120,216,026 - 20,216,745RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,494,730 - 20,495,450UniSTS
ECD06233  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,186,744 - 35,187,458UniSTSGRCh37
Build 362134,108,614 - 34,109,328RGDNCBI36
Celera2120,386,366 - 20,387,080RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,664,807 - 20,665,521UniSTS
ECD06608  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,034,392 - 35,035,096UniSTSGRCh37
Build 362133,956,262 - 33,956,966RGDNCBI36
Celera2120,234,013 - 20,234,717RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,512,719 - 20,513,423UniSTS
ECD06609  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,153,149 - 35,153,853UniSTSGRCh37
Build 362134,075,019 - 34,075,723RGDNCBI36
Celera2120,352,771 - 20,353,475RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,631,182 - 20,631,886UniSTS
ECD06684  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,122,405 - 35,123,107UniSTSGRCh37
Build 362134,044,275 - 34,044,977RGDNCBI36
Celera2120,322,027 - 20,322,729RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,600,437 - 20,601,139UniSTS
ECD06899  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,093,096 - 35,093,792UniSTSGRCh37
Build 362134,014,966 - 34,015,662RGDNCBI36
Celera2120,292,718 - 20,293,414RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,571,093 - 20,571,789UniSTS
ECD06937  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,126,864 - 35,127,559UniSTSGRCh37
Build 362134,048,734 - 34,049,429RGDNCBI36
Celera2120,326,486 - 20,327,181RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,604,896 - 20,605,591UniSTS
ECD07046  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,076,098 - 35,076,790UniSTSGRCh37
Build 362133,997,968 - 33,998,660RGDNCBI36
Celera2120,275,719 - 20,276,411RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,554,350 - 20,555,042UniSTS
ECD07047  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,230,164 - 35,230,856UniSTSGRCh37
Build 362134,152,034 - 34,152,726RGDNCBI36
Celera2120,429,787 - 20,430,479RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,708,309 - 20,709,001UniSTS
ECD07188  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,190,526 - 35,191,214UniSTSGRCh37
Build 362134,112,396 - 34,113,084RGDNCBI36
Celera2120,390,148 - 20,390,836RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,668,547 - 20,669,235UniSTS
ECD07223  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,217,959 - 35,218,646UniSTSGRCh37
Build 362134,139,829 - 34,140,516RGDNCBI36
Celera2120,417,581 - 20,418,268RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,696,105 - 20,696,792UniSTS
ECD07262  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,166,757 - 35,167,443UniSTSGRCh37
Build 362134,088,627 - 34,089,313RGDNCBI36
Celera2120,366,379 - 20,367,065RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,644,755 - 20,645,441UniSTS
ECD07296  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,126,097 - 35,126,782UniSTSGRCh37
Build 362134,047,967 - 34,048,652RGDNCBI36
Celera2120,325,719 - 20,326,404RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,604,129 - 20,604,814UniSTS
ECD07448  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,187,514 - 35,188,195UniSTSGRCh37
Build 362134,109,384 - 34,110,065RGDNCBI36
Celera2120,387,136 - 20,387,817RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,665,577 - 20,666,258UniSTS
ECD07478  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,191,269 - 35,191,949UniSTSGRCh37
Build 362134,113,139 - 34,113,819RGDNCBI36
Celera2120,390,891 - 20,391,571RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,669,290 - 20,669,970UniSTS
ECD07601  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,127,587 - 35,128,264UniSTSGRCh37
Build 362134,049,457 - 34,050,134RGDNCBI36
Celera2120,327,209 - 20,327,886RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,605,619 - 20,606,296UniSTS
ECD07750  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,166,039 - 35,166,712UniSTSGRCh37
Build 362134,087,909 - 34,088,582RGDNCBI36
Celera2120,365,661 - 20,366,334RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,644,037 - 20,644,710UniSTS
ECD07787  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,189,824 - 35,190,496UniSTSGRCh37
Build 362134,111,694 - 34,112,366RGDNCBI36
Celera2120,389,446 - 20,390,118RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,667,845 - 20,668,517UniSTS
ECD07919  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,055,121 - 35,055,789UniSTSGRCh37
Build 362133,976,991 - 33,977,659RGDNCBI36
Celera2120,254,742 - 20,255,410RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,533,434 - 20,534,102UniSTS
ECD07920  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,152,467 - 35,153,135UniSTSGRCh37
Build 362134,074,337 - 34,075,005RGDNCBI36
Celera2120,352,089 - 20,352,757RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,630,500 - 20,631,168UniSTS
ECD08049  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,181,152 - 35,181,817UniSTSGRCh37
Build 362134,103,022 - 34,103,687RGDNCBI36
Celera2120,380,774 - 20,381,439RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,659,215 - 20,659,880UniSTS
ECD08122  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,230,888 - 35,231,551UniSTSGRCh37
Build 362134,152,758 - 34,153,421RGDNCBI36
Celera2120,430,511 - 20,431,174RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,709,033 - 20,709,696UniSTS
ECD08241  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,154,337 - 35,154,997UniSTSGRCh37
Build 362134,076,207 - 34,076,867RGDNCBI36
Celera2120,353,959 - 20,354,619RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,632,370 - 20,633,030UniSTS
ECD08368  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,055,871 - 35,056,527UniSTSGRCh37
Build 362133,977,741 - 33,978,397RGDNCBI36
Celera2120,255,492 - 20,256,148RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,534,184 - 20,534,840UniSTS
ECD08606  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,035,224 - 35,035,874UniSTSGRCh37
Build 362133,957,094 - 33,957,744RGDNCBI36
Celera2120,234,845 - 20,235,495RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,513,551 - 20,514,202UniSTS
ECD08844  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,210,724 - 35,211,368UniSTSGRCh37
Build 362134,132,594 - 34,133,238RGDNCBI36
Celera2120,410,346 - 20,410,990RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,688,870 - 20,689,514UniSTS
ECD08979  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,057,968 - 35,058,608UniSTSGRCh37
Build 362133,979,838 - 33,980,478RGDNCBI36
Celera2120,257,589 - 20,258,229RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,536,281 - 20,536,921UniSTS
ECD09019  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,247,281 - 35,247,920UniSTSGRCh37
Build 362134,169,151 - 34,169,790RGDNCBI36
Celera2120,446,903 - 20,447,542RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,725,429 - 20,726,068UniSTS
ECD09056  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,086,435 - 35,087,073UniSTSGRCh37
Build 362134,008,305 - 34,008,943RGDNCBI36
Celera2120,286,058 - 20,286,696RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,564,500 - 20,565,132UniSTS
ECD09228  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,208,287 - 35,208,921UniSTSGRCh37
Build 362134,130,157 - 34,130,791RGDNCBI36
Celera2120,407,909 - 20,408,543RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,686,433 - 20,687,067UniSTS
ECD09623  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,171,151 - 35,171,775UniSTSGRCh37
Build 362134,093,021 - 34,093,645RGDNCBI36
Celera2120,370,773 - 20,371,397RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,649,150 - 20,649,774UniSTS
ECD10015  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,174,631 - 35,175,244UniSTSGRCh37
Build 362134,096,501 - 34,097,114RGDNCBI36
Celera2120,374,253 - 20,374,866RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,652,631 - 20,653,244UniSTS
ECD10016  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,188,915 - 35,189,528UniSTSGRCh37
Build 362134,110,785 - 34,111,398RGDNCBI36
Celera2120,388,537 - 20,389,150RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,666,936 - 20,667,549UniSTS
ECD10201  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,208,990 - 35,209,598UniSTSGRCh37
Build 362134,130,860 - 34,131,468RGDNCBI36
Celera2120,408,612 - 20,409,220RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,687,136 - 20,687,744UniSTS
ECD10239  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,169,726 - 35,170,333UniSTSGRCh37
Build 362134,091,596 - 34,092,203RGDNCBI36
Celera2120,369,348 - 20,369,955RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,647,725 - 20,648,332UniSTS
ECD10461  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,040,759 - 35,041,360UniSTSGRCh37
Build 362133,962,629 - 33,963,230RGDNCBI36
Celera2120,240,380 - 20,240,981RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,519,087 - 20,519,688UniSTS
ECD10530  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,040,120 - 35,040,719UniSTSGRCh37
Build 362133,961,990 - 33,962,589RGDNCBI36
Celera2120,239,741 - 20,240,340RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,518,448 - 20,519,047UniSTS
ECD10654  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,138,598 - 35,139,193UniSTSGRCh37
Build 362134,060,468 - 34,061,063RGDNCBI36
Celera2120,338,220 - 20,338,815RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,616,631 - 20,617,226UniSTS
ECD10725  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,216,217 - 35,216,810UniSTSGRCh37
Build 362134,138,087 - 34,138,680RGDNCBI36
Celera2120,415,839 - 20,416,432RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,694,363 - 20,694,956UniSTS
ECD10923  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,013,469 - 35,014,056UniSTSGRCh37
Build 362133,935,339 - 33,935,926RGDNCBI36
Celera2120,213,090 - 20,213,677RGD
Cytogenetic Map21q22.1-q22.2UniSTS
Cytogenetic Map21q21.3UniSTS
HuRef2120,491,794 - 20,492,381UniSTS
ECD10924  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,014,138 - 35,014,725UniSTSGRCh37
Build 362133,936,008 - 33,936,595RGDNCBI36
Celera2120,213,759 - 20,214,346RGD
Cytogenetic Map21q22.1-q22.2UniSTS
Cytogenetic Map21q21.3UniSTS
HuRef2120,492,463 - 20,493,050UniSTS
ECD10925  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,087,450 - 35,088,037UniSTSGRCh37
Build 362134,009,320 - 34,009,907RGDNCBI36
Celera2120,287,073 - 20,287,659RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,565,509 - 20,566,095UniSTS
ECD11067  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,227,680 - 35,228,263UniSTSGRCh37
Build 362134,149,550 - 34,150,133RGDNCBI36
Celera2120,427,303 - 20,427,886RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,705,827 - 20,706,410UniSTS
ECD11099  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,161,301 - 35,161,883UniSTSGRCh37
Build 362134,083,171 - 34,083,753RGDNCBI36
Celera2120,360,923 - 20,361,505RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,639,303 - 20,639,885UniSTS
ECD11180  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,161,946 - 35,162,526UniSTSGRCh37
Build 362134,083,816 - 34,084,396RGDNCBI36
Celera2120,361,568 - 20,362,148RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,639,948 - 20,640,528UniSTS
ECD11246  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,146,284 - 35,146,862UniSTSGRCh37
Build 362134,068,154 - 34,068,732RGDNCBI36
Celera2120,345,906 - 20,346,484RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,624,317 - 20,624,895UniSTS
ECD11430  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,174,042 - 35,174,614UniSTSGRCh37
Build 362134,095,912 - 34,096,484RGDNCBI36
Celera2120,373,664 - 20,374,236RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,652,042 - 20,652,614UniSTS
ECD11465  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,056,611 - 35,057,182UniSTSGRCh37
Build 362133,978,481 - 33,979,052RGDNCBI36
Celera2120,256,232 - 20,256,803RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,534,924 - 20,535,495UniSTS
ECD11466  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,213,667 - 35,214,238UniSTSGRCh37
Build 362134,135,537 - 34,136,108RGDNCBI36
Celera2120,413,289 - 20,413,860RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,691,813 - 20,692,384UniSTS
ECD11598  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,200,328 - 35,200,895UniSTSGRCh37
Build 362134,122,198 - 34,122,765RGDNCBI36
Celera2120,399,950 - 20,400,517RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,678,348 - 20,678,915UniSTS
ECD11642  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,169,141 - 35,169,707UniSTSGRCh37
Build 362134,091,011 - 34,091,577RGDNCBI36
Celera2120,368,763 - 20,369,329RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,647,140 - 20,647,706UniSTS
ECD11778  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,143,982 - 35,144,544UniSTSGRCh37
Build 362134,065,852 - 34,066,414RGDNCBI36
Celera2120,343,604 - 20,344,166RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,622,015 - 20,622,577UniSTS
ECD11808  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,199,753 - 35,200,314UniSTSGRCh37
Build 362134,121,623 - 34,122,184RGDNCBI36
Celera2120,399,375 - 20,399,936RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,677,773 - 20,678,334UniSTS
ECD12269  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,046,109 - 35,046,657UniSTSGRCh37
Build 362133,967,979 - 33,968,527RGDNCBI36
Celera2120,245,730 - 20,246,278RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,524,437 - 20,524,985UniSTS
ECD12270  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,137,934 - 35,138,482UniSTSGRCh37
Build 362134,059,804 - 34,060,352RGDNCBI36
Celera2120,337,556 - 20,338,104RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,615,967 - 20,616,515UniSTS
ECD12713  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,022,761 - 35,023,297UniSTSGRCh37
Build 362133,944,631 - 33,945,167RGDNCBI36
Celera2120,222,382 - 20,222,918RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,501,087 - 20,501,623UniSTS
ECD12797  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,216,908 - 35,217,442UniSTSGRCh37
Build 362134,138,778 - 34,139,312RGDNCBI36
Celera2120,416,530 - 20,417,064RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,695,054 - 20,695,588UniSTS
ECD12879  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,143,406 - 35,143,938UniSTSGRCh37
Build 362134,065,276 - 34,065,808RGDNCBI36
Celera2120,343,028 - 20,343,560RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,621,439 - 20,621,971UniSTS
ECD12918  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,179,127 - 35,179,658UniSTSGRCh37
Build 362134,100,997 - 34,101,528RGDNCBI36
Celera2120,378,749 - 20,379,280RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,657,190 - 20,657,721UniSTS
ECD13102  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,130,726 - 35,131,252UniSTSGRCh37
Build 362134,052,596 - 34,053,122RGDNCBI36
Celera2120,330,348 - 20,330,874RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,608,758 - 20,609,284UniSTS
ECD13103  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,214,837 - 35,215,363UniSTSGRCh37
Build 362134,136,707 - 34,137,233RGDNCBI36
Celera2120,414,459 - 20,414,985RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,692,983 - 20,693,509UniSTS
ECD13139  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,095,096 - 35,095,621UniSTSGRCh37
Build 362134,016,966 - 34,017,491RGDNCBI36
Celera2120,294,718 - 20,295,243RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,573,126 - 20,573,651UniSTS
ECD13226  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,252,333 - 35,252,856UniSTSGRCh37
Build 362134,174,203 - 34,174,726RGDNCBI36
Celera2120,451,917 - 20,452,440RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,730,397 - 20,730,920UniSTS
ECD13258  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,252,883 - 35,253,405UniSTSGRCh37
Build 362134,174,753 - 34,175,275RGDNCBI36
Celera2120,452,467 - 20,452,989RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,730,947 - 20,731,469UniSTS
ECD13495  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,109,328 - 35,109,844UniSTSGRCh37
Build 362134,031,198 - 34,031,714RGDNCBI36
Celera2120,308,950 - 20,309,466RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,587,361 - 20,587,877UniSTS
ECD13573  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,058,733 - 35,059,247UniSTSGRCh37
Build 362133,980,603 - 33,981,117RGDNCBI36
Celera2120,258,354 - 20,258,868RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,537,046 - 20,537,560UniSTS
ECD13574  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,178,538 - 35,179,052UniSTSGRCh37
Build 362134,100,408 - 34,100,922RGDNCBI36
Celera2120,378,160 - 20,378,674RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,656,601 - 20,657,115UniSTS
ECD13779  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,114,739 - 35,115,248UniSTSGRCh37
Build 362134,036,609 - 34,037,118RGDNCBI36
Celera2120,314,361 - 20,314,870RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,592,772 - 20,593,281UniSTS
ECD13824  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,141,078 - 35,141,586UniSTSGRCh37
Build 362134,062,948 - 34,063,456RGDNCBI36
Celera2120,340,700 - 20,341,208RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,619,111 - 20,619,619UniSTS
ECD14188  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,215,499 - 35,215,998UniSTSGRCh37
Build 362134,137,369 - 34,137,868RGDNCBI36
Celera2120,415,121 - 20,415,620RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,693,645 - 20,694,144UniSTS
ECD14235  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,059,753 - 35,060,251UniSTSGRCh37
Build 362133,981,623 - 33,982,121RGDNCBI36
Celera2120,259,374 - 20,259,872RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,538,057 - 20,538,555UniSTS
ECD14633  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,060,265 - 35,060,754UniSTSGRCh37
Build 362133,982,135 - 33,982,624RGDNCBI36
Celera2120,259,886 - 20,260,375RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,538,569 - 20,539,058UniSTS
ECD14634  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,108,455 - 35,108,944UniSTSGRCh37
Build 362134,030,325 - 34,030,814RGDNCBI36
Celera2120,308,077 - 20,308,566RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,586,487 - 20,586,977UniSTS
ECD14813  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,027,216 - 35,027,701UniSTSGRCh37
GRCh372135,027,216 - 35,028,821UniSTSGRCh37
Build 362133,949,086 - 33,949,571RGDNCBI36
Celera2120,226,837 - 20,228,442UniSTS
Celera2120,226,837 - 20,227,322RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,505,542 - 20,506,027UniSTS
HuRef2120,505,542 - 20,507,147UniSTS
ECD14852  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,135,953 - 35,136,437UniSTSGRCh37
Build 362134,057,823 - 34,058,307RGDNCBI36
Celera2120,335,575 - 20,336,059RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,613,986 - 20,614,470UniSTS
ECD14853  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,171,867 - 35,172,351UniSTSGRCh37
Build 362134,093,737 - 34,094,221RGDNCBI36
Celera2120,371,489 - 20,371,973RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,649,866 - 20,650,350UniSTS
ECD14985  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,146,950 - 35,147,431UniSTSGRCh37
Build 362134,068,820 - 34,069,301RGDNCBI36
Celera2120,346,572 - 20,347,053RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,624,983 - 20,625,464UniSTS
ECD15059  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,026,714 - 35,027,193UniSTSGRCh37
Build 362133,948,584 - 33,949,063RGDNCBI36
Celera2120,226,335 - 20,226,814RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,505,040 - 20,505,519UniSTS
ECD15153  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,018,358 - 35,018,835UniSTSGRCh37
Build 362133,940,228 - 33,940,705RGDNCBI36
Celera2120,217,979 - 20,218,456RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,496,684 - 20,497,161UniSTS
ECD15154  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,057,422 - 35,057,899UniSTSGRCh37
Build 362133,979,292 - 33,979,769RGDNCBI36
Celera2120,257,043 - 20,257,520RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,535,735 - 20,536,212UniSTS
ECD15239  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,106,086 - 35,106,561UniSTSGRCh37
Build 362134,027,956 - 34,028,431RGDNCBI36
Celera2120,305,708 - 20,306,183RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,584,118 - 20,584,593UniSTS
ECD15389  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,210,190 - 35,210,661UniSTSGRCh37
Build 362134,132,060 - 34,132,531RGDNCBI36
Celera2120,409,812 - 20,410,283RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,688,336 - 20,688,807UniSTS
ECD15426  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,167,770 - 35,168,240UniSTSGRCh37
Build 362134,089,640 - 34,090,110RGDNCBI36
Celera2120,367,392 - 20,367,862RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,645,768 - 20,646,238UniSTS
ECD15461  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,235,181 - 35,235,650UniSTSGRCh37
Build 362134,157,051 - 34,157,520RGDNCBI36
Celera2120,434,804 - 20,435,273RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,713,327 - 20,713,796UniSTS
ECD15649  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,209,698 - 35,210,163UniSTSGRCh37
Build 362134,131,568 - 34,132,033RGDNCBI36
Celera2120,409,320 - 20,409,785RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,687,844 - 20,688,309UniSTS
ECD15650  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,234,498 - 35,234,963UniSTSGRCh37
Build 362134,156,368 - 34,156,833RGDNCBI36
Celera2120,434,121 - 20,434,586RGD
Cytogenetic Map21q22.1-q22.2UniSTS
ECD15733  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,228,964 - 35,229,427UniSTSGRCh37
Build 362134,150,834 - 34,151,297RGDNCBI36
Celera2120,428,587 - 20,429,050RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,707,111 - 20,707,572UniSTS
ECD16255  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,020,388 - 35,020,836UniSTSGRCh37
Build 362133,942,258 - 33,942,706RGDNCBI36
Celera2120,220,009 - 20,220,457RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,498,714 - 20,499,162UniSTS
ECD16372  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,024,802 - 35,025,245UniSTSGRCh37
Build 362133,946,672 - 33,947,115RGDNCBI36
Celera2120,224,423 - 20,224,866RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,503,128 - 20,503,571UniSTS
ECD16718  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,094,515 - 35,094,943UniSTSGRCh37
Build 362134,016,385 - 34,016,813RGDNCBI36
Celera2120,294,137 - 20,294,565RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,572,545 - 20,572,973UniSTS
ECD16719  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,113,361 - 35,113,789UniSTSGRCh37
Build 362134,035,231 - 34,035,659RGDNCBI36
Celera2120,312,983 - 20,313,411RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,591,394 - 20,591,822UniSTS
ECD16768  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,023,671 - 35,024,097UniSTSGRCh37
Build 362133,945,541 - 33,945,967RGDNCBI36
Celera2120,223,292 - 20,223,718RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,501,997 - 20,502,423UniSTS
ECD17148  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,092,021 - 35,092,432UniSTSGRCh37
Build 362134,013,891 - 34,014,302RGDNCBI36
Celera2120,291,643 - 20,292,054RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,570,018 - 20,570,429UniSTS
ECD17335  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,231,771 - 35,232,174UniSTSGRCh37
Build 362134,153,641 - 34,154,044RGDNCBI36
Celera2120,431,394 - 20,431,797RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,709,916 - 20,710,320UniSTS
ECD17350  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,213,182 - 35,213,584UniSTSGRCh37
Build 362134,135,052 - 34,135,454RGDNCBI36
Celera2120,412,804 - 20,413,206RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,691,328 - 20,691,730UniSTS
ECD17422  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,229,574 - 35,229,973UniSTSGRCh37
Build 362134,151,444 - 34,151,843RGDNCBI36
Celera2120,429,197 - 20,429,596RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,707,719 - 20,708,118UniSTS
ECD17452  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,047,123 - 35,047,521UniSTSGRCh37
Build 362133,968,993 - 33,969,391RGDNCBI36
Celera2120,246,744 - 20,247,142RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,525,451 - 20,525,849UniSTS
ECD17542  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,096,446 - 35,096,840UniSTSGRCh37
Build 362134,018,316 - 34,018,710RGDNCBI36
Celera2120,296,068 - 20,296,462RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,574,476 - 20,574,870UniSTS
ECD17543  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,218,791 - 35,219,185UniSTSGRCh37
Build 362134,140,661 - 34,141,055RGDNCBI36
Celera2120,418,413 - 20,418,807RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,696,937 - 20,697,331UniSTS
ECD17566  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,186,164 - 35,186,497UniSTSGRCh37
GRCh372135,186,104 - 35,186,497UniSTSGRCh37
Build 362134,107,974 - 34,108,367RGDNCBI36
Celera2120,385,726 - 20,386,119RGD
Celera2120,385,786 - 20,386,119UniSTS
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,664,167 - 20,664,560UniSTS
HuRef2120,664,227 - 20,664,560UniSTS
ECD17597  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,193,397 - 35,193,789UniSTSGRCh37
Build 362134,115,267 - 34,115,659RGDNCBI36
Celera2120,393,019 - 20,393,411RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,671,418 - 20,671,809UniSTS
ECD17877  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,177,416 - 35,177,797UniSTSGRCh37
Build 362134,099,286 - 34,099,667RGDNCBI36
Celera2120,377,038 - 20,377,419RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,655,416 - 20,655,797UniSTS
ECD18320  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,103,345 - 35,103,709UniSTSGRCh37
Build 362134,025,215 - 34,025,579RGDNCBI36
Celera2120,302,967 - 20,303,331RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,581,376 - 20,581,740UniSTS
ECD18392  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,117,912 - 35,118,273UniSTSGRCh37
Build 362134,039,782 - 34,040,143RGDNCBI36
Celera2120,317,534 - 20,317,895RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,595,945 - 20,596,306UniSTS
ECD18454  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,092,550 - 35,092,909UniSTSGRCh37
Build 362134,014,420 - 34,014,779RGDNCBI36
Celera2120,292,172 - 20,292,531RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,570,547 - 20,570,906UniSTS
ECD18455  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,176,120 - 35,176,479UniSTSGRCh37
Build 362134,097,990 - 34,098,349RGDNCBI36
Celera2120,375,742 - 20,376,101RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,654,120 - 20,654,479UniSTS
ECD18514  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,246,582 - 35,246,939UniSTSGRCh37
Build 362134,168,452 - 34,168,809RGDNCBI36
Celera2120,446,204 - 20,446,561RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,724,727 - 20,725,084UniSTS
ECD18537  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,078,662 - 35,079,018UniSTSGRCh37
Build 362134,000,532 - 34,000,888RGDNCBI36
Celera2120,278,283 - 20,278,639RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,556,726 - 20,557,082UniSTS
ECD18582  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,156,018 - 35,156,372UniSTSGRCh37
Build 362134,077,888 - 34,078,242RGDNCBI36
Celera2120,355,640 - 20,355,994RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,634,050 - 20,634,404UniSTS
ECD18617  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,155,521 - 35,155,874UniSTSGRCh37
Build 362134,077,391 - 34,077,744RGDNCBI36
Celera2120,355,143 - 20,355,496RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,633,554 - 20,633,907UniSTS
ECD18701  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,205,358 - 35,205,708UniSTSGRCh37
Build 362134,127,228 - 34,127,578RGDNCBI36
Celera2120,404,980 - 20,405,330RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,683,378 - 20,683,728UniSTS
ECD18870  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,212,298 - 35,212,642UniSTSGRCh37
Build 362134,134,168 - 34,134,512RGDNCBI36
Celera2120,411,920 - 20,412,264RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,690,444 - 20,690,788UniSTS
ECD18919  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,028,034 - 35,028,376UniSTSGRCh37
Build 362133,949,904 - 33,950,246RGDNCBI36
Celera2120,227,655 - 20,227,997RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,506,360 - 20,506,702UniSTS
ECD19108  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,211,810 - 35,212,144UniSTSGRCh37
Build 362134,133,680 - 34,134,014RGDNCBI36
Celera2120,411,432 - 20,411,766RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,689,956 - 20,690,290UniSTS
ECD19478  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,176,739 - 35,177,059UniSTSGRCh37
Build 362134,098,609 - 34,098,929RGDNCBI36
Celera2120,376,361 - 20,376,681RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,654,739 - 20,655,059UniSTS
ECD19542  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,022,379 - 35,022,697UniSTSGRCh37
Build 362133,944,249 - 33,944,567RGDNCBI36
Celera2120,222,000 - 20,222,318RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,500,705 - 20,501,023UniSTS
ECD19573  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,116,425 - 35,116,742UniSTSGRCh37
Build 362134,038,295 - 34,038,612RGDNCBI36
Celera2120,316,047 - 20,316,364RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,594,458 - 20,594,775UniSTS
ECD19677  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,133,021 - 35,133,334UniSTSGRCh37
Build 362134,054,891 - 34,055,204RGDNCBI36
Celera2120,332,643 - 20,332,956RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,611,053 - 20,611,366UniSTS
ECD20300  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,097,938 - 35,098,227UniSTSGRCh37
Build 362134,019,808 - 34,020,097RGDNCBI36
Celera2120,297,560 - 20,297,849RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,575,968 - 20,576,257UniSTS
ECD20515  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,072,712 - 35,072,993UniSTSGRCh37
Build 362133,994,582 - 33,994,863RGDNCBI36
Celera2120,272,333 - 20,272,614RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,551,021 - 20,551,302UniSTS
ECD20686  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,214,505 - 35,214,780UniSTSGRCh37
Build 362134,136,375 - 34,136,650RGDNCBI36
Celera2120,414,127 - 20,414,402RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,692,651 - 20,692,926UniSTS
ECD20724  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,029,590 - 35,029,864UniSTSGRCh37
Build 362133,951,460 - 33,951,734RGDNCBI36
Celera2120,229,211 - 20,229,485RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,507,916 - 20,508,190UniSTS
ECD20725  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,052,936 - 35,053,210UniSTSGRCh37
Build 362133,974,806 - 33,975,080RGDNCBI36
Celera2120,252,557 - 20,252,831RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,531,266 - 20,531,534UniSTS
ECD20785  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,042,065 - 35,042,337UniSTSGRCh37
Build 362133,963,935 - 33,964,207RGDNCBI36
Celera2120,241,686 - 20,241,958RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,520,393 - 20,520,665UniSTS
ECD20887  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,164,903 - 35,165,171UniSTSGRCh37
Build 362134,086,773 - 34,087,041RGDNCBI36
Celera2120,364,525 - 20,364,793RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,642,901 - 20,643,169UniSTS
ECD20912  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,245,456 - 35,245,723UniSTSGRCh37
Build 362134,167,326 - 34,167,593RGDNCBI36
Celera2120,445,078 - 20,445,345RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,723,601 - 20,723,868UniSTS
ECD20942  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,075,664 - 35,075,930UniSTSGRCh37
Build 362133,997,534 - 33,997,800RGDNCBI36
Celera2120,275,285 - 20,275,551RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,553,916 - 20,554,182UniSTS
ECD20943  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,220,985 - 35,221,251UniSTSGRCh37
Build 362134,142,855 - 34,143,121RGDNCBI36
Celera2120,420,607 - 20,420,873RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,699,131 - 20,699,397UniSTS
ECD21138  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,111,430 - 35,111,690UniSTSGRCh37
Build 362134,033,300 - 34,033,560RGDNCBI36
Celera2120,311,052 - 20,311,312RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,589,463 - 20,589,723UniSTS
ECD21157  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,136,514 - 35,136,773UniSTSGRCh37
Build 362134,058,384 - 34,058,643RGDNCBI36
Celera2120,336,136 - 20,336,395RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,614,547 - 20,614,806UniSTS
ECD21215  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,137,026 - 35,137,283UniSTSGRCh37
Build 362134,058,896 - 34,059,153RGDNCBI36
Celera2120,336,648 - 20,336,905RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,615,059 - 20,615,316UniSTS
ECD21236  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,052,354 - 35,052,610UniSTSGRCh37
Build 362133,974,224 - 33,974,480RGDNCBI36
Celera2120,251,975 - 20,252,231RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,530,684 - 20,530,940UniSTS
ECD21261  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,251,678 - 35,251,933UniSTSGRCh37
Build 362134,173,548 - 34,173,803RGDNCBI36
Celera2120,451,262 - 20,451,517RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,729,742 - 20,729,997UniSTS
ECD21308  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,250,810 - 35,251,063UniSTSGRCh37
Build 362134,172,680 - 34,172,933RGDNCBI36
Celera2120,450,394 - 20,450,647RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,728,874 - 20,729,127UniSTS
ECD21376  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,179,952 - 35,180,203UniSTSGRCh37
Build 362134,101,822 - 34,102,073RGDNCBI36
Celera2120,379,574 - 20,379,825RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,658,015 - 20,658,266UniSTS
ECD21449  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,032,334 - 35,032,583UniSTSGRCh37
Build 362133,954,204 - 33,954,453RGDNCBI36
Celera2120,231,955 - 20,232,204RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,510,661 - 20,510,910UniSTS
ECD21696  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,253,737 - 35,253,979UniSTSGRCh37
Build 362134,175,607 - 34,175,849RGDNCBI36
Celera2120,453,321 - 20,453,563RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,731,801 - 20,732,043UniSTS
ECD21733  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,173,518 - 35,173,759UniSTSGRCh37
Build 362134,095,388 - 34,095,629RGDNCBI36
Celera2120,373,140 - 20,373,381RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,651,518 - 20,651,759UniSTS
ECD21734  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,232,670 - 35,232,911UniSTSGRCh37
Build 362134,154,540 - 34,154,781RGDNCBI36
Celera2120,432,293 - 20,432,534RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,710,816 - 20,711,057UniSTS
ECD21913  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,063,172 - 35,063,407UniSTSGRCh37
Build 362133,985,042 - 33,985,277RGDNCBI36
Celera2120,262,793 - 20,263,028RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,541,480 - 20,541,715UniSTS
ECD22134  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,185,156 - 35,185,384UniSTSGRCh37
Build 362134,107,026 - 34,107,254RGDNCBI36
Celera2120,384,778 - 20,385,006RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,663,219 - 20,663,447UniSTS
ECD22190  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,096,158 - 35,096,384UniSTSGRCh37
Build 362134,018,028 - 34,018,254RGDNCBI36
Celera2120,295,780 - 20,296,006RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,574,188 - 20,574,414UniSTS
ECD22259  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,050,809 - 35,051,033UniSTSGRCh37
Build 362133,972,679 - 33,972,903RGDNCBI36
Celera2120,250,430 - 20,250,654RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,529,138 - 20,529,362UniSTS
ECD22260  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,168,612 - 35,168,836UniSTSGRCh37
Build 362134,090,482 - 34,090,706RGDNCBI36
Celera2120,368,234 - 20,368,458RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,646,611 - 20,646,835UniSTS
ECD22299  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,061,469 - 35,061,692UniSTSGRCh37
Build 362133,983,339 - 33,983,562RGDNCBI36
Celera2120,261,090 - 20,261,313RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,539,773 - 20,539,996UniSTS
ECD22300  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,077,451 - 35,077,674UniSTSGRCh37
Build 362133,999,321 - 33,999,544RGDNCBI36
Celera2120,277,072 - 20,277,295RGD
Cytogenetic Map21q22.1-q22.2UniSTS
ECD22363  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,048,836 - 35,049,057UniSTSGRCh37
Build 362133,970,706 - 33,970,927RGDNCBI36
Celera2120,248,457 - 20,248,678RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,527,164 - 20,527,385UniSTS
ECD22437  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,131,784 - 35,132,003UniSTSGRCh37
Build 362134,053,654 - 34,053,873RGDNCBI36
Celera2120,331,406 - 20,331,625RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,609,816 - 20,610,035UniSTS
ECD22531  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,106,648 - 35,106,864UniSTSGRCh37
Build 362134,028,518 - 34,028,734RGDNCBI36
Celera2120,306,270 - 20,306,486RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,584,680 - 20,584,896UniSTS
ECD22640  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,105,670 - 35,105,883UniSTSGRCh37
Build 362134,027,540 - 34,027,753RGDNCBI36
Celera2120,305,292 - 20,305,505RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,583,701 - 20,583,914UniSTS
ECD22813  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,065,424 - 35,065,631UniSTSGRCh37
Build 362133,987,294 - 33,987,501RGDNCBI36
Celera2120,265,045 - 20,265,252RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,543,732 - 20,543,939UniSTS
ECD22939  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,060,862 - 35,061,065UniSTSGRCh37
Build 362133,982,732 - 33,982,935RGDNCBI36
Celera2120,260,483 - 20,260,686RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,539,166 - 20,539,369UniSTS
ECD22940  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,085,924 - 35,086,127UniSTSGRCh37
Build 362134,007,794 - 34,007,997RGDNCBI36
Celera2120,285,547 - 20,285,750RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,563,988 - 20,564,191UniSTS
ECD22975  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,188,516 - 35,188,718UniSTSGRCh37
Build 362134,110,386 - 34,110,588RGDNCBI36
Celera2120,388,138 - 20,388,340RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,666,579 - 20,666,781UniSTS
ECD23121  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,053,402 - 35,053,600UniSTSGRCh37
Build 362133,975,272 - 33,975,470RGDNCBI36
Celera2120,253,023 - 20,253,221RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,531,726 - 20,531,924UniSTS
ECD23163  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,065,968 - 35,066,165UniSTSGRCh37
Build 362133,987,838 - 33,988,035RGDNCBI36
Celera2120,265,589 - 20,265,786RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,544,276 - 20,544,473UniSTS
ECD23198  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,054,290 - 35,054,486UniSTSGRCh37
Build 362133,976,160 - 33,976,356RGDNCBI36
Celera2120,253,911 - 20,254,107RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,532,603 - 20,532,799UniSTS
ECD23321  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,148,086 - 35,148,278UniSTSGRCh37
Build 362134,069,956 - 34,070,148RGDNCBI36
Celera2120,347,708 - 20,347,900RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,626,119 - 20,626,311UniSTS
ECD23369  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,078,060 - 35,078,251UniSTSGRCh37
Build 362133,999,930 - 34,000,121RGDNCBI36
Celera2120,277,681 - 20,277,872RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,556,124 - 20,556,315UniSTS
ECD23557  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,037,059 - 35,037,244UniSTSGRCh37
Build 362133,958,929 - 33,959,114RGDNCBI36
Celera2120,236,680 - 20,236,865RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,515,387 - 20,515,572UniSTS
ECD23645  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,105,266 - 35,105,448UniSTSGRCh37
Build 362134,027,136 - 34,027,318RGDNCBI36
Celera2120,304,888 - 20,305,070RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,583,297 - 20,583,479UniSTS
ECD23743  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,025,605 - 35,025,783UniSTSGRCh37
Build 362133,947,475 - 33,947,653RGDNCBI36
Celera2120,225,226 - 20,225,404RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,503,931 - 20,504,109UniSTS
ECD23848  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,090,194 - 35,090,367UniSTSGRCh37
Build 362134,012,064 - 34,012,237RGDNCBI36
Celera2120,289,816 - 20,289,989RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,568,191 - 20,568,364UniSTS
ECD23849  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,090,990 - 35,091,163UniSTSGRCh37
Build 362134,012,860 - 34,013,033RGDNCBI36
Celera2120,290,612 - 20,290,785RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,568,987 - 20,569,160UniSTS
ECD24066  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,098,639 - 35,098,801UniSTSGRCh37
Build 362134,020,509 - 34,020,671RGDNCBI36
Celera2120,298,261 - 20,298,423RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,576,669 - 20,576,831UniSTS
ECD24121  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,079,381 - 35,079,540UniSTSGRCh37
Build 362134,001,251 - 34,001,410RGDNCBI36
Celera2120,279,002 - 20,279,161RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,557,445 - 20,557,604UniSTS
ECD24165  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,028,692 - 35,028,848UniSTSGRCh37
Build 362133,950,562 - 33,950,718RGDNCBI36
Celera2120,228,313 - 20,228,469RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,507,018 - 20,507,174UniSTS
ECD24260  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,242,386 - 35,242,534UniSTSGRCh37
Build 362134,164,256 - 34,164,404RGDNCBI36
Celera2120,442,008 - 20,442,156RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,720,531 - 20,720,679UniSTS
ECD24387  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,046,854 - 35,046,989UniSTSGRCh37
Build 362133,968,724 - 33,968,859RGDNCBI36
Celera2120,246,475 - 20,246,610RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,525,182 - 20,525,317UniSTS
ECD24435  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,069,746 - 35,069,874UniSTSGRCh37
Build 362133,991,616 - 33,991,744RGDNCBI36
Celera2120,269,367 - 20,269,495RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,548,055 - 20,548,183UniSTS
ECD24515  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,181,936 - 35,182,045UniSTSGRCh37
Build 362134,103,806 - 34,103,915RGDNCBI36
Celera2120,381,558 - 20,381,667RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,659,999 - 20,660,108UniSTS
REN86049  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,012,855 - 35,013,101UniSTSGRCh37
Build 362133,934,725 - 33,934,971RGDNCBI36
Celera2120,212,476 - 20,212,722RGD
Cytogenetic Map21q22.1-q22.2UniSTS
Cytogenetic Map21q21.3UniSTS
HuRef2120,491,180 - 20,491,426UniSTS
REN86050  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,013,099 - 35,013,361UniSTSGRCh37
Build 362133,934,969 - 33,935,231RGDNCBI36
Celera2120,212,720 - 20,212,982RGD
Cytogenetic Map21q22.1-q22.2UniSTS
Cytogenetic Map21q21.3UniSTS
HuRef2120,491,424 - 20,491,686UniSTS
REN86051  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,013,348 - 35,013,606UniSTSGRCh37
Build 362133,935,218 - 33,935,476RGDNCBI36
Celera2120,212,969 - 20,213,227RGD
Cytogenetic Map21q22.1-q22.2UniSTS
Cytogenetic Map21q21.3UniSTS
HuRef2120,491,673 - 20,491,931UniSTS
REN86052  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,013,583 - 35,013,824UniSTSGRCh37
Build 362133,935,453 - 33,935,694RGDNCBI36
Celera2120,213,204 - 20,213,445RGD
Cytogenetic Map21q22.1-q22.2UniSTS
Cytogenetic Map21q21.3UniSTS
HuRef2120,491,908 - 20,492,149UniSTS
REN86053  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,013,802 - 35,014,051UniSTSGRCh37
Build 362133,935,672 - 33,935,921RGDNCBI36
Celera2120,213,423 - 20,213,672RGD
Cytogenetic Map21q22.1-q22.2UniSTS
Cytogenetic Map21q21.3UniSTS
HuRef2120,492,127 - 20,492,376UniSTS
REN86054  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,014,030 - 35,014,279UniSTSGRCh37
Build 362133,935,900 - 33,936,149RGDNCBI36
Celera2120,213,651 - 20,213,900RGD
Cytogenetic Map21q22.1-q22.2UniSTS
Cytogenetic Map21q21.3UniSTS
HuRef2120,492,355 - 20,492,604UniSTS
REN86055  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,014,267 - 35,014,509UniSTSGRCh37
Build 362133,936,137 - 33,936,379RGDNCBI36
Celera2120,213,888 - 20,214,130RGD
Cytogenetic Map21q22.1-q22.2UniSTS
Cytogenetic Map21q21.3UniSTS
HuRef2120,492,592 - 20,492,834UniSTS
REN86056  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,014,477 - 35,014,726UniSTSGRCh37
Build 362133,936,347 - 33,936,596RGDNCBI36
Celera2120,214,098 - 20,214,347RGD
Cytogenetic Map21q22.1-q22.2UniSTS
Cytogenetic Map21q21.3UniSTS
HuRef2120,492,802 - 20,493,051UniSTS
REN86057  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,014,607 - 35,014,862UniSTSGRCh37
Build 362133,936,477 - 33,936,732RGDNCBI36
Celera2120,214,228 - 20,214,483RGD
Cytogenetic Map21q22.1-q22.2UniSTS
Cytogenetic Map21q21.3UniSTS
HuRef2120,492,932 - 20,493,187UniSTS
REN86058  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,014,793 - 35,015,038UniSTSGRCh37
Build 362133,936,663 - 33,936,908RGDNCBI36
Celera2120,214,414 - 20,214,659RGD
Cytogenetic Map21q22.1-q22.2UniSTS
Cytogenetic Map21q21.3UniSTS
HuRef2120,493,118 - 20,493,363UniSTS
REN86059  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,014,965 - 35,015,218UniSTSGRCh37
Build 362133,936,835 - 33,937,088RGDNCBI36
Celera2120,214,586 - 20,214,839RGD
Cytogenetic Map21q22.1-q22.2UniSTS
Cytogenetic Map21q21.3UniSTS
HuRef2120,493,290 - 20,493,543UniSTS
REN86060  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,015,518 - 35,015,749UniSTSGRCh37
Build 362133,937,388 - 33,937,619RGDNCBI36
Celera2120,215,139 - 20,215,370RGD
Cytogenetic Map21q22.1-q22.2UniSTS
Cytogenetic Map21q21.3UniSTS
HuRef2120,493,843 - 20,494,074UniSTS
REN86061  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,015,734 - 35,015,987UniSTSGRCh37
Build 362133,937,604 - 33,937,857RGDNCBI36
Celera2120,215,355 - 20,215,608RGD
Cytogenetic Map21q22.1-q22.2UniSTS
Cytogenetic Map21q21.3UniSTS
HuRef2120,494,059 - 20,494,312UniSTS
REN86062  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,015,974 - 35,016,230UniSTSGRCh37
Build 362133,937,844 - 33,938,100RGDNCBI36
Celera2120,215,595 - 20,215,851RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,494,299 - 20,494,555UniSTS
REN86063  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,016,173 - 35,016,438UniSTSGRCh37
Build 362133,938,043 - 33,938,308RGDNCBI36
Celera2120,215,794 - 20,216,059RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,494,498 - 20,494,763UniSTS
REN86064  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,016,416 - 35,016,666UniSTSGRCh37
Build 362133,938,286 - 33,938,536RGDNCBI36
Celera2120,216,037 - 20,216,287RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,494,741 - 20,494,991UniSTS
REN86065  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,016,643 - 35,016,897UniSTSGRCh37
Build 362133,938,513 - 33,938,767RGDNCBI36
Celera2120,216,264 - 20,216,518RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,494,968 - 20,495,222UniSTS
REN86066  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,016,890 - 35,017,124UniSTSGRCh37
Build 362133,938,760 - 33,938,994RGDNCBI36
Celera2120,216,511 - 20,216,745RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,495,215 - 20,495,450UniSTS
REN86067  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,017,104 - 35,017,365UniSTSGRCh37
Build 362133,938,974 - 33,939,235RGDNCBI36
Celera2120,216,725 - 20,216,986RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,495,430 - 20,495,691UniSTS
REN86068  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,017,348 - 35,017,596UniSTSGRCh37
Build 362133,939,218 - 33,939,466RGDNCBI36
Celera2120,216,969 - 20,217,217RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,495,674 - 20,495,922UniSTS
REN86069  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,017,581 - 35,017,836UniSTSGRCh37
Build 362133,939,451 - 33,939,706RGDNCBI36
Celera2120,217,202 - 20,217,457RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,495,907 - 20,496,162UniSTS
REN86070  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,017,833 - 35,018,077UniSTSGRCh37
Build 362133,939,703 - 33,939,947RGDNCBI36
Celera2120,217,454 - 20,217,698RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,496,159 - 20,496,403UniSTS
REN86071  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,018,055 - 35,018,305UniSTSGRCh37
Build 362133,939,925 - 33,940,175RGDNCBI36
Celera2120,217,676 - 20,217,926RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,496,381 - 20,496,631UniSTS
REN86072  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,018,283 - 35,018,507UniSTSGRCh37
Build 362133,940,153 - 33,940,377RGDNCBI36
Celera2120,217,904 - 20,218,128RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,496,609 - 20,496,833UniSTS
REN86073  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,018,491 - 35,018,756UniSTSGRCh37
Build 362133,940,361 - 33,940,626RGDNCBI36
Celera2120,218,112 - 20,218,377RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,496,817 - 20,497,082UniSTS
REN86074  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,018,693 - 35,018,930UniSTSGRCh37
Build 362133,940,563 - 33,940,800RGDNCBI36
Celera2120,218,314 - 20,218,551RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,497,019 - 20,497,256UniSTS
REN86075  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,018,907 - 35,019,173UniSTSGRCh37
Build 362133,940,777 - 33,941,043RGDNCBI36
Celera2120,218,528 - 20,218,794RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,497,233 - 20,497,499UniSTS
REN86076  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,019,069 - 35,019,340UniSTSGRCh37
Build 362133,940,939 - 33,941,210RGDNCBI36
Celera2120,218,690 - 20,218,961RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,497,395 - 20,497,666UniSTS
REN86077  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,019,311 - 35,019,576UniSTSGRCh37
Build 362133,941,181 - 33,941,446RGDNCBI36
Celera2120,218,932 - 20,219,197RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,497,637 - 20,497,902UniSTS
REN86078  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,019,567 - 35,019,797UniSTSGRCh37
Build 362133,941,437 - 33,941,667RGDNCBI36
Celera2120,219,188 - 20,219,418RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,497,893 - 20,498,123UniSTS
REN86079  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,019,773 - 35,020,037UniSTSGRCh37
Build 362133,941,643 - 33,941,907RGDNCBI36
Celera2120,219,394 - 20,219,658RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,498,099 - 20,498,363UniSTS
REN86080  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,020,014 - 35,020,281UniSTSGRCh37
Build 362133,941,884 - 33,942,151RGDNCBI36
Celera2120,219,635 - 20,219,902RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,498,340 - 20,498,607UniSTS
REN86081  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,020,265 - 35,020,523UniSTSGRCh37
Build 362133,942,135 - 33,942,393RGDNCBI36
Celera2120,219,886 - 20,220,144RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,498,591 - 20,498,849UniSTS
REN86082  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,020,507 - 35,020,765UniSTSGRCh37
Build 362133,942,377 - 33,942,635RGDNCBI36
Celera2120,220,128 - 20,220,386RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,498,833 - 20,499,091UniSTS
REN86083  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,020,681 - 35,020,919UniSTSGRCh37
Build 362133,942,551 - 33,942,789RGDNCBI36
Celera2120,220,302 - 20,220,540RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,499,007 - 20,499,245UniSTS
REN86084  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,020,887 - 35,021,111UniSTSGRCh37
Build 362133,942,757 - 33,942,981RGDNCBI36
Celera2120,220,508 - 20,220,732RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,499,213 - 20,499,437UniSTS
REN86085  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,021,060 - 35,021,317UniSTSGRCh37
Build 362133,942,930 - 33,943,187RGDNCBI36
Celera2120,220,681 - 20,220,938RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,499,386 - 20,499,643UniSTS
REN86086  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,021,293 - 35,021,559UniSTSGRCh37
GRCh372135,021,293 - 35,021,502UniSTSGRCh37
Build 362133,943,163 - 33,943,372RGDNCBI36
Celera2120,220,914 - 20,221,123RGD
Celera2120,220,914 - 20,221,180UniSTS
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,499,619 - 20,499,828UniSTS
HuRef2120,499,619 - 20,499,885UniSTS
REN86087  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,021,551 - 35,021,804UniSTSGRCh37
Build 362133,943,421 - 33,943,674RGDNCBI36
Celera2120,221,172 - 20,221,425RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,499,877 - 20,500,130UniSTS
REN86088  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,021,793 - 35,022,044UniSTSGRCh37
Build 362133,943,663 - 33,943,914RGDNCBI36
Celera2120,221,414 - 20,221,665RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,500,119 - 20,500,370UniSTS
REN86089  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,022,018 - 35,022,257UniSTSGRCh37
Build 362133,943,888 - 33,944,127RGDNCBI36
Celera2120,221,639 - 20,221,878RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,500,344 - 20,500,583UniSTS
REN86090  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,022,233 - 35,022,463UniSTSGRCh37
Build 362133,944,103 - 33,944,333RGDNCBI36
Celera2120,221,854 - 20,222,084RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,500,559 - 20,500,789UniSTS
REN86091  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,022,439 - 35,022,667UniSTSGRCh37
Build 362133,944,309 - 33,944,537RGDNCBI36
Celera2120,222,060 - 20,222,288RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,500,765 - 20,500,993UniSTS
REN86092  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,022,644 - 35,022,905UniSTSGRCh37
Build 362133,944,514 - 33,944,775RGDNCBI36
Celera2120,222,265 - 20,222,526RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,500,970 - 20,501,231UniSTS
REN86093  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,022,882 - 35,023,118UniSTSGRCh37
Build 362133,944,752 - 33,944,988RGDNCBI36
Celera2120,222,503 - 20,222,739RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,501,208 - 20,501,444UniSTS
REN86094  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,023,098 - 35,023,347UniSTSGRCh37
Build 362133,944,968 - 33,945,217RGDNCBI36
Celera2120,222,719 - 20,222,968RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,501,424 - 20,501,673UniSTS
REN86095  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,023,323 - 35,023,560UniSTSGRCh37
Build 362133,945,193 - 33,945,430RGDNCBI36
Celera2120,222,944 - 20,223,181RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,501,649 - 20,501,886UniSTS
REN86096  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,023,545 - 35,023,797UniSTSGRCh37
Build 362133,945,415 - 33,945,667RGDNCBI36
Celera2120,223,166 - 20,223,418RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,501,871 - 20,502,123UniSTS
REN86097  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,023,774 - 35,024,033UniSTSGRCh37
Build 362133,945,644 - 33,945,903RGDNCBI36
Celera2120,223,395 - 20,223,654RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,502,100 - 20,502,359UniSTS
REN86098  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,024,017 - 35,024,241UniSTSGRCh37
Build 362133,945,887 - 33,946,111RGDNCBI36
Celera2120,223,638 - 20,223,862RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,502,343 - 20,502,567UniSTS
REN86099  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,024,230 - 35,024,485UniSTSGRCh37
Build 362133,946,100 - 33,946,355RGDNCBI36
Celera2120,223,851 - 20,224,106RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,502,556 - 20,502,811UniSTS
REN86100  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,024,462 - 35,024,727UniSTSGRCh37
Build 362133,946,332 - 33,946,597RGDNCBI36
Celera2120,224,083 - 20,224,348RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,502,788 - 20,503,053UniSTS
REN86101  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,024,720 - 35,024,972UniSTSGRCh37
Build 362133,946,590 - 33,946,842RGDNCBI36
Celera2120,224,341 - 20,224,593RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,503,046 - 20,503,298UniSTS
REN86102  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,024,968 - 35,025,236UniSTSGRCh37
Build 362133,946,838 - 33,947,106RGDNCBI36
Celera2120,224,589 - 20,224,857RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,503,294 - 20,503,562UniSTS
REN86103  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,025,117 - 35,025,341UniSTSGRCh37
Build 362133,946,987 - 33,947,211RGDNCBI36
Celera2120,224,738 - 20,224,962RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,503,443 - 20,503,667UniSTS
REN86104  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,026,152 - 35,026,380UniSTSGRCh37
Build 362133,948,022 - 33,948,250RGDNCBI36
Celera2120,225,773 - 20,226,001RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,504,478 - 20,504,706UniSTS
REN86105  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,026,359 - 35,026,603UniSTSGRCh37
Build 362133,948,229 - 33,948,473RGDNCBI36
Celera2120,225,980 - 20,226,224RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,504,685 - 20,504,929UniSTS
REN86106  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,026,587 - 35,026,837UniSTSGRCh37
Build 362133,948,457 - 33,948,707RGDNCBI36
Celera2120,226,208 - 20,226,458RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,504,913 - 20,505,163UniSTS
REN86107  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,026,788 - 35,027,036UniSTSGRCh37
Build 362133,948,658 - 33,948,906RGDNCBI36
Celera2120,226,409 - 20,226,657RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,505,114 - 20,505,362UniSTS
REN86108  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,026,994 - 35,027,243UniSTSGRCh37
Build 362133,948,864 - 33,949,113RGDNCBI36
Celera2120,226,615 - 20,226,864RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,505,320 - 20,505,569UniSTS
REN86109  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,027,229 - 35,027,478UniSTSGRCh37
Build 362133,949,099 - 33,949,348RGDNCBI36
Celera2120,226,850 - 20,227,099RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,505,555 - 20,505,804UniSTS
REN86110  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,027,451 - 35,027,709UniSTSGRCh37
GRCh372135,027,451 - 35,028,829UniSTSGRCh37
Build 362133,949,321 - 33,949,579RGDNCBI36
Celera2120,227,072 - 20,228,450UniSTS
Celera2120,227,072 - 20,227,330RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,505,777 - 20,506,035UniSTS
HuRef2120,505,777 - 20,507,155UniSTS
REN86111  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,027,708 - 35,027,976UniSTSGRCh37
Build 362133,949,578 - 33,949,846RGDNCBI36
Celera2120,227,329 - 20,227,597RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,506,034 - 20,506,302UniSTS
REN86112  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,027,971 - 35,028,227UniSTSGRCh37
Build 362133,949,841 - 33,950,097RGDNCBI36
Celera2120,227,592 - 20,227,848RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,506,297 - 20,506,553UniSTS
REN86113  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,028,149 - 35,028,414UniSTSGRCh37
Build 362133,950,019 - 33,950,284RGDNCBI36
Celera2120,227,770 - 20,228,035RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,506,475 - 20,506,740UniSTS
REN86114  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,028,401 - 35,028,641UniSTSGRCh37
Build 362133,950,271 - 33,950,511RGDNCBI36
Celera2120,228,022 - 20,228,262RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,506,727 - 20,506,967UniSTS
REN86115  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,028,613 - 35,028,851UniSTSGRCh37
Build 362133,950,483 - 33,950,721RGDNCBI36
Celera2120,228,234 - 20,228,472RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,506,939 - 20,507,177UniSTS
REN86116  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,028,804 - 35,029,056UniSTSGRCh37
GRCh372135,027,684 - 35,029,056UniSTSGRCh37
Build 362133,950,674 - 33,950,926RGDNCBI36
Celera2120,227,305 - 20,228,677UniSTS
Celera2120,228,425 - 20,228,677RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,507,130 - 20,507,382UniSTS
HuRef2120,506,010 - 20,507,382UniSTS
REN86117  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,029,370 - 35,029,609UniSTSGRCh37
Build 362133,951,240 - 33,951,479RGDNCBI36
Celera2120,228,991 - 20,229,230RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,507,696 - 20,507,935UniSTS
REN86118  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,029,588 - 35,029,860UniSTSGRCh37
Build 362133,951,458 - 33,951,730RGDNCBI36
Celera2120,229,209 - 20,229,481RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,507,914 - 20,508,186UniSTS
REN86119  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,029,817 - 35,030,080UniSTSGRCh37
Build 362133,951,687 - 33,951,950RGDNCBI36
Celera2120,229,438 - 20,229,701RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,508,143 - 20,508,406UniSTS
REN86120  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,029,991 - 35,030,250UniSTSGRCh37
Build 362133,951,861 - 33,952,120RGDNCBI36
Celera2120,229,612 - 20,229,871RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,508,317 - 20,508,576UniSTS
REN86121  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,030,150 - 35,030,390UniSTSGRCh37
Build 362133,952,020 - 33,952,260RGDNCBI36
Celera2120,229,771 - 20,230,011RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,508,476 - 20,508,716UniSTS
REN86122  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,030,374 - 35,030,637UniSTSGRCh37
Build 362133,952,244 - 33,952,507RGDNCBI36
Celera2120,229,995 - 20,230,258RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,508,700 - 20,508,963UniSTS
REN86123  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,030,628 - 35,030,882UniSTSGRCh37
Build 362133,952,498 - 33,952,752RGDNCBI36
Celera2120,230,249 - 20,230,503RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,508,954 - 20,509,208UniSTS
REN86124  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,030,880 - 35,031,127UniSTSGRCh37
Build 362133,952,750 - 33,952,997RGDNCBI36
Celera2120,230,501 - 20,230,748RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,509,206 - 20,509,453UniSTS
REN86125  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,031,102 - 35,031,355UniSTSGRCh37
Build 362133,952,972 - 33,953,225RGDNCBI36
Celera2120,230,723 - 20,230,976RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,509,428 - 20,509,681UniSTS
REN86126  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,031,319 - 35,031,580UniSTSGRCh37
Build 362133,953,189 - 33,953,450RGDNCBI36
Celera2120,230,940 - 20,231,201RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,509,645 - 20,509,906UniSTS
REN86127  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,031,557 - 35,031,806UniSTSGRCh37
Build 362133,953,427 - 33,953,676RGDNCBI36
Celera2120,231,178 - 20,231,427RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,509,883 - 20,510,132UniSTS
REN86128  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,031,746 - 35,032,007UniSTSGRCh37
Build 362133,953,616 - 33,953,877RGDNCBI36
Celera2120,231,367 - 20,231,628RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,510,072 - 20,510,333UniSTS
REN86129  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,031,987 - 35,032,242UniSTSGRCh37
Build 362133,953,857 - 33,954,112RGDNCBI36
Celera2120,231,608 - 20,231,863RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,510,313 - 20,510,569UniSTS
REN86130  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,032,216 - 35,032,470UniSTSGRCh37
Build 362133,954,086 - 33,954,340RGDNCBI36
Celera2120,231,837 - 20,232,091RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,510,543 - 20,510,797UniSTS
REN86131  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,032,456 - 35,032,699UniSTSGRCh37
Build 362133,954,326 - 33,954,569RGDNCBI36
Celera2120,232,077 - 20,232,320RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,510,783 - 20,511,026UniSTS
REN86132  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,032,693 - 35,032,933UniSTSGRCh37
Build 362133,954,563 - 33,954,803RGDNCBI36
Celera2120,232,314 - 20,232,554RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,511,020 - 20,511,260UniSTS
REN86133  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,032,905 - 35,033,169UniSTSGRCh37
Build 362133,954,775 - 33,955,039RGDNCBI36
Celera2120,232,526 - 20,232,790RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,511,232 - 20,511,496UniSTS
REN86134  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,033,153 - 35,033,408UniSTSGRCh37
Build 362133,955,023 - 33,955,278RGDNCBI36
Celera2120,232,774 - 20,233,029RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,511,480 - 20,511,735UniSTS
REN86135  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,033,388 - 35,033,640UniSTSGRCh37
Build 362133,955,258 - 33,955,510RGDNCBI36
Celera2120,233,009 - 20,233,261RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,511,715 - 20,511,967UniSTS
REN86136  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,033,597 - 35,033,847UniSTSGRCh37
Build 362133,955,467 - 33,955,717RGDNCBI36
Celera2120,233,218 - 20,233,468RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,511,924 - 20,512,174UniSTS
REN86137  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,033,824 - 35,034,075UniSTSGRCh37
Build 362133,955,694 - 33,955,945RGDNCBI36
Celera2120,233,445 - 20,233,696RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,512,151 - 20,512,402UniSTS
REN86138  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,034,031 - 35,034,272UniSTSGRCh37
Build 362133,955,901 - 33,956,142RGDNCBI36
Celera2120,233,652 - 20,233,893RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,512,358 - 20,512,599UniSTS
REN86139  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,034,250 - 35,034,492UniSTSGRCh37
Build 362133,956,120 - 33,956,362RGDNCBI36
Celera2120,233,871 - 20,234,113RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,512,577 - 20,512,819UniSTS
REN86140  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,034,464 - 35,034,699UniSTSGRCh37
Build 362133,956,334 - 33,956,569RGDNCBI36
Celera2120,234,085 - 20,234,320RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,512,791 - 20,513,026UniSTS
REN86141  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,034,663 - 35,034,910UniSTSGRCh37
Build 362133,956,533 - 33,956,780RGDNCBI36
Celera2120,234,284 - 20,234,531RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,512,990 - 20,513,237UniSTS
REN86142  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,034,899 - 35,035,148UniSTSGRCh37
Build 362133,956,769 - 33,957,018RGDNCBI36
Celera2120,234,520 - 20,234,769RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,513,226 - 20,513,475UniSTS
REN86143  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,035,131 - 35,035,395UniSTSGRCh37
Build 362133,957,001 - 33,957,265RGDNCBI36
Celera2120,234,752 - 20,235,016RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,513,458 - 20,513,722UniSTS
REN86144  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,035,389 - 35,035,653UniSTSGRCh37
Build 362133,957,259 - 33,957,523RGDNCBI36
Celera2120,235,010 - 20,235,274RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,513,716 - 20,513,980UniSTS
REN86145  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,035,625 - 35,035,883UniSTSGRCh37
Build 362133,957,495 - 33,957,753RGDNCBI36
Celera2120,235,246 - 20,235,504RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,513,952 - 20,514,211UniSTS
REN86146  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,035,676 - 35,035,906UniSTSGRCh37
Build 362133,957,546 - 33,957,776RGDNCBI36
Celera2120,235,297 - 20,235,527RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,514,003 - 20,514,234UniSTS
REN86147  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,036,201 - 35,036,430UniSTSGRCh37
Build 362133,958,071 - 33,958,300RGDNCBI36
Celera2120,235,822 - 20,236,051RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,514,529 - 20,514,758UniSTS
REN86148  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,036,392 - 35,036,648UniSTSGRCh37
Build 362133,958,262 - 33,958,518RGDNCBI36
Celera2120,236,013 - 20,236,269RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,514,720 - 20,514,976UniSTS
REN86149  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,036,631 - 35,036,882UniSTSGRCh37
Build 362133,958,501 - 33,958,752RGDNCBI36
Celera2120,236,252 - 20,236,503RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,514,959 - 20,515,210UniSTS
REN86150  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,036,859 - 35,037,094UniSTSGRCh37
Build 362133,958,729 - 33,958,964RGDNCBI36
Celera2120,236,480 - 20,236,715RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,515,187 - 20,515,422UniSTS
REN86151  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,037,067 - 35,037,296UniSTSGRCh37
Build 362133,958,937 - 33,959,166RGDNCBI36
Celera2120,236,688 - 20,236,917RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,515,395 - 20,515,624UniSTS
REN86152  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,037,587 - 35,037,811UniSTSGRCh37
Build 362133,959,457 - 33,959,681RGDNCBI36
Celera2120,237,208 - 20,237,432RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,515,915 - 20,516,139UniSTS
REN86153  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,037,713 - 35,037,969UniSTSGRCh37
Build 362133,959,583 - 33,959,839RGDNCBI36
Celera2120,237,334 - 20,237,590RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,516,041 - 20,516,297UniSTS
REN86154  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,037,912 - 35,038,168UniSTSGRCh37
Build 362133,959,782 - 33,960,038RGDNCBI36
Celera2120,237,533 - 20,237,789RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,516,240 - 20,516,496UniSTS
REN86155  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,038,133 - 35,038,357UniSTSGRCh37
Build 362133,960,003 - 33,960,227RGDNCBI36
Celera2120,237,754 - 20,237,978RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,516,461 - 20,516,685UniSTS
REN86156  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,038,390 - 35,038,637UniSTSGRCh37
Build 362133,960,260 - 33,960,507RGDNCBI36
Celera2120,238,011 - 20,238,258RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,516,718 - 20,516,965UniSTS
REN86157  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,038,618 - 35,038,867UniSTSGRCh37
Build 362133,960,488 - 33,960,737RGDNCBI36
Celera2120,238,239 - 20,238,488RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,516,946 - 20,517,195UniSTS
REN86158  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,038,860 - 35,039,096UniSTSGRCh37
Build 362133,960,730 - 33,960,966RGDNCBI36
Celera2120,238,481 - 20,238,717RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,517,188 - 20,517,424UniSTS
REN86159  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,039,048 - 35,039,281UniSTSGRCh37
Build 362133,960,918 - 33,961,151RGDNCBI36
Celera2120,238,669 - 20,238,902RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,517,376 - 20,517,609UniSTS
REN86160  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,039,255 - 35,039,499UniSTSGRCh37
Build 362133,961,125 - 33,961,369RGDNCBI36
Celera2120,238,876 - 20,239,120RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,517,583 - 20,517,827UniSTS
REN86161  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,039,423 - 35,039,650UniSTSGRCh37
Build 362133,961,293 - 33,961,520RGDNCBI36
Celera2120,239,044 - 20,239,271RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,517,751 - 20,517,978UniSTS
REN86162  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,039,627 - 35,039,872UniSTSGRCh37
Build 362133,961,497 - 33,961,742RGDNCBI36
Celera2120,239,248 - 20,239,493RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,517,955 - 20,518,200UniSTS
REN86163  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,039,849 - 35,040,074UniSTSGRCh37
Build 362133,961,719 - 33,961,944RGDNCBI36
Celera2120,239,470 - 20,239,695RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,518,177 - 20,518,402UniSTS
REN86164  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,040,040 - 35,040,286UniSTSGRCh37
Build 362133,961,910 - 33,962,156RGDNCBI36
Celera2120,239,661 - 20,239,907RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,518,368 - 20,518,614UniSTS
REN86165  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,040,259 - 35,040,502UniSTSGRCh37
Build 362133,962,129 - 33,962,372RGDNCBI36
Celera2120,239,880 - 20,240,123RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,518,587 - 20,518,830UniSTS
REN86166  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,040,479 - 35,040,751UniSTSGRCh37
Build 362133,962,349 - 33,962,621RGDNCBI36
Celera2120,240,100 - 20,240,372RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,518,807 - 20,519,079UniSTS
REN86167  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,040,738 - 35,040,986UniSTSGRCh37
Build 362133,962,608 - 33,962,856RGDNCBI36
Celera2120,240,359 - 20,240,607RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,519,066 - 20,519,314UniSTS
REN86168  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,040,963 - 35,041,198UniSTSGRCh37
Build 362133,962,833 - 33,963,068RGDNCBI36
Celera2120,240,584 - 20,240,819RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,519,291 - 20,519,526UniSTS
REN86169  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,041,177 - 35,041,401UniSTSGRCh37
Build 362133,963,047 - 33,963,271RGDNCBI36
Celera2120,240,798 - 20,241,022RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,519,505 - 20,519,729UniSTS
REN86170  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,042,037 - 35,042,261UniSTSGRCh37
Build 362133,963,907 - 33,964,131RGDNCBI36
Celera2120,241,658 - 20,241,882RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,520,365 - 20,520,589UniSTS
REN86171  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,042,229 - 35,042,480UniSTSGRCh37
Build 362133,964,099 - 33,964,350RGDNCBI36
Celera2120,241,850 - 20,242,101RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,520,557 - 20,520,808UniSTS
REN86172  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,042,429 - 35,042,675UniSTSGRCh37
Build 362133,964,299 - 33,964,545RGDNCBI36
Celera2120,242,050 - 20,242,296RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,520,757 - 20,521,003UniSTS
REN86173  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,042,647 - 35,042,888UniSTSGRCh37
Build 362133,964,517 - 33,964,758RGDNCBI36
Celera2120,242,268 - 20,242,509RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,520,975 - 20,521,216UniSTS
REN86174  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,042,884 - 35,043,122UniSTSGRCh37
Build 362133,964,754 - 33,964,992RGDNCBI36
Celera2120,242,505 - 20,242,743RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,521,212 - 20,521,450UniSTS
REN86175  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,043,099 - 35,043,340UniSTSGRCh37
Build 362133,964,969 - 33,965,210RGDNCBI36
Celera2120,242,720 - 20,242,961RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,521,427 - 20,521,668UniSTS
REN86176  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,043,332 - 35,043,572UniSTSGRCh37
Build 362133,965,202 - 33,965,442RGDNCBI36
Celera2120,242,953 - 20,243,193RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,521,660 - 20,521,900UniSTS
REN86177  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,043,419 - 35,043,668UniSTSGRCh37
Build 362133,965,289 - 33,965,538RGDNCBI36
Celera2120,243,040 - 20,243,289RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,521,747 - 20,521,996UniSTS
REN86178  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,044,014 - 35,044,273UniSTSGRCh37
Build 362133,965,884 - 33,966,143RGDNCBI36
Celera2120,243,635 - 20,243,894RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,522,342 - 20,522,601UniSTS
REN86179  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,044,275 - 35,044,504UniSTSGRCh37
Build 362133,966,145 - 33,966,374RGDNCBI36
Celera2120,243,896 - 20,244,125RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,522,603 - 20,522,832UniSTS
REN86180  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,044,536 - 35,044,798UniSTSGRCh37
Build 362133,966,406 - 33,966,668RGDNCBI36
Celera2120,244,157 - 20,244,419RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,522,864 - 20,523,126UniSTS
REN86181  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,044,785 - 35,045,017UniSTSGRCh37
Build 362133,966,655 - 33,966,887RGDNCBI36
Celera2120,244,406 - 20,244,638RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,523,113 - 20,523,345UniSTS
REN86182  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,045,270 - 35,045,522UniSTSGRCh37
Build 362133,967,140 - 33,967,392RGDNCBI36
Celera2120,244,891 - 20,245,143RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,523,598 - 20,523,850UniSTS
REN86183  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,045,499 - 35,045,737UniSTSGRCh37
Build 362133,967,369 - 33,967,607RGDNCBI36
Celera2120,245,120 - 20,245,358RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,523,827 - 20,524,065UniSTS
REN86184  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,045,736 - 35,045,987UniSTSGRCh37
Build 362133,967,606 - 33,967,857RGDNCBI36
Celera2120,245,357 - 20,245,608RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,524,064 - 20,524,315UniSTS
REN86185  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,045,963 - 35,046,187UniSTSGRCh37
Build 362133,967,833 - 33,968,057RGDNCBI36
Celera2120,245,584 - 20,245,808RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,524,291 - 20,524,515UniSTS
REN86186  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,046,157 - 35,046,414UniSTSGRCh37
Build 362133,968,027 - 33,968,284RGDNCBI36
Celera2120,245,778 - 20,246,035RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,524,485 - 20,524,742UniSTS
REN86187  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,046,413 - 35,046,655UniSTSGRCh37
Build 362133,968,283 - 33,968,525RGDNCBI36
Celera2120,246,034 - 20,246,276RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,524,741 - 20,524,983UniSTS
REN86188  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,046,631 - 35,046,899UniSTSGRCh37
Build 362133,968,501 - 33,968,769RGDNCBI36
Celera2120,246,252 - 20,246,520RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,524,959 - 20,525,227UniSTS
REN86189  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,046,878 - 35,047,111UniSTSGRCh37
Build 362133,968,748 - 33,968,981RGDNCBI36
Celera2120,246,499 - 20,246,732RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,525,206 - 20,525,439UniSTS
REN86190  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,047,101 - 35,047,353UniSTSGRCh37
Build 362133,968,971 - 33,969,223RGDNCBI36
Celera2120,246,722 - 20,246,974RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,525,429 - 20,525,681UniSTS
REN86191  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,047,300 - 35,047,571UniSTSGRCh37
Build 362133,969,170 - 33,969,441RGDNCBI36
Celera2120,246,921 - 20,247,192RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,525,628 - 20,525,899UniSTS
REN86192  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,047,431 - 35,047,678UniSTSGRCh37
Build 362133,969,301 - 33,969,548RGDNCBI36
Celera2120,247,052 - 20,247,299RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,525,759 - 20,526,006UniSTS
REN86193  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,047,799 - 35,048,025UniSTSGRCh37
Build 362133,969,669 - 33,969,895RGDNCBI36
Celera2120,247,420 - 20,247,646RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,526,127 - 20,526,353UniSTS
REN86194  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,048,010 - 35,048,253UniSTSGRCh37
Build 362133,969,880 - 33,970,123RGDNCBI36
Celera2120,247,631 - 20,247,874RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,526,338 - 20,526,581UniSTS
REN86195  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,048,137 - 35,048,377UniSTSGRCh37
Build 362133,970,007 - 33,970,247RGDNCBI36
Celera2120,247,758 - 20,247,998RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,526,465 - 20,526,705UniSTS
REN86196  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,048,352 - 35,048,595UniSTSGRCh37
Build 362133,970,222 - 33,970,465RGDNCBI36
Celera2120,247,973 - 20,248,216RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,526,680 - 20,526,923UniSTS
REN86197  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,048,437 - 35,048,683UniSTSGRCh37
Build 362133,970,307 - 33,970,553RGDNCBI36
Celera2120,248,058 - 20,248,304RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,526,765 - 20,527,011UniSTS
REN86198  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,048,639 - 35,048,907UniSTSGRCh37
Build 362133,970,509 - 33,970,777RGDNCBI36
Celera2120,248,260 - 20,248,528RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,526,967 - 20,527,235UniSTS
REN86199  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,048,882 - 35,049,123UniSTSGRCh37
Build 362133,970,752 - 33,970,993RGDNCBI36
Celera2120,248,503 - 20,248,744RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,527,210 - 20,527,451UniSTS
REN86200  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,048,987 - 35,049,227UniSTSGRCh37
Build 362133,970,857 - 33,971,097RGDNCBI36
Celera2120,248,608 - 20,248,848RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,527,315 - 20,527,555UniSTS
REN86201  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,049,470 - 35,049,699UniSTSGRCh37
Build 362133,971,340 - 33,971,569RGDNCBI36
Celera2120,249,091 - 20,249,320RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,527,798 - 20,528,027UniSTS
REN86202  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,049,620 - 35,049,887UniSTSGRCh37
Build 362133,971,490 - 33,971,757RGDNCBI36
Celera2120,249,241 - 20,249,508RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,527,948 - 20,528,215UniSTS
REN86203  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,049,863 - 35,050,090UniSTSGRCh37
Build 362133,971,733 - 33,971,960RGDNCBI36
Celera2120,249,484 - 20,249,711RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,528,191 - 20,528,418UniSTS
REN86204  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,050,070 - 35,050,340UniSTSGRCh37
Build 362133,971,940 - 33,972,210RGDNCBI36
Celera2120,249,691 - 20,249,961RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,528,398 - 20,528,669UniSTS
REN86205  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,050,314 - 35,050,556UniSTSGRCh37
Build 362133,972,184 - 33,972,426RGDNCBI36
Celera2120,249,935 - 20,250,177RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,528,643 - 20,528,885UniSTS
REN86206  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,050,548 - 35,050,776UniSTSGRCh37
Build 362133,972,418 - 33,972,646RGDNCBI36
Celera2120,250,169 - 20,250,397RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,528,877 - 20,529,105UniSTS
REN86207  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,050,753 - 35,051,003UniSTSGRCh37
Build 362133,972,623 - 33,972,873RGDNCBI36
Celera2120,250,374 - 20,250,624RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,529,082 - 20,529,332UniSTS
REN86208  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,050,797 - 35,051,034UniSTSGRCh37
Build 362133,972,667 - 33,972,904RGDNCBI36
Celera2120,250,418 - 20,250,655RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,529,126 - 20,529,363UniSTS
REN86209  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,051,014 - 35,051,241UniSTSGRCh37
Build 362133,972,884 - 33,973,111RGDNCBI36
Celera2120,250,635 - 20,250,862RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,529,343 - 20,529,570UniSTS
REN86210  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,051,218 - 35,051,464UniSTSGRCh37
Build 362133,973,088 - 33,973,334RGDNCBI36
Celera2120,250,839 - 20,251,085RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,529,547 - 20,529,793UniSTS
REN86211  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,051,441 - 35,051,704UniSTSGRCh37
Build 362133,973,311 - 33,973,574RGDNCBI36
Celera2120,251,062 - 20,251,325RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,529,770 - 20,530,033UniSTS
REN86212  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,051,683 - 35,051,907UniSTSGRCh37
Build 362133,973,553 - 33,973,777RGDNCBI36
Celera2120,251,304 - 20,251,528RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,530,012 - 20,530,236UniSTS
REN86213  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,051,841 - 35,052,079UniSTSGRCh37
Build 362133,973,711 - 33,973,949RGDNCBI36
Celera2120,251,462 - 20,251,700RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,530,170 - 20,530,409UniSTS
REN86214  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,052,296 - 35,052,527UniSTSGRCh37
Build 362133,974,166 - 33,974,397RGDNCBI36
Celera2120,251,917 - 20,252,148RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,530,626 - 20,530,857UniSTS
REN86215  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,052,334 - 35,052,601UniSTSGRCh37
Build 362133,974,204 - 33,974,471RGDNCBI36
Celera2120,251,955 - 20,252,222RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,530,664 - 20,530,931UniSTS
REN86216  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,052,935 - 35,053,165UniSTSGRCh37
Build 362133,974,805 - 33,975,035RGDNCBI36
Celera2120,252,556 - 20,252,786RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,531,265 - 20,531,489UniSTS
REN86217  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,053,132 - 35,053,383UniSTSGRCh37
Build 362133,975,002 - 33,975,253RGDNCBI36
Celera2120,252,753 - 20,253,004RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,531,456 - 20,531,707UniSTS
REN86218  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,053,362 - 35,053,627UniSTSGRCh37
Build 362133,975,232 - 33,975,497RGDNCBI36
Celera2120,252,983 - 20,253,248RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,531,686 - 20,531,951UniSTS
REN86219  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,053,512 - 35,053,772UniSTSGRCh37
Build 362133,975,382 - 33,975,642RGDNCBI36
Celera2120,253,133 - 20,253,393RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,531,836 - 20,532,096UniSTS
REN86220  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,053,664 - 35,053,912UniSTSGRCh37
Build 362133,975,534 - 33,975,782RGDNCBI36
Celera2120,253,285 - 20,253,533RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,531,988 - 20,532,235UniSTS
REN86221  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,054,031 - 35,054,294UniSTSGRCh37
Build 362133,975,901 - 33,976,164RGDNCBI36
Celera2120,253,652 - 20,253,915RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,532,344 - 20,532,607UniSTS
REN86222  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,054,277 - 35,054,523UniSTSGRCh37
Build 362133,976,147 - 33,976,393RGDNCBI36
Celera2120,253,898 - 20,254,144RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,532,590 - 20,532,836UniSTS
REN86223  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,054,420 - 35,054,653UniSTSGRCh37
Build 362133,976,290 - 33,976,523RGDNCBI36
Celera2120,254,041 - 20,254,274RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,532,733 - 20,532,966UniSTS
REN86224  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,054,928 - 35,055,163UniSTSGRCh37
Build 362133,976,798 - 33,977,033RGDNCBI36
Celera2120,254,549 - 20,254,784RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,533,241 - 20,533,476UniSTS
REN86225  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,055,158 - 35,055,407UniSTSGRCh37
Build 362133,977,028 - 33,977,277RGDNCBI36
Celera2120,254,779 - 20,255,028RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,533,471 - 20,533,720UniSTS
REN86226  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,055,393 - 35,055,643UniSTSGRCh37
Build 362133,977,263 - 33,977,513RGDNCBI36
Celera2120,255,014 - 20,255,264RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,533,706 - 20,533,956UniSTS
REN86227  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,055,619 - 35,055,853UniSTSGRCh37
Build 362133,977,489 - 33,977,723RGDNCBI36
Celera2120,255,240 - 20,255,474RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,533,932 - 20,534,166UniSTS
REN86228  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,055,828 - 35,056,068UniSTSGRCh37
Build 362133,977,698 - 33,977,938RGDNCBI36
Celera2120,255,449 - 20,255,689RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,534,141 - 20,534,381UniSTS
REN86229  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,056,045 - 35,056,293UniSTSGRCh37
Build 362133,977,915 - 33,978,163RGDNCBI36
Celera2120,255,666 - 20,255,914RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,534,358 - 20,534,606UniSTS
REN86230  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,056,266 - 35,056,524UniSTSGRCh37
Build 362133,978,136 - 33,978,394RGDNCBI36
Celera2120,255,887 - 20,256,145RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,534,579 - 20,534,837UniSTS
REN86231  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,056,519 - 35,056,751UniSTSGRCh37
Build 362133,978,389 - 33,978,621RGDNCBI36
Celera2120,256,140 - 20,256,372RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,534,832 - 20,535,064UniSTS
REN86232  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,056,711 - 35,056,946UniSTSGRCh37
Build 362133,978,581 - 33,978,816RGDNCBI36
Celera2120,256,332 - 20,256,567RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,535,024 - 20,535,259UniSTS
REN86233  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,056,898 - 35,057,122UniSTSGRCh37
Build 362133,978,768 - 33,978,992RGDNCBI36
Celera2120,256,519 - 20,256,743RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,535,211 - 20,535,435UniSTS
REN86234  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,057,088 - 35,057,360UniSTSGRCh37
Build 362133,978,958 - 33,979,230RGDNCBI36
Celera2120,256,709 - 20,256,981RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,535,401 - 20,535,673UniSTS
REN86235  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,057,339 - 35,057,590UniSTSGRCh37
Build 362133,979,209 - 33,979,460RGDNCBI36
Celera2120,256,960 - 20,257,211RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,535,652 - 20,535,903UniSTS
REN86236  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,057,570 - 35,057,808UniSTSGRCh37
Build 362133,979,440 - 33,979,678RGDNCBI36
Celera2120,257,191 - 20,257,429RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,535,883 - 20,536,121UniSTS
REN86237  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,057,785 - 35,058,034UniSTSGRCh37
Build 362133,979,655 - 33,979,904RGDNCBI36
Celera2120,257,406 - 20,257,655RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,536,098 - 20,536,347UniSTS
REN86238  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,058,011 - 35,058,266UniSTSGRCh37
Build 362133,979,881 - 33,980,136RGDNCBI36
Celera2120,257,632 - 20,257,887RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,536,324 - 20,536,579UniSTS
REN86239  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,058,245 - 35,058,478UniSTSGRCh37
Build 362133,980,115 - 33,980,348RGDNCBI36
Celera2120,257,866 - 20,258,099RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,536,558 - 20,536,791UniSTS
REN86240  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,058,389 - 35,058,622UniSTSGRCh37
Build 362133,980,259 - 33,980,492RGDNCBI36
Celera2120,258,010 - 20,258,243RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,536,702 - 20,536,935UniSTS
REN86241  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,058,586 - 35,058,835UniSTSGRCh37
Build 362133,980,456 - 33,980,705RGDNCBI36
Celera2120,258,207 - 20,258,456RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,536,899 - 20,537,148UniSTS
REN86242  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,058,792 - 35,059,042UniSTSGRCh37
Build 362133,980,662 - 33,980,912RGDNCBI36
Celera2120,258,413 - 20,258,663RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,537,105 - 20,537,355UniSTS
REN86243  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,059,036 - 35,059,283UniSTSGRCh37
Build 362133,980,906 - 33,981,153RGDNCBI36
Celera2120,258,657 - 20,258,904RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,537,349 - 20,537,596UniSTS
REN86244  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,059,138 - 35,059,363UniSTSGRCh37
Build 362133,981,008 - 33,981,233RGDNCBI36
Celera2120,258,759 - 20,258,984RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,537,451 - 20,537,676UniSTS
REN86245  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,059,332 - 35,059,574UniSTSGRCh37
Build 362133,981,202 - 33,981,444RGDNCBI36
Celera2120,258,953 - 20,259,195RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,537,645 - 20,537,887UniSTS
REN86246  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,059,550 - 35,059,774UniSTSGRCh37
Build 362133,981,420 - 33,981,644RGDNCBI36
Celera2120,259,171 - 20,259,395RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,537,863 - 20,538,078UniSTS
REN86247  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,059,749 - 35,059,991UniSTSGRCh37
Build 362133,981,619 - 33,981,861RGDNCBI36
Celera2120,259,370 - 20,259,612RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,538,053 - 20,538,295UniSTS
REN86248  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,059,959 - 35,060,183UniSTSGRCh37
Build 362133,981,829 - 33,982,053RGDNCBI36
Celera2120,259,580 - 20,259,804RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,538,263 - 20,538,487UniSTS
REN86249  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,060,158 - 35,060,422UniSTSGRCh37
Build 362133,982,028 - 33,982,292RGDNCBI36
Celera2120,259,779 - 20,260,043RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,538,462 - 20,538,726UniSTS
REN86250  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,060,419 - 35,060,652UniSTSGRCh37
Build 362133,982,289 - 33,982,522RGDNCBI36
Celera2120,260,040 - 20,260,273RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,538,723 - 20,538,956UniSTS
REN86251  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,060,635 - 35,060,886UniSTSGRCh37
Build 362133,982,505 - 33,982,756RGDNCBI36
Celera2120,260,256 - 20,260,507RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,538,939 - 20,539,190UniSTS
REN86252  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,060,867 - 35,061,092UniSTSGRCh37
Build 362133,982,737 - 33,982,962RGDNCBI36
Celera2120,260,488 - 20,260,713RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,539,171 - 20,539,396UniSTS
REN86253  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,061,051 - 35,061,275UniSTSGRCh37
Build 362133,982,921 - 33,983,145RGDNCBI36
Celera2120,260,672 - 20,260,896RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,539,355 - 20,539,579UniSTS
REN86254  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,061,236 - 35,061,481UniSTSGRCh37
Build 362133,983,106 - 33,983,351RGDNCBI36
Celera2120,260,857 - 20,261,102RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,539,540 - 20,539,785UniSTS
REN86255  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,061,464 - 35,061,705UniSTSGRCh37
Build 362133,983,334 - 33,983,575RGDNCBI36
Celera2120,261,085 - 20,261,326RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,539,768 - 20,540,009UniSTS
REN86256  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,061,668 - 35,061,896UniSTSGRCh37
Build 362133,983,538 - 33,983,766RGDNCBI36
Celera2120,261,289 - 20,261,517RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,539,972 - 20,540,200UniSTS
REN86257  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,062,940 - 35,063,189UniSTSGRCh37
Build 362133,984,810 - 33,985,059RGDNCBI36
Celera2120,262,561 - 20,262,810RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,541,244 - 20,541,497UniSTS
REN86258  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,063,183 - 35,063,437UniSTSGRCh37
Build 362133,985,053 - 33,985,307RGDNCBI36
Celera2120,262,804 - 20,263,058RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,541,491 - 20,541,745UniSTS
REN86259  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,063,425 - 35,063,668UniSTSGRCh37
Build 362133,985,295 - 33,985,538RGDNCBI36
Celera2120,263,046 - 20,263,289RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,541,733 - 20,541,976UniSTS
REN86260  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,063,649 - 35,063,891UniSTSGRCh37
Build 362133,985,519 - 33,985,761RGDNCBI36
Celera2120,263,270 - 20,263,512RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,541,957 - 20,542,199UniSTS
REN86261  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,063,868 - 35,064,129UniSTSGRCh37
Build 362133,985,738 - 33,985,999RGDNCBI36
Celera2120,263,489 - 20,263,750RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,542,176 - 20,542,437UniSTS
REN86262  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,064,044 - 35,064,298UniSTSGRCh37
Build 362133,985,914 - 33,986,168RGDNCBI36
Celera2120,263,665 - 20,263,919RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,542,352 - 20,542,606UniSTS
REN86263  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,064,275 - 35,064,518UniSTSGRCh37
Build 362133,986,145 - 33,986,388RGDNCBI36
Celera2120,263,896 - 20,264,139RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,542,583 - 20,542,826UniSTS
REN86264  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,064,509 - 35,064,754UniSTSGRCh37
Build 362133,986,379 - 33,986,624RGDNCBI36
Celera2120,264,130 - 20,264,375RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,542,817 - 20,543,062UniSTS
REN86265  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,064,635 - 35,064,862UniSTSGRCh37
Build 362133,986,505 - 33,986,732RGDNCBI36
Celera2120,264,256 - 20,264,483RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,542,943 - 20,543,170UniSTS
REN86266  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,064,829 - 35,065,053UniSTSGRCh37
Build 362133,986,699 - 33,986,923RGDNCBI36
Celera2120,264,450 - 20,264,674RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,543,137 - 20,543,361UniSTS
REN86267  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,065,211 - 35,065,462UniSTSGRCh37
Build 362133,987,081 - 33,987,332RGDNCBI36
Celera2120,264,832 - 20,265,083RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,543,519 - 20,543,770UniSTS
REN86268  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,065,438 - 35,065,711UniSTSGRCh37
Build 362133,987,308 - 33,987,581RGDNCBI36
Celera2120,265,059 - 20,265,332RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,543,746 - 20,544,019UniSTS
REN86269  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,065,678 - 35,065,921UniSTSGRCh37
Build 362133,987,548 - 33,987,791RGDNCBI36
Celera2120,265,299 - 20,265,542RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,543,986 - 20,544,229UniSTS
REN86270  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,065,895 - 35,066,137UniSTSGRCh37
Build 362133,987,765 - 33,988,007RGDNCBI36
Celera2120,265,516 - 20,265,758RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,544,203 - 20,544,445UniSTS
REN86271  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,066,061 - 35,066,287UniSTSGRCh37
Build 362133,987,931 - 33,988,157RGDNCBI36
Celera2120,265,682 - 20,265,908RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,544,369 - 20,544,595UniSTS
REN86272  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,066,252 - 35,066,488UniSTSGRCh37
Build 362133,988,122 - 33,988,358RGDNCBI36
Celera2120,265,873 - 20,266,109RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,544,560 - 20,544,796UniSTS
REN86273  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,066,471 - 35,066,732UniSTSGRCh37
Build 362133,988,341 - 33,988,602RGDNCBI36
Celera2120,266,092 - 20,266,353RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,544,779 - 20,545,040UniSTS
REN86274  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,066,626 - 35,066,850UniSTSGRCh37
Build 362133,988,496 - 33,988,720RGDNCBI36
Celera2120,266,247 - 20,266,471RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,544,934 - 20,545,158UniSTS
REN86275  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,066,776 - 35,067,034UniSTSGRCh37
Build 362133,988,646 - 33,988,904RGDNCBI36
Celera2120,266,397 - 20,266,655RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,545,084 - 20,545,342UniSTS
REN86276  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,067,019 - 35,067,245UniSTSGRCh37
Build 362133,988,889 - 33,989,115RGDNCBI36
Celera2120,266,640 - 20,266,866RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,545,327 - 20,545,553UniSTS
REN86277  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,067,223 - 35,067,472UniSTSGRCh37
Build 362133,989,093 - 33,989,342RGDNCBI36
Celera2120,266,844 - 20,267,093RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,545,531 - 20,545,780UniSTS
REN86278  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,067,460 - 35,067,702UniSTSGRCh37
Build 362133,989,330 - 33,989,572RGDNCBI36
Celera2120,267,081 - 20,267,323RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,545,768 - 20,546,010UniSTS
REN86279  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,067,697 - 35,067,949UniSTSGRCh37
Build 362133,989,567 - 33,989,819RGDNCBI36
Celera2120,267,318 - 20,267,570RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,546,005 - 20,546,257UniSTS
REN86280  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,067,928 - 35,068,178UniSTSGRCh37
Build 362133,989,798 - 33,990,048RGDNCBI36
Celera2120,267,549 - 20,267,799RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,546,236 - 20,546,486UniSTS
REN86281  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,068,152 - 35,068,388UniSTSGRCh37
Build 362133,990,022 - 33,990,258RGDNCBI36
Celera2120,267,773 - 20,268,009RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,546,460 - 20,546,696UniSTS
REN86282  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,068,366 - 35,068,625UniSTSGRCh37
Build 362133,990,236 - 33,990,495RGDNCBI36
Celera2120,267,987 - 20,268,246RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,546,674 - 20,546,933UniSTS
REN86283  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,068,616 - 35,068,862UniSTSGRCh37
Build 362133,990,486 - 33,990,732RGDNCBI36
Celera2120,268,237 - 20,268,483RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,546,924 - 20,547,170UniSTS
REN86284  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,068,858 - 35,069,109UniSTSGRCh37
Build 362133,990,728 - 33,990,979RGDNCBI36
Celera2120,268,479 - 20,268,730RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,547,166 - 20,547,417UniSTS
REN86285  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,069,097 - 35,069,335UniSTSGRCh37
Build 362133,990,967 - 33,991,205RGDNCBI36
Celera2120,268,718 - 20,268,956RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,547,405 - 20,547,643UniSTS
REN86286  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,069,264 - 35,069,489UniSTSGRCh37
Build 362133,991,134 - 33,991,359RGDNCBI36
Celera2120,268,885 - 20,269,110RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,547,572 - 20,547,797UniSTS
REN86287  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,069,467 - 35,069,702UniSTSGRCh37
Build 362133,991,337 - 33,991,572RGDNCBI36
Celera2120,269,088 - 20,269,323RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,547,775 - 20,548,011UniSTS
REN86288  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,069,671 - 35,069,932UniSTSGRCh37
Build 362133,991,541 - 33,991,802RGDNCBI36
Celera2120,269,292 - 20,269,553RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,547,980 - 20,548,241UniSTS
REN86289  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,069,897 - 35,070,167UniSTSGRCh37
Build 362133,991,767 - 33,992,037RGDNCBI36
Celera2120,269,518 - 20,269,788RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,548,206 - 20,548,476UniSTS
REN86290  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,070,145 - 35,070,396UniSTSGRCh37
Build 362133,992,015 - 33,992,266RGDNCBI36
Celera2120,269,766 - 20,270,017RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,548,454 - 20,548,705UniSTS
REN86291  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,070,376 - 35,070,600UniSTSGRCh37
Build 362133,992,246 - 33,992,470RGDNCBI36
Celera2120,269,997 - 20,270,221RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,548,685 - 20,548,909UniSTS
REN86292  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,070,573 - 35,070,819UniSTSGRCh37
Build 362133,992,443 - 33,992,689RGDNCBI36
Celera2120,270,194 - 20,270,440RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,548,882 - 20,549,128UniSTS
REN86293  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,070,793 - 35,071,037UniSTSGRCh37
Build 362133,992,663 - 33,992,907RGDNCBI36
Celera2120,270,414 - 20,270,658RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,549,102 - 20,549,346UniSTS
REN86294  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,071,022 - 35,071,271UniSTSGRCh37
Build 362133,992,892 - 33,993,141RGDNCBI36
Celera2120,270,643 - 20,270,892RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,549,331 - 20,549,580UniSTS
REN86295  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,071,236 - 35,071,483UniSTSGRCh37
Build 362133,993,106 - 33,993,353RGDNCBI36
Celera2120,270,857 - 20,271,104RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,549,545 - 20,549,792UniSTS
REN86296  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,071,479 - 35,071,728UniSTSGRCh37
Build 362133,993,349 - 33,993,598RGDNCBI36
Celera2120,271,100 - 20,271,349RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,549,788 - 20,550,037UniSTS
REN86297  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,071,717 - 35,071,973UniSTSGRCh37
Build 362133,993,587 - 33,993,843RGDNCBI36
Celera2120,271,338 - 20,271,594RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,550,026 - 20,550,282UniSTS
REN86298  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,071,940 - 35,072,173UniSTSGRCh37
Build 362133,993,810 - 33,994,043RGDNCBI36
Celera2120,271,561 - 20,271,794RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,550,249 - 20,550,482UniSTS
REN86299  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,072,147 - 35,072,373UniSTSGRCh37
Build 362133,994,017 - 33,994,243RGDNCBI36
Celera2120,271,768 - 20,271,994RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,550,456 - 20,550,682UniSTS
REN86300  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,072,194 - 35,072,433UniSTSGRCh37
GRCh37690,537,525 - 90,538,607UniSTSGRCh37
Build 362133,994,064 - 33,994,303RGDNCBI36
Celera690,956,470 - 90,957,552UniSTS
Celera2120,271,815 - 20,272,054RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,550,503 - 20,550,742UniSTS
HuRef687,754,898 - 87,755,980UniSTS
REN86301  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,072,460 - 35,072,701UniSTSGRCh37
Build 362133,994,330 - 33,994,571RGDNCBI36
Celera2120,272,081 - 20,272,322RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,550,769 - 20,551,010UniSTS
REN86302  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,072,685 - 35,072,941UniSTSGRCh37
Build 362133,994,555 - 33,994,811RGDNCBI36
Celera2120,272,306 - 20,272,562RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,550,994 - 20,551,250UniSTS
REN86303  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,072,903 - 35,073,171UniSTSGRCh37
Build 362133,994,773 - 33,995,041RGDNCBI36
Celera2120,272,524 - 20,272,792RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,551,212 - 20,551,480UniSTS
REN86304  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,073,168 - 35,073,392UniSTSGRCh37
Build 362133,995,038 - 33,995,262RGDNCBI36
Celera2120,272,789 - 20,273,013RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,551,477 - 20,551,699UniSTS
REN86305  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,073,285 - 35,073,534UniSTSGRCh37
Build 362133,995,155 - 33,995,404RGDNCBI36
Celera2120,272,906 - 20,273,155RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,551,592 - 20,551,841UniSTS
REN86306  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,073,514 - 35,073,770UniSTSGRCh37
Build 362133,995,384 - 33,995,640RGDNCBI36
Celera2120,273,135 - 20,273,391RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,551,821 - 20,552,077UniSTS
REN86307  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,073,632 - 35,073,885UniSTSGRCh37
Build 362133,995,502 - 33,995,755RGDNCBI36
Celera2120,273,253 - 20,273,506RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,551,939 - 20,552,192UniSTS
REN86309  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,074,740 - 35,074,964UniSTSGRCh37
Build 362133,996,610 - 33,996,834RGDNCBI36
Celera2120,274,361 - 20,274,585RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,552,990 - 20,553,214UniSTS
REN86310  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,074,851 - 35,075,111UniSTSGRCh37
Build 362133,996,721 - 33,996,981RGDNCBI36
Celera2120,274,472 - 20,274,732RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,553,101 - 20,553,361UniSTS
REN86311  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,075,309 - 35,075,536UniSTSGRCh37
Build 362133,997,179 - 33,997,406RGDNCBI36
Celera2120,274,930 - 20,275,157RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,553,559 - 20,553,788UniSTS
REN86312  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,075,504 - 35,075,753UniSTSGRCh37
Build 362133,997,374 - 33,997,623RGDNCBI36
Celera2120,275,125 - 20,275,374RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,553,756 - 20,554,005UniSTS
REN86313  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,075,727 - 35,075,997UniSTSGRCh37
Build 362133,997,597 - 33,997,867RGDNCBI36
Celera2120,275,348 - 20,275,618RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,553,979 - 20,554,249UniSTS
REN86314  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,075,974 - 35,076,233UniSTSGRCh37
Build 362133,997,844 - 33,998,103RGDNCBI36
Celera2120,275,595 - 20,275,854RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,554,226 - 20,554,485UniSTS
REN86315  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,076,214 - 35,076,445UniSTSGRCh37
Build 362133,998,084 - 33,998,315RGDNCBI36
Celera2120,275,835 - 20,276,066RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,554,466 - 20,554,697UniSTS
REN86316  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,076,430 - 35,076,679UniSTSGRCh37
Build 362133,998,300 - 33,998,549RGDNCBI36
Celera2120,276,051 - 20,276,300RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,554,682 - 20,554,931UniSTS
REN86317  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,076,653 - 35,076,920UniSTSGRCh37
Build 362133,998,523 - 33,998,790RGDNCBI36
Celera2120,276,274 - 20,276,541RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,554,905 - 20,555,172UniSTS
REN86318  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,076,885 - 35,077,115UniSTSGRCh37
Build 362133,998,755 - 33,998,985RGDNCBI36
Celera2120,276,506 - 20,276,736RGD
REN86319  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,077,431 - 35,077,673UniSTSGRCh37
Build 362133,999,301 - 33,999,543RGDNCBI36
Celera2120,277,052 - 20,277,294RGD
Cytogenetic Map21q22.1-q22.2UniSTS
REN86320  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,077,984 - 35,078,211UniSTSGRCh37
Build 362133,999,854 - 34,000,081RGDNCBI36
Celera2120,277,605 - 20,277,832RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,556,048 - 20,556,275UniSTS
REN86321  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,078,127 - 35,078,375UniSTSGRCh37
Build 362133,999,997 - 34,000,245RGDNCBI36
Celera2120,277,748 - 20,277,996RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,556,191 - 20,556,439UniSTS
REN86322  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,078,600 - 35,078,862UniSTSGRCh37
Build 362134,000,470 - 34,000,732RGDNCBI36
Celera2120,278,221 - 20,278,483RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,556,664 - 20,556,926UniSTS
REN86323  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,078,834 - 35,079,058UniSTSGRCh37
Build 362134,000,704 - 34,000,928RGDNCBI36
Celera2120,278,455 - 20,278,679RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,556,898 - 20,557,122UniSTS
REN86324  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,078,949 - 35,079,175UniSTSGRCh37
Build 362134,000,819 - 34,001,045RGDNCBI36
Celera2120,278,570 - 20,278,796RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,557,013 - 20,557,239UniSTS
REN86325  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,079,159 - 35,079,406UniSTSGRCh37
Build 362134,001,029 - 34,001,276RGDNCBI36
Celera2120,278,780 - 20,279,027RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,557,223 - 20,557,470UniSTS
REN86326  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,079,319 - 35,079,543UniSTSGRCh37
Build 362134,001,189 - 34,001,413RGDNCBI36
Celera2120,278,940 - 20,279,164RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,557,383 - 20,557,607UniSTS
REN86327  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,079,516 - 35,079,781UniSTSGRCh37
Build 362134,001,386 - 34,001,651RGDNCBI36
Celera2120,279,137 - 20,279,402RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,557,580 - 20,557,845UniSTS
REN86328  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,079,766 - 35,080,019UniSTSGRCh37
Build 362134,001,636 - 34,001,889RGDNCBI36
Celera2120,279,387 - 20,279,640RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,557,830 - 20,558,083UniSTS
REN86329  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,080,014 - 35,080,251UniSTSGRCh37
Build 362134,001,884 - 34,002,121RGDNCBI36
Celera2120,279,635 - 20,279,872RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,558,078 - 20,558,315UniSTS
REN86330  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,080,218 - 35,080,466UniSTSGRCh37
Build 362134,002,088 - 34,002,336RGDNCBI36
Celera2120,279,839 - 20,280,087RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,558,282 - 20,558,530UniSTS
REN86331  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,080,441 - 35,080,691UniSTSGRCh37
Build 362134,002,311 - 34,002,561RGDNCBI36
Celera2120,280,062 - 20,280,312RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,558,505 - 20,558,755UniSTS
REN86332  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,080,998 - 35,081,222UniSTSGRCh37
Build 362134,002,868 - 34,003,092RGDNCBI36
Celera2120,280,620 - 20,280,844RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,559,063 - 20,559,287UniSTS
REN86333  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,081,188 - 35,081,452UniSTSGRCh37
Build 362134,003,058 - 34,003,322RGDNCBI36
Celera2120,280,810 - 20,281,074RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,559,253 - 20,559,517UniSTS
REN86334  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,081,434 - 35,081,676UniSTSGRCh37
Build 362134,003,304 - 34,003,546RGDNCBI36
Celera2120,281,056 - 20,281,298RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,559,499 - 20,559,741UniSTS
REN86335  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,081,977 - 35,082,219UniSTSGRCh37
Build 362134,003,847 - 34,004,089RGDNCBI36
Celera2120,281,599 - 20,281,841RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,560,042 - 20,560,284UniSTS
REN86336  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,082,136 - 35,082,380UniSTSGRCh37
Build 362134,004,006 - 34,004,250RGDNCBI36
Celera2120,281,758 - 20,282,002RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,560,201 - 20,560,445UniSTS
REN86337  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,082,687 - 35,082,928UniSTSGRCh37
Build 362134,004,557 - 34,004,798RGDNCBI36
Celera2120,282,309 - 20,282,550RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,560,752 - 20,560,993UniSTS
REN86338  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,082,810 - 35,083,081UniSTSGRCh37
Build 362134,004,680 - 34,004,951RGDNCBI36
Celera2120,282,432 - 20,282,703RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,560,875 - 20,561,146UniSTS
REN86339  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,083,068 - 35,083,311UniSTSGRCh37
Build 362134,004,938 - 34,005,181RGDNCBI36
Celera2120,282,690 - 20,282,933RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,561,133 - 20,561,376UniSTS
REN86340  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,083,288 - 35,083,517UniSTSGRCh37
Build 362134,005,158 - 34,005,387RGDNCBI36
Celera2120,282,910 - 20,283,139RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,561,353 - 20,561,582UniSTS
REN86341  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,083,492 - 35,083,717UniSTSGRCh37
Build 362134,005,362 - 34,005,587RGDNCBI36
Celera2120,283,114 - 20,283,339RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,561,557 - 20,561,782UniSTS
REN86342  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,083,705 - 35,083,969UniSTSGRCh37
Build 362134,005,575 - 34,005,839RGDNCBI36
Celera2120,283,327 - 20,283,591RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,561,770 - 20,562,034UniSTS
REN86343  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,083,903 - 35,084,148UniSTSGRCh37
Build 362134,005,773 - 34,006,018RGDNCBI36
Celera2120,283,525 - 20,283,770RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,561,968 - 20,562,211UniSTS
REN86344  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,084,120 - 35,084,389UniSTSGRCh37
Build 362134,005,990 - 34,006,259RGDNCBI36
Celera2120,283,742 - 20,284,011RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,562,183 - 20,562,452UniSTS
REN86345  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,084,371 - 35,084,623UniSTSGRCh37
Build 362134,006,241 - 34,006,493RGDNCBI36
Celera2120,283,993 - 20,284,245RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,562,434 - 20,562,686UniSTS
REN86346  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,084,615 - 35,084,866UniSTSGRCh37
Build 362134,006,485 - 34,006,736RGDNCBI36
Celera2120,284,237 - 20,284,488RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,562,678 - 20,562,929UniSTS
REN86347  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,084,843 - 35,085,105UniSTSGRCh37
Build 362134,006,713 - 34,006,975RGDNCBI36
Celera2120,284,465 - 20,284,727RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,562,906 - 20,563,168UniSTS
REN86348  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,084,994 - 35,085,256UniSTSGRCh37
Build 362134,006,864 - 34,007,126RGDNCBI36
Celera2120,284,616 - 20,284,878RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,563,057 - 20,563,319UniSTS
REN86349  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,085,818 - 35,086,053UniSTSGRCh37
Build 362134,007,688 - 34,007,923RGDNCBI36
Cytogenetic Map21q22.1-q22.2UniSTS
REN86350  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,085,903 - 35,086,127UniSTSGRCh37
Build 362134,007,773 - 34,007,997RGDNCBI36
Celera2120,285,526 - 20,285,750RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,563,967 - 20,564,191UniSTS
REN86351  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,086,089 - 35,086,328UniSTSGRCh37
Build 362134,007,959 - 34,008,198RGDNCBI36
Celera2120,285,712 - 20,285,951RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,564,153 - 20,564,393UniSTS
REN86352  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,086,434 - 35,086,680UniSTSGRCh37
Build 362134,008,304 - 34,008,550RGDNCBI36
Celera2120,286,057 - 20,286,303RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,564,499 - 20,564,745UniSTS
REN86353  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,086,677 - 35,086,901UniSTSGRCh37
Build 362134,008,547 - 34,008,771RGDNCBI36
Celera2120,286,300 - 20,286,524RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,564,742 - 20,564,966UniSTS
REN86354  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,086,865 - 35,087,105UniSTSGRCh37
Build 362134,008,735 - 34,008,975RGDNCBI36
Celera2120,286,488 - 20,286,728RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,564,930 - 20,565,164UniSTS
REN86355  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,087,082 - 35,087,314UniSTSGRCh37
Build 362134,008,952 - 34,009,184RGDNCBI36
Celera2120,286,705 - 20,286,937RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,565,141 - 20,565,373UniSTS
REN86356  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,087,272 - 35,087,539UniSTSGRCh37
Build 362134,009,142 - 34,009,409RGDNCBI36
Celera2120,286,895 - 20,287,162RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,565,331 - 20,565,598UniSTS
REN86357  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,087,497 - 35,087,723UniSTSGRCh37
Build 362134,009,367 - 34,009,593RGDNCBI36
Celera2120,287,120 - 20,287,345RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,565,556 - 20,565,781UniSTS
REN86358  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,087,689 - 35,087,925UniSTSGRCh37
Build 362134,009,559 - 34,009,795RGDNCBI36
Celera2120,287,311 - 20,287,547RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,565,747 - 20,565,983UniSTS
REN86359  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,087,860 - 35,088,112UniSTSGRCh37
Build 362134,009,730 - 34,009,982RGDNCBI36
Celera2120,287,482 - 20,287,734RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,565,918 - 20,566,170UniSTS
REN86360  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,088,081 - 35,088,347UniSTSGRCh37
Build 362134,009,951 - 34,010,217RGDNCBI36
Celera2120,287,703 - 20,287,969RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,566,139 - 20,566,405UniSTS
REN86361  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,088,328 - 35,088,582UniSTSGRCh37
Build 362134,010,198 - 34,010,452RGDNCBI36
Celera2120,287,950 - 20,288,204RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,566,386 - 20,566,640UniSTS
REN86362  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,088,572 - 35,088,816UniSTSGRCh37
Build 362134,010,442 - 34,010,686RGDNCBI36
Celera2120,288,194 - 20,288,438RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,566,630 - 20,566,874UniSTS
REN86363  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,088,777 - 35,089,029UniSTSGRCh37
Build 362134,010,647 - 34,010,899RGDNCBI36
Celera2120,288,399 - 20,288,651RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,566,835 - 20,567,087UniSTS
REN86364  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,089,301 - 35,089,543UniSTSGRCh37
Build 362134,011,171 - 34,011,413RGDNCBI36
Celera2120,288,923 - 20,289,165RGD
Cytogenetic Map21q22.1-q22.2UniSTS
REN86365  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,089,334 - 35,089,583UniSTSGRCh37
Build 362134,011,204 - 34,011,453RGDNCBI36
Celera2120,288,956 - 20,289,205RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,567,392 - 20,567,580UniSTS
REN86366  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,089,595 - 35,089,843UniSTSGRCh37
Build 362134,011,465 - 34,011,713RGDNCBI36
Celera2120,289,217 - 20,289,465RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,567,592 - 20,567,840UniSTS
REN86367  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,089,828 - 35,090,070UniSTSGRCh37
Build 362134,011,698 - 34,011,940RGDNCBI36
Celera2120,289,450 - 20,289,692RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,567,825 - 20,568,067UniSTS
REN86368  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,090,034 - 35,090,287UniSTSGRCh37
Build 362134,011,904 - 34,012,157RGDNCBI36
Celera2120,289,656 - 20,289,909RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,568,031 - 20,568,284UniSTS
REN86369  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,090,275 - 35,090,499UniSTSGRCh37
Build 362134,012,145 - 34,012,369RGDNCBI36
Celera2120,289,897 - 20,290,121RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,568,272 - 20,568,496UniSTS
REN86370  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,090,435 - 35,090,688UniSTSGRCh37
Build 362134,012,305 - 34,012,558RGDNCBI36
Celera2120,290,057 - 20,290,310RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,568,432 - 20,568,685UniSTS
REN86371  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,090,657 - 35,090,929UniSTSGRCh37
Build 362134,012,527 - 34,012,799RGDNCBI36
Celera2120,290,279 - 20,290,551RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,568,654 - 20,568,926UniSTS
REN86372  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,090,917 - 35,091,167UniSTSGRCh37
Build 362134,012,787 - 34,013,037RGDNCBI36
Celera2120,290,539 - 20,290,789RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,568,914 - 20,569,164UniSTS
REN86373  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,091,146 - 35,091,371UniSTSGRCh37
Build 362134,013,016 - 34,013,241RGDNCBI36
Celera2120,290,768 - 20,290,993RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,569,143 - 20,569,368UniSTS
REN86374  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,091,184 - 35,091,419UniSTSGRCh37
Build 362134,013,054 - 34,013,289RGDNCBI36
Celera2120,290,806 - 20,291,041RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,569,181 - 20,569,416UniSTS
REN86375  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,091,779 - 35,092,011UniSTSGRCh37
Build 362134,013,649 - 34,013,881RGDNCBI36
Celera2120,291,401 - 20,291,633RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,569,776 - 20,570,008UniSTS
REN86376  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,091,988 - 35,092,260UniSTSGRCh37
Build 362134,013,858 - 34,014,130RGDNCBI36
Celera2120,291,610 - 20,291,882RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,569,985 - 20,570,257UniSTS
REN86377  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,092,238 - 35,092,473UniSTSGRCh37
Build 362134,014,108 - 34,014,343RGDNCBI36
Celera2120,291,860 - 20,292,095RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,570,235 - 20,570,470UniSTS
REN86378  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,092,467 - 35,092,695UniSTSGRCh37
Build 362134,014,337 - 34,014,565RGDNCBI36
Celera2120,292,089 - 20,292,317RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,570,464 - 20,570,692UniSTS
REN86379  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,092,653 - 35,092,909UniSTSGRCh37
Build 362134,014,523 - 34,014,779RGDNCBI36
Celera2120,292,275 - 20,292,531RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,570,650 - 20,570,906UniSTS
REN86380  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,092,885 - 35,093,118UniSTSGRCh37
Build 362134,014,755 - 34,014,988RGDNCBI36
Celera2120,292,507 - 20,292,740RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,570,882 - 20,571,115UniSTS
REN86381  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,093,108 - 35,093,362UniSTSGRCh37
Build 362134,014,978 - 34,015,232RGDNCBI36
Celera2120,292,730 - 20,292,984RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,571,105 - 20,571,359UniSTS
REN86382  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,093,340 - 35,093,565UniSTSGRCh37
Build 362134,015,210 - 34,015,435RGDNCBI36
Celera2120,292,962 - 20,293,187RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,571,337 - 20,571,562UniSTS
REN86383  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,093,526 - 35,093,788UniSTSGRCh37
Build 362134,015,396 - 34,015,658RGDNCBI36
Celera2120,293,148 - 20,293,410RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,571,523 - 20,571,785UniSTS
REN86384  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,093,617 - 35,093,848UniSTSGRCh37
Build 362134,015,487 - 34,015,718RGDNCBI36
Celera2120,293,239 - 20,293,470RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,571,614 - 20,571,845UniSTS
REN86385  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,093,789 - 35,094,034UniSTSGRCh37
Build 362134,015,659 - 34,015,904RGDNCBI36
Celera2120,293,411 - 20,293,656RGD
Cytogenetic Map21q22.1-q22.2UniSTS
REN86386  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,094,290 - 35,094,514UniSTSGRCh37
Build 362134,016,160 - 34,016,384RGDNCBI36
Celera2120,293,912 - 20,294,136RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,572,320 - 20,572,544UniSTS
REN86387  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,094,506 - 35,094,738UniSTSGRCh37
Build 362134,016,376 - 34,016,608RGDNCBI36
Celera2120,294,128 - 20,294,360RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,572,536 - 20,572,768UniSTS
REN86388  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,094,729 - 35,094,953UniSTSGRCh37
Build 362134,016,599 - 34,016,823RGDNCBI36
Celera2120,294,351 - 20,294,575RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,572,759 - 20,572,983UniSTS
REN86389  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,094,925 - 35,095,178UniSTSGRCh37
Build 362134,016,795 - 34,017,048RGDNCBI36
Celera2120,294,547 - 20,294,800RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,572,955 - 20,573,208UniSTS
REN86390  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,095,160 - 35,095,384UniSTSGRCh37
Build 362134,017,030 - 34,017,254RGDNCBI36
Celera2120,294,782 - 20,295,006RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,573,190 - 20,573,414UniSTS
REN86391  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,095,360 - 35,095,617UniSTSGRCh37
Build 362134,017,230 - 34,017,487RGDNCBI36
Celera2120,294,982 - 20,295,239RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,573,390 - 20,573,647UniSTS
REN86392  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,095,420 - 35,095,644UniSTSGRCh37
Build 362134,017,290 - 34,017,514RGDNCBI36
Celera2120,295,042 - 20,295,266RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,573,450 - 20,573,674UniSTS
REN86393  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,095,932 - 35,096,170UniSTSGRCh37
Build 362134,017,802 - 34,018,040RGDNCBI36
Celera2120,295,554 - 20,295,792RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,573,962 - 20,574,200UniSTS
REN86394  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,096,163 - 35,096,398UniSTSGRCh37
Build 362134,018,033 - 34,018,268RGDNCBI36
Celera2120,295,785 - 20,296,020RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,574,193 - 20,574,428UniSTS
REN86395  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,096,369 - 35,096,622UniSTSGRCh37
Build 362134,018,239 - 34,018,492RGDNCBI36
Celera2120,295,991 - 20,296,244RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,574,399 - 20,574,652UniSTS
REN86396  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,096,611 - 35,096,860UniSTSGRCh37
Build 362134,018,481 - 34,018,730RGDNCBI36
Celera2120,296,233 - 20,296,482RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,574,641 - 20,574,890UniSTS
REN86397  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,096,837 - 35,097,086UniSTSGRCh37
Build 362134,018,707 - 34,018,956RGDNCBI36
Celera2120,296,459 - 20,296,708RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,574,867 - 20,575,116UniSTS
REN86398  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,097,073 - 35,097,337UniSTSGRCh37
Build 362134,018,943 - 34,019,207RGDNCBI36
Celera2120,296,695 - 20,296,959RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,575,103 - 20,575,367UniSTS
REN86399  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,097,845 - 35,098,071UniSTSGRCh37
Build 362134,019,715 - 34,019,941RGDNCBI36
Celera2120,297,467 - 20,297,693RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,575,875 - 20,576,101UniSTS
REN86400  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,098,048 - 35,098,280UniSTSGRCh37
Build 362134,019,918 - 34,020,150RGDNCBI36
Celera2120,297,670 - 20,297,902RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,576,078 - 20,576,310UniSTS
REN86401  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,098,085 - 35,098,327UniSTSGRCh37
Build 362134,019,955 - 34,020,197RGDNCBI36
Celera2120,297,707 - 20,297,949RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,576,115 - 20,576,357UniSTS
REN86402  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,098,454 - 35,098,710UniSTSGRCh37
Build 362134,020,324 - 34,020,580RGDNCBI36
Celera2120,298,076 - 20,298,332RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,576,484 - 20,576,740UniSTS
REN86403  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,098,698 - 35,098,932UniSTSGRCh37
Build 362134,020,568 - 34,020,802RGDNCBI36
Celera2120,298,320 - 20,298,554RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,576,728 - 20,576,962UniSTS
REN86404  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,098,910 - 35,099,142UniSTSGRCh37
Build 362134,020,780 - 34,021,012RGDNCBI36
Celera2120,298,532 - 20,298,764RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,576,940 - 20,577,172UniSTS
REN86405  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,099,138 - 35,099,378UniSTSGRCh37
Build 362134,021,008 - 34,021,248RGDNCBI36
Celera2120,298,760 - 20,299,000RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,577,168 - 20,577,408UniSTS
REN86406  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,099,355 - 35,099,603UniSTSGRCh37
Build 362134,021,225 - 34,021,473RGDNCBI36
Celera2120,298,977 - 20,299,225RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,577,385 - 20,577,633UniSTS
REN86407  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,099,580 - 35,099,828UniSTSGRCh37
Build 362134,021,450 - 34,021,698RGDNCBI36
Celera2120,299,202 - 20,299,450RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,577,610 - 20,577,858UniSTS
REN86408  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,099,808 - 35,100,043UniSTSGRCh37
Build 362134,021,678 - 34,021,913RGDNCBI36
Celera2120,299,430 - 20,299,665RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,577,838 - 20,578,073UniSTS
REN86409  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,100,026 - 35,100,251UniSTSGRCh37
Build 362134,021,896 - 34,022,121RGDNCBI36
Celera2120,299,648 - 20,299,873RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,578,056 - 20,578,281UniSTS
REN86410  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,100,167 - 35,100,416UniSTSGRCh37
Build 362134,022,037 - 34,022,286RGDNCBI36
Celera2120,299,789 - 20,300,038RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,578,197 - 20,578,446UniSTS
REN86411  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,100,386 - 35,100,649UniSTSGRCh37
Build 362134,022,256 - 34,022,519RGDNCBI36
Celera2120,300,008 - 20,300,271RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,578,416 - 20,578,679UniSTS
REN86412  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,100,622 - 35,100,864UniSTSGRCh37
Build 362134,022,492 - 34,022,734RGDNCBI36
Celera2120,300,244 - 20,300,486RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,578,652 - 20,578,894UniSTS
REN86413  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,100,830 - 35,101,064UniSTSGRCh37
Build 362134,022,700 - 34,022,934RGDNCBI36
Celera2120,300,452 - 20,300,686RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,578,860 - 20,579,094UniSTS
REN86414  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,101,041 - 35,101,305UniSTSGRCh37
Build 362134,022,911 - 34,023,175RGDNCBI36
Celera2120,300,663 - 20,300,927RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,579,071 - 20,579,335UniSTS
REN86415  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,101,231 - 35,101,481UniSTSGRCh37
Build 362134,023,101 - 34,023,351RGDNCBI36
Celera2120,300,853 - 20,301,103RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,579,261 - 20,579,511UniSTS
REN86416  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,101,458 - 35,101,691UniSTSGRCh37
Build 362134,023,328 - 34,023,561RGDNCBI36
Celera2120,301,080 - 20,301,313RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,579,488 - 20,579,721UniSTS
REN86417  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,101,667 - 35,101,932UniSTSGRCh37
Build 362134,023,537 - 34,023,802RGDNCBI36
Celera2120,301,289 - 20,301,554RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,579,697 - 20,579,962UniSTS
REN86418  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,101,918 - 35,102,170UniSTSGRCh37
Build 362134,023,788 - 34,024,040RGDNCBI36
Celera2120,301,540 - 20,301,792RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,579,948 - 20,580,200UniSTS
REN86419  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,102,134 - 35,102,365UniSTSGRCh37
Build 362134,024,004 - 34,024,235RGDNCBI36
Celera2120,301,756 - 20,301,987RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,580,164 - 20,580,395UniSTS
REN86420  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,102,336 - 35,102,567UniSTSGRCh37
Build 362134,024,206 - 34,024,437RGDNCBI36
Celera2120,301,958 - 20,302,189RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,580,366 - 20,580,597UniSTS
REN86421  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,102,410 - 35,102,668UniSTSGRCh37
Build 362134,024,280 - 34,024,538RGDNCBI36
Celera2120,302,032 - 20,302,290RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,580,440 - 20,580,698UniSTS
REN86422  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,103,295 - 35,103,546UniSTSGRCh37
Build 362134,025,165 - 34,025,416RGDNCBI36
Celera2120,302,917 - 20,303,168RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,581,326 - 20,581,577UniSTS
REN86423  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,103,543 - 35,103,770UniSTSGRCh37
Build 362134,025,413 - 34,025,640RGDNCBI36
Celera2120,303,165 - 20,303,392RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,581,574 - 20,581,801UniSTS
REN86424  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,103,748 - 35,104,012UniSTSGRCh37
Build 362134,025,618 - 34,025,882RGDNCBI36
Celera2120,303,370 - 20,303,634RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,581,779 - 20,582,043UniSTS
REN86425  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,104,006 - 35,104,250UniSTSGRCh37
Build 362134,025,876 - 34,026,120RGDNCBI36
Celera2120,303,628 - 20,303,872RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,582,037 - 20,582,281UniSTS
REN86426  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,104,226 - 35,104,480UniSTSGRCh37
Build 362134,026,096 - 34,026,350RGDNCBI36
Celera2120,303,848 - 20,304,102RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,582,257 - 20,582,511UniSTS
REN86427  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,104,438 - 35,104,701UniSTSGRCh37
Build 362134,026,308 - 34,026,571RGDNCBI36
Celera2120,304,060 - 20,304,323RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,582,469 - 20,582,732UniSTS
REN86428  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,104,680 - 35,104,936UniSTSGRCh37
Build 362134,026,550 - 34,026,806RGDNCBI36
Celera2120,304,302 - 20,304,558RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,582,711 - 20,582,967UniSTS
REN86429  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,104,915 - 35,105,145UniSTSGRCh37
Build 362134,026,785 - 34,027,015RGDNCBI36
Celera2120,304,537 - 20,304,767RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,582,946 - 20,583,176UniSTS
REN86430  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,105,119 - 35,105,360UniSTSGRCh37
Build 362134,026,989 - 34,027,230RGDNCBI36
Celera2120,304,741 - 20,304,982RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,583,150 - 20,583,391UniSTS
REN86431  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,105,341 - 35,105,610UniSTSGRCh37
Build 362134,027,211 - 34,027,480RGDNCBI36
Celera2120,304,963 - 20,305,232RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,583,372 - 20,583,641UniSTS
REN86432  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,105,511 - 35,105,770UniSTSGRCh37
Build 362134,027,381 - 34,027,640RGDNCBI36
Celera2120,305,133 - 20,305,392RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,583,542 - 20,583,801UniSTS
REN86433  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,105,743 - 35,105,998UniSTSGRCh37
Build 362134,027,613 - 34,027,868RGDNCBI36
Celera2120,305,365 - 20,305,620RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,583,774 - 20,584,030UniSTS
REN86434  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,105,952 - 35,106,199UniSTSGRCh37
Build 362134,027,822 - 34,028,069RGDNCBI36
Celera2120,305,574 - 20,305,821RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,583,984 - 20,584,231UniSTS
REN86435  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,106,137 - 35,106,361UniSTSGRCh37
Build 362134,028,007 - 34,028,231RGDNCBI36
Celera2120,305,759 - 20,305,983RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,584,169 - 20,584,393UniSTS
REN86436  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,106,331 - 35,106,583UniSTSGRCh37
Build 362134,028,201 - 34,028,453RGDNCBI36
Celera2120,305,953 - 20,306,205RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,584,363 - 20,584,615UniSTS
REN86437  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,106,528 - 35,106,753UniSTSGRCh37
Build 362134,028,398 - 34,028,623RGDNCBI36
Celera2120,306,150 - 20,306,375RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,584,560 - 20,584,785UniSTS
REN86438  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,106,734 - 35,106,966UniSTSGRCh37
Build 362134,028,604 - 34,028,836RGDNCBI36
Celera2120,306,356 - 20,306,588RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,584,766 - 20,584,998UniSTS
REN86439  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,106,953 - 35,107,211UniSTSGRCh37
Build 362134,028,823 - 34,029,081RGDNCBI36
Celera2120,306,575 - 20,306,833RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,584,985 - 20,585,243UniSTS
REN86440  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,107,190 - 35,107,453UniSTSGRCh37
Build 362134,029,060 - 34,029,323RGDNCBI36
Celera2120,306,812 - 20,307,075RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,585,222 - 20,585,485UniSTS
REN86441  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,107,436 - 35,107,688UniSTSGRCh37
Build 362134,029,306 - 34,029,558RGDNCBI36
Celera2120,307,058 - 20,307,310RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,585,468 - 20,585,720UniSTS
REN86442  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,107,685 - 35,107,910UniSTSGRCh37
Build 362134,029,555 - 34,029,780RGDNCBI36
Celera2120,307,307 - 20,307,532RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,585,717 - 20,585,942UniSTS
REN86443  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,107,800 - 35,108,032UniSTSGRCh37
Build 362134,029,670 - 34,029,902RGDNCBI36
Celera2120,307,422 - 20,307,654RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,585,832 - 20,586,064UniSTS
REN86444  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,108,287 - 35,108,513UniSTSGRCh37
Build 362134,030,157 - 34,030,383RGDNCBI36
Celera2120,307,909 - 20,308,135RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,586,319 - 20,586,545UniSTS
REN86445  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,108,490 - 35,108,751UniSTSGRCh37
Build 362134,030,360 - 34,030,621RGDNCBI36
Celera2120,308,112 - 20,308,373RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,586,522 - 20,586,783UniSTS
REN86446  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,108,728 - 35,108,974UniSTSGRCh37
Build 362134,030,598 - 34,030,844RGDNCBI36
Celera2120,308,350 - 20,308,596RGD
Cytogenetic Map21q22.1-q22.2UniSTS
REN86447  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,108,865 - 35,109,091UniSTSGRCh37
Build 362134,030,735 - 34,030,961RGDNCBI36
Celera2120,308,487 - 20,308,713RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,586,898 - 20,587,124UniSTS
REN86448  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,109,092 - 35,109,331UniSTSGRCh37
Build 362134,030,962 - 34,031,201RGDNCBI36
Celera2120,308,714 - 20,308,953RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,587,125 - 20,587,364UniSTS
REN86449  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,109,317 - 35,109,546UniSTSGRCh37
Build 362134,031,187 - 34,031,416RGDNCBI36
Celera2120,308,939 - 20,309,168RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,587,350 - 20,587,579UniSTS
REN86450  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,109,536 - 35,109,799UniSTSGRCh37
Build 362134,031,406 - 34,031,669RGDNCBI36
Celera2120,309,158 - 20,309,421RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,587,569 - 20,587,832UniSTS
REN86451  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,109,685 - 35,109,923UniSTSGRCh37
Build 362134,031,555 - 34,031,793RGDNCBI36
Celera2120,309,307 - 20,309,545RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,587,718 - 20,587,956UniSTS
REN86452  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,110,195 - 35,110,446UniSTSGRCh37
Build 362134,032,065 - 34,032,316RGDNCBI36
Celera2120,309,817 - 20,310,068RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,588,228 - 20,588,479UniSTS
REN86453  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,110,429 - 35,110,673UniSTSGRCh37
Build 362134,032,299 - 34,032,543RGDNCBI36
Celera2120,310,051 - 20,310,295RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,588,462 - 20,588,706UniSTS
REN86454  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,110,517 - 35,110,741UniSTSGRCh37
Build 362134,032,387 - 34,032,611RGDNCBI36
Celera2120,310,139 - 20,310,363RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,588,550 - 20,588,774UniSTS
REN86455  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,110,801 - 35,111,047UniSTSGRCh37
Build 362134,032,671 - 34,032,917RGDNCBI36
Celera2120,310,423 - 20,310,669RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,588,834 - 20,589,080UniSTS
REN86456  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,111,028 - 35,111,272UniSTSGRCh37
Build 362134,032,898 - 34,033,142RGDNCBI36
Celera2120,310,650 - 20,310,894RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,589,061 - 20,589,305UniSTS
REN86457  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,111,243 - 35,111,494UniSTSGRCh37
Build 362134,033,113 - 34,033,364RGDNCBI36
Celera2120,310,865 - 20,311,116RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,589,276 - 20,589,527UniSTS
REN86458  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,111,465 - 35,111,701UniSTSGRCh37
Build 362134,033,335 - 34,033,571RGDNCBI36
Celera2120,311,087 - 20,311,323RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,589,498 - 20,589,734UniSTS
REN86459  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,111,675 - 35,111,923UniSTSGRCh37
Build 362134,033,545 - 34,033,793RGDNCBI36
Celera2120,311,297 - 20,311,545RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,589,708 - 20,589,956UniSTS
REN86460  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,111,908 - 35,112,151UniSTSGRCh37
Build 362134,033,778 - 34,034,021RGDNCBI36
Celera2120,311,530 - 20,311,773RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,589,941 - 20,590,184UniSTS
REN86461  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,112,135 - 35,112,394UniSTSGRCh37
Build 362134,034,005 - 34,034,264RGDNCBI36
Celera2120,311,757 - 20,312,016RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,590,168 - 20,590,427UniSTS
REN86462  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,112,381 - 35,112,624UniSTSGRCh37
Build 362134,034,251 - 34,034,494RGDNCBI36
Celera2120,312,003 - 20,312,246RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,590,414 - 20,590,657UniSTS
REN86463  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,112,608 - 35,112,864UniSTSGRCh37
Build 362134,034,478 - 34,034,734RGDNCBI36
Celera2120,312,230 - 20,312,486RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,590,641 - 20,590,897UniSTS
REN86464  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,112,849 - 35,113,095UniSTSGRCh37
Build 362134,034,719 - 34,034,965RGDNCBI36
Celera2120,312,471 - 20,312,717RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,590,882 - 20,591,128UniSTS
REN86465  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,113,067 - 35,113,312UniSTSGRCh37
Build 362134,034,937 - 34,035,182RGDNCBI36
Celera2120,312,689 - 20,312,934RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,591,100 - 20,591,345UniSTS
REN86466  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,113,150 - 35,113,413UniSTSGRCh37
Build 362134,035,020 - 34,035,283RGDNCBI36
Celera2120,312,772 - 20,313,035RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,591,183 - 20,591,446UniSTS
REN86467  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,113,352 - 35,113,603UniSTSGRCh37
Build 362134,035,222 - 34,035,473RGDNCBI36
Celera2120,312,974 - 20,313,225RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,591,385 - 20,591,636UniSTS
REN86468  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,113,572 - 35,113,796UniSTSGRCh37
Build 362134,035,442 - 34,035,666RGDNCBI36
Celera2120,313,194 - 20,313,418RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,591,605 - 20,591,829UniSTS
REN86469  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,114,726 - 35,114,951UniSTSGRCh37
Build 362134,036,596 - 34,036,821RGDNCBI36
Celera2120,314,348 - 20,314,573RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,592,759 - 20,592,984UniSTS
REN86470  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,114,925 - 35,115,174UniSTSGRCh37
Build 362134,036,795 - 34,037,044RGDNCBI36
Celera2120,314,547 - 20,314,796RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,592,958 - 20,593,207UniSTS
REN86471  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,115,168 - 35,115,417UniSTSGRCh37
Build 362134,037,038 - 34,037,287RGDNCBI36
Celera2120,314,790 - 20,315,039RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,593,201 - 20,593,450UniSTS
REN86472  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,115,244 - 35,115,496UniSTSGRCh37
Build 362134,037,114 - 34,037,366RGDNCBI36
Celera2120,314,866 - 20,315,118RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,593,277 - 20,593,529UniSTS
REN86473  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,115,744 - 35,115,987UniSTSGRCh37
Build 362134,037,614 - 34,037,857RGDNCBI36
Celera2120,315,366 - 20,315,609RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,593,777 - 20,594,020UniSTS
REN86474  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,115,972 - 35,116,197UniSTSGRCh37
Build 362134,037,842 - 34,038,067RGDNCBI36
Celera2120,315,594 - 20,315,819RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,594,005 - 20,594,230UniSTS
REN86475  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,116,166 - 35,116,419UniSTSGRCh37
Build 362134,038,036 - 34,038,289RGDNCBI36
Celera2120,315,788 - 20,316,041RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,594,199 - 20,594,452UniSTS
REN86476  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,116,396 - 35,116,644UniSTSGRCh37
Build 362134,038,266 - 34,038,514RGDNCBI36
Celera2120,316,018 - 20,316,266RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,594,429 - 20,594,677UniSTS
REN86477  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,116,621 - 35,116,864UniSTSGRCh37
Build 362134,038,491 - 34,038,734RGDNCBI36
Celera2120,316,243 - 20,316,486RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,594,654 - 20,594,897UniSTS
REN86478  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,116,843 - 35,117,095UniSTSGRCh37
Build 362134,038,713 - 34,038,965RGDNCBI36
Celera2120,316,465 - 20,316,717RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,594,876 - 20,595,128UniSTS
REN86479  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,117,072 - 35,117,312UniSTSGRCh37
Build 362134,038,942 - 34,039,182RGDNCBI36
Celera2120,316,694 - 20,316,934RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,595,105 - 20,595,345UniSTS
REN86480  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,117,273 - 35,117,514UniSTSGRCh37
Build 362134,039,143 - 34,039,384RGDNCBI36
Celera2120,316,895 - 20,317,136RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,595,306 - 20,595,547UniSTS
REN86481  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,117,501 - 35,117,742UniSTSGRCh37
Build 362134,039,371 - 34,039,612RGDNCBI36
Celera2120,317,123 - 20,317,364RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,595,534 - 20,595,775UniSTS
REN86482  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,117,719 - 35,117,963UniSTSGRCh37
Build 362134,039,589 - 34,039,833RGDNCBI36
Celera2120,317,341 - 20,317,585RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,595,752 - 20,595,996UniSTS
REN86483  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,117,937 - 35,118,188UniSTSGRCh37
Build 362134,039,807 - 34,040,058RGDNCBI36
Celera2120,317,559 - 20,317,810RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,595,970 - 20,596,221UniSTS
REN86484  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,118,167 - 35,118,391UniSTSGRCh37
Build 362134,040,037 - 34,040,261RGDNCBI36
Celera2120,317,789 - 20,318,013RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,596,200 - 20,596,424UniSTS
REN86485  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,118,374 - 35,118,638UniSTSGRCh37
Build 362134,040,244 - 34,040,508RGDNCBI36
Celera2120,317,996 - 20,318,260RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,596,407 - 20,596,671UniSTS
REN86486  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,118,615 - 35,118,868UniSTSGRCh37
Build 362134,040,485 - 34,040,738RGDNCBI36
Celera2120,318,237 - 20,318,490RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,596,648 - 20,596,901UniSTS
REN86487  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,118,839 - 35,119,105UniSTSGRCh37
Build 362134,040,709 - 34,040,975RGDNCBI36
Celera2120,318,461 - 20,318,727RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,596,872 - 20,597,138UniSTS
REN86488  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,118,917 - 35,119,186UniSTSGRCh37
Build 362134,040,787 - 34,041,056RGDNCBI36
Celera2120,318,539 - 20,318,808RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,596,950 - 20,597,219UniSTS
REN86489  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,119,337 - 35,119,562UniSTSGRCh37
Build 362134,041,207 - 34,041,432RGDNCBI36
Celera2120,318,959 - 20,319,184RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,597,370 - 20,597,595UniSTS
REN86490  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,119,538 - 35,119,802UniSTSGRCh37
Build 362134,041,408 - 34,041,672RGDNCBI36
Celera2120,319,160 - 20,319,424RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,597,571 - 20,597,835UniSTS
REN86491  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,119,782 - 35,120,034UniSTSGRCh37
Build 362134,041,652 - 34,041,904RGDNCBI36
Celera2120,319,404 - 20,319,656RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,597,815 - 20,598,067UniSTS
REN86492  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,119,953 - 35,120,180UniSTSGRCh37
Build 362134,041,823 - 34,042,050RGDNCBI36
Celera2120,319,575 - 20,319,802RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,597,986 - 20,598,213UniSTS
REN86493  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,120,151 - 35,120,380UniSTSGRCh37
Build 362134,042,021 - 34,042,250RGDNCBI36
Celera2120,319,773 - 20,320,002RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,598,184 - 20,598,413UniSTS
REN86494  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,120,367 - 35,120,636UniSTSGRCh37
Build 362134,042,237 - 34,042,506RGDNCBI36
Celera2120,319,989 - 20,320,258RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,598,400 - 20,598,669UniSTS
REN86495  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,120,601 - 35,120,843UniSTSGRCh37
Build 362134,042,471 - 34,042,713RGDNCBI36
Celera2120,320,223 - 20,320,465RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,598,634 - 20,598,876UniSTS
REN86496  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,120,817 - 35,121,042UniSTSGRCh37
Build 362134,042,687 - 34,042,912RGDNCBI36
Celera2120,320,439 - 20,320,664RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,598,850 - 20,599,075UniSTS
REN86497  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,121,017 - 35,121,263UniSTSGRCh37
Build 362134,042,887 - 34,043,133RGDNCBI36
Celera2120,320,639 - 20,320,885RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,599,050 - 20,599,296UniSTS
REN86498  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,121,203 - 35,121,437UniSTSGRCh37
Build 362134,043,073 - 34,043,307RGDNCBI36
Celera2120,320,825 - 20,321,059RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,599,236 - 20,599,469UniSTS
REN86499  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,121,408 - 35,121,670UniSTSGRCh37
Build 362134,043,278 - 34,043,540RGDNCBI36
Celera2120,321,030 - 20,321,292RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,599,440 - 20,599,702UniSTS
REN86500  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,121,971 - 35,122,199UniSTSGRCh37
Build 362134,043,841 - 34,044,069RGDNCBI36
Celera2120,321,593 - 20,321,821RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,600,003 - 20,600,231UniSTS
REN86501  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,122,182 - 35,122,437UniSTSGRCh37
Build 362134,044,052 - 34,044,307RGDNCBI36
Celera2120,321,804 - 20,322,059RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,600,214 - 20,600,469UniSTS
REN86502  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,122,414 - 35,122,658UniSTSGRCh37
Build 362134,044,284 - 34,044,528RGDNCBI36
Celera2120,322,036 - 20,322,280RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,600,446 - 20,600,690UniSTS
REN86503  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,122,635 - 35,122,895UniSTSGRCh37
Build 362134,044,505 - 34,044,765RGDNCBI36
Celera2120,322,257 - 20,322,517RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,600,667 - 20,600,927UniSTS
REN86504  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,122,889 - 35,123,128UniSTSGRCh37
Build 362134,044,759 - 34,044,998RGDNCBI36
Celera2120,322,511 - 20,322,750RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,600,921 - 20,601,160UniSTS
REN86505  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,123,117 - 35,123,341UniSTSGRCh37
Build 362134,044,987 - 34,045,211RGDNCBI36
Celera2120,322,739 - 20,322,963RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,601,149 - 20,601,373UniSTS
REN86506  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,123,315 - 35,123,575UniSTSGRCh37
Build 362134,045,185 - 34,045,445RGDNCBI36
Celera2120,322,937 - 20,323,197RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,601,347 - 20,601,607UniSTS
REN86507  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,123,527 - 35,123,777UniSTSGRCh37
Build 362134,045,397 - 34,045,647RGDNCBI36
Celera2120,323,149 - 20,323,399RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,601,559 - 20,601,809UniSTS
REN86508  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,123,747 - 35,123,984UniSTSGRCh37
Build 362134,045,617 - 34,045,854RGDNCBI36
Celera2120,323,369 - 20,323,606RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,601,779 - 20,602,016UniSTS
REN86509  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,123,955 - 35,124,205UniSTSGRCh37
Build 362134,045,825 - 34,046,075RGDNCBI36
Celera2120,323,577 - 20,323,827RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,601,987 - 20,602,237UniSTS
REN86510  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,124,197 - 35,124,421UniSTSGRCh37
Build 362134,046,067 - 34,046,291RGDNCBI36
Celera2120,323,819 - 20,324,043RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,602,229 - 20,602,453UniSTS
REN86511  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,124,397 - 35,124,622UniSTSGRCh37
Build 362134,046,267 - 34,046,492RGDNCBI36
Celera2120,324,019 - 20,324,244RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,602,429 - 20,602,654UniSTS
REN86512  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,124,592 - 35,124,858UniSTSGRCh37
Build 362134,046,462 - 34,046,728RGDNCBI36
Celera2120,324,214 - 20,324,480RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,602,624 - 20,602,890UniSTS
REN86513  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,124,833 - 35,125,058UniSTSGRCh37
Build 362134,046,703 - 34,046,928RGDNCBI36
Celera2120,324,455 - 20,324,680RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,602,865 - 20,603,090UniSTS
REN86514  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,125,008 - 35,125,268UniSTSGRCh37
Build 362134,046,878 - 34,047,138RGDNCBI36
Celera2120,324,630 - 20,324,890RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,603,040 - 20,603,300UniSTS
REN86515  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,125,245 - 35,125,475UniSTSGRCh37
Build 362134,047,115 - 34,047,345RGDNCBI36
Celera2120,324,867 - 20,325,097RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,603,277 - 20,603,507UniSTS
REN86516  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,125,466 - 35,125,725UniSTSGRCh37
Build 362134,047,336 - 34,047,595RGDNCBI36
Celera2120,325,088 - 20,325,347RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,603,498 - 20,603,757UniSTS
REN86517  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,125,544 - 35,125,794UniSTSGRCh37
Build 362134,047,414 - 34,047,664RGDNCBI36
Celera2120,325,166 - 20,325,416RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,603,576 - 20,603,826UniSTS
REN86518  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,126,044 - 35,126,301UniSTSGRCh37
Build 362134,047,914 - 34,048,171RGDNCBI36
Celera2120,325,666 - 20,325,923RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,604,076 - 20,604,333UniSTS
REN86519  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,126,278 - 35,126,528UniSTSGRCh37
Build 362134,048,148 - 34,048,398RGDNCBI36
Celera2120,325,900 - 20,326,150RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,604,310 - 20,604,560UniSTS
REN86520  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,126,505 - 35,126,754UniSTSGRCh37
Build 362134,048,375 - 34,048,624RGDNCBI36
Celera2120,326,127 - 20,326,376RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,604,537 - 20,604,786UniSTS
REN86521  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,126,727 - 35,126,993UniSTSGRCh37
Build 362134,048,597 - 34,048,863RGDNCBI36
Celera2120,326,349 - 20,326,615RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,604,759 - 20,605,025UniSTS
REN86522  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,126,962 - 35,127,222UniSTSGRCh37
Build 362134,048,832 - 34,049,092RGDNCBI36
Celera2120,326,584 - 20,326,844RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,604,994 - 20,605,254UniSTS
REN86523  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,127,198 - 35,127,426UniSTSGRCh37
Build 362134,049,068 - 34,049,296RGDNCBI36
Celera2120,326,820 - 20,327,048RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,605,230 - 20,605,458UniSTS
REN86524  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,127,396 - 35,127,639UniSTSGRCh37
Build 362134,049,266 - 34,049,509RGDNCBI36
Celera2120,327,018 - 20,327,261RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,605,428 - 20,605,671UniSTS
REN86525  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,127,636 - 35,127,890UniSTSGRCh37
Build 362134,049,506 - 34,049,760RGDNCBI36
Celera2120,327,258 - 20,327,512RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,605,668 - 20,605,922UniSTS
REN86526  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,127,868 - 35,128,118UniSTSGRCh37
Build 362134,049,738 - 34,049,988RGDNCBI36
Celera2120,327,490 - 20,327,740RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,605,900 - 20,606,150UniSTS
REN86527  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,128,099 - 35,128,338UniSTSGRCh37
Build 362134,049,969 - 34,050,208RGDNCBI36
Celera2120,327,721 - 20,327,960RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,606,131 - 20,606,370UniSTS
REN86528  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,128,137 - 35,128,371UniSTSGRCh37
Build 362134,050,007 - 34,050,241RGDNCBI36
Celera2120,327,759 - 20,327,993RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,606,169 - 20,606,403UniSTS
REN86529  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,128,642 - 35,128,905UniSTSGRCh37
Build 362134,050,512 - 34,050,775RGDNCBI36
Celera2120,328,264 - 20,328,527RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,606,674 - 20,606,937UniSTS
REN86530  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,128,752 - 35,128,990UniSTSGRCh37
Build 362134,050,622 - 34,050,860RGDNCBI36
Celera2120,328,374 - 20,328,612RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,606,784 - 20,607,022UniSTS
REN86531  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,129,367 - 35,129,593UniSTSGRCh37
Build 362134,051,237 - 34,051,463RGDNCBI36
Celera2120,328,989 - 20,329,215RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,607,399 - 20,607,625UniSTS
REN86532  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,129,558 - 35,129,793UniSTSGRCh37
Build 362134,051,428 - 34,051,663RGDNCBI36
Celera2120,329,180 - 20,329,415RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,607,590 - 20,607,825UniSTS
REN86533  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,129,756 - 35,130,012UniSTSGRCh37
Build 362134,051,626 - 34,051,882RGDNCBI36
Celera2120,329,378 - 20,329,634RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,607,788 - 20,608,044UniSTS
REN86534  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,129,991 - 35,130,229UniSTSGRCh37
Build 362134,051,861 - 34,052,099RGDNCBI36
Celera2120,329,613 - 20,329,851RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,608,023 - 20,608,261UniSTS
REN86535  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,130,200 - 35,130,454UniSTSGRCh37
Build 362134,052,070 - 34,052,324RGDNCBI36
Celera2120,329,822 - 20,330,076RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,608,232 - 20,608,486UniSTS
REN86536  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,130,486 - 35,130,731UniSTSGRCh37
Build 362134,052,356 - 34,052,601RGDNCBI36
Celera2120,330,108 - 20,330,353RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,608,518 - 20,608,763UniSTS
REN86537  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,130,707 - 35,130,943UniSTSGRCh37
Build 362134,052,577 - 34,052,813RGDNCBI36
Celera2120,330,329 - 20,330,565RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,608,739 - 20,608,975UniSTS
REN86538  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,130,920 - 35,131,188UniSTSGRCh37
Build 362134,052,790 - 34,053,058RGDNCBI36
Celera2120,330,542 - 20,330,810RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,608,952 - 20,609,220UniSTS
REN86539  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,131,180 - 35,131,418UniSTSGRCh37
Build 362134,053,050 - 34,053,288RGDNCBI36
Celera2120,330,802 - 20,331,040RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,609,212 - 20,609,450UniSTS
REN86540  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,131,349 - 35,131,617UniSTSGRCh37
Build 362134,053,219 - 34,053,487RGDNCBI36
Celera2120,330,971 - 20,331,239RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,609,381 - 20,609,649UniSTS
REN86541  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,131,596 - 35,131,846UniSTSGRCh37
Build 362134,053,466 - 34,053,716RGDNCBI36
Celera2120,331,218 - 20,331,468RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,609,628 - 20,609,878UniSTS
REN86542  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,131,819 - 35,132,065UniSTSGRCh37
Build 362134,053,689 - 34,053,935RGDNCBI36
Celera2120,331,441 - 20,331,687RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,609,851 - 20,610,097UniSTS
REN86543  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,131,889 - 35,132,127UniSTSGRCh37
Build 362134,053,759 - 34,053,997RGDNCBI36
Celera2120,331,511 - 20,331,749RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,609,921 - 20,610,159UniSTS
REN86544  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,132,095 - 35,132,335UniSTSGRCh37
Build 362134,053,965 - 34,054,205RGDNCBI36
Celera2120,331,717 - 20,331,957RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,610,127 - 20,610,367UniSTS
REN86545  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,132,389 - 35,132,621UniSTSGRCh37
Build 362134,054,259 - 34,054,491RGDNCBI36
Celera2120,332,011 - 20,332,243RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,610,421 - 20,610,653UniSTS
REN86546  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,132,587 - 35,132,829UniSTSGRCh37
Build 362134,054,457 - 34,054,699RGDNCBI36
Celera2120,332,209 - 20,332,451RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,610,619 - 20,610,861UniSTS
REN86547  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,132,804 - 35,133,052UniSTSGRCh37
Build 362134,054,674 - 34,054,922RGDNCBI36
Celera2120,332,426 - 20,332,674RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,610,836 - 20,611,084UniSTS
REN86548  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,133,028 - 35,133,265UniSTSGRCh37
Build 362134,054,898 - 34,055,135RGDNCBI36
Celera2120,332,650 - 20,332,887RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,611,060 - 20,611,297UniSTS
REN86549  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,133,250 - 35,133,513UniSTSGRCh37
Build 362134,055,120 - 34,055,383RGDNCBI36
Celera2120,332,872 - 20,333,135RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,611,282 - 20,611,545UniSTS
REN86550  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,133,506 - 35,133,769UniSTSGRCh37
Build 362134,055,376 - 34,055,639RGDNCBI36
Celera2120,333,128 - 20,333,391RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,611,538 - 20,611,801UniSTS
REN86551  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,133,764 - 35,133,988UniSTSGRCh37
Build 362134,055,634 - 34,055,858RGDNCBI36
Celera2120,333,386 - 20,333,610RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,611,796 - 20,612,020UniSTS
REN86552  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,133,977 - 35,134,223UniSTSGRCh37
Build 362134,055,847 - 34,056,093RGDNCBI36
Celera2120,333,599 - 20,333,845RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,612,009 - 20,612,256UniSTS
REN86553  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,134,221 - 35,134,468UniSTSGRCh37
Build 362134,056,091 - 34,056,338RGDNCBI36
Celera2120,333,843 - 20,334,090RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,612,254 - 20,612,501UniSTS
REN86554  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,134,325 - 35,134,571UniSTSGRCh37
Build 362134,056,195 - 34,056,441RGDNCBI36
Celera2120,333,947 - 20,334,193RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,612,358 - 20,612,604UniSTS
REN86555  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,134,995 - 35,135,246UniSTSGRCh37
Build 362134,056,865 - 34,057,116RGDNCBI36
Celera2120,334,617 - 20,334,868RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,613,028 - 20,613,279UniSTS
REN86556  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,135,054 - 35,135,285UniSTSGRCh37
Build 362134,056,924 - 34,057,155RGDNCBI36
Celera2120,334,676 - 20,334,907RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,613,087 - 20,613,318UniSTS
REN86557  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,135,280 - 35,135,513UniSTSGRCh37
Build 362134,057,150 - 34,057,383RGDNCBI36
Celera2120,334,902 - 20,335,135RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,613,313 - 20,613,546UniSTS
REN86558  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,135,474 - 35,135,719UniSTSGRCh37
Build 362134,057,344 - 34,057,589RGDNCBI36
Celera2120,335,096 - 20,335,341RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,613,507 - 20,613,752UniSTS
REN86559  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,135,677 - 35,135,926UniSTSGRCh37
Build 362134,057,547 - 34,057,796RGDNCBI36
Celera2120,335,299 - 20,335,548RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,613,710 - 20,613,959UniSTS
REN86560  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,135,886 - 35,136,143UniSTSGRCh37
Build 362134,057,756 - 34,058,013RGDNCBI36
Celera2120,335,508 - 20,335,765RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,613,919 - 20,614,176UniSTS
REN86561  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,136,137 - 35,136,386UniSTSGRCh37
Build 362134,058,007 - 34,058,256RGDNCBI36
Celera2120,335,759 - 20,336,008RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,614,170 - 20,614,419UniSTS
REN86562  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,136,330 - 35,136,554UniSTSGRCh37
Build 362134,058,200 - 34,058,424RGDNCBI36
Celera2120,335,952 - 20,336,176RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,614,363 - 20,614,587UniSTS
REN86563  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,136,542 - 35,136,784UniSTSGRCh37
Build 362134,058,412 - 34,058,654RGDNCBI36
Celera2120,336,164 - 20,336,406RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,614,575 - 20,614,817UniSTS
REN86564  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,136,756 - 35,137,007UniSTSGRCh37
Build 362134,058,626 - 34,058,877RGDNCBI36
Celera2120,336,378 - 20,336,629RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,614,789 - 20,615,040UniSTS
REN86565  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,136,980 - 35,137,226UniSTSGRCh37
Build 362134,058,850 - 34,059,096RGDNCBI36
Celera2120,336,602 - 20,336,848RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,615,013 - 20,615,259UniSTS
REN86566  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,137,211 - 35,137,438UniSTSGRCh37
Build 362134,059,081 - 34,059,308RGDNCBI36
Celera2120,336,833 - 20,337,060RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,615,244 - 20,615,471UniSTS
REN86567  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,137,371 - 35,137,605UniSTSGRCh37
Build 362134,059,241 - 34,059,475RGDNCBI36
Celera2120,336,993 - 20,337,227RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,615,404 - 20,615,638UniSTS
REN86568  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,137,558 - 35,137,815UniSTSGRCh37
Build 362134,059,428 - 34,059,685RGDNCBI36
Celera2120,337,180 - 20,337,437RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,615,591 - 20,615,848UniSTS
REN86569  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,137,802 - 35,138,003UniSTSGRCh37
GRCh372135,137,769 - 35,138,003UniSTSGRCh37
Build 362134,059,639 - 34,059,873RGDNCBI36
Celera2120,337,391 - 20,337,625RGD
Celera2120,337,424 - 20,337,625UniSTS
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,615,802 - 20,616,036UniSTS
HuRef2120,615,835 - 20,616,036UniSTS
REN86570  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,137,985 - 35,138,235UniSTSGRCh37
Build 362134,059,855 - 34,060,105RGDNCBI36
Celera2120,337,607 - 20,337,857RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,616,018 - 20,616,268UniSTS
REN86571  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,138,217 - 35,138,482UniSTSGRCh37
Build 362134,060,087 - 34,060,352RGDNCBI36
Celera2120,337,839 - 20,338,104RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,616,250 - 20,616,515UniSTS
REN86572  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,138,459 - 35,138,701UniSTSGRCh37
Build 362134,060,329 - 34,060,571RGDNCBI36
Celera2120,338,081 - 20,338,323RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,616,492 - 20,616,734UniSTS
REN86573  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,138,682 - 35,138,951UniSTSGRCh37
Build 362134,060,552 - 34,060,821RGDNCBI36
Celera2120,338,304 - 20,338,573RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,616,715 - 20,616,984UniSTS
REN86574  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,138,940 - 35,139,195UniSTSGRCh37
Build 362134,060,810 - 34,061,065RGDNCBI36
Celera2120,338,562 - 20,338,817RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,616,973 - 20,617,228UniSTS
REN86575  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,139,524 - 35,139,781UniSTSGRCh37
Build 362134,061,394 - 34,061,651RGDNCBI36
Celera2120,339,146 - 20,339,403RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,617,557 - 20,617,814UniSTS
REN86576  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,139,750 - 35,139,974UniSTSGRCh37
Build 362134,061,620 - 34,061,844RGDNCBI36
Celera2120,339,372 - 20,339,596RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,617,783 - 20,618,007UniSTS
REN86577  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,139,892 - 35,140,133UniSTSGRCh37
Build 362134,061,762 - 34,062,003RGDNCBI36
Celera2120,339,514 - 20,339,755RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,617,925 - 20,618,166UniSTS
REN86578  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,140,087 - 35,140,357UniSTSGRCh37
Build 362134,061,957 - 34,062,227RGDNCBI36
Celera2120,339,709 - 20,339,979RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,618,120 - 20,618,390UniSTS
REN86579  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,140,337 - 35,140,561UniSTSGRCh37
Build 362134,062,207 - 34,062,431RGDNCBI36
Celera2120,339,959 - 20,340,183RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,618,370 - 20,618,594UniSTS
REN86580  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,140,432 - 35,140,657UniSTSGRCh37
Build 362134,062,302 - 34,062,527RGDNCBI36
Celera2120,340,054 - 20,340,279RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,618,465 - 20,618,690UniSTS
REN86581  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,140,873 - 35,141,107UniSTSGRCh37
Build 362134,062,743 - 34,062,977RGDNCBI36
Celera2120,340,495 - 20,340,729RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,618,906 - 20,619,140UniSTS
REN86582  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,141,090 - 35,141,341UniSTSGRCh37
Build 362134,062,960 - 34,063,211RGDNCBI36
Celera2120,340,712 - 20,340,963RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,619,123 - 20,619,374UniSTS
REN86583  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,141,334 - 35,141,583UniSTSGRCh37
Build 362134,063,204 - 34,063,453RGDNCBI36
Celera2120,340,956 - 20,341,205RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,619,367 - 20,619,616UniSTS
REN86584  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,141,562 - 35,141,816UniSTSGRCh37
Build 362134,063,432 - 34,063,686RGDNCBI36
Celera2120,341,184 - 20,341,438RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,619,595 - 20,619,849UniSTS
REN86585  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,141,805 - 35,142,038UniSTSGRCh37
Build 362134,063,675 - 34,063,908RGDNCBI36
Celera2120,341,427 - 20,341,660RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,619,838 - 20,620,071UniSTS
REN86586  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,142,016 - 35,142,246UniSTSGRCh37
Build 362134,063,886 - 34,064,116RGDNCBI36
Celera2120,341,638 - 20,341,868RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,620,049 - 20,620,279UniSTS
REN86587  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,142,295 - 35,142,538UniSTSGRCh37
Build 362134,064,165 - 34,064,408RGDNCBI36
Celera2120,341,917 - 20,342,160RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,620,328 - 20,620,571UniSTS
REN86588  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,142,659 - 35,142,883UniSTSGRCh37
Build 362134,064,529 - 34,064,753RGDNCBI36
Celera2120,342,281 - 20,342,505RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,620,692 - 20,620,916UniSTS
REN86589  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,142,849 - 35,143,113UniSTSGRCh37
Build 362134,064,719 - 34,064,983RGDNCBI36
Celera2120,342,471 - 20,342,735RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,620,882 - 20,621,146UniSTS
REN86590  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,142,975 - 35,143,215UniSTSGRCh37
Build 362134,064,845 - 34,065,085RGDNCBI36
Celera2120,342,597 - 20,342,837RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,621,008 - 20,621,248UniSTS
REN86591  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,143,191 - 35,143,427UniSTSGRCh37
Build 362134,065,061 - 34,065,297RGDNCBI36
Celera2120,342,813 - 20,343,049RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,621,224 - 20,621,460UniSTS
REN86592  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,143,426 - 35,143,686UniSTSGRCh37
Build 362134,065,296 - 34,065,556RGDNCBI36
Celera2120,343,048 - 20,343,308RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,621,459 - 20,621,719UniSTS
REN86593  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,143,683 - 35,143,929UniSTSGRCh37
Build 362134,065,553 - 34,065,799RGDNCBI36
Celera2120,343,305 - 20,343,551RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,621,716 - 20,621,962UniSTS
REN86594  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,143,904 - 35,144,138UniSTSGRCh37
Build 362134,065,774 - 34,066,008RGDNCBI36
Celera2120,343,526 - 20,343,760RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,621,937 - 20,622,171UniSTS
REN86595  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,144,115 - 35,144,365UniSTSGRCh37
Build 362134,065,985 - 34,066,235RGDNCBI36
Celera2120,343,737 - 20,343,987RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,622,148 - 20,622,398UniSTS
REN86596  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,144,342 - 35,144,567UniSTSGRCh37
Build 362134,066,212 - 34,066,437RGDNCBI36
Celera2120,343,964 - 20,344,189RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,622,375 - 20,622,600UniSTS
REN86597  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,144,531 - 35,144,788UniSTSGRCh37
Build 362134,066,401 - 34,066,658RGDNCBI36
Celera2120,344,153 - 20,344,410RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,622,564 - 20,622,821UniSTS
REN86598  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,144,779 - 35,145,018UniSTSGRCh37
Build 362134,066,649 - 34,066,888RGDNCBI36
Celera2120,344,401 - 20,344,640RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,622,812 - 20,623,051UniSTS
REN86599  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,144,973 - 35,145,241UniSTSGRCh37
Build 362134,066,843 - 34,067,111RGDNCBI36
Celera2120,344,595 - 20,344,863RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,623,006 - 20,623,274UniSTS
REN86600  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,145,608 - 35,145,841UniSTSGRCh37
Build 362134,067,478 - 34,067,711RGDNCBI36
Celera2120,345,230 - 20,345,463RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,623,641 - 20,623,874UniSTS
REN86601  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,145,759 - 35,145,991UniSTSGRCh37
Build 362134,067,629 - 34,067,861RGDNCBI36
Celera2120,345,381 - 20,345,613RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,623,792 - 20,624,024UniSTS
REN86602  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,146,279 - 35,146,523UniSTSGRCh37
Build 362134,068,149 - 34,068,393RGDNCBI36
Celera2120,345,901 - 20,346,145RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,624,312 - 20,624,556UniSTS
REN86603  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,146,521 - 35,146,778UniSTSGRCh37
Build 362134,068,391 - 34,068,648RGDNCBI36
Celera2120,346,143 - 20,346,400RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,624,554 - 20,624,811UniSTS
REN86604  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,146,775 - 35,147,036UniSTSGRCh37
Build 362134,068,645 - 34,068,906RGDNCBI36
Celera2120,346,397 - 20,346,658RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,624,808 - 20,625,069UniSTS
REN86605  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,146,943 - 35,147,199UniSTSGRCh37
Build 362134,068,813 - 34,069,069RGDNCBI36
Celera2120,346,565 - 20,346,821RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,624,976 - 20,625,232UniSTS
REN86606  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,147,174 - 35,147,420UniSTSGRCh37
Build 362134,069,044 - 34,069,290RGDNCBI36
Celera2120,346,796 - 20,347,042RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,625,207 - 20,625,453UniSTS
REN86607  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,147,410 - 35,147,669UniSTSGRCh37
Build 362134,069,280 - 34,069,539RGDNCBI36
Celera2120,347,032 - 20,347,291RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,625,443 - 20,625,702UniSTS
REN86608  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,147,659 - 35,147,928UniSTSGRCh37
Build 362134,069,529 - 34,069,798RGDNCBI36
Celera2120,347,281 - 20,347,550RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,625,692 - 20,625,961UniSTS
REN86609  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,147,923 - 35,148,183UniSTSGRCh37
Build 362134,069,793 - 34,070,053RGDNCBI36
Celera2120,347,545 - 20,347,805RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,625,956 - 20,626,216UniSTS
REN86610  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,148,158 - 35,148,411UniSTSGRCh37
Build 362134,070,028 - 34,070,281RGDNCBI36
Celera2120,347,780 - 20,348,033RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,626,191 - 20,626,444UniSTS
REN86611  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,148,406 - 35,148,636UniSTSGRCh37
Build 362134,070,276 - 34,070,506RGDNCBI36
Celera2120,348,028 - 20,348,258RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,626,439 - 20,626,669UniSTS
REN86612  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,148,551 - 35,148,786UniSTSGRCh37
Build 362134,070,421 - 34,070,656RGDNCBI36
Celera2120,348,173 - 20,348,408RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,626,584 - 20,626,820UniSTS
REN86613  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,148,764 - 35,149,002UniSTSGRCh37
Build 362134,070,634 - 34,070,872RGDNCBI36
Celera2120,348,386 - 20,348,624RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,626,798 - 20,627,035UniSTS
REN86614  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,148,961 - 35,149,218UniSTSGRCh37
Build 362134,070,831 - 34,071,088RGDNCBI36
Celera2120,348,583 - 20,348,840RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,626,994 - 20,627,251UniSTS
REN86615  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,149,213 - 35,149,447UniSTSGRCh37
Build 362134,071,083 - 34,071,317RGDNCBI36
Celera2120,348,835 - 20,349,069RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,627,246 - 20,627,480UniSTS
REN86616  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,149,417 - 35,149,660UniSTSGRCh37
Build 362134,071,287 - 34,071,530RGDNCBI36
Celera2120,349,039 - 20,349,282RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,627,450 - 20,627,693UniSTS
REN86617  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,149,635 - 35,149,872UniSTSGRCh37
Build 362134,071,505 - 34,071,742RGDNCBI36
Celera2120,349,257 - 20,349,494RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,627,668 - 20,627,905UniSTS
REN86618  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,149,864 - 35,150,112UniSTSGRCh37
Build 362134,071,734 - 34,071,982RGDNCBI36
Celera2120,349,486 - 20,349,734RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,627,897 - 20,628,145UniSTS
REN86619  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,150,105 - 35,150,337UniSTSGRCh37
Build 362134,071,975 - 34,072,207RGDNCBI36
Celera2120,349,727 - 20,349,959RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,628,138 - 20,628,370UniSTS
REN86620  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,150,317 - 35,150,590UniSTSGRCh37
Build 362134,072,187 - 34,072,460RGDNCBI36
Celera2120,349,939 - 20,350,212RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,628,350 - 20,628,623UniSTS
REN86621  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,150,519 - 35,150,786UniSTSGRCh37
Build 362134,072,389 - 34,072,656RGDNCBI36
Celera2120,350,141 - 20,350,408RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,628,552 - 20,628,819UniSTS
REN86622  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,151,217 - 35,151,454UniSTSGRCh37
Build 362134,073,087 - 34,073,324RGDNCBI36
Celera2120,350,839 - 20,351,076RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,629,250 - 20,629,487UniSTS
REN86623  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,151,438 - 35,151,662UniSTSGRCh37
Build 362134,073,308 - 34,073,532RGDNCBI36
Celera2120,351,060 - 20,351,284RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,629,471 - 20,629,695UniSTS
REN86624  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,151,622 - 35,151,883UniSTSGRCh37
Build 362134,073,492 - 34,073,753RGDNCBI36
Celera2120,351,244 - 20,351,505RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,629,655 - 20,629,916UniSTS
REN86625  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,151,873 - 35,152,100UniSTSGRCh37
Build 362134,073,743 - 34,073,970RGDNCBI36
Celera2120,351,495 - 20,351,722RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,629,906 - 20,630,133UniSTS
REN86626  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,152,036 - 35,152,280UniSTSGRCh37
Build 362134,073,906 - 34,074,150RGDNCBI36
Celera2120,351,658 - 20,351,902RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,630,069 - 20,630,313UniSTS
REN86627  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,152,262 - 35,152,491UniSTSGRCh37
Build 362134,074,132 - 34,074,361RGDNCBI36
Celera2120,351,884 - 20,352,113RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,630,295 - 20,630,524UniSTS
REN86628  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,152,481 - 35,152,724UniSTSGRCh37
Build 362134,074,351 - 34,074,594RGDNCBI36
Celera2120,352,103 - 20,352,346RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,630,514 - 20,630,757UniSTS
REN86629  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,152,697 - 35,152,921UniSTSGRCh37
Build 362134,074,567 - 34,074,791RGDNCBI36
Celera2120,352,319 - 20,352,543RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,630,730 - 20,630,954UniSTS
REN86630  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,152,894 - 35,153,137UniSTSGRCh37
Build 362134,074,764 - 34,075,007RGDNCBI36
Celera2120,352,516 - 20,352,759RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,630,927 - 20,631,170UniSTS
REN86631  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,153,111 - 35,153,379UniSTSGRCh37
Build 362134,074,981 - 34,075,249RGDNCBI36
Celera2120,352,733 - 20,353,001RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,631,144 - 20,631,412UniSTS
REN86632  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,153,370 - 35,153,632UniSTSGRCh37
Build 362134,075,240 - 34,075,502RGDNCBI36
Celera2120,352,992 - 20,353,254RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,631,403 - 20,631,665UniSTS
REN86633  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,153,582 - 35,153,838UniSTSGRCh37
Build 362134,075,452 - 34,075,708RGDNCBI36
Celera2120,353,204 - 20,353,460RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,631,615 - 20,631,871UniSTS
REN86634  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,153,718 - 35,153,969UniSTSGRCh37
Build 362134,075,588 - 34,075,839RGDNCBI36
Celera2120,353,340 - 20,353,591RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,631,751 - 20,632,002UniSTS
REN86635  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,153,948 - 35,154,221UniSTSGRCh37
Build 362134,075,818 - 34,076,091RGDNCBI36
Celera2120,353,570 - 20,353,843RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,631,981 - 20,632,254UniSTS
REN86636  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,154,172 - 35,154,396UniSTSGRCh37
Build 362134,076,042 - 34,076,266RGDNCBI36
Celera2120,353,794 - 20,354,018RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,632,205 - 20,632,429UniSTS
REN86637  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,154,366 - 35,154,626UniSTSGRCh37
Build 362134,076,236 - 34,076,496RGDNCBI36
Celera2120,353,988 - 20,354,248RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,632,399 - 20,632,659UniSTS
REN86638  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,154,625 - 35,154,880UniSTSGRCh37
Build 362134,076,495 - 34,076,750RGDNCBI36
Celera2120,354,247 - 20,354,502RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,632,658 - 20,632,913UniSTS
REN86639  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,154,805 - 35,155,055UniSTSGRCh37
Build 362134,076,675 - 34,076,925RGDNCBI36
Celera2120,354,427 - 20,354,677RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,632,838 - 20,633,088UniSTS
REN86640  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,155,509 - 35,155,737UniSTSGRCh37
Build 362134,077,379 - 34,077,607RGDNCBI36
Celera2120,355,131 - 20,355,359RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,633,542 - 20,633,770UniSTS
REN86641  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,155,715 - 35,155,978UniSTSGRCh37
Build 362134,077,585 - 34,077,848RGDNCBI36
Celera2120,355,337 - 20,355,600RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,633,748 - 20,634,011UniSTS
REN86642  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,155,954 - 35,156,215UniSTSGRCh37
Build 362134,077,824 - 34,078,085RGDNCBI36
Celera2120,355,576 - 20,355,837RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,633,987 - 20,634,247UniSTS
REN86643  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,156,110 - 35,156,361UniSTSGRCh37
Build 362134,077,980 - 34,078,231RGDNCBI36
Celera2120,355,732 - 20,355,983RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,634,142 - 20,634,393UniSTS
REN86644  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,156,360 - 35,156,611UniSTSGRCh37
Build 362134,078,230 - 34,078,481RGDNCBI36
Celera2120,355,982 - 20,356,233RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,634,392 - 20,634,643UniSTS
REN86645  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,156,487 - 35,156,728UniSTSGRCh37
Build 362134,078,357 - 34,078,598RGDNCBI36
Celera2120,356,109 - 20,356,350RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,634,519 - 20,634,770UniSTS
REN86646  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,156,695 - 35,156,950UniSTSGRCh37
Build 362134,078,565 - 34,078,820RGDNCBI36
Celera2120,356,317 - 20,356,572RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,634,737 - 20,634,992UniSTS
REN86647  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,156,934 - 35,157,187UniSTSGRCh37
Build 362134,078,804 - 34,079,057RGDNCBI36
Celera2120,356,556 - 20,356,809RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,634,976 - 20,635,229UniSTS
REN86648  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,157,170 - 35,157,422UniSTSGRCh37
Build 362134,079,040 - 34,079,292RGDNCBI36
Celera2120,356,792 - 20,357,044RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,635,212 - 20,635,464UniSTS
REN86649  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,157,420 - 35,157,680UniSTSGRCh37
Build 362134,079,290 - 34,079,550RGDNCBI36
Celera2120,357,042 - 20,357,302RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,635,462 - 20,635,722UniSTS
REN86650  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,157,679 - 35,157,905UniSTSGRCh37
Build 362134,079,549 - 34,079,775RGDNCBI36
Celera2120,357,301 - 20,357,527RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,635,721 - 20,635,947UniSTS
REN86651  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,157,877 - 35,158,147UniSTSGRCh37
Build 362134,079,747 - 34,080,017RGDNCBI36
Celera2120,357,499 - 20,357,769RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,635,919 - 20,636,189UniSTS
REN86652  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,158,120 - 35,158,374UniSTSGRCh37
Build 362134,079,990 - 34,080,244RGDNCBI36
Celera2120,357,742 - 20,357,996RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,636,162 - 20,636,416UniSTS
REN86653  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,158,332 - 35,158,580UniSTSGRCh37
Build 362134,080,202 - 34,080,450RGDNCBI36
Celera2120,357,954 - 20,358,202RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,636,374 - 20,636,622UniSTS
REN86654  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,158,560 - 35,158,792UniSTSGRCh37
Build 362134,080,430 - 34,080,662RGDNCBI36
Celera2120,358,182 - 20,358,414RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,636,602 - 20,636,834UniSTS
REN86655  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,158,781 - 35,159,025UniSTSGRCh37
Build 362134,080,651 - 34,080,895RGDNCBI36
Celera2120,358,403 - 20,358,647RGD
Cytogenetic Map21q22.1-q22.2UniSTS
REN86656  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,159,002 - 35,159,250UniSTSGRCh37
Build 362134,080,872 - 34,081,120RGDNCBI36
Celera2120,358,624 - 20,358,872RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,637,004 - 20,637,252UniSTS
REN86657  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,159,226 - 35,159,468UniSTSGRCh37
Build 362134,081,096 - 34,081,338RGDNCBI36
Celera2120,358,848 - 20,359,090RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,637,228 - 20,637,470UniSTS
REN86658  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,159,447 - 35,159,720UniSTSGRCh37
Build 362134,081,317 - 34,081,590RGDNCBI36
Celera2120,359,069 - 20,359,342RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,637,449 - 20,637,722UniSTS
REN86659  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,159,697 - 35,159,943UniSTSGRCh37
Build 362134,081,567 - 34,081,813RGDNCBI36
Celera2120,359,319 - 20,359,565RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,637,699 - 20,637,945UniSTS
REN86660  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,159,905 - 35,160,153UniSTSGRCh37
Build 362134,081,775 - 34,082,023RGDNCBI36
Celera2120,359,527 - 20,359,775RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,637,907 - 20,638,155UniSTS
REN86661  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,160,130 - 35,160,361UniSTSGRCh37
Build 362134,082,000 - 34,082,231RGDNCBI36
Celera2120,359,752 - 20,359,983RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,638,132 - 20,638,363UniSTS
REN86662  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,160,339 - 35,160,564UniSTSGRCh37
Build 362134,082,209 - 34,082,434RGDNCBI36
Celera2120,359,961 - 20,360,186RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,638,341 - 20,638,566UniSTS
REN86663  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,160,512 - 35,160,761UniSTSGRCh37
Build 362134,082,382 - 34,082,631RGDNCBI36
Celera2120,360,134 - 20,360,383RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,638,514 - 20,638,763UniSTS
REN86664  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,160,739 - 35,160,994UniSTSGRCh37
Build 362134,082,609 - 34,082,864RGDNCBI36
Celera2120,360,361 - 20,360,616RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,638,741 - 20,638,996UniSTS
REN86665  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,160,950 - 35,161,200UniSTSGRCh37
Build 362134,082,820 - 34,083,070RGDNCBI36
Celera2120,360,572 - 20,360,822RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,638,952 - 20,639,202UniSTS
REN86666  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,161,190 - 35,161,445UniSTSGRCh37
Build 362134,083,060 - 34,083,315RGDNCBI36
Celera2120,360,812 - 20,361,067RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,639,192 - 20,639,447UniSTS
REN86667  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,161,395 - 35,161,633UniSTSGRCh37
Build 362134,083,265 - 34,083,503RGDNCBI36
Celera2120,361,017 - 20,361,255RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,639,397 - 20,639,635UniSTS
REN86668  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,161,602 - 35,161,871UniSTSGRCh37
Build 362134,083,472 - 34,083,741RGDNCBI36
Celera2120,361,224 - 20,361,493RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,639,604 - 20,639,873UniSTS
REN86669  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,161,869 - 35,162,123UniSTSGRCh37
Build 362134,083,739 - 34,083,993RGDNCBI36
Celera2120,361,491 - 20,361,745RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,639,871 - 20,640,125UniSTS
REN86670  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,162,100 - 35,162,357UniSTSGRCh37
Build 362134,083,970 - 34,084,227RGDNCBI36
Celera2120,361,722 - 20,361,979RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,640,102 - 20,640,359UniSTS
REN86671  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,162,330 - 35,162,554UniSTSGRCh37
Build 362134,084,200 - 34,084,424RGDNCBI36
Celera2120,361,952 - 20,362,176RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,640,332 - 20,640,556UniSTS
REN86672  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,162,530 - 35,162,799UniSTSGRCh37
Build 362134,084,400 - 34,084,669RGDNCBI36
Celera2120,362,152 - 20,362,421RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,640,532 - 20,640,797UniSTS
REN86673  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,162,657 - 35,162,929UniSTSGRCh37
Build 362134,084,527 - 34,084,799RGDNCBI36
Celera2120,362,279 - 20,362,551RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,640,655 - 20,640,927UniSTS
REN86674  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,162,915 - 35,163,164UniSTSGRCh37
Build 362134,084,785 - 34,085,034RGDNCBI36
Celera2120,362,537 - 20,362,786RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,640,913 - 20,641,162UniSTS
REN86675  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,163,142 - 35,163,400UniSTSGRCh37
Build 362134,085,012 - 34,085,270RGDNCBI36
Celera2120,362,764 - 20,363,022RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,641,140 - 20,641,398UniSTS
REN86676  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,163,374 - 35,163,624UniSTSGRCh37
Build 362134,085,244 - 34,085,494RGDNCBI36
Celera2120,362,996 - 20,363,246RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,641,372 - 20,641,622UniSTS
REN86677  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,163,527 - 35,163,751UniSTSGRCh37
Build 362134,085,397 - 34,085,621RGDNCBI36
Celera2120,363,149 - 20,363,373RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,641,525 - 20,641,749UniSTS
REN86678  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,163,717 - 35,163,973UniSTSGRCh37
Build 362134,085,587 - 34,085,843RGDNCBI36
Celera2120,363,339 - 20,363,595RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,641,715 - 20,641,971UniSTS
REN86679  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,163,876 - 35,164,105UniSTSGRCh37
Build 362134,085,746 - 34,085,975RGDNCBI36
Celera2120,363,498 - 20,363,727RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,641,874 - 20,642,103UniSTS
REN86680  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,164,025 - 35,164,280UniSTSGRCh37
Build 362134,085,895 - 34,086,150RGDNCBI36
Celera2120,363,647 - 20,363,902RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,642,023 - 20,642,278UniSTS
REN86681  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,164,257 - 35,164,505UniSTSGRCh37
Build 362134,086,127 - 34,086,375RGDNCBI36
Celera2120,363,879 - 20,364,127RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,642,255 - 20,642,503UniSTS
REN86682  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,164,524 - 35,164,748UniSTSGRCh37
Build 362134,086,394 - 34,086,618RGDNCBI36
Celera2120,364,146 - 20,364,370RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,642,522 - 20,642,746UniSTS
REN86683  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,164,720 - 35,164,970UniSTSGRCh37
Build 362134,086,590 - 34,086,840RGDNCBI36
Celera2120,364,342 - 20,364,592RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,642,718 - 20,642,968UniSTS
REN86684  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,164,947 - 35,165,183UniSTSGRCh37
Build 362134,086,817 - 34,087,053RGDNCBI36
Celera2120,364,569 - 20,364,805RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,642,945 - 20,643,181UniSTS
REN86685  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,165,159 - 35,165,430UniSTSGRCh37
Build 362134,087,029 - 34,087,300RGDNCBI36
Celera2120,364,781 - 20,365,052RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,643,157 - 20,643,428UniSTS
REN86686  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,165,399 - 35,165,648UniSTSGRCh37
Build 362134,087,269 - 34,087,518RGDNCBI36
Celera2120,365,021 - 20,365,270RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,643,397 - 20,643,646UniSTS
REN86687  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,165,621 - 35,165,878UniSTSGRCh37
Build 362134,087,491 - 34,087,748RGDNCBI36
Celera2120,365,243 - 20,365,500RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,643,619 - 20,643,876UniSTS
REN86688  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,165,857 - 35,166,108UniSTSGRCh37
Build 362134,087,727 - 34,087,978RGDNCBI36
Celera2120,365,479 - 20,365,730RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,643,855 - 20,644,106UniSTS
REN86689  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,166,085 - 35,166,332UniSTSGRCh37
Build 362134,087,955 - 34,088,202RGDNCBI36
Celera2120,365,707 - 20,365,954RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,644,083 - 20,644,330UniSTS
REN86690  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,166,309 - 35,166,567UniSTSGRCh37
Build 362134,088,179 - 34,088,437RGDNCBI36
Celera2120,365,931 - 20,366,189RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,644,307 - 20,644,565UniSTS
REN86691  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,166,561 - 35,166,814UniSTSGRCh37
Build 362134,088,431 - 34,088,684RGDNCBI36
Celera2120,366,183 - 20,366,436RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,644,559 - 20,644,812UniSTS
REN86692  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,166,798 - 35,167,038UniSTSGRCh37
Build 362134,088,668 - 34,088,908RGDNCBI36
Celera2120,366,420 - 20,366,660RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,644,796 - 20,645,036UniSTS
REN86693  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,167,015 - 35,167,261UniSTSGRCh37
Build 362134,088,885 - 34,089,131RGDNCBI36
Celera2120,366,637 - 20,366,883RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,645,013 - 20,645,259UniSTS
REN86694  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,167,228 - 35,167,482UniSTSGRCh37
Build 362134,089,098 - 34,089,352RGDNCBI36
Celera2120,366,850 - 20,367,104RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,645,226 - 20,645,480UniSTS
REN86695  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,167,339 - 35,167,564UniSTSGRCh37
Build 362134,089,209 - 34,089,434RGDNCBI36
Celera2120,366,961 - 20,367,186RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,645,337 - 20,645,562UniSTS
REN86696  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,167,529 - 35,167,798UniSTSGRCh37
Build 362134,089,399 - 34,089,668RGDNCBI36
Celera2120,367,151 - 20,367,420RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,645,527 - 20,645,796UniSTS
REN86697  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,167,766 - 35,168,008UniSTSGRCh37
Build 362134,089,636 - 34,089,878RGDNCBI36
Celera2120,367,388 - 20,367,630RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,645,764 - 20,646,006UniSTS
REN86698  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,167,982 - 35,168,242UniSTSGRCh37
Build 362134,089,852 - 34,090,112RGDNCBI36
Celera2120,367,604 - 20,367,864RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,645,980 - 20,646,240UniSTS
REN86699  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,168,219 - 35,168,491UniSTSGRCh37
Build 362134,090,089 - 34,090,361RGDNCBI36
Celera2120,367,841 - 20,368,113RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,646,217 - 20,646,490UniSTS
REN86700  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,168,473 - 35,168,730UniSTSGRCh37
Build 362134,090,343 - 34,090,600RGDNCBI36
Celera2120,368,095 - 20,368,352RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,646,472 - 20,646,729UniSTS
REN86701  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,168,708 - 35,168,959UniSTSGRCh37
Build 362134,090,578 - 34,090,829RGDNCBI36
Celera2120,368,330 - 20,368,581RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,646,707 - 20,646,958UniSTS
REN86702  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,168,938 - 35,169,167UniSTSGRCh37
Build 362134,090,808 - 34,091,037RGDNCBI36
Celera2120,368,560 - 20,368,789RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,646,937 - 20,647,166UniSTS
REN86703  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,169,135 - 35,169,401UniSTSGRCh37
Build 362134,091,005 - 34,091,271RGDNCBI36
Celera2120,368,757 - 20,369,023RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,647,134 - 20,647,400UniSTS
REN86704  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,169,377 - 35,169,634UniSTSGRCh37
Build 362134,091,247 - 34,091,504RGDNCBI36
Celera2120,368,999 - 20,369,256RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,647,376 - 20,647,633UniSTS
REN86705  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,169,609 - 35,169,845UniSTSGRCh37
Build 362134,091,479 - 34,091,715RGDNCBI36
Celera2120,369,231 - 20,369,467RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,647,608 - 20,647,844UniSTS
REN86706  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,169,823 - 35,170,050UniSTSGRCh37
Build 362134,091,693 - 34,091,920RGDNCBI36
Celera2120,369,445 - 20,369,672RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,647,822 - 20,648,049UniSTS
REN86707  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,170,002 - 35,170,243UniSTSGRCh37
Build 362134,091,872 - 34,092,113RGDNCBI36
Celera2120,369,624 - 20,369,865RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,648,001 - 20,648,242UniSTS
REN86708  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,170,220 - 35,170,485UniSTSGRCh37
Build 362134,092,090 - 34,092,355RGDNCBI36
Celera2120,369,842 - 20,370,107RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,648,219 - 20,648,484UniSTS
REN86709  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,170,454 - 35,170,689UniSTSGRCh37
Build 362134,092,324 - 34,092,559RGDNCBI36
Celera2120,370,076 - 20,370,311RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,648,453 - 20,648,688UniSTS
REN86710  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,170,517 - 35,170,782UniSTSGRCh37
Build 362134,092,387 - 34,092,652RGDNCBI36
Celera2120,370,139 - 20,370,404RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,648,516 - 20,648,781UniSTS
REN86711  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,170,768 - 35,171,039UniSTSGRCh37
Build 362134,092,638 - 34,092,909RGDNCBI36
Celera2120,370,390 - 20,370,661RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,648,767 - 20,649,038UniSTS
REN86712  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,171,016 - 35,171,257UniSTSGRCh37
Build 362134,092,886 - 34,093,127RGDNCBI36
Celera2120,370,638 - 20,370,879RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,649,015 - 20,649,256UniSTS
REN86713  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,171,238 - 35,171,467UniSTSGRCh37
Build 362134,093,108 - 34,093,337RGDNCBI36
Celera2120,370,860 - 20,371,089RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,649,237 - 20,649,466UniSTS
REN86714  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,171,448 - 35,171,716UniSTSGRCh37
Build 362134,093,318 - 34,093,586RGDNCBI36
Celera2120,371,070 - 20,371,338RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,649,447 - 20,649,715UniSTS
REN86715  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,171,713 - 35,171,971UniSTSGRCh37
Build 362134,093,583 - 34,093,841RGDNCBI36
Celera2120,371,335 - 20,371,593RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,649,712 - 20,649,970UniSTS
REN86716  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,171,948 - 35,172,193UniSTSGRCh37
Build 362134,093,818 - 34,094,063RGDNCBI36
Celera2120,371,570 - 20,371,815RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,649,947 - 20,650,192UniSTS
REN86717  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,172,150 - 35,172,401UniSTSGRCh37
Build 362134,094,020 - 34,094,271RGDNCBI36
Celera2120,371,772 - 20,372,023RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,650,149 - 20,650,400UniSTS
REN86718  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,172,249 - 35,172,474UniSTSGRCh37
Build 362134,094,119 - 34,094,344RGDNCBI36
Celera2120,371,871 - 20,372,096RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,650,248 - 20,650,473UniSTS
REN86719  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,172,438 - 35,172,690UniSTSGRCh37
Build 362134,094,308 - 34,094,560RGDNCBI36
Celera2120,372,060 - 20,372,312RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,650,437 - 20,650,689UniSTS
REN86720  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,172,666 - 35,172,924UniSTSGRCh37
Build 362134,094,536 - 34,094,794RGDNCBI36
Celera2120,372,288 - 20,372,546RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,650,665 - 20,650,923UniSTS
REN86721  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,172,919 - 35,173,159UniSTSGRCh37
Build 362134,094,789 - 34,095,029RGDNCBI36
Celera2120,372,541 - 20,372,781RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,650,918 - 20,651,158UniSTS
REN86722  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,173,130 - 35,173,381UniSTSGRCh37
Build 362134,095,000 - 34,095,251RGDNCBI36
Celera2120,372,752 - 20,373,003RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,651,129 - 20,651,381UniSTS
REN86723  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,173,284 - 35,173,515UniSTSGRCh37
Build 362134,095,154 - 34,095,385RGDNCBI36
Celera2120,372,906 - 20,373,137RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,651,284 - 20,651,515UniSTS
REN86724  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,173,468 - 35,173,738UniSTSGRCh37
Build 362134,095,338 - 34,095,608RGDNCBI36
Celera2120,373,090 - 20,373,360RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,651,468 - 20,651,738UniSTS
REN86725  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,173,679 - 35,173,912UniSTSGRCh37
Build 362134,095,549 - 34,095,782RGDNCBI36
Celera2120,373,301 - 20,373,534RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,651,679 - 20,651,912UniSTS
REN86726  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,173,889 - 35,174,128UniSTSGRCh37
Build 362134,095,759 - 34,095,998RGDNCBI36
Celera2120,373,511 - 20,373,750RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,651,889 - 20,652,128UniSTS
REN86727  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,174,083 - 35,174,307UniSTSGRCh37
Build 362134,095,953 - 34,096,177RGDNCBI36
Celera2120,373,705 - 20,373,929RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,652,083 - 20,652,307UniSTS
REN86728  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,174,291 - 35,174,530UniSTSGRCh37
Build 362134,096,161 - 34,096,400RGDNCBI36
Celera2120,373,913 - 20,374,152RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,652,291 - 20,652,530UniSTS
REN86729  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,174,508 - 35,174,754UniSTSGRCh37
Build 362134,096,378 - 34,096,624RGDNCBI36
Celera2120,374,130 - 20,374,376RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,652,508 - 20,652,754UniSTS
REN86730  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,174,735 - 35,174,993UniSTSGRCh37
Build 362134,096,605 - 34,096,863RGDNCBI36
Celera2120,374,357 - 20,374,615RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,652,735 - 20,652,993UniSTS
REN86731  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,174,969 - 35,175,193UniSTSGRCh37
Build 362134,096,839 - 34,097,063RGDNCBI36
Celera2120,374,591 - 20,374,815RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,652,969 - 20,653,193UniSTS
REN86732  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,175,146 - 35,175,406UniSTSGRCh37
Build 362134,097,016 - 34,097,276RGDNCBI36
Celera2120,374,768 - 20,375,028RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,653,146 - 20,653,406UniSTS
REN86733  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,175,382 - 35,175,643UniSTSGRCh37
Build 362134,097,252 - 34,097,513RGDNCBI36
Celera2120,375,004 - 20,375,265RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,653,382 - 20,653,643UniSTS
REN86734  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,175,620 - 35,175,859UniSTSGRCh37
Build 362134,097,490 - 34,097,729RGDNCBI36
Celera2120,375,242 - 20,375,481RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,653,620 - 20,653,859UniSTS
REN86735  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,175,729 - 35,175,973UniSTSGRCh37
Build 362134,097,599 - 34,097,843RGDNCBI36
Celera2120,375,351 - 20,375,595RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,653,729 - 20,653,973UniSTS
REN86736  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,175,950 - 35,176,212UniSTSGRCh37
Build 362134,097,820 - 34,098,082RGDNCBI36
Celera2120,375,572 - 20,375,834RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,653,950 - 20,654,212UniSTS
REN86737  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,176,189 - 35,176,441UniSTSGRCh37
Build 362134,098,059 - 34,098,311RGDNCBI36
Celera2120,375,811 - 20,376,063RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,654,189 - 20,654,441UniSTS
REN86738  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,176,413 - 35,176,672UniSTSGRCh37
Build 362134,098,283 - 34,098,542RGDNCBI36
Celera2120,376,035 - 20,376,294RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,654,413 - 20,654,672UniSTS
REN86739  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,176,639 - 35,176,886UniSTSGRCh37
Build 362134,098,509 - 34,098,756RGDNCBI36
Celera2120,376,261 - 20,376,508RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,654,639 - 20,654,886UniSTS
REN86740  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,176,863 - 35,177,114UniSTSGRCh37
Build 362134,098,733 - 34,098,984RGDNCBI36
Celera2120,376,485 - 20,376,736RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,654,863 - 20,655,114UniSTS
REN86741  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,177,099 - 35,177,366UniSTSGRCh37
Build 362134,098,969 - 34,099,236RGDNCBI36
Celera2120,376,721 - 20,376,988RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,655,099 - 20,655,366UniSTS
REN86742  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,177,349 - 35,177,595UniSTSGRCh37
Build 362134,099,219 - 34,099,465RGDNCBI36
Celera2120,376,971 - 20,377,217RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,655,349 - 20,655,595UniSTS
REN86743  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,177,572 - 35,177,819UniSTSGRCh37
Build 362134,099,442 - 34,099,689RGDNCBI36
Celera2120,377,194 - 20,377,441RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,655,572 - 20,655,819UniSTS
REN86744  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,177,738 - 35,177,969UniSTSGRCh37
Build 362134,099,608 - 34,099,839RGDNCBI36
Celera2120,377,360 - 20,377,591RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,655,738 - 20,655,969UniSTS
REN86745  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,178,537 - 35,178,786UniSTSGRCh37
Build 362134,100,407 - 34,100,656RGDNCBI36
Celera2120,378,159 - 20,378,408RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,656,600 - 20,656,849UniSTS
REN86746  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,178,779 - 35,179,003UniSTSGRCh37
Build 362134,100,649 - 34,100,873RGDNCBI36
Celera2120,378,401 - 20,378,625RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,656,842 - 20,657,066UniSTS
REN86747  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,178,970 - 35,179,218UniSTSGRCh37
Build 362134,100,840 - 34,101,088RGDNCBI36
Celera2120,378,592 - 20,378,840RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,657,033 - 20,657,281UniSTS
REN86748  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,179,164 - 35,179,422UniSTSGRCh37
Build 362134,101,034 - 34,101,292RGDNCBI36
Celera2120,378,786 - 20,379,044RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,657,227 - 20,657,485UniSTS
REN86749  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,179,333 - 35,179,584UniSTSGRCh37
Build 362134,101,203 - 34,101,454RGDNCBI36
Celera2120,378,955 - 20,379,206RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,657,396 - 20,657,647UniSTS
REN86750  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,179,444 - 35,179,686UniSTSGRCh37
Build 362134,101,314 - 34,101,556RGDNCBI36
Celera2120,379,066 - 20,379,308RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,657,507 - 20,657,749UniSTS
REN86751  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,179,639 - 35,179,867UniSTSGRCh37
Build 362134,101,509 - 34,101,737RGDNCBI36
Celera2120,379,261 - 20,379,489RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,657,702 - 20,657,930UniSTS
REN86752  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,179,857 - 35,180,106UniSTSGRCh37
Build 362134,101,727 - 34,101,976RGDNCBI36
Celera2120,379,479 - 20,379,728RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,657,920 - 20,658,169UniSTS
REN86753  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,179,982 - 35,180,208UniSTSGRCh37
Build 362134,101,852 - 34,102,078RGDNCBI36
Celera2120,379,604 - 20,379,830RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,658,045 - 20,658,271UniSTS
REN86754  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,180,920 - 35,181,144UniSTSGRCh37
Build 362134,102,790 - 34,103,014RGDNCBI36
Celera2120,380,542 - 20,380,766RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,658,983 - 20,659,207UniSTS
REN86755  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,181,110 - 35,181,368UniSTSGRCh37
Build 362134,102,980 - 34,103,238RGDNCBI36
Celera2120,380,732 - 20,380,990RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,659,173 - 20,659,431UniSTS
REN86756  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,181,357 - 35,181,581UniSTSGRCh37
Build 362134,103,227 - 34,103,451RGDNCBI36
Celera2120,380,979 - 20,381,203RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,659,420 - 20,659,644UniSTS
REN86757  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,181,556 - 35,181,813UniSTSGRCh37
Build 362134,103,426 - 34,103,683RGDNCBI36
Celera2120,381,178 - 20,381,435RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,659,619 - 20,659,876UniSTS
REN86758  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,181,807 - 35,182,035UniSTSGRCh37
Build 362134,103,677 - 34,103,905RGDNCBI36
Celera2120,381,429 - 20,381,657RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,659,870 - 20,660,098UniSTS
REN86759  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,182,252 - 35,182,477UniSTSGRCh37
Build 362134,104,122 - 34,104,347RGDNCBI36
Celera2120,381,874 - 20,382,099RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,660,315 - 20,660,540UniSTS
REN86760  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,182,428 - 35,182,673UniSTSGRCh37
Build 362134,104,298 - 34,104,543RGDNCBI36
Celera2120,382,050 - 20,382,295RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,660,491 - 20,660,736UniSTS
REN86761  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,182,670 - 35,182,897UniSTSGRCh37
Build 362134,104,540 - 34,104,767RGDNCBI36
Celera2120,382,292 - 20,382,519RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,660,733 - 20,660,960UniSTS
REN86762  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,182,878 - 35,183,149UniSTSGRCh37
Build 362134,104,748 - 34,105,019RGDNCBI36
Celera2120,382,500 - 20,382,771RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,660,941 - 20,661,212UniSTS
REN86763  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,183,134 - 35,183,384UniSTSGRCh37
Build 362134,105,004 - 34,105,254RGDNCBI36
Celera2120,382,756 - 20,383,006RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,661,197 - 20,661,447UniSTS
REN86764  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,183,361 - 35,183,626UniSTSGRCh37
Build 362134,105,231 - 34,105,496RGDNCBI36
Celera2120,382,983 - 20,383,248RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,661,424 - 20,661,689UniSTS
REN86765  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,183,601 - 35,183,825UniSTSGRCh37
Build 362134,105,471 - 34,105,695RGDNCBI36
Celera2120,383,223 - 20,383,447RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,661,664 - 20,661,888UniSTS
REN86766  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,183,818 - 35,184,059UniSTSGRCh37
Build 362134,105,688 - 34,105,929RGDNCBI36
Celera2120,383,440 - 20,383,681RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,661,881 - 20,662,122UniSTS
REN86767  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,184,036 - 35,184,288UniSTSGRCh37
Build 362134,105,906 - 34,106,158RGDNCBI36
Celera2120,383,658 - 20,383,910RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,662,099 - 20,662,351UniSTS
REN86768  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,184,274 - 35,184,501UniSTSGRCh37
Build 362134,106,144 - 34,106,371RGDNCBI36
Celera2120,383,896 - 20,384,123RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,662,337 - 20,662,564UniSTS
REN86769  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,184,498 - 35,184,723UniSTSGRCh37
Build 362134,106,368 - 34,106,593RGDNCBI36
Celera2120,384,120 - 20,384,345RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,662,561 - 20,662,786UniSTS
REN86770  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,184,570 - 35,184,794UniSTSGRCh37
Build 362134,106,440 - 34,106,664RGDNCBI36
Celera2120,384,192 - 20,384,416RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,662,633 - 20,662,857UniSTS
REN86771  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,184,864 - 35,185,095UniSTSGRCh37
Build 362134,106,734 - 34,106,965RGDNCBI36
Celera2120,384,486 - 20,384,717RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,662,927 - 20,663,158UniSTS
REN86772  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,185,093 - 35,185,352UniSTSGRCh37
Build 362134,106,963 - 34,107,222RGDNCBI36
Celera2120,384,715 - 20,384,974RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,663,156 - 20,663,415UniSTS
REN86773  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,185,328 - 35,185,571UniSTSGRCh37
Build 362134,107,198 - 34,107,441RGDNCBI36
Celera2120,384,950 - 20,385,193RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,663,391 - 20,663,634UniSTS
REN86774  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,185,543 - 35,185,771UniSTSGRCh37
Build 362134,107,413 - 34,107,641RGDNCBI36
Celera2120,385,165 - 20,385,393RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,663,606 - 20,663,834UniSTS
REN86775  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,185,745 - 35,185,982UniSTSGRCh37
Build 362134,107,615 - 34,107,852RGDNCBI36
Celera2120,385,367 - 20,385,604RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,663,808 - 20,664,045UniSTS
REN86776  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,185,955 - 35,186,210UniSTSGRCh37
Build 362134,107,825 - 34,108,080RGDNCBI36
Celera2120,385,577 - 20,385,832RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,664,018 - 20,664,273UniSTS
REN86777  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,186,173 - 35,186,414UniSTSGRCh37
Build 362134,108,043 - 34,108,284RGDNCBI36
Celera2120,385,795 - 20,386,036RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,664,236 - 20,664,477UniSTS
REN86778  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,186,384 - 35,186,646UniSTSGRCh37
Build 362134,108,254 - 34,108,516RGDNCBI36
Celera2120,386,006 - 20,386,268RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,664,447 - 20,664,709UniSTS
REN86779  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,186,624 - 35,186,854UniSTSGRCh37
Build 362134,108,494 - 34,108,724RGDNCBI36
Celera2120,386,246 - 20,386,476RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,664,687 - 20,664,917UniSTS
REN86780  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,186,848 - 35,187,074UniSTSGRCh37
Build 362134,108,718 - 34,108,944RGDNCBI36
Celera2120,386,470 - 20,386,696RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,664,911 - 20,665,137UniSTS
REN86781  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,187,047 - 35,187,294UniSTSGRCh37
Build 362134,108,917 - 34,109,164RGDNCBI36
Celera2120,386,669 - 20,386,916RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,665,110 - 20,665,357UniSTS
REN86782  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,187,272 - 35,187,524UniSTSGRCh37
Build 362134,109,142 - 34,109,394RGDNCBI36
Celera2120,386,894 - 20,387,146RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,665,335 - 20,665,587UniSTS
REN86783  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,187,494 - 35,187,750UniSTSGRCh37
Build 362134,109,364 - 34,109,620RGDNCBI36
Celera2120,387,116 - 20,387,372RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,665,557 - 20,665,813UniSTS
REN86784  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,187,727 - 35,187,973UniSTSGRCh37
Build 362134,109,597 - 34,109,843RGDNCBI36
Celera2120,387,349 - 20,387,595RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,665,790 - 20,666,036UniSTS
REN86785  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,187,956 - 35,188,211UniSTSGRCh37
Build 362134,109,826 - 34,110,081RGDNCBI36
Celera2120,387,578 - 20,387,833RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,666,019 - 20,666,274UniSTS
REN86786  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,188,041 - 35,188,292UniSTSGRCh37
Build 362134,109,911 - 34,110,162RGDNCBI36
Celera2120,387,663 - 20,387,914RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,666,104 - 20,666,355UniSTS
REN86787  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,188,269 - 35,188,536UniSTSGRCh37
Build 362134,110,139 - 34,110,406RGDNCBI36
Celera2120,387,891 - 20,388,158RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,666,332 - 20,666,599UniSTS
REN86788  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,188,515 - 35,188,758UniSTSGRCh37
Build 362134,110,385 - 34,110,628RGDNCBI36
Celera2120,388,137 - 20,388,380RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,666,578 - 20,666,821UniSTS
REN86789  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,188,706 - 35,188,967UniSTSGRCh37
Build 362134,110,576 - 34,110,837RGDNCBI36
Celera2120,388,328 - 20,388,589RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,666,769 - 20,666,988UniSTS
REN86790  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,188,936 - 35,189,179UniSTSGRCh37
Build 362134,110,806 - 34,111,049RGDNCBI36
Celera2120,388,558 - 20,388,801RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,666,957 - 20,667,200UniSTS
REN86791  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,189,156 - 35,189,381UniSTSGRCh37
Build 362134,111,026 - 34,111,251RGDNCBI36
Celera2120,388,778 - 20,389,003RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,667,177 - 20,667,402UniSTS
REN86792  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,189,361 - 35,189,606UniSTSGRCh37
Build 362134,111,231 - 34,111,476RGDNCBI36
Celera2120,388,983 - 20,389,228RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,667,382 - 20,667,627UniSTS
REN86793  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,189,547 - 35,189,793UniSTSGRCh37
Build 362134,111,417 - 34,111,663RGDNCBI36
Celera2120,389,169 - 20,389,415RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,667,568 - 20,667,814UniSTS
REN86794  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,189,761 - 35,190,005UniSTSGRCh37
Build 362134,111,631 - 34,111,875RGDNCBI36
Celera2120,389,383 - 20,389,627RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,667,782 - 20,668,026UniSTS
REN86795  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,189,982 - 35,190,219UniSTSGRCh37
Build 362134,111,852 - 34,112,089RGDNCBI36
Celera2120,389,604 - 20,389,841RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,668,003 - 20,668,240UniSTS
REN86796  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,190,172 - 35,190,420UniSTSGRCh37
Build 362134,112,042 - 34,112,290RGDNCBI36
Celera2120,389,794 - 20,390,042RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,668,193 - 20,668,441UniSTS
REN86797  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,190,397 - 35,190,625UniSTSGRCh37
Build 362134,112,267 - 34,112,495RGDNCBI36
Celera2120,390,019 - 20,390,247RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,668,418 - 20,668,646UniSTS
REN86798  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,190,602 - 35,190,870UniSTSGRCh37
Build 362134,112,472 - 34,112,740RGDNCBI36
Celera2120,390,224 - 20,390,492RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,668,623 - 20,668,891UniSTS
REN86799  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,190,864 - 35,191,129UniSTSGRCh37
Build 362134,112,734 - 34,112,999RGDNCBI36
Celera2120,390,486 - 20,390,751RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,668,885 - 20,669,150UniSTS
REN86800  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,191,105 - 35,191,347UniSTSGRCh37
Build 362134,112,975 - 34,113,217RGDNCBI36
Celera2120,390,727 - 20,390,969RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,669,126 - 20,669,368UniSTS
REN86801  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,191,318 - 35,191,571UniSTSGRCh37
Build 362134,113,188 - 34,113,441RGDNCBI36
Celera2120,390,940 - 20,391,193RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,669,339 - 20,669,592UniSTS
REN86802  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,191,548 - 35,191,795UniSTSGRCh37
Build 362134,113,418 - 34,113,665RGDNCBI36
Celera2120,391,170 - 20,391,417RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,669,569 - 20,669,816UniSTS
REN86803  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,191,772 - 35,192,013UniSTSGRCh37
Build 362134,113,642 - 34,113,883RGDNCBI36
Celera2120,391,394 - 20,391,635RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,669,793 - 20,670,034UniSTS
REN86804  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,192,326 - 35,192,550UniSTSGRCh37
Build 362134,114,196 - 34,114,420RGDNCBI36
Celera2120,391,948 - 20,392,172RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,670,347 - 20,670,571UniSTS
REN86805  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,192,491 - 35,192,751UniSTSGRCh37
Build 362134,114,361 - 34,114,621RGDNCBI36
Celera2120,392,113 - 20,392,373RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,670,512 - 20,670,772UniSTS
REN86806  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,192,671 - 35,192,915UniSTSGRCh37
Build 362134,114,541 - 34,114,785RGDNCBI36
Celera2120,392,293 - 20,392,537RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,670,692 - 20,670,936UniSTS
REN86807  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,192,858 - 35,193,119UniSTSGRCh37
Build 362134,114,728 - 34,114,989RGDNCBI36
Celera2120,392,480 - 20,392,741RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,670,879 - 20,671,140UniSTS
REN86808  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,193,100 - 35,193,357UniSTSGRCh37
Build 362134,114,970 - 34,115,227RGDNCBI36
Celera2120,392,722 - 20,392,979RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,671,121 - 20,671,378UniSTS
REN86809  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,193,348 - 35,193,613UniSTSGRCh37
Build 362134,115,218 - 34,115,483RGDNCBI36
Celera2120,392,970 - 20,393,235RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,671,369 - 20,671,634UniSTS
REN86810  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,193,593 - 35,193,854UniSTSGRCh37
Build 362134,115,463 - 34,115,724RGDNCBI36
Celera2120,393,215 - 20,393,476RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,671,613 - 20,671,874UniSTS
REN86811  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,193,846 - 35,194,079UniSTSGRCh37
Build 362134,115,716 - 34,115,949RGDNCBI36
Celera2120,393,468 - 20,393,701RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,671,866 - 20,672,099UniSTS
REN86812  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,194,031 - 35,194,280UniSTSGRCh37
Build 362134,115,901 - 34,116,150RGDNCBI36
Celera2120,393,653 - 20,393,902RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,672,051 - 20,672,300UniSTS
REN86813  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,194,267 - 35,194,491UniSTSGRCh37
Build 362134,116,137 - 34,116,361RGDNCBI36
Celera2120,393,889 - 20,394,113RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,672,287 - 20,672,511UniSTS
REN86814  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,194,472 - 35,194,700UniSTSGRCh37
Build 362134,116,342 - 34,116,570RGDNCBI36
Celera2120,394,094 - 20,394,322RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,672,492 - 20,672,720UniSTS
REN86815  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,194,650 - 35,194,921UniSTSGRCh37
Build 362134,116,520 - 34,116,791RGDNCBI36
Celera2120,394,272 - 20,394,543RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,672,670 - 20,672,941UniSTS
REN86816  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,194,908 - 35,195,161UniSTSGRCh37
Build 362134,116,778 - 34,117,031RGDNCBI36
Celera2120,394,530 - 20,394,783RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,672,928 - 20,673,181UniSTS
REN86817  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,195,117 - 35,195,387UniSTSGRCh37
Build 362134,116,987 - 34,117,257RGDNCBI36
Celera2120,394,739 - 20,395,009RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,673,137 - 20,673,407UniSTS
REN86818  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,195,386 - 35,195,618UniSTSGRCh37
Build 362134,117,256 - 34,117,488RGDNCBI36
Celera2120,395,008 - 20,395,240RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,673,406 - 20,673,638UniSTS
REN86819  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,195,590 - 35,195,835UniSTSGRCh37
Build 362134,117,460 - 34,117,705RGDNCBI36
Celera2120,395,212 - 20,395,457RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,673,610 - 20,673,855UniSTS
REN86820  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,195,812 - 35,196,062UniSTSGRCh37
Build 362134,117,682 - 34,117,932RGDNCBI36
Celera2120,395,434 - 20,395,684RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,673,832 - 20,674,082UniSTS
REN86821  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,196,049 - 35,196,277UniSTSGRCh37
Build 362134,117,919 - 34,118,147RGDNCBI36
Celera2120,395,671 - 20,395,899RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,674,069 - 20,674,297UniSTS
REN86822  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,196,240 - 35,196,494UniSTSGRCh37
Build 362134,118,110 - 34,118,364RGDNCBI36
Celera2120,395,862 - 20,396,116RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,674,260 - 20,674,514UniSTS
REN86823  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,196,469 - 35,196,718UniSTSGRCh37
Build 362134,118,339 - 34,118,588RGDNCBI36
Celera2120,396,091 - 20,396,340RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,674,489 - 20,674,738UniSTS
REN86824  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,196,692 - 35,196,937UniSTSGRCh37
Build 362134,118,562 - 34,118,807RGDNCBI36
Celera2120,396,314 - 20,396,559RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,674,712 - 20,674,957UniSTS
REN86825  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,196,931 - 35,197,165UniSTSGRCh37
Build 362134,118,801 - 34,119,035RGDNCBI36
Celera2120,396,553 - 20,396,787RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,674,951 - 20,675,185UniSTS
REN86826  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,197,131 - 35,197,373UniSTSGRCh37
Build 362134,119,001 - 34,119,243RGDNCBI36
Celera2120,396,753 - 20,396,995RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,675,151 - 20,675,393UniSTS
REN86827  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,197,363 - 35,197,593UniSTSGRCh37
Build 362134,119,233 - 34,119,463RGDNCBI36
Celera2120,396,985 - 20,397,215RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,675,383 - 20,675,613UniSTS
REN86828  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,197,548 - 35,197,797UniSTSGRCh37
Build 362134,119,418 - 34,119,667RGDNCBI36
Celera2120,397,170 - 20,397,419RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,675,568 - 20,675,817UniSTS
REN86829  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,197,785 - 35,198,031UniSTSGRCh37
Build 362134,119,655 - 34,119,901RGDNCBI36
Celera2120,397,407 - 20,397,653RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,675,805 - 20,676,051UniSTS
REN86830  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,198,008 - 35,198,261UniSTSGRCh37
Build 362134,119,878 - 34,120,131RGDNCBI36
Celera2120,397,630 - 20,397,883RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,676,028 - 20,676,281UniSTS
REN86831  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,198,252 - 35,198,502UniSTSGRCh37
Build 362134,120,122 - 34,120,372RGDNCBI36
Celera2120,397,874 - 20,398,124RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,676,272 - 20,676,522UniSTS
REN86832  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,198,472 - 35,198,705UniSTSGRCh37
Build 362134,120,342 - 34,120,575RGDNCBI36
Celera2120,398,094 - 20,398,327RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,676,492 - 20,676,725UniSTS
REN86833  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,198,682 - 35,198,940UniSTSGRCh37
Build 362134,120,552 - 34,120,810RGDNCBI36
Celera2120,398,304 - 20,398,562RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,676,702 - 20,676,960UniSTS
REN86834  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,198,915 - 35,199,154UniSTSGRCh37
Build 362134,120,785 - 34,121,024RGDNCBI36
Celera2120,398,537 - 20,398,776RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,676,935 - 20,677,174UniSTS
REN86835  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,199,137 - 35,199,378UniSTSGRCh37
Build 362134,121,007 - 34,121,248RGDNCBI36
Celera2120,398,759 - 20,399,000RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,677,157 - 20,677,398UniSTS
REN86836  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,199,293 - 35,199,544UniSTSGRCh37
Build 362134,121,163 - 34,121,414RGDNCBI36
Celera2120,398,915 - 20,399,166RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,677,313 - 20,677,564UniSTS
REN86837  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,199,524 - 35,199,765UniSTSGRCh37
Build 362134,121,394 - 34,121,635RGDNCBI36
Celera2120,399,146 - 20,399,387RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,677,544 - 20,677,785UniSTS
REN86838  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,199,740 - 35,199,984UniSTSGRCh37
Build 362134,121,610 - 34,121,854RGDNCBI36
Celera2120,399,362 - 20,399,606RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,677,760 - 20,678,004UniSTS
REN86839  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,199,969 - 35,200,229UniSTSGRCh37
Build 362134,121,839 - 34,122,099RGDNCBI36
Celera2120,399,591 - 20,399,851RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,677,989 - 20,678,249UniSTS
REN86840  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,200,226 - 35,200,479UniSTSGRCh37
Build 362134,122,096 - 34,122,349RGDNCBI36
Celera2120,399,848 - 20,400,101RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,678,246 - 20,678,499UniSTS
REN86841  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,200,448 - 35,200,695UniSTSGRCh37
Build 362134,122,318 - 34,122,565RGDNCBI36
Celera2120,400,070 - 20,400,317RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,678,468 - 20,678,715UniSTS
REN86842  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,200,674 - 35,200,917UniSTSGRCh37
Build 362134,122,544 - 34,122,787RGDNCBI36
Celera2120,400,296 - 20,400,539RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,678,694 - 20,678,937UniSTS
REN86843  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,200,910 - 35,201,159UniSTSGRCh37
Build 362134,122,780 - 34,123,029RGDNCBI36
Celera2120,400,532 - 20,400,781RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,678,930 - 20,679,179UniSTS
REN86844  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,201,124 - 35,201,375UniSTSGRCh37
Build 362134,122,994 - 34,123,245RGDNCBI36
Celera2120,400,746 - 20,400,997RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,679,144 - 20,679,395UniSTS
REN86845  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,201,358 - 35,201,607UniSTSGRCh37
Build 362134,123,228 - 34,123,477RGDNCBI36
Celera2120,400,980 - 20,401,229RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,679,378 - 20,679,627UniSTS
REN86846  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,201,599 - 35,201,849UniSTSGRCh37
Build 362134,123,469 - 34,123,719RGDNCBI36
Celera2120,401,221 - 20,401,471RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,679,619 - 20,679,869UniSTS
REN86847  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,201,820 - 35,202,062UniSTSGRCh37
Build 362134,123,690 - 34,123,932RGDNCBI36
Celera2120,401,442 - 20,401,684RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,679,840 - 20,680,082UniSTS
REN86848  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,202,039 - 35,202,277UniSTSGRCh37
Build 362134,123,909 - 34,124,147RGDNCBI36
Celera2120,401,661 - 20,401,899RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,680,059 - 20,680,297UniSTS
REN86849  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,202,210 - 35,202,446UniSTSGRCh37
Build 362134,124,080 - 34,124,316RGDNCBI36
Celera2120,401,832 - 20,402,068RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,680,230 - 20,680,466UniSTS
REN86850  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,202,423 - 35,202,673UniSTSGRCh37
Build 362134,124,293 - 34,124,543RGDNCBI36
Celera2120,402,045 - 20,402,295RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,680,443 - 20,680,693UniSTS
REN86851  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,202,666 - 35,202,897UniSTSGRCh37
Build 362134,124,536 - 34,124,767RGDNCBI36
Celera2120,402,288 - 20,402,519RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,680,686 - 20,680,917UniSTS
REN86852  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,202,868 - 35,203,137UniSTSGRCh37
Build 362134,124,738 - 34,125,007RGDNCBI36
Celera2120,402,490 - 20,402,759RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,680,888 - 20,681,157UniSTS
REN86853  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,203,112 - 35,203,343UniSTSGRCh37
Build 362134,124,982 - 34,125,213RGDNCBI36
Celera2120,402,734 - 20,402,965RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,681,132 - 20,681,363UniSTS
REN86854  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,203,313 - 35,203,581UniSTSGRCh37
Build 362134,125,183 - 34,125,451RGDNCBI36
Celera2120,402,935 - 20,403,203RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,681,333 - 20,681,601UniSTS
REN86855  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,203,556 - 35,203,805UniSTSGRCh37
Build 362134,125,426 - 34,125,675RGDNCBI36
Celera2120,403,178 - 20,403,427RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,681,576 - 20,681,825UniSTS
REN86856  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,203,777 - 35,204,026UniSTSGRCh37
Build 362134,125,647 - 34,125,896RGDNCBI36
Celera2120,403,399 - 20,403,648RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,681,797 - 20,682,046UniSTS
REN86857  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,204,003 - 35,204,268UniSTSGRCh37
Build 362134,125,873 - 34,126,138RGDNCBI36
Celera2120,403,625 - 20,403,890RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,682,023 - 20,682,288UniSTS
REN86858  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,204,258 - 35,204,502UniSTSGRCh37
Build 362134,126,128 - 34,126,372RGDNCBI36
Celera2120,403,880 - 20,404,124RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,682,278 - 20,682,522UniSTS
REN86859  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,204,476 - 35,204,712UniSTSGRCh37
Build 362134,126,346 - 34,126,582RGDNCBI36
Celera2120,404,098 - 20,404,334RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,682,496 - 20,682,732UniSTS
REN86860  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,204,687 - 35,204,955UniSTSGRCh37
Build 362134,126,557 - 34,126,825RGDNCBI36
Celera2120,404,309 - 20,404,577RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,682,707 - 20,682,975UniSTS
REN86861  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,204,951 - 35,205,200UniSTSGRCh37
Build 362134,126,821 - 34,127,070RGDNCBI36
Celera2120,404,573 - 20,404,822RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,682,971 - 20,683,220UniSTS
REN86862  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,205,190 - 35,205,435UniSTSGRCh37
Build 362134,127,060 - 34,127,305RGDNCBI36
Celera2120,404,812 - 20,405,057RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,683,210 - 20,683,455UniSTS
REN86863  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,205,428 - 35,205,675UniSTSGRCh37
Build 362134,127,298 - 34,127,545RGDNCBI36
Celera2120,405,050 - 20,405,297RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,683,448 - 20,683,695UniSTS
REN86864  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,205,652 - 35,205,895UniSTSGRCh37
Build 362134,127,522 - 34,127,765RGDNCBI36
Celera2120,405,274 - 20,405,517RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,683,672 - 20,683,915UniSTS
REN86865  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,205,827 - 35,206,058UniSTSGRCh37
Build 362134,127,697 - 34,127,928RGDNCBI36
Celera2120,405,449 - 20,405,680RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,683,847 - 20,684,078UniSTS
REN86866  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,206,039 - 35,206,271UniSTSGRCh37
Build 362134,127,909 - 34,128,141RGDNCBI36
Celera2120,405,661 - 20,405,893RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,684,059 - 20,684,291UniSTS
REN86867  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,206,252 - 35,206,494UniSTSGRCh37
Build 362134,128,122 - 34,128,364RGDNCBI36
Celera2120,405,874 - 20,406,116RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,684,272 - 20,684,514UniSTS
REN86868  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,206,479 - 35,206,749UniSTSGRCh37
Build 362134,128,349 - 34,128,619RGDNCBI36
Celera2120,406,101 - 20,406,371RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,684,499 - 20,684,769UniSTS
REN86869  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,206,731 - 35,206,981UniSTSGRCh37
Build 362134,128,601 - 34,128,851RGDNCBI36
Celera2120,406,353 - 20,406,603RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,684,751 - 20,685,127UniSTS
REN86870  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,206,940 - 35,207,192UniSTSGRCh37
Build 362134,128,810 - 34,129,062RGDNCBI36
Celera2120,406,562 - 20,406,814RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,685,086 - 20,685,338UniSTS
REN86871  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,207,166 - 35,207,416UniSTSGRCh37
Build 362134,129,036 - 34,129,286RGDNCBI36
Celera2120,406,788 - 20,407,038RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,685,312 - 20,685,562UniSTS
REN86872  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,207,394 - 35,207,651UniSTSGRCh37
Build 362134,129,264 - 34,129,521RGDNCBI36
Celera2120,407,016 - 20,407,273RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,685,540 - 20,685,797UniSTS
REN86873  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,207,618 - 35,207,886UniSTSGRCh37
Build 362134,129,488 - 34,129,756RGDNCBI36
Celera2120,407,240 - 20,407,508RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,685,764 - 20,686,032UniSTS
REN86874  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,207,738 - 35,207,962UniSTSGRCh37
Build 362134,129,608 - 34,129,832RGDNCBI36
Celera2120,407,360 - 20,407,584RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,685,884 - 20,686,108UniSTS
REN86875  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,207,907 - 35,208,161UniSTSGRCh37
Build 362134,129,777 - 34,130,031RGDNCBI36
Celera2120,407,529 - 20,407,783RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,686,053 - 20,686,307UniSTS
REN86876  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,208,266 - 35,208,495UniSTSGRCh37
Build 362134,130,136 - 34,130,365RGDNCBI36
Celera2120,407,888 - 20,408,117RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,686,412 - 20,686,641UniSTS
REN86877  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,208,484 - 35,208,749UniSTSGRCh37
Build 362134,130,354 - 34,130,619RGDNCBI36
Celera2120,408,106 - 20,408,371RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,686,630 - 20,686,895UniSTS
REN86878  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,208,739 - 35,208,989UniSTSGRCh37
Build 362134,130,609 - 34,130,859RGDNCBI36
Celera2120,408,361 - 20,408,611RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,686,885 - 20,687,135UniSTS
REN86879  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,208,966 - 35,209,225UniSTSGRCh37
Build 362134,130,836 - 34,131,095RGDNCBI36
Celera2120,408,588 - 20,408,847RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,687,112 - 20,687,371UniSTS
REN86880  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,209,182 - 35,209,421UniSTSGRCh37
Build 362134,131,052 - 34,131,291RGDNCBI36
Celera2120,408,804 - 20,409,043RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,687,328 - 20,687,567UniSTS
REN86881  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37510,664,327 - 10,664,574UniSTSGRCh37
GRCh372135,209,318 - 35,209,565UniSTSGRCh37
Build 36510,717,327 - 10,717,574RGDNCBI36
Celera510,701,470 - 10,701,717RGD
Celera2120,408,940 - 20,409,187UniSTS
Cytogenetic Map5p15.2UniSTS
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef510,647,136 - 10,647,383UniSTS
HuRef2120,687,464 - 20,687,711UniSTS
REN86882  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,209,543 - 35,209,805UniSTSGRCh37
Build 362134,131,413 - 34,131,675RGDNCBI36
Celera2120,409,165 - 20,409,427RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,687,689 - 20,687,951UniSTS
REN86883  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,209,781 - 35,210,035UniSTSGRCh37
Build 362134,131,651 - 34,131,905RGDNCBI36
Celera2120,409,403 - 20,409,657RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,687,927 - 20,688,181UniSTS
REN86884  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,209,990 - 35,210,219UniSTSGRCh37
Build 362134,131,860 - 34,132,089RGDNCBI36
Celera2120,409,612 - 20,409,841RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,688,136 - 20,688,365UniSTS
REN86885  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,210,196 - 35,210,448UniSTSGRCh37
Build 362134,132,066 - 34,132,318RGDNCBI36
Celera2120,409,818 - 20,410,070RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,688,342 - 20,688,594UniSTS
REN86886  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,210,427 - 35,210,695UniSTSGRCh37
Build 362134,132,297 - 34,132,565RGDNCBI36
Celera2120,410,049 - 20,410,317RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,688,573 - 20,688,841UniSTS
REN86887  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,210,662 - 35,210,926UniSTSGRCh37
Build 362134,132,532 - 34,132,796RGDNCBI36
Celera2120,410,284 - 20,410,548RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,688,808 - 20,689,072UniSTS
REN86888  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,210,902 - 35,211,149UniSTSGRCh37
Build 362134,132,772 - 34,133,019RGDNCBI36
Celera2120,410,524 - 20,410,771RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,689,048 - 20,689,295UniSTS
REN86889  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,211,140 - 35,211,395UniSTSGRCh37
Build 362134,133,010 - 34,133,265RGDNCBI36
Celera2120,410,762 - 20,411,017RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,689,286 - 20,689,541UniSTS
REN86890  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,211,377 - 35,211,617UniSTSGRCh37
Build 362134,133,247 - 34,133,487RGDNCBI36
Celera2120,410,999 - 20,411,239RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,689,523 - 20,689,763UniSTS
REN86891  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,211,605 - 35,211,866UniSTSGRCh37
Build 362134,133,475 - 34,133,736RGDNCBI36
Celera2120,411,227 - 20,411,488RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,689,751 - 20,690,012UniSTS
REN86892  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,211,861 - 35,212,111UniSTSGRCh37
Build 362134,133,731 - 34,133,981RGDNCBI36
Celera2120,411,483 - 20,411,733RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,690,007 - 20,690,257UniSTS
REN86893  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,212,101 - 35,212,347UniSTSGRCh37
Build 362134,133,971 - 34,134,217RGDNCBI36
Celera2120,411,723 - 20,411,969RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,690,247 - 20,690,493UniSTS
REN86894  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,212,320 - 35,212,564UniSTSGRCh37
Build 362134,134,190 - 34,134,434RGDNCBI36
Celera2120,411,942 - 20,412,186RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,690,466 - 20,690,710UniSTS
REN86895  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,212,540 - 35,212,769UniSTSGRCh37
Build 362134,134,410 - 34,134,639RGDNCBI36
Celera2120,412,162 - 20,412,391RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,690,686 - 20,690,915UniSTS
REN86896  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,212,606 - 35,212,844UniSTSGRCh37
Build 362134,134,476 - 34,134,714RGDNCBI36
Celera2120,412,228 - 20,412,466RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,690,752 - 20,690,990UniSTS
REN86897  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,212,952 - 35,213,200UniSTSGRCh37
Build 362134,134,822 - 34,135,070RGDNCBI36
Celera2120,412,574 - 20,412,822RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,691,098 - 20,691,346UniSTS
REN86898  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,213,195 - 35,213,421UniSTSGRCh37
Build 362134,135,065 - 34,135,291RGDNCBI36
Celera2120,412,817 - 20,413,043RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,691,341 - 20,691,567UniSTS
REN86899  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,213,407 - 35,213,660UniSTSGRCh37
Build 362134,135,277 - 34,135,530RGDNCBI36
Celera2120,413,029 - 20,413,282RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,691,553 - 20,691,806UniSTS
REN86900  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,213,631 - 35,213,865UniSTSGRCh37
Build 362134,135,501 - 34,135,735RGDNCBI36
Celera2120,413,253 - 20,413,487RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,691,777 - 20,692,011UniSTS
REN86901  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,213,844 - 35,214,093UniSTSGRCh37
Build 362134,135,714 - 34,135,963RGDNCBI36
Celera2120,413,466 - 20,413,715RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,691,990 - 20,692,239UniSTS
REN86902  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,214,028 - 35,214,277UniSTSGRCh37
Build 362134,135,898 - 34,136,147RGDNCBI36
Celera2120,413,650 - 20,413,899RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,692,174 - 20,692,423UniSTS
REN86903  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,214,152 - 35,214,401UniSTSGRCh37
Build 362134,136,022 - 34,136,271RGDNCBI36
Celera2120,413,774 - 20,414,023RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,692,298 - 20,692,547UniSTS
REN86904  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,214,508 - 35,214,742UniSTSGRCh37
Build 362134,136,378 - 34,136,612RGDNCBI36
Celera2120,414,130 - 20,414,364RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,692,654 - 20,692,888UniSTS
REN86905  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,214,731 - 35,214,972UniSTSGRCh37
Build 362134,136,601 - 34,136,842RGDNCBI36
Celera2120,414,353 - 20,414,594RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,692,877 - 20,693,118UniSTS
REN86906  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,214,963 - 35,215,201UniSTSGRCh37
Build 362134,136,833 - 34,137,071RGDNCBI36
Celera2120,414,585 - 20,414,823RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,693,109 - 20,693,347UniSTS
REN86907  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,215,174 - 35,215,421UniSTSGRCh37
Build 362134,137,044 - 34,137,291RGDNCBI36
Celera2120,414,796 - 20,415,043RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,693,320 - 20,693,567UniSTS
REN86908  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,215,396 - 35,215,637UniSTSGRCh37
Build 362134,137,266 - 34,137,507RGDNCBI36
Celera2120,415,018 - 20,415,259RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,693,542 - 20,693,783UniSTS
REN86909  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,215,609 - 35,215,840UniSTSGRCh37
Build 362134,137,479 - 34,137,710RGDNCBI36
Celera2120,415,231 - 20,415,462RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,693,755 - 20,693,986UniSTS
REN86910  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,215,817 - 35,216,045UniSTSGRCh37
Build 362134,137,687 - 34,137,915RGDNCBI36
Celera2120,415,439 - 20,415,667RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,693,963 - 20,694,191UniSTS
REN86911  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,215,998 - 35,216,237UniSTSGRCh37
Build 362134,137,868 - 34,138,107RGDNCBI36
Celera2120,415,620 - 20,415,859RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,694,144 - 20,694,383UniSTS
REN86912  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,216,214 - 35,216,440UniSTSGRCh37
Build 362134,138,084 - 34,138,310RGDNCBI36
Celera2120,415,836 - 20,416,062RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,694,360 - 20,694,586UniSTS
REN86913  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,216,400 - 35,216,657UniSTSGRCh37
Build 362134,138,270 - 34,138,527RGDNCBI36
Celera2120,416,022 - 20,416,279RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,694,546 - 20,694,803UniSTS
REN86914  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,216,649 - 35,216,900UniSTSGRCh37
Build 362134,138,519 - 34,138,770RGDNCBI36
Celera2120,416,271 - 20,416,522RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,694,795 - 20,695,046UniSTS
REN86915  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,216,778 - 35,217,002UniSTSGRCh37
Build 362134,138,648 - 34,138,872RGDNCBI36
Celera2120,416,400 - 20,416,624RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,694,924 - 20,695,148UniSTS
REN86916  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,216,977 - 35,217,250UniSTSGRCh37
Build 362134,138,847 - 34,139,120RGDNCBI36
Celera2120,416,599 - 20,416,872RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,695,123 - 20,695,396UniSTS
REN86917  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,217,232 - 35,217,475UniSTSGRCh37
Build 362134,139,102 - 34,139,345RGDNCBI36
Celera2120,416,854 - 20,417,097RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,695,378 - 20,695,621UniSTS
REN86918  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,217,452 - 35,217,698UniSTSGRCh37
Build 362134,139,322 - 34,139,568RGDNCBI36
Celera2120,417,074 - 20,417,320RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,695,598 - 20,695,844UniSTS
REN86919  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,217,673 - 35,217,925UniSTSGRCh37
Build 362134,139,543 - 34,139,795RGDNCBI36
Celera2120,417,295 - 20,417,547RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,695,819 - 20,696,071UniSTS
REN86920  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,217,903 - 35,218,158UniSTSGRCh37
Build 362134,139,773 - 34,140,028RGDNCBI36
Celera2120,417,525 - 20,417,780RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,696,049 - 20,696,304UniSTS
REN86921  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,218,135 - 35,218,384UniSTSGRCh37
Build 362134,140,005 - 34,140,254RGDNCBI36
Celera2120,417,757 - 20,418,006RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,696,281 - 20,696,530UniSTS
REN86922  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,218,329 - 35,218,591UniSTSGRCh37
Build 362134,140,199 - 34,140,461RGDNCBI36
Celera2120,417,951 - 20,418,213RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,696,475 - 20,696,737UniSTS
REN86923  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,218,570 - 35,218,809UniSTSGRCh37
Build 362134,140,440 - 34,140,679RGDNCBI36
Celera2120,418,192 - 20,418,431RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,696,716 - 20,696,955UniSTS
REN86924  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,218,770 - 35,218,995UniSTSGRCh37
Build 362134,140,640 - 34,140,865RGDNCBI36
Celera2120,418,392 - 20,418,617RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,696,916 - 20,697,141UniSTS
REN86925  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,218,982 - 35,219,225UniSTSGRCh37
Build 362134,140,852 - 34,141,095RGDNCBI36
Celera2120,418,604 - 20,418,847RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,697,128 - 20,697,371UniSTS
REN86926  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,219,201 - 35,219,454UniSTSGRCh37
Build 362134,141,071 - 34,141,324RGDNCBI36
Celera2120,418,823 - 20,419,076RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,697,347 - 20,697,600UniSTS
REN86927  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,219,445 - 35,219,680UniSTSGRCh37
Build 362134,141,315 - 34,141,550RGDNCBI36
Celera2120,419,067 - 20,419,302RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,697,591 - 20,697,826UniSTS
REN86928  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,219,648 - 35,219,889UniSTSGRCh37
Build 362134,141,518 - 34,141,759RGDNCBI36
Celera2120,419,270 - 20,419,511RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,697,794 - 20,698,035UniSTS
REN86929  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,219,860 - 35,220,113UniSTSGRCh37
Build 362134,141,730 - 34,141,983RGDNCBI36
Celera2120,419,482 - 20,419,735RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,698,006 - 20,698,259UniSTS
REN86930  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,220,092 - 35,220,355UniSTSGRCh37
Build 362134,141,962 - 34,142,225RGDNCBI36
Celera2120,419,714 - 20,419,977RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,698,238 - 20,698,501UniSTS
REN86931  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,220,304 - 35,220,549UniSTSGRCh37
Build 362134,142,174 - 34,142,419RGDNCBI36
Celera2120,419,926 - 20,420,171RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,698,450 - 20,698,695UniSTS
REN86932  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,220,527 - 35,220,785UniSTSGRCh37
Build 362134,142,397 - 34,142,655RGDNCBI36
Celera2120,420,149 - 20,420,407RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,698,673 - 20,698,931UniSTS
REN86933  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,220,762 - 35,221,002UniSTSGRCh37
Build 362134,142,632 - 34,142,872RGDNCBI36
Celera2120,420,384 - 20,420,624RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,698,908 - 20,699,148UniSTS
REN86934  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,220,990 - 35,221,238UniSTSGRCh37
Build 362134,142,860 - 34,143,108RGDNCBI36
Celera2120,420,612 - 20,420,860RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,699,136 - 20,699,384UniSTS
REN86935  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,221,020 - 35,221,273UniSTSGRCh37
Build 362134,142,890 - 34,143,143RGDNCBI36
Celera2120,420,642 - 20,420,895RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,699,166 - 20,699,419UniSTS
REN86936  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,221,900 - 35,222,150UniSTSGRCh37
Build 362134,143,770 - 34,144,020RGDNCBI36
Celera2120,421,522 - 20,421,772RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,700,046 - 20,700,296UniSTS
REN86937  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,222,131 - 35,222,370UniSTSGRCh37
Build 362134,144,001 - 34,144,240RGDNCBI36
Celera2120,421,753 - 20,421,992RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,700,277 - 20,700,516UniSTS
REN86938  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,222,347 - 35,222,580UniSTSGRCh37
Build 362134,144,217 - 34,144,450RGDNCBI36
Celera2120,421,969 - 20,422,202RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,700,493 - 20,700,726UniSTS
REN86939  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,222,554 - 35,222,800UniSTSGRCh37
Build 362134,144,424 - 34,144,670RGDNCBI36
Celera2120,422,176 - 20,422,422RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,700,700 - 20,700,946UniSTS
REN86940  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,222,778 - 35,223,030UniSTSGRCh37
Build 362134,144,648 - 34,144,900RGDNCBI36
Celera2120,422,400 - 20,422,652RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,700,924 - 20,701,176UniSTS
REN86941  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,223,022 - 35,223,276UniSTSGRCh37
Build 362134,144,892 - 34,145,146RGDNCBI36
Celera2120,422,644 - 20,422,898RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,701,168 - 20,701,422UniSTS
REN86942  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,223,253 - 35,223,495UniSTSGRCh37
Build 362134,145,123 - 34,145,365RGDNCBI36
Celera2120,422,875 - 20,423,117RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,701,399 - 20,701,641UniSTS
REN86943  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,223,468 - 35,223,692UniSTSGRCh37
Build 362134,145,338 - 34,145,562RGDNCBI36
Celera2120,423,090 - 20,423,314RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,701,614 - 20,701,838UniSTS
REN86944  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,224,266 - 35,224,500UniSTSGRCh37
Build 362134,146,136 - 34,146,370RGDNCBI36
Celera2120,423,889 - 20,424,123RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,702,413 - 20,702,647UniSTS
REN86945  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,224,473 - 35,224,724UniSTSGRCh37
Build 362134,146,343 - 34,146,594RGDNCBI36
Celera2120,424,096 - 20,424,347RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,702,620 - 20,702,871UniSTS
REN86946  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,224,713 - 35,224,964UniSTSGRCh37
Build 362134,146,583 - 34,146,834RGDNCBI36
Celera2120,424,336 - 20,424,587RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,702,860 - 20,703,111UniSTS
REN86947  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,224,948 - 35,225,176UniSTSGRCh37
Build 362134,146,818 - 34,147,046RGDNCBI36
Celera2120,424,571 - 20,424,799RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,703,095 - 20,703,323UniSTS
REN86948  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,225,152 - 35,225,382UniSTSGRCh37
Build 362134,147,022 - 34,147,252RGDNCBI36
Celera2120,424,775 - 20,425,005RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,703,299 - 20,703,529UniSTS
REN86949  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,225,339 - 35,225,568UniSTSGRCh37
Build 362134,147,209 - 34,147,438RGDNCBI36
Celera2120,424,962 - 20,425,191RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,703,486 - 20,703,715UniSTS
REN86950  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,225,519 - 35,225,775UniSTSGRCh37
Build 362134,147,389 - 34,147,645RGDNCBI36
Celera2120,425,142 - 20,425,398RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,703,666 - 20,703,922UniSTS
REN86951  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,225,759 - 35,226,007UniSTSGRCh37
Build 362134,147,629 - 34,147,877RGDNCBI36
Celera2120,425,382 - 20,425,630RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,703,906 - 20,704,154UniSTS
REN86952  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,225,977 - 35,226,206UniSTSGRCh37
Build 362134,147,847 - 34,148,076RGDNCBI36
Celera2120,425,600 - 20,425,829RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,704,124 - 20,704,353UniSTS
REN86953  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,226,186 - 35,226,438UniSTSGRCh37
Build 362134,148,056 - 34,148,308RGDNCBI36
Celera2120,425,809 - 20,426,061RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,704,333 - 20,704,585UniSTS
REN86954  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,226,415 - 35,226,660UniSTSGRCh37
Build 362134,148,285 - 34,148,530RGDNCBI36
Celera2120,426,038 - 20,426,283RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,704,562 - 20,704,807UniSTS
REN86955  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,226,633 - 35,226,892UniSTSGRCh37
Build 362134,148,503 - 34,148,762RGDNCBI36
Celera2120,426,256 - 20,426,515RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,704,780 - 20,705,039UniSTS
REN86956  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,226,884 - 35,227,131UniSTSGRCh37
Build 362134,148,754 - 34,149,001RGDNCBI36
Celera2120,426,507 - 20,426,754RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,705,031 - 20,705,278UniSTS
REN86957  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,227,120 - 35,227,372UniSTSGRCh37
Build 362134,148,990 - 34,149,242RGDNCBI36
Celera2120,426,743 - 20,426,995RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,705,267 - 20,705,519UniSTS
REN86958  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,227,350 - 35,227,619UniSTSGRCh37
Build 362134,149,220 - 34,149,489RGDNCBI36
Celera2120,426,973 - 20,427,242RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,705,497 - 20,705,766UniSTS
REN86959  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,227,607 - 35,227,858UniSTSGRCh37
Build 362134,149,477 - 34,149,728RGDNCBI36
Celera2120,427,230 - 20,427,481RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,705,754 - 20,706,005UniSTS
REN86960  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,227,809 - 35,228,064UniSTSGRCh37
Build 362134,149,679 - 34,149,934RGDNCBI36
Celera2120,427,432 - 20,427,687RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,705,956 - 20,706,211UniSTS
REN86961  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,228,045 - 35,228,269UniSTSGRCh37
Build 362134,149,915 - 34,150,139RGDNCBI36
Celera2120,427,668 - 20,427,892RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,706,192 - 20,706,416UniSTS
REN86962  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,228,247 - 35,228,513UniSTSGRCh37
Build 362134,150,117 - 34,150,383RGDNCBI36
Celera2120,427,870 - 20,428,136RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,706,394 - 20,706,660UniSTS
REN86963  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,228,494 - 35,228,758UniSTSGRCh37
Build 362134,150,364 - 34,150,628RGDNCBI36
Celera2120,428,117 - 20,428,381RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,706,641 - 20,706,905UniSTS
REN86964  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,228,735 - 35,228,990UniSTSGRCh37
Build 362134,150,605 - 34,150,860RGDNCBI36
Celera2120,428,358 - 20,428,613RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,706,882 - 20,707,137UniSTS
REN86965  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,228,904 - 35,229,151UniSTSGRCh37
Build 362134,150,774 - 34,151,021RGDNCBI36
Celera2120,428,527 - 20,428,774RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,707,051 - 20,707,296UniSTS
REN86966  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,229,119 - 35,229,387UniSTSGRCh37
Build 362134,150,989 - 34,151,257RGDNCBI36
Celera2120,428,742 - 20,429,010RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,707,264 - 20,707,532UniSTS
REN86967  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,229,364 - 35,229,599UniSTSGRCh37
Build 362134,151,234 - 34,151,469RGDNCBI36
Celera2120,428,987 - 20,429,222RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,707,509 - 20,707,744UniSTS
REN86968  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,229,576 - 35,229,826UniSTSGRCh37
Build 362134,151,446 - 34,151,696RGDNCBI36
Celera2120,429,199 - 20,429,449RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,707,721 - 20,707,971UniSTS
REN86969  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,229,790 - 35,230,014UniSTSGRCh37
Build 362134,151,660 - 34,151,884RGDNCBI36
Celera2120,429,413 - 20,429,637RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,707,935 - 20,708,159UniSTS
REN86970  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,229,991 - 35,230,248UniSTSGRCh37
Build 362134,151,861 - 34,152,118RGDNCBI36
Celera2120,429,614 - 20,429,871RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,708,136 - 20,708,393UniSTS
REN86971  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,230,221 - 35,230,470UniSTSGRCh37
Build 362134,152,091 - 34,152,340RGDNCBI36
Celera2120,429,844 - 20,430,093RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,708,366 - 20,708,615UniSTS
REN86972  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,230,448 - 35,230,696UniSTSGRCh37
Build 362134,152,318 - 34,152,566RGDNCBI36
Celera2120,430,071 - 20,430,319RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,708,593 - 20,708,841UniSTS
REN86973  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,230,676 - 35,230,906UniSTSGRCh37
Build 362134,152,546 - 34,152,776RGDNCBI36
Celera2120,430,299 - 20,430,529RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,708,821 - 20,709,051UniSTS
REN86974  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,230,887 - 35,231,119UniSTSGRCh37
Build 362134,152,757 - 34,152,989RGDNCBI36
Celera2120,430,510 - 20,430,742RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,709,032 - 20,709,264UniSTS
REN86975  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,231,083 - 35,231,351UniSTSGRCh37
Build 362134,152,953 - 34,153,221RGDNCBI36
Celera2120,430,706 - 20,430,974RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,709,228 - 20,709,496UniSTS
REN86976  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,231,337 - 35,231,591UniSTSGRCh37
Build 362134,153,207 - 34,153,461RGDNCBI36
Celera2120,430,960 - 20,431,214RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,709,482 - 20,709,736UniSTS
REN86977  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,231,568 - 35,231,806UniSTSGRCh37
Build 362134,153,438 - 34,153,676RGDNCBI36
Celera2120,431,191 - 20,431,429RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,709,713 - 20,709,951UniSTS
REN86978  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,231,777 - 35,232,016UniSTSGRCh37
Build 362134,153,647 - 34,153,886RGDNCBI36
Celera2120,431,400 - 20,431,639RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,709,922 - 20,710,162UniSTS
REN86979  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,231,963 - 35,232,231UniSTSGRCh37
Build 362134,153,833 - 34,154,101RGDNCBI36
Celera2120,431,586 - 20,431,854RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,710,109 - 20,710,377UniSTS
REN86980  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,232,208 - 35,232,480UniSTSGRCh37
Build 362134,154,078 - 34,154,350RGDNCBI36
Celera2120,431,831 - 20,432,103RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,710,354 - 20,710,626UniSTS
REN86981  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,232,458 - 35,232,689UniSTSGRCh37
Build 362134,154,328 - 34,154,559RGDNCBI36
Celera2120,432,081 - 20,432,312RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,710,604 - 20,710,835UniSTS
REN86982  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,232,668 - 35,232,921UniSTSGRCh37
Build 362134,154,538 - 34,154,791RGDNCBI36
Celera2120,432,291 - 20,432,544RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,710,814 - 20,711,067UniSTS
REN86983  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,232,898 - 35,233,155UniSTSGRCh37
Build 362134,154,768 - 34,155,025RGDNCBI36
Celera2120,432,521 - 20,432,778RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,711,044 - 20,711,301UniSTS
REN86984  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,233,144 - 35,233,387UniSTSGRCh37
Build 362134,155,014 - 34,155,257RGDNCBI36
Celera2120,432,767 - 20,433,010RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,711,290 - 20,711,533UniSTS
REN86985  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,233,382 - 35,233,631UniSTSGRCh37
Build 362134,155,252 - 34,155,501RGDNCBI36
Celera2120,433,005 - 20,433,254RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,711,528 - 20,711,777UniSTS
REN86986  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,233,608 - 35,233,877UniSTSGRCh37
Build 362134,155,478 - 34,155,747RGDNCBI36
Celera2120,433,231 - 20,433,500RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,711,754 - 20,712,023UniSTS
REN86987  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,233,718 - 35,233,968UniSTSGRCh37
Build 362134,155,588 - 34,155,838RGDNCBI36
Celera2120,433,341 - 20,433,591RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,711,864 - 20,712,114UniSTS
REN86988  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,234,334 - 35,234,576UniSTSGRCh37
Build 362134,156,204 - 34,156,446RGDNCBI36
Celera2120,433,957 - 20,434,199RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,712,481 - 20,712,722UniSTS
REN86989  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,234,553 - 35,234,785UniSTSGRCh37
Build 362134,156,423 - 34,156,655RGDNCBI36
Celera2120,434,176 - 20,434,408RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,712,699 - 20,712,931UniSTS
REN86990  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,234,763 - 35,235,025UniSTSGRCh37
Build 362134,156,633 - 34,156,895RGDNCBI36
Celera2120,434,386 - 20,434,648RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,712,909 - 20,713,171UniSTS
REN86991  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,235,024 - 35,235,250UniSTSGRCh37
Build 362134,156,894 - 34,157,120RGDNCBI36
Celera2120,434,647 - 20,434,873RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,713,170 - 20,713,396UniSTS
REN86992  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,235,222 - 35,235,481UniSTSGRCh37
Build 362134,157,092 - 34,157,351RGDNCBI36
Celera2120,434,845 - 20,435,104RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,713,368 - 20,713,627UniSTS
REN86993  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,235,410 - 35,235,653UniSTSGRCh37
Build 362134,157,280 - 34,157,523RGDNCBI36
Celera2120,435,033 - 20,435,276RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,713,556 - 20,713,799UniSTS
REN86994  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,235,626 - 35,235,879UniSTSGRCh37
Build 362134,157,496 - 34,157,749RGDNCBI36
Celera2120,435,249 - 20,435,502RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,713,772 - 20,714,025UniSTS
REN86995  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,235,856 - 35,236,119UniSTSGRCh37
Build 362134,157,726 - 34,157,989RGDNCBI36
Celera2120,435,479 - 20,435,742RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,714,002 - 20,714,265UniSTS
REN86996  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,236,095 - 35,236,355UniSTSGRCh37
Build 362134,157,965 - 34,158,225RGDNCBI36
Celera2120,435,718 - 20,435,978RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,714,241 - 20,714,501UniSTS
REN86997  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,236,330 - 35,236,586UniSTSGRCh37
Build 362134,158,200 - 34,158,456RGDNCBI36
Celera2120,435,953 - 20,436,209RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,714,476 - 20,714,732UniSTS
REN86998  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,236,563 - 35,236,826UniSTSGRCh37
Build 362134,158,433 - 34,158,696RGDNCBI36
Celera2120,436,186 - 20,436,449RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,714,709 - 20,714,972UniSTS
REN86999  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,236,800 - 35,237,060UniSTSGRCh37
Build 362134,158,670 - 34,158,930RGDNCBI36
Celera2120,436,423 - 20,436,683RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,714,946 - 20,715,206UniSTS
REN87000  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,237,053 - 35,237,285UniSTSGRCh37
Build 362134,158,923 - 34,159,155RGDNCBI36
Celera2120,436,676 - 20,436,908RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,715,199 - 20,715,431UniSTS
REN87001  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,237,268 - 35,237,518UniSTSGRCh37
Build 362134,159,138 - 34,159,388RGDNCBI36
Celera2120,436,891 - 20,437,141RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,715,414 - 20,715,664UniSTS
REN87002  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,237,498 - 35,237,743UniSTSGRCh37
Build 362134,159,368 - 34,159,613RGDNCBI36
Celera2120,437,121 - 20,437,366RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,715,644 - 20,715,889UniSTS
REN87003  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,237,720 - 35,237,984UniSTSGRCh37
Build 362134,159,590 - 34,159,854RGDNCBI36
Celera2120,437,343 - 20,437,607RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,715,866 - 20,716,130UniSTS
REN87004  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,237,948 - 35,238,178UniSTSGRCh37
Build 362134,159,818 - 34,160,048RGDNCBI36
Celera2120,437,571 - 20,437,801RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,716,094 - 20,716,324UniSTS
REN87005  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,238,172 - 35,238,409UniSTSGRCh37
Build 362134,160,042 - 34,160,279RGDNCBI36
Celera2120,437,795 - 20,438,032RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,716,318 - 20,716,555UniSTS
REN87006  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,238,398 - 35,238,643UniSTSGRCh37
Build 362134,160,268 - 34,160,513RGDNCBI36
Celera2120,438,021 - 20,438,266RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,716,544 - 20,716,789UniSTS
REN87007  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,238,627 - 35,238,883UniSTSGRCh37
Build 362134,160,497 - 34,160,753RGDNCBI36
Celera2120,438,250 - 20,438,506RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,716,773 - 20,717,029UniSTS
REN87008  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,238,865 - 35,239,127UniSTSGRCh37
Build 362134,160,735 - 34,160,997RGDNCBI36
Celera2120,438,488 - 20,438,750RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,717,011 - 20,717,273UniSTS
REN87009  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,239,105 - 35,239,366UniSTSGRCh37
Build 362134,160,975 - 34,161,236RGDNCBI36
Celera2120,438,728 - 20,438,989RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,717,251 - 20,717,512UniSTS
REN87010  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,239,350 - 35,239,605UniSTSGRCh37
Build 362134,161,220 - 34,161,475RGDNCBI36
Celera2120,438,973 - 20,439,228RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,717,496 - 20,717,751UniSTS
REN87011  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,239,602 - 35,239,826UniSTSGRCh37
Build 362134,161,472 - 34,161,696RGDNCBI36
Celera2120,439,225 - 20,439,449RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,717,748 - 20,717,972UniSTS
REN87012  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,239,737 - 35,239,986UniSTSGRCh37
Build 362134,161,607 - 34,161,856RGDNCBI36
Celera2120,439,360 - 20,439,608RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,717,883 - 20,718,131UniSTS
REN87013  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,241,178 - 35,241,403UniSTSGRCh37
Build 362134,163,048 - 34,163,273RGDNCBI36
Celera2120,440,800 - 20,441,025RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,719,323 - 20,719,548UniSTS
REN87014  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,241,401 - 35,241,625UniSTSGRCh37
Build 362134,163,271 - 34,163,495RGDNCBI36
Celera2120,441,023 - 20,441,247RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,719,546 - 20,719,770UniSTS
REN87015  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,241,599 - 35,241,834UniSTSGRCh37
Build 362134,163,469 - 34,163,704RGDNCBI36
Celera2120,441,221 - 20,441,456RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,719,744 - 20,719,979UniSTS
REN87016  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,241,822 - 35,242,057UniSTSGRCh37
Build 362134,163,692 - 34,163,927RGDNCBI36
Celera2120,441,444 - 20,441,679RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,719,967 - 20,720,202UniSTS
REN87017  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,242,045 - 35,242,276UniSTSGRCh37
Build 362134,163,915 - 34,164,146RGDNCBI36
Celera2120,441,667 - 20,441,898RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,720,190 - 20,720,421UniSTS
REN87018  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,242,234 - 35,242,475UniSTSGRCh37
Build 362134,164,104 - 34,164,345RGDNCBI36
Celera2120,441,856 - 20,442,097RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,720,379 - 20,720,620UniSTS
REN87019  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,242,429 - 35,242,685UniSTSGRCh37
Build 362134,164,299 - 34,164,555RGDNCBI36
Celera2120,442,051 - 20,442,307RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,720,574 - 20,720,830UniSTS
REN87020  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,242,647 - 35,242,898UniSTSGRCh37
Build 362134,164,517 - 34,164,768RGDNCBI36
Celera2120,442,269 - 20,442,520RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,720,792 - 20,721,043UniSTS
REN87021  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,242,856 - 35,243,115UniSTSGRCh37
Build 362134,164,726 - 34,164,985RGDNCBI36
Celera2120,442,478 - 20,442,737RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,721,001 - 20,721,260UniSTS
REN87022  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,243,092 - 35,243,325UniSTSGRCh37
Build 362134,164,962 - 34,165,195RGDNCBI36
Celera2120,442,714 - 20,442,947RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,721,237 - 20,721,470UniSTS
REN87023  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,243,286 - 35,243,524UniSTSGRCh37
Build 362134,165,156 - 34,165,394RGDNCBI36
Celera2120,442,908 - 20,443,146RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,721,431 - 20,721,669UniSTS
REN87024  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,243,459 - 35,243,690UniSTSGRCh37
Build 362134,165,329 - 34,165,560RGDNCBI36
Celera2120,443,081 - 20,443,312RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,721,604 - 20,721,835UniSTS
REN87025  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,243,961 - 35,244,188UniSTSGRCh37
Build 362134,165,831 - 34,166,058RGDNCBI36
Celera2120,443,583 - 20,443,810RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,722,106 - 20,722,333UniSTS
REN87026  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,244,161 - 35,244,425UniSTSGRCh37
Build 362134,166,031 - 34,166,295RGDNCBI36
Celera2120,443,783 - 20,444,047RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,722,306 - 20,722,570UniSTS
REN87027  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,244,418 - 35,244,688UniSTSGRCh37
Build 362134,166,288 - 34,166,558RGDNCBI36
Celera2120,444,040 - 20,444,310RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,722,563 - 20,722,833UniSTS
REN87028  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,244,543 - 35,244,767UniSTSGRCh37
Build 362134,166,413 - 34,166,637RGDNCBI36
Celera2120,444,165 - 20,444,389RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,722,688 - 20,722,912UniSTS
REN87029  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,244,732 - 35,244,989UniSTSGRCh37
Build 362134,166,602 - 34,166,859RGDNCBI36
Celera2120,444,354 - 20,444,611RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,722,877 - 20,723,134UniSTS
REN87030  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,244,983 - 35,245,242UniSTSGRCh37
Build 362134,166,853 - 34,167,112RGDNCBI36
Celera2120,444,605 - 20,444,864RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,723,128 - 20,723,387UniSTS
REN87031  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,245,212 - 35,245,437UniSTSGRCh37
Build 362134,167,082 - 34,167,307RGDNCBI36
Celera2120,444,834 - 20,445,059RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,723,357 - 20,723,582UniSTS
REN87032  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,245,420 - 35,245,668UniSTSGRCh37
Build 362134,167,290 - 34,167,538RGDNCBI36
Celera2120,445,042 - 20,445,290RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,723,565 - 20,723,813UniSTS
REN87033  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,245,646 - 35,245,896UniSTSGRCh37
Build 362134,167,516 - 34,167,766RGDNCBI36
Celera2120,445,268 - 20,445,518RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,723,791 - 20,724,041UniSTS
REN87034  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,246,486 - 35,246,710UniSTSGRCh37
Build 362134,168,356 - 34,168,580RGDNCBI36
Celera2120,446,108 - 20,446,332RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,724,631 - 20,724,855UniSTS
REN87035  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,246,682 - 35,246,940UniSTSGRCh37
Build 362134,168,552 - 34,168,810RGDNCBI36
Celera2120,446,304 - 20,446,562RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,724,827 - 20,725,085UniSTS
REN87036  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,246,760 - 35,247,000UniSTSGRCh37
Build 362134,168,630 - 34,168,870RGDNCBI36
Celera2120,446,382 - 20,446,622RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,724,905 - 20,725,148UniSTS
REN87037  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,247,249 - 35,247,491UniSTSGRCh37
Build 362134,169,119 - 34,169,361RGDNCBI36
Celera2120,446,871 - 20,447,113RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,725,397 - 20,725,639UniSTS
REN87038  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,247,489 - 35,247,736UniSTSGRCh37
Build 362134,169,359 - 34,169,606RGDNCBI36
Celera2120,447,111 - 20,447,358RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,725,637 - 20,725,884UniSTS
REN87039  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,247,723 - 35,247,977UniSTSGRCh37
Build 362134,169,593 - 34,169,847RGDNCBI36
Celera2120,447,345 - 20,447,599RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,725,871 - 20,726,125UniSTS
REN87040  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,247,757 - 35,247,989UniSTSGRCh37
Build 362134,169,627 - 34,169,859RGDNCBI36
Celera2120,447,379 - 20,447,611RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,725,905 - 20,726,137UniSTS
REN87041  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,248,669 - 35,248,893UniSTSGRCh37
Build 362134,170,539 - 34,170,763RGDNCBI36
Celera2120,448,253 - 20,448,477RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,726,738 - 20,726,962UniSTS
REN87042  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,248,862 - 35,249,125UniSTSGRCh37
Build 362134,170,732 - 34,170,995RGDNCBI36
Celera2120,448,446 - 20,448,709RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,726,931 - 20,727,194UniSTS
REN87043  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,249,102 - 35,249,360UniSTSGRCh37
Build 362134,170,972 - 34,171,230RGDNCBI36
Celera2120,448,686 - 20,448,944RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,727,171 - 20,727,429UniSTS
REN87044  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,249,627 - 35,249,851UniSTSGRCh37
Build 362134,171,497 - 34,171,721RGDNCBI36
Celera2120,449,211 - 20,449,435RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,727,709 - 20,727,933UniSTS
REN87045  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,249,821 - 35,250,051UniSTSGRCh37
Build 362134,171,691 - 34,171,921RGDNCBI36
Celera2120,449,405 - 20,449,635RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,727,903 - 20,728,133UniSTS
REN87046  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,250,036 - 35,250,286UniSTSGRCh37
Build 362134,171,906 - 34,172,156RGDNCBI36
Celera2120,449,620 - 20,449,870RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,728,118 - 20,728,356UniSTS
REN87047  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,250,221 - 35,250,445UniSTSGRCh37
Build 362134,172,091 - 34,172,315RGDNCBI36
Celera2120,449,805 - 20,450,029RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,728,291 - 20,728,509UniSTS
REN87048  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,250,422 - 35,250,691UniSTSGRCh37
Build 362134,172,292 - 34,172,561RGDNCBI36
Celera2120,450,006 - 20,450,275RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,728,486 - 20,728,755UniSTS
REN87049  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,250,680 - 35,250,914UniSTSGRCh37
Build 362134,172,550 - 34,172,784RGDNCBI36
Celera2120,450,264 - 20,450,498RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,728,744 - 20,728,978UniSTS
REN87050  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,250,897 - 35,251,121UniSTSGRCh37
Build 362134,172,767 - 34,172,991RGDNCBI36
Celera2120,450,481 - 20,450,705RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,728,961 - 20,729,185UniSTS
REN87051  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,251,095 - 35,251,348UniSTSGRCh37
Build 362134,172,965 - 34,173,218RGDNCBI36
Celera2120,450,679 - 20,450,932RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,729,159 - 20,729,412UniSTS
REN87052  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,251,282 - 35,251,522UniSTSGRCh37
Build 362134,173,152 - 34,173,392RGDNCBI36
Celera2120,450,866 - 20,451,106RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,729,346 - 20,729,586UniSTS
REN87053  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,251,372 - 35,251,627UniSTSGRCh37
Build 362134,173,242 - 34,173,497RGDNCBI36
Celera2120,450,956 - 20,451,211RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,729,436 - 20,729,691UniSTS
REN87054  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,251,606 - 35,251,840UniSTSGRCh37
Build 362134,173,476 - 34,173,710RGDNCBI36
Celera2120,451,190 - 20,451,424RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,729,670 - 20,729,904UniSTS
REN87055  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,251,727 - 35,251,992UniSTSGRCh37
Build 362134,173,597 - 34,173,862RGDNCBI36
Celera2120,451,311 - 20,451,576RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,729,791 - 20,730,056UniSTS
REN87056  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,251,925 - 35,252,152UniSTSGRCh37
Build 362134,173,795 - 34,174,022RGDNCBI36
Celera2120,451,509 - 20,451,736RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,729,989 - 20,730,216UniSTS
REN87057  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,252,119 - 35,252,367UniSTSGRCh37
Build 362134,173,989 - 34,174,237RGDNCBI36
Celera2120,451,703 - 20,451,951RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,730,183 - 20,730,431UniSTS
REN87058  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,252,338 - 35,252,581UniSTSGRCh37
Build 362134,174,208 - 34,174,451RGDNCBI36
Celera2120,451,922 - 20,452,165RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,730,402 - 20,730,645UniSTS
REN87059  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,252,561 - 35,252,817UniSTSGRCh37
Build 362134,174,431 - 34,174,687RGDNCBI36
Celera2120,452,145 - 20,452,401RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,730,625 - 20,730,881UniSTS
REN87060  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,252,786 - 35,253,032UniSTSGRCh37
Build 362134,174,656 - 34,174,902RGDNCBI36
Celera2120,452,370 - 20,452,616RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,730,850 - 20,731,096UniSTS
REN87061  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,253,009 - 35,253,251UniSTSGRCh37
Build 362134,174,879 - 34,175,121RGDNCBI36
Celera2120,452,593 - 20,452,835RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,731,073 - 20,731,315UniSTS
REN87062  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,253,198 - 35,253,443UniSTSGRCh37
Build 362134,175,068 - 34,175,313RGDNCBI36
Celera2120,452,782 - 20,453,027RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,731,262 - 20,731,507UniSTS
REN87063  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,253,574 - 35,253,811UniSTSGRCh37
Build 362134,175,444 - 34,175,681RGDNCBI36
Celera2120,453,158 - 20,453,395RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,731,638 - 20,731,875UniSTS
REN87064  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,253,804 - 35,254,056UniSTSGRCh37
Build 362134,175,674 - 34,175,926RGDNCBI36
Celera2120,453,388 - 20,453,640RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,731,868 - 20,732,120UniSTS
REN87065  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,253,971 - 35,254,215UniSTSGRCh37
Build 362134,175,841 - 34,176,085RGDNCBI36
Celera2120,453,555 - 20,453,799RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,732,035 - 20,732,279UniSTS
REN87066  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,254,177 - 35,254,405UniSTSGRCh37
Build 362134,176,047 - 34,176,275RGDNCBI36
Celera2120,453,761 - 20,453,989RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,732,241 - 20,732,469UniSTS
REN87067  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,254,404 - 35,254,662UniSTSGRCh37
Build 362134,176,274 - 34,176,532RGDNCBI36
Celera2120,453,988 - 20,454,246RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,732,468 - 20,732,726UniSTS
REN87068  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,254,658 - 35,254,903UniSTSGRCh37
Build 362134,176,528 - 34,176,773RGDNCBI36
Celera2120,454,242 - 20,454,487RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,732,722 - 20,732,967UniSTS
REN87069  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,254,880 - 35,255,138UniSTSGRCh37
Build 362134,176,750 - 34,177,008RGDNCBI36
Celera2120,454,464 - 20,454,722RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,732,944 - 20,733,202UniSTS
REN87070  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,255,111 - 35,255,364UniSTSGRCh37
Build 362134,176,981 - 34,177,234RGDNCBI36
Celera2120,454,695 - 20,454,948RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,733,175 - 20,733,428UniSTS
REN87071  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,255,341 - 35,255,606UniSTSGRCh37
Build 362134,177,211 - 34,177,476RGDNCBI36
Celera2120,454,925 - 20,455,190RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,733,405 - 20,733,670UniSTS
REN87072  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,255,582 - 35,255,814UniSTSGRCh37
Build 362134,177,452 - 34,177,684RGDNCBI36
Celera2120,455,166 - 20,455,398RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,733,646 - 20,733,878UniSTS
REN87073  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,255,777 - 35,256,039UniSTSGRCh37
Build 362134,177,647 - 34,177,909RGDNCBI36
Celera2120,455,361 - 20,455,623RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,733,841 - 20,734,103UniSTS
REN87074  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,255,929 - 35,256,181UniSTSGRCh37
Build 362134,177,799 - 34,178,051RGDNCBI36
Celera2120,455,513 - 20,455,765RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,733,993 - 20,734,245UniSTS
REN87075  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,256,098 - 35,256,352UniSTSGRCh37
Build 362134,177,968 - 34,178,222RGDNCBI36
Celera2120,455,682 - 20,455,936RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,734,162 - 20,734,417UniSTS
REN87076  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,256,323 - 35,256,573UniSTSGRCh37
Build 362134,178,193 - 34,178,443RGDNCBI36
Celera2120,455,907 - 20,456,157RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,734,388 - 20,734,638UniSTS
REN87077  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,256,552 - 35,256,793UniSTSGRCh37
Build 362134,178,422 - 34,178,663RGDNCBI36
Celera2120,456,136 - 20,456,377RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,734,617 - 20,734,858UniSTS
REN87078  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,256,767 - 35,257,018UniSTSGRCh37
Build 362134,178,637 - 34,178,888RGDNCBI36
Celera2120,456,351 - 20,456,602RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,734,832 - 20,735,083UniSTS
REN87079  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,257,015 - 35,257,276UniSTSGRCh37
Build 362134,178,885 - 34,179,146RGDNCBI36
Celera2120,456,599 - 20,456,860RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,735,080 - 20,735,341UniSTS
REN87080  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,257,272 - 35,257,521UniSTSGRCh37
Build 362134,179,142 - 34,179,391RGDNCBI36
Celera2120,456,856 - 20,457,105RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,735,337 - 20,735,586UniSTS
REN87081  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,257,488 - 35,257,724UniSTSGRCh37
Build 362134,179,358 - 34,179,594RGDNCBI36
Celera2120,457,072 - 20,457,308RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,735,553 - 20,735,789UniSTS
REN87082  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,257,702 - 35,257,956UniSTSGRCh37
Build 362134,179,572 - 34,179,826RGDNCBI36
Celera2120,457,286 - 20,457,540RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,735,767 - 20,736,021UniSTS
REN87083  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,257,940 - 35,258,203UniSTSGRCh37
Build 362134,179,810 - 34,180,073RGDNCBI36
Celera2120,457,524 - 20,457,787RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,736,005 - 20,736,268UniSTS
REN87084  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,258,181 - 35,258,423UniSTSGRCh37
Build 362134,180,051 - 34,180,293RGDNCBI36
Celera2120,457,765 - 20,458,007RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,736,246 - 20,736,488UniSTS
REN87085  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,258,394 - 35,258,627UniSTSGRCh37
Build 362134,180,264 - 34,180,497RGDNCBI36
Celera2120,457,978 - 20,458,211RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,736,459 - 20,736,692UniSTS
REN87086  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,258,605 - 35,258,847UniSTSGRCh37
Build 362134,180,475 - 34,180,717RGDNCBI36
Celera2120,458,189 - 20,458,431RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,736,670 - 20,736,912UniSTS
REN87087  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,258,843 - 35,259,086UniSTSGRCh37
Build 362134,180,713 - 34,180,956RGDNCBI36
Celera2120,458,427 - 20,458,670RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,736,908 - 20,737,151UniSTS
REN87088  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,259,059 - 35,259,320UniSTSGRCh37
Build 362134,180,929 - 34,181,190RGDNCBI36
Celera2120,458,643 - 20,458,904RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,737,124 - 20,737,385UniSTS
REN87089  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,259,123 - 35,259,350UniSTSGRCh37
Build 362134,180,993 - 34,181,220RGDNCBI36
Celera2120,458,707 - 20,458,934RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,737,188 - 20,737,415UniSTS
REN87090  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,259,569 - 35,259,811UniSTSGRCh37
Build 362134,181,439 - 34,181,681RGDNCBI36
Celera2120,459,153 - 20,459,395RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,737,634 - 20,737,878UniSTS
REN87091  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,259,793 - 35,260,056UniSTSGRCh37
Build 362134,181,663 - 34,181,926RGDNCBI36
Celera2120,459,377 - 20,459,640RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,737,860 - 20,738,123UniSTS
REN87092  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,260,030 - 35,260,290UniSTSGRCh37
Build 362134,181,900 - 34,182,160RGDNCBI36
Celera2120,459,614 - 20,459,874RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,738,097 - 20,738,357UniSTS
REN87093  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,260,272 - 35,260,540UniSTSGRCh37
Build 362134,182,142 - 34,182,410RGDNCBI36
Celera2120,459,856 - 20,460,124RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,738,339 - 20,738,599UniSTS
REN87094  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,260,517 - 35,260,762UniSTSGRCh37
Build 362134,182,387 - 34,182,632RGDNCBI36
Celera2120,460,101 - 20,460,346RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,738,576 - 20,738,821UniSTS
REN87095  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,260,742 - 35,260,996UniSTSGRCh37
Build 362134,182,612 - 34,182,866RGDNCBI36
Celera2120,460,326 - 20,460,580RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,738,801 - 20,739,055UniSTS
REN87096  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,260,975 - 35,261,214UniSTSGRCh37
Build 362134,182,845 - 34,183,084RGDNCBI36
Celera2120,460,559 - 20,460,798RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,739,034 - 20,739,273UniSTS
REN87097  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,261,177 - 35,261,425UniSTSGRCh37
Build 362134,183,047 - 34,183,295RGDNCBI36
Celera2120,460,761 - 20,461,009RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,739,236 - 20,739,484UniSTS
REN87098  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,261,398 - 35,261,654UniSTSGRCh37
Build 362134,183,268 - 34,183,524RGDNCBI36
Celera2120,460,982 - 20,461,238RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,739,457 - 20,739,713UniSTS
REN87099  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,261,647 - 35,261,902UniSTSGRCh37
Build 362134,183,517 - 34,183,772RGDNCBI36
Celera2120,461,231 - 20,461,486RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,739,706 - 20,739,961UniSTS
REN87100  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,261,845 - 35,262,093UniSTSGRCh37
Build 362134,183,715 - 34,183,963RGDNCBI36
Celera2120,461,429 - 20,461,677RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,739,904 - 20,740,152UniSTS
REN87101  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,262,070 - 35,262,324UniSTSGRCh37
Build 362134,183,940 - 34,184,194RGDNCBI36
Celera2120,461,654 - 20,461,908RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,740,129 - 20,740,383UniSTS
REN87102  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,262,296 - 35,262,529UniSTSGRCh37
Build 362134,184,166 - 34,184,399RGDNCBI36
Celera2120,461,880 - 20,462,113RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,740,355 - 20,740,588UniSTS
stSG607333  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,013,785 - 35,014,812UniSTSGRCh37
Build 362133,935,655 - 33,936,682RGDNCBI36
Celera2120,213,406 - 20,214,433RGD
HuRef2120,492,110 - 20,493,137UniSTS
stSG607335  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,015,909 - 35,017,073UniSTSGRCh37
Build 362133,937,779 - 33,938,943RGDNCBI36
Celera2120,215,530 - 20,216,694RGD
HuRef2120,494,234 - 20,495,399UniSTS
stSG607336  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,017,054 - 35,018,545UniSTSGRCh37
Build 362133,938,924 - 33,940,415RGDNCBI36
Celera2120,216,675 - 20,218,166RGD
HuRef2120,495,380 - 20,496,871UniSTS
stSG607337  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,018,000 - 35,019,049UniSTSGRCh37
Build 362133,939,870 - 33,940,919RGDNCBI36
Celera2120,217,621 - 20,218,670RGD
HuRef2120,496,326 - 20,497,375UniSTS
stSG607338  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,019,030 - 35,020,417UniSTSGRCh37
Build 362133,940,900 - 33,942,287RGDNCBI36
Celera2120,218,651 - 20,220,038RGD
HuRef2120,497,356 - 20,498,743UniSTS
stSG607340  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,020,632 - 35,021,874UniSTSGRCh37
Build 362133,942,502 - 33,943,744RGDNCBI36
Celera2120,220,253 - 20,221,495RGD
HuRef2120,498,958 - 20,500,200UniSTS
stSG607341  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,021,855 - 35,023,298UniSTSGRCh37
Build 362133,943,725 - 33,945,168RGDNCBI36
Celera2120,221,476 - 20,222,919RGD
HuRef2120,500,181 - 20,501,624UniSTS
stSG607342  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,023,279 - 35,024,461UniSTSGRCh37
Build 362133,945,149 - 33,946,331RGDNCBI36
Celera2120,222,900 - 20,224,082RGD
HuRef2120,501,605 - 20,502,787UniSTS
stSG607343  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,024,447 - 35,025,670UniSTSGRCh37
Build 362133,946,317 - 33,947,540RGDNCBI36
Celera2120,224,068 - 20,225,291RGD
HuRef2120,502,773 - 20,503,996UniSTS
stSG607344  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,025,665 - 35,026,848UniSTSGRCh37
Build 362133,947,535 - 33,948,718RGDNCBI36
Celera2120,225,286 - 20,226,469RGD
HuRef2120,503,991 - 20,505,174UniSTS
stSG607345  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,026,836 - 35,027,036UniSTSGRCh37
Build 362133,948,706 - 33,948,906RGDNCBI36
Celera2120,226,457 - 20,226,657RGD
HuRef2120,505,162 - 20,505,362UniSTS
stSG607346  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,027,051 - 35,028,310UniSTSGRCh37
Build 362133,948,921 - 33,950,180RGDNCBI36
Celera2120,226,672 - 20,227,931RGD
HuRef2120,505,377 - 20,506,636UniSTS
stSG607347  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,028,357 - 35,029,777UniSTSGRCh37
Build 362133,950,227 - 33,951,647RGDNCBI36
Celera2120,227,978 - 20,229,398RGD
HuRef2120,506,683 - 20,508,103UniSTS
stSG607348  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,029,801 - 35,031,006UniSTSGRCh37
Build 362133,951,671 - 33,952,876RGDNCBI36
Celera2120,229,422 - 20,230,627RGD
HuRef2120,508,127 - 20,509,332UniSTS
stSG607349  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,030,992 - 35,032,479UniSTSGRCh37
Build 362133,952,862 - 33,954,349RGDNCBI36
Celera2120,230,613 - 20,232,100RGD
HuRef2120,509,318 - 20,510,806UniSTS
stSG607350  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,034,387 - 35,035,408UniSTSGRCh37
Build 362133,956,257 - 33,957,278RGDNCBI36
Celera2120,234,008 - 20,235,029RGD
HuRef2120,512,714 - 20,513,735UniSTS
stSG607351  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,035,389 - 35,036,390UniSTSGRCh37
Build 362133,957,259 - 33,958,260RGDNCBI36
Celera2120,235,010 - 20,236,011RGD
HuRef2120,513,716 - 20,514,718UniSTS
stSG607352  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,036,246 - 35,037,245UniSTSGRCh37
Build 362133,958,116 - 33,959,115RGDNCBI36
Celera2120,235,867 - 20,236,866RGD
HuRef2120,514,574 - 20,515,573UniSTS
stSG607353  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,038,974 - 35,040,139UniSTSGRCh37
Build 362133,960,844 - 33,962,009RGDNCBI36
Celera2120,238,595 - 20,239,760RGD
HuRef2120,517,302 - 20,518,467UniSTS
stSG607354  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,040,120 - 35,041,134UniSTSGRCh37
Build 362133,961,990 - 33,963,004RGDNCBI36
Celera2120,239,741 - 20,240,755RGD
HuRef2120,518,448 - 20,519,462UniSTS
stSG607355  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,041,123 - 35,042,173UniSTSGRCh37
Build 362133,962,993 - 33,964,043RGDNCBI36
Celera2120,240,744 - 20,241,794RGD
HuRef2120,519,451 - 20,520,501UniSTS
stSG607356  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,042,152 - 35,043,151UniSTSGRCh37
Build 362133,964,022 - 33,965,021RGDNCBI36
Celera2120,241,773 - 20,242,772RGD
HuRef2120,520,480 - 20,521,479UniSTS
stSG607357  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,045,808 - 35,046,937UniSTSGRCh37
Build 362133,967,678 - 33,968,807RGDNCBI36
Celera2120,245,429 - 20,246,558RGD
HuRef2120,524,136 - 20,525,265UniSTS
stSG607358  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,046,921 - 35,047,932UniSTSGRCh37
Build 362133,968,791 - 33,969,802RGDNCBI36
Celera2120,246,542 - 20,247,553RGD
HuRef2120,525,249 - 20,526,260UniSTS
stSG607361  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,050,884 - 35,051,952UniSTSGRCh37
Build 362133,972,754 - 33,973,822RGDNCBI36
Celera2120,250,505 - 20,251,573RGD
HuRef2120,529,213 - 20,530,281UniSTS
stSG607362  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,051,925 - 35,053,018UniSTSGRCh37
Build 362133,973,795 - 33,974,888RGDNCBI36
Celera2120,251,546 - 20,252,639RGD
stSG607364  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,054,328 - 35,055,441UniSTSGRCh37
Build 362133,976,198 - 33,977,311RGDNCBI36
Celera2120,253,949 - 20,255,062RGD
HuRef2120,532,641 - 20,533,754UniSTS
stSG607365  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,055,422 - 35,056,528UniSTSGRCh37
Build 362133,977,292 - 33,978,398RGDNCBI36
Celera2120,255,043 - 20,256,149RGD
HuRef2120,533,735 - 20,534,841UniSTS
stSG607366  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,056,508 - 35,057,899UniSTSGRCh37
Build 362133,978,378 - 33,979,769RGDNCBI36
Celera2120,256,129 - 20,257,520RGD
HuRef2120,534,821 - 20,536,212UniSTS
stSG607367  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,057,882 - 35,059,247UniSTSGRCh37
Build 362133,979,752 - 33,981,117RGDNCBI36
Celera2120,257,503 - 20,258,868RGD
HuRef2120,536,195 - 20,537,560UniSTS
stSG607369  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,060,553 - 35,061,686UniSTSGRCh37
Build 362133,982,423 - 33,983,556RGDNCBI36
Celera2120,260,174 - 20,261,307RGD
HuRef2120,538,857 - 20,539,990UniSTS
stSG607370  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,063,251 - 35,064,681UniSTSGRCh37
Build 362133,985,121 - 33,986,551RGDNCBI36
Celera2120,262,872 - 20,264,302RGD
HuRef2120,541,559 - 20,542,989UniSTS
stSG607371  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,064,664 - 35,065,992UniSTSGRCh37
Build 362133,986,534 - 33,987,862RGDNCBI36
Celera2120,264,285 - 20,265,613RGD
HuRef2120,542,972 - 20,544,300UniSTS
stSG607372  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,066,091 - 35,067,588UniSTSGRCh37
Build 362133,987,961 - 33,989,458RGDNCBI36
Celera2120,265,712 - 20,267,209RGD
HuRef2120,544,399 - 20,545,896UniSTS
stSG607373  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,067,567 - 35,069,033UniSTSGRCh37
Build 362133,989,437 - 33,990,903RGDNCBI36
Celera2120,267,188 - 20,268,654RGD
HuRef2120,545,875 - 20,547,341UniSTS
stSG607374  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,069,014 - 35,070,096UniSTSGRCh37
Build 362133,990,884 - 33,991,966RGDNCBI36
Celera2120,268,635 - 20,269,717RGD
HuRef2120,547,322 - 20,548,405UniSTS
stSG607375  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,070,078 - 35,071,169UniSTSGRCh37
Build 362133,991,948 - 33,993,039RGDNCBI36
Celera2120,269,699 - 20,270,790RGD
HuRef2120,548,387 - 20,549,478UniSTS
stSG607376  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,071,065 - 35,072,068UniSTSGRCh37
Build 362133,992,935 - 33,993,938RGDNCBI36
Celera2120,270,686 - 20,271,689RGD
HuRef2120,549,374 - 20,550,377UniSTS
stSG607378  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,073,397 - 35,074,770UniSTSGRCh37
Build 362133,995,267 - 33,996,640RGDNCBI36
Celera2120,273,018 - 20,274,391RGD
HuRef2120,551,704 - 20,553,020UniSTS
stSG607379  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,074,751 - 35,076,184UniSTSGRCh37
Build 362133,996,621 - 33,998,054RGDNCBI36
Celera2120,274,372 - 20,275,805RGD
HuRef2120,553,001 - 20,554,436UniSTS
stSG607380  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,076,165 - 35,077,482UniSTSGRCh37
Build 362133,998,035 - 33,999,352RGDNCBI36
Celera2120,275,786 - 20,277,103RGD
stSG607381  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,077,464 - 35,078,678UniSTSGRCh37
Build 362133,999,334 - 34,000,548RGDNCBI36
Celera2120,277,085 - 20,278,299RGD
stSG607382  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,078,231 - 35,079,435UniSTSGRCh37
Build 362134,000,101 - 34,001,305RGDNCBI36
Celera2120,277,852 - 20,279,056RGD
HuRef2120,556,295 - 20,557,499UniSTS
stSG607383  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,085,154 - 35,086,456UniSTSGRCh37
Build 362134,007,024 - 34,008,326RGDNCBI36
Celera2120,284,776 - 20,286,079RGD
HuRef2120,563,217 - 20,564,521UniSTS
stSG607384  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,086,607 - 35,087,928UniSTSGRCh37
Build 362134,008,477 - 34,009,798RGDNCBI36
Celera2120,286,230 - 20,287,550RGD
HuRef2120,564,672 - 20,565,986UniSTS
stSG607385  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,087,909 - 35,088,918UniSTSGRCh37
Build 362134,009,779 - 34,010,788RGDNCBI36
Celera2120,287,531 - 20,288,540RGD
HuRef2120,565,967 - 20,566,976UniSTS
stSG607386  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,088,898 - 35,090,267UniSTSGRCh37
Build 362134,010,768 - 34,012,137RGDNCBI36
Celera2120,288,520 - 20,289,889RGD
HuRef2120,566,956 - 20,568,264UniSTS
stSG607387  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,090,248 - 35,091,001UniSTSGRCh37
Build 362134,012,118 - 34,012,871RGDNCBI36
Celera2120,289,870 - 20,290,623RGD
HuRef2120,568,245 - 20,568,998UniSTS
stSG607388  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,091,085 - 35,092,172UniSTSGRCh37
Build 362134,012,955 - 34,014,042RGDNCBI36
Celera2120,290,707 - 20,291,794RGD
HuRef2120,569,082 - 20,570,169UniSTS
stSG607389  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,092,286 - 35,093,664UniSTSGRCh37
Build 362134,014,156 - 34,015,534RGDNCBI36
Celera2120,291,908 - 20,293,286RGD
HuRef2120,570,283 - 20,571,661UniSTS
stSG607391  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,094,736 - 35,096,182UniSTSGRCh37
Build 362134,016,606 - 34,018,052RGDNCBI36
Celera2120,294,358 - 20,295,804RGD
HuRef2120,572,766 - 20,574,212UniSTS
stSG607392  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,095,613 - 35,096,624UniSTSGRCh37
Build 362134,017,483 - 34,018,494RGDNCBI36
Celera2120,295,235 - 20,296,246RGD
HuRef2120,573,643 - 20,574,654UniSTS
stSG607393  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,096,605 - 35,097,957UniSTSGRCh37
Build 362134,018,475 - 34,019,827RGDNCBI36
Celera2120,296,227 - 20,297,579RGD
HuRef2120,574,635 - 20,575,987UniSTS
stSG607394  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,097,940 - 35,099,364UniSTSGRCh37
Build 362134,019,810 - 34,021,234RGDNCBI36
Celera2120,297,562 - 20,298,986RGD
HuRef2120,575,970 - 20,577,394UniSTS
stSG607395  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,098,775 - 35,099,898UniSTSGRCh37
Build 362134,020,645 - 34,021,768RGDNCBI36
Celera2120,298,397 - 20,299,520RGD
HuRef2120,576,805 - 20,577,928UniSTS
stSG607396  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,099,882 - 35,101,338UniSTSGRCh37
Build 362134,021,752 - 34,023,208RGDNCBI36
Celera2120,299,504 - 20,300,960RGD
HuRef2120,577,912 - 20,579,368UniSTS
stSG607398  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,103,590 - 35,104,877UniSTSGRCh37
Build 362134,025,460 - 34,026,747RGDNCBI36
Celera2120,303,212 - 20,304,499RGD
HuRef2120,581,621 - 20,582,908UniSTS
stSG607399  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,104,859 - 35,106,114UniSTSGRCh37
Build 362134,026,729 - 34,027,984RGDNCBI36
Celera2120,304,481 - 20,305,736RGD
HuRef2120,582,890 - 20,584,146UniSTS
stSG607400  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,106,095 - 35,107,459UniSTSGRCh37
Build 362134,027,965 - 34,029,329RGDNCBI36
Celera2120,305,717 - 20,307,081RGD
HuRef2120,584,127 - 20,585,491UniSTS
stSG607401  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,107,440 - 35,108,750UniSTSGRCh37
Build 362134,029,310 - 34,030,620RGDNCBI36
Celera2120,307,062 - 20,308,372RGD
HuRef2120,585,472 - 20,586,782UniSTS
stSG607403  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,109,823 - 35,111,046UniSTSGRCh37
Build 362134,031,693 - 34,032,916RGDNCBI36
Celera2120,309,445 - 20,310,668RGD
HuRef2120,587,856 - 20,589,079UniSTS
stSG607404  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,110,521 - 35,111,639UniSTSGRCh37
Build 362134,032,391 - 34,033,509RGDNCBI36
Celera2120,310,143 - 20,311,261RGD
HuRef2120,588,554 - 20,589,672UniSTS
stSG607405  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,111,622 - 35,112,972UniSTSGRCh37
Build 362134,033,492 - 34,034,842RGDNCBI36
Celera2120,311,244 - 20,312,594RGD
HuRef2120,589,655 - 20,591,005UniSTS
stSG607406  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,112,964 - 35,114,285UniSTSGRCh37
Build 362134,034,834 - 34,036,155RGDNCBI36
Celera2120,312,586 - 20,313,907RGD
HuRef2120,590,997 - 20,592,318UniSTS
stSG607407  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,114,266 - 35,115,427UniSTSGRCh37
Build 362134,036,136 - 34,037,297RGDNCBI36
Celera2120,313,888 - 20,315,049RGD
HuRef2120,592,299 - 20,593,460UniSTS
stSG607408  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,115,406 - 35,116,444UniSTSGRCh37
Build 362134,037,276 - 34,038,314RGDNCBI36
Celera2120,315,028 - 20,316,066RGD
HuRef2120,593,439 - 20,594,477UniSTS
stSG607409  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,116,428 - 35,117,710UniSTSGRCh37
Build 362134,038,298 - 34,039,580RGDNCBI36
Celera2120,316,050 - 20,317,332RGD
HuRef2120,594,461 - 20,595,743UniSTS
stSG607410  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,117,691 - 35,118,403UniSTSGRCh37
Build 362134,039,561 - 34,040,273RGDNCBI36
Celera2120,317,313 - 20,318,025RGD
HuRef2120,595,724 - 20,596,436UniSTS
stSG607411  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,121,197 - 35,122,432UniSTSGRCh37
Build 362134,043,067 - 34,044,302RGDNCBI36
Celera2120,320,819 - 20,322,054RGD
HuRef2120,599,230 - 20,600,464UniSTS
stSG607412  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,122,479 - 35,123,589UniSTSGRCh37
Build 362134,044,349 - 34,045,459RGDNCBI36
Celera2120,322,101 - 20,323,211RGD
HuRef2120,600,511 - 20,601,621UniSTS
stSG607413  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,123,589 - 35,124,799UniSTSGRCh37
Build 362134,045,459 - 34,046,669RGDNCBI36
Celera2120,323,211 - 20,324,421RGD
HuRef2120,601,621 - 20,602,831UniSTS
stSG607414  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,124,788 - 35,126,282UniSTSGRCh37
Build 362134,046,658 - 34,048,152RGDNCBI36
Celera2120,324,410 - 20,325,904RGD
HuRef2120,602,820 - 20,604,314UniSTS
stSG607415  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,126,449 - 35,127,606UniSTSGRCh37
Build 362134,048,319 - 34,049,476RGDNCBI36
Celera2120,326,071 - 20,327,228RGD
HuRef2120,604,481 - 20,605,638UniSTS
stSG607416  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,127,587 - 35,128,754UniSTSGRCh37
Build 362134,049,457 - 34,050,624RGDNCBI36
Celera2120,327,209 - 20,328,376RGD
HuRef2120,605,619 - 20,606,786UniSTS
stSG607417  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,128,754 - 35,129,952UniSTSGRCh37
Build 362134,050,624 - 34,051,822RGDNCBI36
Celera2120,328,376 - 20,329,574RGD
HuRef2120,606,786 - 20,607,984UniSTS
stSG607419  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,130,925 - 35,131,995UniSTSGRCh37
Build 362134,052,795 - 34,053,865RGDNCBI36
Celera2120,330,547 - 20,331,617RGD
HuRef2120,608,957 - 20,610,027UniSTS
stSG607420  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,131,977 - 35,133,136UniSTSGRCh37
Build 362134,053,847 - 34,055,006RGDNCBI36
Celera2120,331,599 - 20,332,758RGD
HuRef2120,610,009 - 20,611,168UniSTS
stSG607421  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,133,117 - 35,134,166UniSTSGRCh37
Build 362134,054,987 - 34,056,036RGDNCBI36
Celera2120,332,739 - 20,333,788RGD
HuRef2120,611,149 - 20,612,199UniSTS
stSG607422  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,134,147 - 35,135,515UniSTSGRCh37
Build 362134,056,017 - 34,057,385RGDNCBI36
Celera2120,333,769 - 20,335,137RGD
HuRef2120,612,180 - 20,613,548UniSTS
stSG607423  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,135,496 - 35,136,729UniSTSGRCh37
Build 362134,057,366 - 34,058,599RGDNCBI36
Celera2120,335,118 - 20,336,351RGD
HuRef2120,613,529 - 20,614,762UniSTS
stSG607424  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,136,710 - 35,137,809UniSTSGRCh37
Build 362134,058,580 - 34,059,679RGDNCBI36
Celera2120,336,332 - 20,337,431RGD
HuRef2120,614,743 - 20,615,842UniSTS
stSG607425  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,137,790 - 35,139,043UniSTSGRCh37
Build 362134,059,660 - 34,060,913RGDNCBI36
Celera2120,337,412 - 20,338,665RGD
HuRef2120,615,823 - 20,617,076UniSTS
stSG607426  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,139,030 - 35,140,032UniSTSGRCh37
Build 362134,060,900 - 34,061,902RGDNCBI36
Celera2120,338,652 - 20,339,654RGD
HuRef2120,617,063 - 20,618,065UniSTS
stSG607427  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,140,013 - 35,141,442UniSTSGRCh37
Build 362134,061,883 - 34,063,312RGDNCBI36
Celera2120,339,635 - 20,341,064RGD
HuRef2120,618,046 - 20,619,475UniSTS
stSG607428  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,143,406 - 35,144,432UniSTSGRCh37
Build 362134,065,276 - 34,066,302RGDNCBI36
Celera2120,343,028 - 20,344,054RGD
HuRef2120,621,439 - 20,622,465UniSTS
stSG607429  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,144,413 - 35,145,670UniSTSGRCh37
Build 362134,066,283 - 34,067,540RGDNCBI36
Celera2120,344,035 - 20,345,292RGD
HuRef2120,622,446 - 20,623,703UniSTS
stSG607430  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,145,649 - 35,147,069UniSTSGRCh37
Build 362134,067,519 - 34,068,939RGDNCBI36
Celera2120,345,271 - 20,346,691RGD
HuRef2120,623,682 - 20,625,102UniSTS
stSG607431  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,147,062 - 35,148,236UniSTSGRCh37
Build 362134,068,932 - 34,070,106RGDNCBI36
Celera2120,346,684 - 20,347,858RGD
HuRef2120,625,095 - 20,626,269UniSTS
stSG607432  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,152,069 - 35,153,155UniSTSGRCh37
Build 362134,073,939 - 34,075,025RGDNCBI36
Celera2120,351,691 - 20,352,777RGD
HuRef2120,630,102 - 20,631,188UniSTS
stSG607433  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,153,136 - 35,154,467UniSTSGRCh37
Build 362134,075,006 - 34,076,337RGDNCBI36
Celera2120,352,758 - 20,354,089RGD
HuRef2120,631,169 - 20,632,500UniSTS
stSG607434  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,154,448 - 35,155,735UniSTSGRCh37
Build 362134,076,318 - 34,077,605RGDNCBI36
Celera2120,354,070 - 20,355,357RGD
HuRef2120,632,481 - 20,633,768UniSTS
stSG607435  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,156,018 - 35,157,235UniSTSGRCh37
Build 362134,077,888 - 34,079,105RGDNCBI36
Celera2120,355,640 - 20,356,857RGD
HuRef2120,634,050 - 20,635,277UniSTS
stSG607436  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,157,216 - 35,158,330UniSTSGRCh37
Build 362134,079,086 - 34,080,200RGDNCBI36
Celera2120,356,838 - 20,357,952RGD
HuRef2120,635,258 - 20,636,372UniSTS
stSG607437  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,158,311 - 35,159,552UniSTSGRCh37
Build 362134,080,181 - 34,081,422RGDNCBI36
Celera2120,357,933 - 20,359,174RGD
HuRef2120,636,353 - 20,637,554UniSTS
stSG607438  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,159,560 - 35,160,600UniSTSGRCh37
Build 362134,081,430 - 34,082,470RGDNCBI36
Celera2120,359,182 - 20,360,222RGD
HuRef2120,637,562 - 20,638,602UniSTS
stSG607439  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,160,595 - 35,161,798UniSTSGRCh37
Build 362134,082,465 - 34,083,668RGDNCBI36
Celera2120,360,217 - 20,361,420RGD
HuRef2120,638,597 - 20,639,800UniSTS
stSG607440  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,161,779 - 35,163,114UniSTSGRCh37
Build 362134,083,649 - 34,084,984RGDNCBI36
Celera2120,361,401 - 20,362,736RGD
HuRef2120,639,781 - 20,641,112UniSTS
stSG607441  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,163,095 - 35,164,095UniSTSGRCh37
Build 362134,084,965 - 34,085,965RGDNCBI36
Celera2120,362,717 - 20,363,717RGD
HuRef2120,641,093 - 20,642,093UniSTS
stSG607442  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,164,077 - 35,165,560UniSTSGRCh37
Build 362134,085,947 - 34,087,430RGDNCBI36
Celera2120,363,699 - 20,365,182RGD
HuRef2120,642,075 - 20,643,558UniSTS
stSG607443  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,165,541 - 35,166,849UniSTSGRCh37
Build 362134,087,411 - 34,088,719RGDNCBI36
Celera2120,365,163 - 20,366,471RGD
HuRef2120,643,539 - 20,644,847UniSTS
stSG607444  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,166,830 - 35,168,009UniSTSGRCh37
Build 362134,088,700 - 34,089,879RGDNCBI36
Celera2120,366,452 - 20,367,631RGD
HuRef2120,644,828 - 20,646,007UniSTS
stSG607445  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,167,990 - 35,169,285UniSTSGRCh37
Build 362134,089,860 - 34,091,155RGDNCBI36
Celera2120,367,612 - 20,368,907RGD
HuRef2120,645,988 - 20,647,284UniSTS
stSG607446  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,169,268 - 35,170,328UniSTSGRCh37
Build 362134,091,138 - 34,092,198RGDNCBI36
Celera2120,368,890 - 20,369,950RGD
HuRef2120,647,267 - 20,648,327UniSTS
stSG607447  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,170,311 - 35,171,359UniSTSGRCh37
Build 362134,092,181 - 34,093,229RGDNCBI36
Celera2120,369,933 - 20,370,981RGD
HuRef2120,648,310 - 20,649,358UniSTS
stSG607448  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,171,340 - 35,172,714UniSTSGRCh37
Build 362134,093,210 - 34,094,584RGDNCBI36
Celera2120,370,962 - 20,372,336RGD
HuRef2120,649,339 - 20,650,713UniSTS
stSG607449  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,172,695 - 35,173,759UniSTSGRCh37
Build 362134,094,565 - 34,095,629RGDNCBI36
Celera2120,372,317 - 20,373,381RGD
HuRef2120,650,694 - 20,651,759UniSTS
stSG607450  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,173,740 - 35,175,009UniSTSGRCh37
Build 362134,095,610 - 34,096,879RGDNCBI36
Celera2120,373,362 - 20,374,631RGD
HuRef2120,651,740 - 20,653,009UniSTS
stSG607451  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,174,990 - 35,176,182UniSTSGRCh37
Build 362134,096,860 - 34,098,052RGDNCBI36
Celera2120,374,612 - 20,375,804RGD
HuRef2120,652,990 - 20,654,182UniSTS
stSG607452  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,176,163 - 35,177,460UniSTSGRCh37
Build 362134,098,033 - 34,099,330RGDNCBI36
Celera2120,375,785 - 20,377,082RGD
HuRef2120,654,163 - 20,655,460UniSTS
stSG607453  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,177,447 - 35,178,860UniSTSGRCh37
Build 362134,099,317 - 34,100,730RGDNCBI36
Celera2120,377,069 - 20,378,482RGD
HuRef2120,655,447 - 20,656,923UniSTS
stSG607454  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,178,841 - 35,180,137UniSTSGRCh37
Build 362134,100,711 - 34,102,007RGDNCBI36
Celera2120,378,463 - 20,379,759RGD
HuRef2120,656,904 - 20,658,200UniSTS
stSG607455  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,180,125 - 35,181,448UniSTSGRCh37
Build 362134,101,995 - 34,103,318RGDNCBI36
Celera2120,379,747 - 20,381,070RGD
HuRef2120,658,188 - 20,659,511UniSTS
stSG607456  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,181,429 - 35,182,775UniSTSGRCh37
Build 362134,103,299 - 34,104,645RGDNCBI36
Celera2120,381,051 - 20,382,397RGD
HuRef2120,659,492 - 20,660,838UniSTS
stSG607457  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,182,766 - 35,184,072UniSTSGRCh37
Build 362134,104,636 - 34,105,942RGDNCBI36
Celera2120,382,388 - 20,383,694RGD
HuRef2120,660,829 - 20,662,135UniSTS
stSG607458  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,184,050 - 35,185,353UniSTSGRCh37
Build 362134,105,920 - 34,107,223RGDNCBI36
Celera2120,383,672 - 20,384,975RGD
HuRef2120,662,113 - 20,663,416UniSTS
stSG607460  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,186,449 - 35,187,458UniSTSGRCh37
Build 362134,108,319 - 34,109,328RGDNCBI36
Celera2120,386,071 - 20,387,080RGD
HuRef2120,664,512 - 20,665,521UniSTS
stSG607461  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,187,468 - 35,188,941UniSTSGRCh37
Build 362134,109,338 - 34,110,811RGDNCBI36
Celera2120,387,090 - 20,388,563RGD
HuRef2120,665,531 - 20,666,962UniSTS
stSG607463  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,190,451 - 35,191,642UniSTSGRCh37
Build 362134,112,321 - 34,113,512RGDNCBI36
Celera2120,390,073 - 20,391,264RGD
HuRef2120,668,472 - 20,669,663UniSTS
stSG607464  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,191,626 - 35,192,643UniSTSGRCh37
Build 362134,113,496 - 34,114,513RGDNCBI36
Celera2120,391,248 - 20,392,265RGD
HuRef2120,669,647 - 20,670,664UniSTS
stSG607465  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,192,627 - 35,193,983UniSTSGRCh37
Build 362134,114,497 - 34,115,853RGDNCBI36
Celera2120,392,249 - 20,393,605RGD
HuRef2120,670,648 - 20,672,003UniSTS
stSG607466  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,193,964 - 35,195,387UniSTSGRCh37
Build 362134,115,834 - 34,117,257RGDNCBI36
Celera2120,393,586 - 20,395,009RGD
HuRef2120,671,984 - 20,673,407UniSTS
stSG607467  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,195,367 - 35,195,547UniSTSGRCh37
Build 362134,117,237 - 34,117,417RGDNCBI36
Celera2120,394,989 - 20,395,169RGD
HuRef2120,673,387 - 20,673,567UniSTS
stSG607468  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,195,551 - 35,196,877UniSTSGRCh37
Build 362134,117,421 - 34,118,747RGDNCBI36
Celera2120,395,173 - 20,396,499RGD
HuRef2120,673,571 - 20,674,897UniSTS
stSG607469  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,196,858 - 35,197,951UniSTSGRCh37
Build 362134,118,728 - 34,119,821RGDNCBI36
Celera2120,396,480 - 20,397,573RGD
HuRef2120,674,878 - 20,675,971UniSTS
stSG607470  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,197,936 - 35,199,239UniSTSGRCh37
Build 362134,119,806 - 34,121,109RGDNCBI36
Celera2120,397,558 - 20,398,861RGD
HuRef2120,675,956 - 20,677,259UniSTS
stSG607471  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,199,220 - 35,200,649UniSTSGRCh37
Build 362134,121,090 - 34,122,519RGDNCBI36
Celera2120,398,842 - 20,400,271RGD
HuRef2120,677,240 - 20,678,669UniSTS
stSG607472  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,200,645 - 35,201,695UniSTSGRCh37
Build 362134,122,515 - 34,123,565RGDNCBI36
Celera2120,400,267 - 20,401,317RGD
HuRef2120,678,665 - 20,679,715UniSTS
stSG607473  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,201,533 - 35,202,570UniSTSGRCh37
Build 362134,123,403 - 34,124,440RGDNCBI36
Celera2120,401,155 - 20,402,192RGD
HuRef2120,679,553 - 20,680,590UniSTS
stSG607474  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,202,549 - 35,204,019UniSTSGRCh37
Build 362134,124,419 - 34,125,889RGDNCBI36
Celera2120,402,171 - 20,403,641RGD
HuRef2120,680,569 - 20,682,039UniSTS
stSG607475  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,204,000 - 35,205,154UniSTSGRCh37
Build 362134,125,870 - 34,127,024RGDNCBI36
Celera2120,403,622 - 20,404,776RGD
HuRef2120,682,020 - 20,683,174UniSTS
stSG607477  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,206,414 - 35,206,650UniSTSGRCh37
Build 362134,128,284 - 34,128,520RGDNCBI36
Celera2120,406,036 - 20,406,272RGD
HuRef2120,684,434 - 20,684,670UniSTS
stSG607478  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,206,659 - 35,207,659UniSTSGRCh37
Build 362134,128,529 - 34,129,529RGDNCBI36
Celera2120,406,281 - 20,407,281RGD
HuRef2120,684,679 - 20,685,805UniSTS
stSG607479  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,207,640 - 35,209,006UniSTSGRCh37
Build 362134,129,510 - 34,130,876RGDNCBI36
Celera2120,407,262 - 20,408,628RGD
HuRef2120,685,786 - 20,687,152UniSTS
stSG607480  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,208,990 - 35,210,066UniSTSGRCh37
Build 362134,130,860 - 34,131,936RGDNCBI36
Celera2120,408,612 - 20,409,688RGD
HuRef2120,687,136 - 20,688,212UniSTS
stSG607481  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,210,047 - 35,211,142UniSTSGRCh37
Build 362134,131,917 - 34,133,012RGDNCBI36
Celera2120,409,669 - 20,410,764RGD
HuRef2120,688,193 - 20,689,288UniSTS
stSG607482  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,211,123 - 35,212,347UniSTSGRCh37
Build 362134,132,993 - 34,134,217RGDNCBI36
Celera2120,410,745 - 20,411,969RGD
HuRef2120,689,269 - 20,690,493UniSTS
stSG607483  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,212,328 - 35,213,686UniSTSGRCh37
Build 362134,134,198 - 34,135,556RGDNCBI36
Celera2120,411,950 - 20,413,308RGD
HuRef2120,690,474 - 20,691,832UniSTS
stSG607485  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,214,798 - 35,215,893UniSTSGRCh37
Build 362134,136,668 - 34,137,763RGDNCBI36
Celera2120,414,420 - 20,415,515RGD
HuRef2120,692,944 - 20,694,039UniSTS
stSG607486  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,215,874 - 35,216,967UniSTSGRCh37
Build 362134,137,744 - 34,138,837RGDNCBI36
Celera2120,415,496 - 20,416,589RGD
HuRef2120,694,020 - 20,695,113UniSTS
stSG607487  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,216,967 - 35,218,013UniSTSGRCh37
Build 362134,138,837 - 34,139,883RGDNCBI36
Celera2120,416,589 - 20,417,635RGD
HuRef2120,695,113 - 20,696,159UniSTS
stSG607488  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,218,039 - 35,219,148UniSTSGRCh37
Build 362134,139,909 - 34,141,018RGDNCBI36
Celera2120,417,661 - 20,418,770RGD
HuRef2120,696,185 - 20,697,294UniSTS
stSG607489  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,219,132 - 35,220,160UniSTSGRCh37
Build 362134,141,002 - 34,142,030RGDNCBI36
Celera2120,418,754 - 20,419,782RGD
HuRef2120,697,278 - 20,698,306UniSTS
stSG607490  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,220,143 - 35,221,203UniSTSGRCh37
Build 362134,142,013 - 34,143,073RGDNCBI36
Celera2120,419,765 - 20,420,825RGD
HuRef2120,698,289 - 20,699,349UniSTS
stSG607491  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,221,187 - 35,222,272UniSTSGRCh37
Build 362134,143,057 - 34,144,142RGDNCBI36
Celera2120,420,809 - 20,421,894RGD
HuRef2120,699,333 - 20,700,418UniSTS
stSG607492  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,222,253 - 35,223,407UniSTSGRCh37
Build 362134,144,123 - 34,145,277RGDNCBI36
Celera2120,421,875 - 20,423,029RGD
HuRef2120,700,399 - 20,701,553UniSTS
stSG607494  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,224,675 - 35,226,172UniSTSGRCh37
Build 362134,146,545 - 34,148,042RGDNCBI36
Celera2120,424,298 - 20,425,795RGD
HuRef2120,702,822 - 20,704,319UniSTS
stSG607495  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,226,174 - 35,227,208UniSTSGRCh37
Build 362134,148,044 - 34,149,078RGDNCBI36
Celera2120,425,797 - 20,426,831RGD
HuRef2120,704,321 - 20,705,355UniSTS
stSG607496  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,227,189 - 35,228,263UniSTSGRCh37
Build 362134,149,059 - 34,150,133RGDNCBI36
Celera2120,426,812 - 20,427,886RGD
HuRef2120,705,336 - 20,706,410UniSTS
stSG607497  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,228,448 - 35,229,580UniSTSGRCh37
Build 362134,150,318 - 34,151,450RGDNCBI36
Celera2120,428,071 - 20,429,203RGD
HuRef2120,706,595 - 20,707,725UniSTS
stSG607498  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,229,573 - 35,229,808UniSTSGRCh37
Build 362134,151,443 - 34,151,678RGDNCBI36
Celera2120,429,196 - 20,429,431RGD
HuRef2120,707,718 - 20,707,953UniSTS
stSG607499  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,229,809 - 35,230,891UniSTSGRCh37
Build 362134,151,679 - 34,152,761RGDNCBI36
Celera2120,429,432 - 20,430,514RGD
HuRef2120,707,954 - 20,709,036UniSTS
stSG607500  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,230,872 - 35,232,079UniSTSGRCh37
Build 362134,152,742 - 34,153,949RGDNCBI36
Celera2120,430,495 - 20,431,702RGD
HuRef2120,709,017 - 20,710,225UniSTS
stSG607501  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,232,060 - 35,233,203UniSTSGRCh37
Build 362134,153,930 - 34,155,073RGDNCBI36
Celera2120,431,683 - 20,432,826RGD
HuRef2120,710,206 - 20,711,349UniSTS
stSG607502  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,233,184 - 35,234,517UniSTSGRCh37
Build 362134,155,054 - 34,156,387RGDNCBI36
Celera2120,432,807 - 20,434,140RGD
stSG607505  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,236,552 - 35,238,013UniSTSGRCh37
Build 362134,158,422 - 34,159,883RGDNCBI36
Celera2120,436,175 - 20,437,636RGD
HuRef2120,714,698 - 20,716,159UniSTS
stSG607506  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,237,994 - 35,239,004UniSTSGRCh37
Build 362134,159,864 - 34,160,874RGDNCBI36
Celera2120,437,617 - 20,438,627RGD
HuRef2120,716,140 - 20,717,150UniSTS
stSG607510  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,242,392 - 35,243,657UniSTSGRCh37
Build 362134,164,262 - 34,165,527RGDNCBI36
Celera2120,442,014 - 20,443,279RGD
HuRef2120,720,537 - 20,721,802UniSTS
stSG607511  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,243,656 - 35,244,663UniSTSGRCh37
Build 362134,165,526 - 34,166,533RGDNCBI36
Celera2120,443,278 - 20,444,285RGD
HuRef2120,721,801 - 20,722,808UniSTS
stSG607512  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,244,652 - 35,245,652UniSTSGRCh37
Build 362134,166,522 - 34,167,522RGDNCBI36
Celera2120,444,274 - 20,445,274RGD
HuRef2120,722,797 - 20,723,797UniSTS
stSG607513  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,245,633 - 35,246,853UniSTSGRCh37
Build 362134,167,503 - 34,168,723RGDNCBI36
Celera2120,445,255 - 20,446,475RGD
HuRef2120,723,778 - 20,724,998UniSTS
stSG607515  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,247,619 - 35,248,629UniSTSGRCh37
Build 362134,169,489 - 34,170,499RGDNCBI36
Celera2120,447,241 - 20,448,213RGD
HuRef2120,725,767 - 20,726,698UniSTS
stSG607517  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,249,757 - 35,250,967UniSTSGRCh37
Build 362134,171,627 - 34,172,837RGDNCBI36
Celera2120,449,341 - 20,450,551RGD
HuRef2120,727,839 - 20,729,031UniSTS
stSG607518  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,250,948 - 35,251,968UniSTSGRCh37
Build 362134,172,818 - 34,173,838RGDNCBI36
Celera2120,450,532 - 20,451,552RGD
HuRef2120,729,012 - 20,730,032UniSTS
stSG607519  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,251,949 - 35,253,045UniSTSGRCh37
Build 362134,173,819 - 34,174,915RGDNCBI36
Celera2120,451,533 - 20,452,629RGD
HuRef2120,730,013 - 20,731,109UniSTS
stSG607520  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,253,026 - 35,254,321UniSTSGRCh37
Build 362134,174,896 - 34,176,191RGDNCBI36
Celera2120,452,610 - 20,453,905RGD
HuRef2120,731,090 - 20,732,385UniSTS
stSG607521  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,254,304 - 35,254,488UniSTSGRCh37
Build 362134,176,174 - 34,176,358RGDNCBI36
Celera2120,453,888 - 20,454,072RGD
HuRef2120,732,368 - 20,732,552UniSTS
stSG607522  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,254,489 - 35,255,804UniSTSGRCh37
Build 362134,176,359 - 34,177,674RGDNCBI36
Celera2120,454,073 - 20,455,388RGD
HuRef2120,732,553 - 20,733,868UniSTS
stSG607523  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,255,881 - 35,256,994UniSTSGRCh37
Build 362134,177,751 - 34,178,864RGDNCBI36
Celera2120,455,465 - 20,456,578RGD
HuRef2120,733,945 - 20,735,059UniSTS
stSG607524  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,256,975 - 35,258,033UniSTSGRCh37
Build 362134,178,845 - 34,179,903RGDNCBI36
Celera2120,456,559 - 20,457,617RGD
HuRef2120,735,040 - 20,736,098UniSTS
stSG607525  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,258,014 - 35,259,051UniSTSGRCh37
Build 362134,179,884 - 34,180,921RGDNCBI36
Celera2120,457,598 - 20,458,635RGD
HuRef2120,736,079 - 20,737,116UniSTS
stSG607526  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,259,032 - 35,260,295UniSTSGRCh37
Build 362134,180,902 - 34,182,165RGDNCBI36
Celera2120,458,616 - 20,459,879RGD
HuRef2120,737,097 - 20,738,362UniSTS
stSG607527  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,260,277 - 35,261,686UniSTSGRCh37
Build 362134,182,147 - 34,183,556RGDNCBI36
Celera2120,459,861 - 20,461,270RGD
HuRef2120,738,344 - 20,739,745UniSTS
ITSN1_8621  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,209,995 - 35,210,774UniSTSGRCh37
Build 362134,131,865 - 34,132,644RGDNCBI36
Celera2120,409,617 - 20,410,396RGD
HuRef2120,688,141 - 20,688,920UniSTS
D21S1975  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,249,182 - 35,249,327UniSTSGRCh37
Build 362134,171,052 - 34,171,197RGDNCBI36
Celera2120,448,766 - 20,448,911RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,727,251 - 20,727,396UniSTS
TNG Radiation Hybrid Map2111922.0UniSTS
SHGC-87604  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,148,415 - 35,148,540UniSTSGRCh37
Build 362134,070,285 - 34,070,410RGDNCBI36
Celera2120,348,037 - 20,348,162RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,626,448 - 20,626,573UniSTS
TNG Radiation Hybrid Map2111838.0UniSTS
GeneMap99-GB4 RH Map21176.9UniSTS
NCBI RH Map21261.9UniSTS
STS-F02358  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,210,471 - 35,210,693UniSTSGRCh37
Build 362134,132,341 - 34,132,563RGDNCBI36
Celera2120,410,093 - 20,410,315RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,688,617 - 20,688,839UniSTS
GeneMap99-GB4 RH Map21154.82UniSTS
NCBI RH Map21246.2UniSTS
SHGC-51824  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,250,840 - 35,250,967UniSTSGRCh37
Build 362134,172,710 - 34,172,837RGDNCBI36
Celera2120,450,424 - 20,450,551RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,728,904 - 20,729,031UniSTS
TNG Radiation Hybrid Map2111926.0UniSTS
SHGC-87572  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,127,204 - 35,127,363UniSTSGRCh37
Build 362134,049,074 - 34,049,233RGDNCBI36
Celera2120,326,826 - 20,326,985RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,605,236 - 20,605,395UniSTS
TNG Radiation Hybrid Map2111825.0UniSTS
GeneMap99-GB4 RH Map21157.95UniSTS
NCBI RH Map21258.5UniSTS
RH16546  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,118,531 - 35,118,715UniSTSGRCh37
Build 362134,040,401 - 34,040,585RGDNCBI36
Celera2120,318,153 - 20,318,337RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,596,564 - 20,596,748UniSTS
GeneMap99-GB4 RH Map21157.95UniSTS
NCBI RH Map21258.5UniSTS
SHGC-51883  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,047,906 - 35,048,025UniSTSGRCh37
Build 362133,969,776 - 33,969,895RGDNCBI36
Celera2120,247,527 - 20,247,646RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,526,234 - 20,526,353UniSTS
TNG Radiation Hybrid Map2111765.0UniSTS
SHGC-37625  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372135,200,140 - 35,200,240UniSTSGRCh37
Build 362134,122,010 - 34,122,110RGDNCBI36
Celera2120,399,762 - 20,399,862RGD
Cytogenetic Map21q22.1-q22.2UniSTS
HuRef2120,678,160 - 20,678,260UniSTS
TNG Radiation Hybrid Map2111866.0UniSTS
Stanford-G3 RH Map21903.0UniSTS
NCBI RH Map21255.0UniSTS
GeneMap99-G3 RH Map21903.0UniSTS
D21S1254  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map21q22.1-q22.2UniSTS
TNG Radiation Hybrid Map2111773.0UniSTS
Stanford-G3 RH Map21872.0UniSTS
NCBI RH Map21248.9UniSTS
GeneMap99-G3 RH Map21872.0UniSTS
D21S235  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map21q22.1-q22.2UniSTS
D21S235  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map21q22.1-q22.2UniSTS


Expression


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

alimentary part of gastrointestinal system circulatory system endocrine system exocrine system hemolymphoid system hepatobiliary system integumental system musculoskeletal system nervous system renal system reproductive system respiratory system sensory system visual system adipose tissue appendage entire extraembryonic component pharyngeal arch
High
Medium 94 671 63 30 20 33 1719 56 1614 63 401 128 4 1025 906 3
Low 2344 1897 1663 594 1231 432 2636 2099 2120 356 1057 1483 170 1 179 1882 3 2
Below cutoff 422 699 1 41 2 2

Sequence

Nucleotide Sequences
RefSeq Transcripts NG_029504 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001001132 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001331008 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001331009 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001331010 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001331011 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001331012 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_003024 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011529692 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011529693 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017028428 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017028429 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017028430 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017028431 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017028432 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017028433 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017028434 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017028435 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017028436 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017028437 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017028438 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017028440 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017028441 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047440943 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047440944 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047440945 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047440946 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047440947 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047440948 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047440949 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047440950 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047440951 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054324760 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054324761 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054324762 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054324763 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054324764 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054324765 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054324766 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054324767 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054324768 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054324769 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054324770 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054324771 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054324772 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054324773 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054324774 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054324775 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054324776 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054324777 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054324778 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054324779 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054324780 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054324781 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054324782 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054324783 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_001754889 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_001754890 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_244289 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AF064243 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF064244 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF085873 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF114487 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF114488 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF180522 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AH007026 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AI857585 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK027846 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK056104 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK074554 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK075290 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK300274 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AP000308 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AP000309 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AP000310 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AP000311 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AP000312 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AP000313 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AP001718 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AY138139 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AY254341 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AY340592 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AY340593 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AY603418 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AY603419 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AY605091 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AY605092 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AY639648 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AY639649 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AY639650 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AY639651 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AY639652 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AY639653 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC013578 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC020269 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC039036 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC058925 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC073744 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC116185 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC116186 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC117560 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BX538175 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BX648852 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471079 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068257 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CX163355 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DQ340865 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DQ386455 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DQ679754 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DQ679755 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DQ679756 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DQ679757 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  EU107386 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  EU117382 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  EU120733 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  EU120734 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  EU120735 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  EU120736 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  EU140799 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  EU140800 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  EU152331 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  EU191901 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  GU245887 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  GU939616 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  GU939617 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  GU939618 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  GU939621 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF457227 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF511399 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF511404 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  LS482389 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  U61166 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000379960   ⟹   ENSP00000369294
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2133,750,107 - 33,836,635 (+)Ensembl
RefSeq Acc Id: ENST00000381283   ⟹   ENSP00000370683
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2133,718,797 - 33,772,282 (+)Ensembl
RefSeq Acc Id: ENST00000381284   ⟹   ENSP00000370684
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2133,858,697 - 33,886,354 (+)Ensembl
RefSeq Acc Id: ENST00000381285   ⟹   ENSP00000370685
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2133,642,478 - 33,889,305 (+)Ensembl
RefSeq Acc Id: ENST00000381291   ⟹   ENSP00000370691
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2133,642,478 - 33,838,494 (+)Ensembl
RefSeq Acc Id: ENST00000381318   ⟹   ENSP00000370719
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2133,642,501 - 33,899,861 (+)Ensembl
RefSeq Acc Id: ENST00000399338   ⟹   ENSP00000382275
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2133,718,810 - 33,817,614 (+)Ensembl
RefSeq Acc Id: ENST00000399349   ⟹   ENSP00000382286
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2133,642,498 - 33,838,496 (+)Ensembl
RefSeq Acc Id: ENST00000399352   ⟹   ENSP00000382289
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2133,642,496 - 33,838,498 (+)Ensembl
RefSeq Acc Id: ENST00000399353   ⟹   ENSP00000382290
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2133,642,400 - 33,837,018 (+)Ensembl
RefSeq Acc Id: ENST00000399355   ⟹   ENSP00000382292
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2133,642,498 - 33,837,293 (+)Ensembl
RefSeq Acc Id: ENST00000399367   ⟹   ENSP00000382301
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2133,642,483 - 33,888,608 (+)Ensembl
RefSeq Acc Id: ENST00000415023   ⟹   ENSP00000409800
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2133,875,360 - 33,886,354 (+)Ensembl
RefSeq Acc Id: ENST00000419241   ⟹   ENSP00000415302
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2133,797,554 - 33,817,416 (+)Ensembl
RefSeq Acc Id: ENST00000420666   ⟹   ENSP00000408319
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2133,875,358 - 33,886,377 (+)Ensembl
RefSeq Acc Id: ENST00000428240
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2133,818,452 - 33,829,686 (+)Ensembl
RefSeq Acc Id: ENST00000437126   ⟹   ENSP00000413290
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2133,818,383 - 33,834,396 (+)Ensembl
RefSeq Acc Id: ENST00000440794   ⟹   ENSP00000396054
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2133,799,923 - 33,817,736 (+)Ensembl
RefSeq Acc Id: ENST00000444491   ⟹   ENSP00000400079
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2133,642,452 - 33,735,204 (+)Ensembl
RefSeq Acc Id: ENST00000451686   ⟹   ENSP00000407132
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2133,642,542 - 33,735,093 (+)Ensembl
RefSeq Acc Id: ENST00000456489   ⟹   ENSP00000411464
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2133,735,041 - 33,735,626 (+)Ensembl
RefSeq Acc Id: ENST00000462212
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2133,829,006 - 33,837,038 (+)Ensembl
RefSeq Acc Id: ENST00000465143
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2133,811,204 - 33,814,507 (+)Ensembl
RefSeq Acc Id: ENST00000470742
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2133,642,453 - 33,721,991 (+)Ensembl
RefSeq Acc Id: ENST00000472548
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2133,829,006 - 33,837,038 (+)Ensembl
RefSeq Acc Id: ENST00000474132
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2133,774,363 - 33,775,079 (+)Ensembl
RefSeq Acc Id: ENST00000475422
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2133,829,006 - 33,856,793 (+)Ensembl
RefSeq Acc Id: ENST00000479424
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2133,829,006 - 33,837,038 (+)Ensembl
RefSeq Acc Id: ENST00000487427
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2133,818,026 - 33,829,029 (+)Ensembl
RefSeq Acc Id: ENST00000488166
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2133,754,183 - 33,772,300 (+)Ensembl
RefSeq Acc Id: ENST00000489261
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2133,829,006 - 33,856,793 (+)Ensembl
RefSeq Acc Id: ENST00000495656
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2133,829,006 - 33,856,793 (+)Ensembl
RefSeq Acc Id: NM_001001132   ⟹   NP_001001132
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382133,642,501 - 33,838,498 (+)NCBI
GRCh372135,014,706 - 35,261,609 (+)NCBI
Build 362133,936,654 - 34,132,672 (+)NCBI Archive
HuRef2120,493,109 - 20,739,668 (+)ENTREZGENE
CHM1_12134,577,248 - 34,773,229 (+)NCBI
T2T-CHM13v2.02132,024,315 - 32,220,296 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001331008   ⟹   NP_001317937
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382133,642,501 - 33,838,498 (+)NCBI
T2T-CHM13v2.02132,024,315 - 32,220,296 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001331009   ⟹   NP_001317938
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382133,642,501 - 33,838,498 (+)NCBI
T2T-CHM13v2.02132,024,315 - 32,220,296 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001331010   ⟹   NP_001317939
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382133,642,501 - 33,899,861 (+)NCBI
T2T-CHM13v2.02132,024,315 - 32,281,564 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001331011   ⟹   NP_001317940
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382133,642,501 - 33,838,498 (+)NCBI
T2T-CHM13v2.02132,024,315 - 32,220,296 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001331012   ⟹   NP_001317941
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382133,642,501 - 33,838,498 (+)NCBI
T2T-CHM13v2.02132,024,315 - 32,220,296 (+)NCBI
Sequence:
RefSeq Acc Id: NM_003024   ⟹   NP_003015
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382133,642,501 - 33,899,861 (+)NCBI
GRCh372135,014,706 - 35,261,609 (+)NCBI
Build 362133,936,654 - 34,183,479 (+)NCBI Archive
HuRef2120,493,109 - 20,739,668 (+)ENTREZGENE
CHM1_12134,577,248 - 34,824,084 (+)NCBI
T2T-CHM13v2.02132,024,315 - 32,281,564 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011529692   ⟹   XP_011527994
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382133,642,501 - 33,838,498 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011529693   ⟹   XP_011527995
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382133,642,501 - 33,817,736 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017028428   ⟹   XP_016883917
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382133,642,501 - 33,899,861 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017028429   ⟹   XP_016883918
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382133,642,501 - 33,899,861 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017028430   ⟹   XP_016883919
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382133,642,501 - 33,899,861 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017028431   ⟹   XP_016883920
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382133,642,501 - 33,899,861 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017028432   ⟹   XP_016883921
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382133,642,501 - 33,899,861 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017028433   ⟹   XP_016883922
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382133,642,501 - 33,899,861 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017028434   ⟹   XP_016883923
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382133,642,501 - 33,899,861 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017028435   ⟹   XP_016883924
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382133,642,501 - 33,899,861 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017028436   ⟹   XP_016883925
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382133,642,501 - 33,899,861 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017028438   ⟹   XP_016883927
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382133,642,501 - 33,838,498 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017028440   ⟹   XP_016883929
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382133,642,501 - 33,838,498 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017028441   ⟹   XP_016883930
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382133,642,501 - 33,817,736 (+)NCBI
Sequence:
RefSeq Acc Id: XM_047440943   ⟹   XP_047296899
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382133,705,662 - 33,899,861 (+)NCBI
RefSeq Acc Id: XM_047440944   ⟹   XP_047296900
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382133,705,662 - 33,838,498 (+)NCBI
RefSeq Acc Id: XM_047440945   ⟹   XP_047296901
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382133,642,501 - 33,838,498 (+)NCBI
RefSeq Acc Id: XM_047440946   ⟹   XP_047296902
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382133,705,662 - 33,838,498 (+)NCBI
RefSeq Acc Id: XM_047440947   ⟹   XP_047296903
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382133,705,662 - 33,838,498 (+)NCBI
RefSeq Acc Id: XM_047440948   ⟹   XP_047296904
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382133,705,662 - 33,817,736 (+)NCBI
RefSeq Acc Id: XM_047440949   ⟹   XP_047296905
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382133,642,501 - 33,829,731 (+)NCBI
RefSeq Acc Id: XM_047440950   ⟹   XP_047296906
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382133,642,501 - 33,829,731 (+)NCBI
RefSeq Acc Id: XM_047440951   ⟹   XP_047296907
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382133,642,501 - 33,817,736 (+)NCBI
RefSeq Acc Id: XM_054324760   ⟹   XP_054180735
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.02132,024,315 - 32,281,564 (+)NCBI
RefSeq Acc Id: XM_054324761   ⟹   XP_054180736
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.02132,024,315 - 32,281,564 (+)NCBI
RefSeq Acc Id: XM_054324762   ⟹   XP_054180737
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.02132,024,315 - 32,281,564 (+)NCBI
RefSeq Acc Id: XM_054324763   ⟹   XP_054180738
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.02132,087,442 - 32,281,564 (+)NCBI
RefSeq Acc Id: XM_054324764   ⟹   XP_054180739
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.02132,024,315 - 32,281,564 (+)NCBI
RefSeq Acc Id: XM_054324765   ⟹   XP_054180740
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.02132,024,315 - 32,281,564 (+)NCBI
RefSeq Acc Id: XM_054324766   ⟹   XP_054180741
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.02132,024,315 - 32,281,564 (+)NCBI
RefSeq Acc Id: XM_054324767   ⟹   XP_054180742
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.02132,024,315 - 32,281,564 (+)NCBI
RefSeq Acc Id: XM_054324768   ⟹   XP_054180743
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.02132,024,315 - 32,281,564 (+)NCBI
RefSeq Acc Id: XM_054324769   ⟹   XP_054180744
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.02132,024,315 - 32,281,564 (+)NCBI
RefSeq Acc Id: XM_054324770   ⟹   XP_054180745
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.02132,087,442 - 32,220,296 (+)NCBI
RefSeq Acc Id: XM_054324771   ⟹   XP_054180746
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.02132,024,315 - 32,220,296 (+)NCBI
RefSeq Acc Id: XM_054324772   ⟹   XP_054180747
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.02132,147,735 - 32,281,564 (+)NCBI
RefSeq Acc Id: XM_054324773   ⟹   XP_054180748
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.02132,024,315 - 32,220,296 (+)NCBI
RefSeq Acc Id: XM_054324774   ⟹   XP_054180749
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.02132,087,442 - 32,220,296 (+)NCBI
RefSeq Acc Id: XM_054324775   ⟹   XP_054180750
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.02132,087,442 - 32,220,296 (+)NCBI
RefSeq Acc Id: XM_054324776   ⟹   XP_054180751
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.02132,024,315 - 32,220,296 (+)NCBI
RefSeq Acc Id: XM_054324777   ⟹   XP_054180752
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.02132,024,315 - 32,220,296 (+)NCBI
RefSeq Acc Id: XM_054324778   ⟹   XP_054180753
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.02132,024,315 - 32,200,115 (+)NCBI
RefSeq Acc Id: XM_054324779   ⟹   XP_054180754
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.02132,024,315 - 32,200,115 (+)NCBI
RefSeq Acc Id: XM_054324780   ⟹   XP_054180755
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.02132,087,442 - 32,200,115 (+)NCBI
RefSeq Acc Id: XM_054324781   ⟹   XP_054180756
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.02132,024,315 - 32,211,529 (+)NCBI
RefSeq Acc Id: XM_054324782   ⟹   XP_054180757
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.02132,024,315 - 32,211,529 (+)NCBI
RefSeq Acc Id: XM_054324783   ⟹   XP_054180758
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.02132,024,315 - 32,200,115 (+)NCBI
Protein Sequences
Protein RefSeqs NP_001001132 (Get FASTA)   NCBI Sequence Viewer  
  NP_001317937 (Get FASTA)   NCBI Sequence Viewer  
  NP_001317938 (Get FASTA)   NCBI Sequence Viewer  
  NP_001317939 (Get FASTA)   NCBI Sequence Viewer  
  NP_001317940 (Get FASTA)   NCBI Sequence Viewer  
  NP_001317941 (Get FASTA)   NCBI Sequence Viewer  
  NP_003015 (Get FASTA)   NCBI Sequence Viewer  
  XP_011527994 (Get FASTA)   NCBI Sequence Viewer  
  XP_011527995 (Get FASTA)   NCBI Sequence Viewer  
  XP_016883917 (Get FASTA)   NCBI Sequence Viewer  
  XP_016883918 (Get FASTA)   NCBI Sequence Viewer  
  XP_016883919 (Get FASTA)   NCBI Sequence Viewer  
  XP_016883920 (Get FASTA)   NCBI Sequence Viewer  
  XP_016883921 (Get FASTA)   NCBI Sequence Viewer  
  XP_016883922 (Get FASTA)   NCBI Sequence Viewer  
  XP_016883923 (Get FASTA)   NCBI Sequence Viewer  
  XP_016883924 (Get FASTA)   NCBI Sequence Viewer  
  XP_016883925 (Get FASTA)   NCBI Sequence Viewer  
  XP_016883927 (Get FASTA)   NCBI Sequence Viewer  
  XP_016883929 (Get FASTA)   NCBI Sequence Viewer  
  XP_016883930 (Get FASTA)   NCBI Sequence Viewer  
  XP_047296899 (Get FASTA)   NCBI Sequence Viewer  
  XP_047296900 (Get FASTA)   NCBI Sequence Viewer  
  XP_047296901 (Get FASTA)   NCBI Sequence Viewer  
  XP_047296902 (Get FASTA)   NCBI Sequence Viewer  
  XP_047296903 (Get FASTA)   NCBI Sequence Viewer  
  XP_047296904 (Get FASTA)   NCBI Sequence Viewer  
  XP_047296905 (Get FASTA)   NCBI Sequence Viewer  
  XP_047296906 (Get FASTA)   NCBI Sequence Viewer  
  XP_047296907 (Get FASTA)   NCBI Sequence Viewer  
  XP_054180735 (Get FASTA)   NCBI Sequence Viewer  
  XP_054180736 (Get FASTA)   NCBI Sequence Viewer  
  XP_054180737 (Get FASTA)   NCBI Sequence Viewer  
  XP_054180738 (Get FASTA)   NCBI Sequence Viewer  
  XP_054180739 (Get FASTA)   NCBI Sequence Viewer  
  XP_054180740 (Get FASTA)   NCBI Sequence Viewer  
  XP_054180741 (Get FASTA)   NCBI Sequence Viewer  
  XP_054180742 (Get FASTA)   NCBI Sequence Viewer  
  XP_054180743 (Get FASTA)   NCBI Sequence Viewer  
  XP_054180744 (Get FASTA)   NCBI Sequence Viewer  
  XP_054180745 (Get FASTA)   NCBI Sequence Viewer  
  XP_054180746 (Get FASTA)   NCBI Sequence Viewer  
  XP_054180747 (Get FASTA)   NCBI Sequence Viewer  
  XP_054180748 (Get FASTA)   NCBI Sequence Viewer  
  XP_054180749 (Get FASTA)   NCBI Sequence Viewer  
  XP_054180750 (Get FASTA)   NCBI Sequence Viewer  
  XP_054180751 (Get FASTA)   NCBI Sequence Viewer  
  XP_054180752 (Get FASTA)   NCBI Sequence Viewer  
  XP_054180753 (Get FASTA)   NCBI Sequence Viewer  
  XP_054180754 (Get FASTA)   NCBI Sequence Viewer  
  XP_054180755 (Get FASTA)   NCBI Sequence Viewer  
  XP_054180756 (Get FASTA)   NCBI Sequence Viewer  
  XP_054180757 (Get FASTA)   NCBI Sequence Viewer  
  XP_054180758 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAC50592 (Get FASTA)   NCBI Sequence Viewer  
  AAC78610 (Get FASTA)   NCBI Sequence Viewer  
  AAC78611 (Get FASTA)   NCBI Sequence Viewer  
  AAC80436 (Get FASTA)   NCBI Sequence Viewer  
  AAC80437 (Get FASTA)   NCBI Sequence Viewer  
  AAD29952 (Get FASTA)   NCBI Sequence Viewer  
  AAD29953 (Get FASTA)   NCBI Sequence Viewer  
  AAD53183 (Get FASTA)   NCBI Sequence Viewer  
  AAH39036 (Get FASTA)   NCBI Sequence Viewer  
  AAH58925 (Get FASTA)   NCBI Sequence Viewer  
  AAH73744 (Get FASTA)   NCBI Sequence Viewer  
  AAI16186 (Get FASTA)   NCBI Sequence Viewer  
  AAI16187 (Get FASTA)   NCBI Sequence Viewer  
  AAI17561 (Get FASTA)   NCBI Sequence Viewer  
  AAN11307 (Get FASTA)   NCBI Sequence Viewer  
  AAP13099 (Get FASTA)   NCBI Sequence Viewer  
  AAQ19991 (Get FASTA)   NCBI Sequence Viewer  
  AAQ19992 (Get FASTA)   NCBI Sequence Viewer  
  AAT28305 (Get FASTA)   NCBI Sequence Viewer  
  AAT28306 (Get FASTA)   NCBI Sequence Viewer  
  AAT36645 (Get FASTA)   NCBI Sequence Viewer  
  AAT36646 (Get FASTA)   NCBI Sequence Viewer  
  ABC69037 (Get FASTA)   NCBI Sequence Viewer  
  ABD72328 (Get FASTA)   NCBI Sequence Viewer  
  ABG74695 (Get FASTA)   NCBI Sequence Viewer  
  ABG74696 (Get FASTA)   NCBI Sequence Viewer  
  ABG74697 (Get FASTA)   NCBI Sequence Viewer  
  ABG74698 (Get FASTA)   NCBI Sequence Viewer  
  ABV03351 (Get FASTA)   NCBI Sequence Viewer  
  ABV21755 (Get FASTA)   NCBI Sequence Viewer  
  ABV24866 (Get FASTA)   NCBI Sequence Viewer  
  ABV24867 (Get FASTA)   NCBI Sequence Viewer  
  ABV24868 (Get FASTA)   NCBI Sequence Viewer  
  ABV24869 (Get FASTA)   NCBI Sequence Viewer  
  ABV58335 (Get FASTA)   NCBI Sequence Viewer  
  ABV58336 (Get FASTA)   NCBI Sequence Viewer  
  ABV69555 (Get FASTA)   NCBI Sequence Viewer  
  ABW71829 (Get FASTA)   NCBI Sequence Viewer  
  ADF97294 (Get FASTA)   NCBI Sequence Viewer  
  ADF97295 (Get FASTA)   NCBI Sequence Viewer  
  ADF97296 (Get FASTA)   NCBI Sequence Viewer  
  ADF97297 (Get FASTA)   NCBI Sequence Viewer  
  BAG62034 (Get FASTA)   NCBI Sequence Viewer  
  CAD98050 (Get FASTA)   NCBI Sequence Viewer  
  EAX09805 (Get FASTA)   NCBI Sequence Viewer  
  EAX09806 (Get FASTA)   NCBI Sequence Viewer  
  EAX09807 (Get FASTA)   NCBI Sequence Viewer  
  EAX09808 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000369294.6
  ENSP00000370683.3
  ENSP00000370684.3
  ENSP00000370685
  ENSP00000370685.5
  ENSP00000370691
  ENSP00000370691.4
  ENSP00000370719
  ENSP00000370719.3
  ENSP00000382275
  ENSP00000382275.4
  ENSP00000382286
  ENSP00000382286.1
  ENSP00000382289
  ENSP00000382289.1
  ENSP00000382290
  ENSP00000382290.1
  ENSP00000382292
  ENSP00000382292.2
  ENSP00000382301
  ENSP00000382301.3
  ENSP00000396054.1
  ENSP00000400079.1
  ENSP00000407132.1
  ENSP00000408319.1
  ENSP00000409800.1
  ENSP00000411464.1
  ENSP00000413290.1
  ENSP00000415302.1
GenBank Protein Q15811 (Get FASTA)   NCBI Sequence Viewer  
  SPT35766 (Get FASTA)   NCBI Sequence Viewer  
Reference Protein Sequences
RefSeq Acc Id: NP_003015   ⟸   NM_003024
- Peptide Label: isoform ITSN-l
- UniProtKB: Q9UNK2 (UniProtKB/Swiss-Prot),   Q9UNK1 (UniProtKB/Swiss-Prot),   Q9UK60 (UniProtKB/Swiss-Prot),   Q9UET5 (UniProtKB/Swiss-Prot),   Q20BK3 (UniProtKB/Swiss-Prot),   Q1ED40 (UniProtKB/Swiss-Prot),   Q14BD3 (UniProtKB/Swiss-Prot),   Q0PW97 (UniProtKB/Swiss-Prot),   Q0PW95 (UniProtKB/Swiss-Prot),   Q0PW94 (UniProtKB/Swiss-Prot),   O95216 (UniProtKB/Swiss-Prot),   E9PHV2 (UniProtKB/Swiss-Prot),   E9PG01 (UniProtKB/Swiss-Prot),   E9PE44 (UniProtKB/Swiss-Prot),   E7ERJ1 (UniProtKB/Swiss-Prot),   B4DTM2 (UniProtKB/Swiss-Prot),   A8DCP3 (UniProtKB/Swiss-Prot),   A8D7D0 (UniProtKB/Swiss-Prot),   A8CTY7 (UniProtKB/Swiss-Prot),   A8CTY3 (UniProtKB/Swiss-Prot),   A8CTX8 (UniProtKB/Swiss-Prot),   A7Y322 (UniProtKB/Swiss-Prot),   Q9UQ92 (UniProtKB/Swiss-Prot),   Q15811 (UniProtKB/Swiss-Prot),   Q14BD4 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001001132   ⟸   NM_001001132
- Peptide Label: isoform ITSN-s
- UniProtKB: Q0PW96 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_011527994   ⟸   XM_011529692
- Peptide Label: isoform X15
- UniProtKB: Q0PW96 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_011527995   ⟸   XM_011529693
- Peptide Label: isoform X17
- UniProtKB: A8CTZ0 (UniProtKB/TrEMBL),   E9PD98 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016883920   ⟸   XM_017028431
- Peptide Label: isoform X4
- UniProtKB: Q14BD4 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016883922   ⟸   XM_017028433
- Peptide Label: isoform X6
- UniProtKB: Q14BD4 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016883921   ⟸   XM_017028432
- Peptide Label: isoform X5
- UniProtKB: Q14BD4 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016883923   ⟸   XM_017028434
- Peptide Label: isoform X7
- UniProtKB: Q14BD4 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016883918   ⟸   XM_017028429
- Peptide Label: isoform X2
- UniProtKB: A0A2X0TVY8 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016883924   ⟸   XM_017028435
- Peptide Label: isoform X8
- UniProtKB: A0A2X0TVY8 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016883919   ⟸   XM_017028430
- Peptide Label: isoform X3
- UniProtKB: Q14BD4 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016883925   ⟸   XM_017028436
- Peptide Label: isoform X9
- UniProtKB: Q14BD4 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016883927   ⟸   XM_017028438
- Peptide Label: isoform X11
- UniProtKB: A7XZY7 (UniProtKB/TrEMBL),   Q0PW96 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016883929   ⟸   XM_017028440
- Peptide Label: isoform X14
- UniProtKB: Q0PW96 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016883930   ⟸   XM_017028441
- Peptide Label: isoform X16
- UniProtKB: A8CTZ0 (UniProtKB/TrEMBL),   E9PD98 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016883917   ⟸   XM_017028428
- Peptide Label: isoform X1
- UniProtKB: Q9UNK2 (UniProtKB/Swiss-Prot),   Q9UNK1 (UniProtKB/Swiss-Prot),   Q9UK60 (UniProtKB/Swiss-Prot),   Q9UET5 (UniProtKB/Swiss-Prot),   Q20BK3 (UniProtKB/Swiss-Prot),   Q1ED40 (UniProtKB/Swiss-Prot),   Q14BD3 (UniProtKB/Swiss-Prot),   Q0PW97 (UniProtKB/Swiss-Prot),   Q0PW95 (UniProtKB/Swiss-Prot),   Q0PW94 (UniProtKB/Swiss-Prot),   O95216 (UniProtKB/Swiss-Prot),   E9PHV2 (UniProtKB/Swiss-Prot),   E9PG01 (UniProtKB/Swiss-Prot),   E9PE44 (UniProtKB/Swiss-Prot),   E7ERJ1 (UniProtKB/Swiss-Prot),   B4DTM2 (UniProtKB/Swiss-Prot),   A8DCP3 (UniProtKB/Swiss-Prot),   A8D7D0 (UniProtKB/Swiss-Prot),   A8CTY7 (UniProtKB/Swiss-Prot),   A8CTY3 (UniProtKB/Swiss-Prot),   A8CTX8 (UniProtKB/Swiss-Prot),   A7Y322 (UniProtKB/Swiss-Prot),   Q9UQ92 (UniProtKB/Swiss-Prot),   Q15811 (UniProtKB/Swiss-Prot),   Q14BD4 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001317939   ⟸   NM_001331010
- Peptide Label: isoform 5
- UniProtKB: Q14BD4 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001317937   ⟸   NM_001331008
- Peptide Label: isoform 3
- UniProtKB: F8W7U0 (UniProtKB/TrEMBL),   Q0PW96 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001317938   ⟸   NM_001331009
- Peptide Label: isoform 4
- UniProtKB: Q0PW96 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001317940   ⟸   NM_001331011
- Peptide Label: isoform 6
- UniProtKB: Q0PW96 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001317941   ⟸   NM_001331012
- Peptide Label: isoform 7
- UniProtKB: Q0PW96 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: ENSP00000382286   ⟸   ENST00000399349
RefSeq Acc Id: ENSP00000382275   ⟸   ENST00000399338
RefSeq Acc Id: ENSP00000382301   ⟸   ENST00000399367
RefSeq Acc Id: ENSP00000382289   ⟸   ENST00000399352
RefSeq Acc Id: ENSP00000382290   ⟸   ENST00000399353
RefSeq Acc Id: ENSP00000382292   ⟸   ENST00000399355
RefSeq Acc Id: ENSP00000407132   ⟸   ENST00000451686
RefSeq Acc Id: ENSP00000396054   ⟸   ENST00000440794
RefSeq Acc Id: ENSP00000409800   ⟸   ENST00000415023
RefSeq Acc Id: ENSP00000411464   ⟸   ENST00000456489
RefSeq Acc Id: ENSP00000369294   ⟸   ENST00000379960
RefSeq Acc Id: ENSP00000415302   ⟸   ENST00000419241
RefSeq Acc Id: ENSP00000400079   ⟸   ENST00000444491
RefSeq Acc Id: ENSP00000408319   ⟸   ENST00000420666
RefSeq Acc Id: ENSP00000370719   ⟸   ENST00000381318
RefSeq Acc Id: ENSP00000370684   ⟸   ENST00000381284
RefSeq Acc Id: ENSP00000370685   ⟸   ENST00000381285
RefSeq Acc Id: ENSP00000370683   ⟸   ENST00000381283
RefSeq Acc Id: ENSP00000370691   ⟸   ENST00000381291
RefSeq Acc Id: ENSP00000413290   ⟸   ENST00000437126
RefSeq Acc Id: XP_047296901   ⟸   XM_047440945
- Peptide Label: isoform X10
RefSeq Acc Id: XP_047296905   ⟸   XM_047440949
- Peptide Label: isoform X18
RefSeq Acc Id: XP_047296906   ⟸   XM_047440950
- Peptide Label: isoform X19
RefSeq Acc Id: XP_047296907   ⟸   XM_047440951
- Peptide Label: isoform X20
RefSeq Acc Id: XP_047296899   ⟸   XM_047440943
- Peptide Label: isoform X3
RefSeq Acc Id: XP_047296900   ⟸   XM_047440944
- Peptide Label: isoform X10
RefSeq Acc Id: XP_047296903   ⟸   XM_047440947
- Peptide Label: isoform X13
RefSeq Acc Id: XP_047296902   ⟸   XM_047440946
- Peptide Label: isoform X12
RefSeq Acc Id: XP_047296904   ⟸   XM_047440948
- Peptide Label: isoform X17
RefSeq Acc Id: XP_054180735   ⟸   XM_054324760
- Peptide Label: isoform X1
- UniProtKB: Q9UNK2 (UniProtKB/Swiss-Prot),   Q9UNK1 (UniProtKB/Swiss-Prot),   Q9UK60 (UniProtKB/Swiss-Prot),   Q9UET5 (UniProtKB/Swiss-Prot),   Q20BK3 (UniProtKB/Swiss-Prot),   Q1ED40 (UniProtKB/Swiss-Prot),   Q15811 (UniProtKB/Swiss-Prot),   Q14BD3 (UniProtKB/Swiss-Prot),   Q0PW97 (UniProtKB/Swiss-Prot),   Q0PW95 (UniProtKB/Swiss-Prot),   Q0PW94 (UniProtKB/Swiss-Prot),   O95216 (UniProtKB/Swiss-Prot),   E9PHV2 (UniProtKB/Swiss-Prot),   E9PG01 (UniProtKB/Swiss-Prot),   E9PE44 (UniProtKB/Swiss-Prot),   E7ERJ1 (UniProtKB/Swiss-Prot),   B4DTM2 (UniProtKB/Swiss-Prot),   A8DCP3 (UniProtKB/Swiss-Prot),   A8D7D0 (UniProtKB/Swiss-Prot),   A8CTY7 (UniProtKB/Swiss-Prot),   A8CTY3 (UniProtKB/Swiss-Prot),   A8CTX8 (UniProtKB/Swiss-Prot),   A7Y322 (UniProtKB/Swiss-Prot),   Q9UQ92 (UniProtKB/Swiss-Prot)
RefSeq Acc Id: XP_054180739   ⟸   XM_054324764
- Peptide Label: isoform X4
RefSeq Acc Id: XP_054180741   ⟸   XM_054324766
- Peptide Label: isoform X6
RefSeq Acc Id: XP_054180740   ⟸   XM_054324765
- Peptide Label: isoform X5
RefSeq Acc Id: XP_054180742   ⟸   XM_054324767
- Peptide Label: isoform X7
RefSeq Acc Id: XP_054180736   ⟸   XM_054324761
- Peptide Label: isoform X2
RefSeq Acc Id: XP_054180743   ⟸   XM_054324768
- Peptide Label: isoform X8
RefSeq Acc Id: XP_054180737   ⟸   XM_054324762
- Peptide Label: isoform X3
RefSeq Acc Id: XP_054180744   ⟸   XM_054324769
- Peptide Label: isoform X9
RefSeq Acc Id: XP_054180746   ⟸   XM_054324771
- Peptide Label: isoform X10
RefSeq Acc Id: XP_054180748   ⟸   XM_054324773
- Peptide Label: isoform X11
- UniProtKB: A7XZY7 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054180751   ⟸   XM_054324776
- Peptide Label: isoform X14
RefSeq Acc Id: XP_054180752   ⟸   XM_054324777
- Peptide Label: isoform X15
RefSeq Acc Id: XP_054180756   ⟸   XM_054324781
- Peptide Label: isoform X18
RefSeq Acc Id: XP_054180757   ⟸   XM_054324782
- Peptide Label: isoform X19
RefSeq Acc Id: XP_054180753   ⟸   XM_054324778
- Peptide Label: isoform X16
RefSeq Acc Id: XP_054180754   ⟸   XM_054324779
- Peptide Label: isoform X17
RefSeq Acc Id: XP_054180758   ⟸   XM_054324783
- Peptide Label: isoform X20
RefSeq Acc Id: XP_054180738   ⟸   XM_054324763
- Peptide Label: isoform X3
RefSeq Acc Id: XP_054180745   ⟸   XM_054324770
- Peptide Label: isoform X10
RefSeq Acc Id: XP_054180750   ⟸   XM_054324775
- Peptide Label: isoform X13
RefSeq Acc Id: XP_054180749   ⟸   XM_054324774
- Peptide Label: isoform X12
RefSeq Acc Id: XP_054180755   ⟸   XM_054324780
- Peptide Label: isoform X17
RefSeq Acc Id: XP_054180747   ⟸   XM_054324772
- Peptide Label: isoform X21
Protein Domains
C2   DH   EF-hand   EH   PH   SH3

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q15811-F1-model_v2 AlphaFold Q15811 1-1721 view protein structure

Promoters
RGD ID:13602704
Promoter ID:EPDNEW_H27535
Type:multiple initiation site
Name:ITSN1_2
Description:intersectin 1
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H27536  EPDNEW_H27537  
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh382133,642,212 - 33,642,272EPDNEW
RGD ID:13602702
Promoter ID:EPDNEW_H27536
Type:initiation region
Name:ITSN1_1
Description:intersectin 1
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H27535  EPDNEW_H27537  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh382133,642,503 - 33,642,563EPDNEW
RGD ID:13602706
Promoter ID:EPDNEW_H27537
Type:multiple initiation site
Name:ITSN1_3
Description:intersectin 1
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H27536  EPDNEW_H27535  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh382133,687,103 - 33,687,163EPDNEW
RGD ID:6799460
Promoter ID:HG_KWN:40692
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   CD4+TCell_2Hour,   HeLa_S3,   Jurkat,   K562,   Lymphoblastoid,   NB4
Transcripts:ENST00000290244,   ENST00000361534,   ENST00000381283,   ENST00000381285,   ENST00000381288,   ENST00000381291,   ENST00000381540,   ENST00000399338,   ENST00000399367,   NM_001001132,   OTTHUMT00000140070,   OTTHUMT00000141278,   OTTHUMT00000141282,   OTTHUMT00000141283,   OTTHUMT00000141369,   OTTHUMT00000141371,   OTTHUMT00000141373,   OTTHUMT00000315799,   OTTHUMT00000315800,   OTTHUMT00000315801,   OTTHUMT00000337115,   OTTHUMT00000337118,   UC002YSR.1,   UC002YSS.1,   UC002YST.1,   UC002YSU.2,   UC002YSV.2,   UC002YSX.1,   UC002YSY.1,   UC002YSZ.1,   UC002YTB.1,   UC002YTH.2,   UC010GMG.1,   UC010GMH.1,   UC010GMI.1,   UC010GMJ.1
Position:
Human AssemblyChrPosition (strand)Source
Build 362133,935,821 - 33,937,387 (-)MPROMDB
RGD ID:6799471
Promoter ID:HG_KWN:40701
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:HeLa_S3
Transcripts:OTTHUMT00000313586
Position:
Human AssemblyChrPosition (strand)Source
Build 362134,093,406 - 34,093,906 (+)MPROMDB
RGD ID:6799480
Promoter ID:HG_KWN:40702
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:HeLa_S3
Transcripts:UC002YTF.1
Position:
Human AssemblyChrPosition (strand)Source
Build 362134,095,981 - 34,096,481 (+)MPROMDB
RGD ID:6799481
Promoter ID:HG_KWN:40704
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:HeLa_S3
Transcripts:OTTHUMT00000140998,   OTTHUMT00000140999,   OTTHUMT00000141008,   UC002YTG.1
Position:
Human AssemblyChrPosition (strand)Source
Build 362134,112,036 - 34,112,536 (+)MPROMDB

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:6183 AgrOrtholog
COSMIC ITSN1 COSMIC
Ensembl Genes ENSG00000205726 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000379960.9 UniProtKB/TrEMBL
  ENST00000381283.7 UniProtKB/TrEMBL
  ENST00000381284.7 UniProtKB/TrEMBL
  ENST00000381285 ENTREZGENE
  ENST00000381285.8 UniProtKB/TrEMBL
  ENST00000381291 ENTREZGENE
  ENST00000381291.8 UniProtKB/Swiss-Prot
  ENST00000381318 ENTREZGENE
  ENST00000381318.8 UniProtKB/Swiss-Prot
  ENST00000399338 ENTREZGENE
  ENST00000399338.8 UniProtKB/Swiss-Prot
  ENST00000399349 ENTREZGENE
  ENST00000399349.5 UniProtKB/Swiss-Prot
  ENST00000399352 ENTREZGENE
  ENST00000399352.5 UniProtKB/Swiss-Prot
  ENST00000399353 ENTREZGENE
  ENST00000399353.5 UniProtKB/Swiss-Prot
  ENST00000399355 ENTREZGENE
  ENST00000399355.6 UniProtKB/TrEMBL
  ENST00000399367 ENTREZGENE
  ENST00000399367.7 UniProtKB/Swiss-Prot
  ENST00000415023.1 UniProtKB/TrEMBL
  ENST00000419241.1 UniProtKB/TrEMBL
  ENST00000420666.1 UniProtKB/TrEMBL
  ENST00000437126.5 UniProtKB/TrEMBL
  ENST00000440794.2 UniProtKB/TrEMBL
  ENST00000444491.5 UniProtKB/TrEMBL
  ENST00000451686.5 UniProtKB/TrEMBL
  ENST00000456489.1 UniProtKB/TrEMBL
Gene3D-CATH 1.20.900.10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  2.30.29.30 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  2.60.40.150 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  EF-hand UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SH3 Domains UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000205726 GTEx
HGNC ID HGNC:6183 ENTREZGENE
Human Proteome Map ITSN1 Human Proteome Map
InterPro C2_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  C2_domain_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  DBL_dom_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  DH-domain UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  EF-hand-dom_pair UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  EF_Hand_1_Ca_BS UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  EF_hand_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  EH_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  GDS_CDC24_CS UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  INTAP UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PH-like_dom_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PH_domain UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SH3-like_dom_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SH3_domain UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:6453 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
NCBI Gene 6453 ENTREZGENE
OMIM 602442 OMIM
PANTHER EH DOMAIN UniProtKB/TrEMBL
  INTERSECTIN-1 UniProtKB/TrEMBL
  INTERSECTIN-2 ISOFORM X1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  RHO GUANINE NUCLEOTIDE EXCHANGE FACTOR AT 64C, ISOFORM A UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  RHO-TYPE GUANINE NUCLEOTIDE EXCHANGE FACTOR, ISOFORM F UniProtKB/TrEMBL
  RHO-TYPE GUANINE NUCLEOTIDE EXCHANGE FACTOR, ISOFORM F UniProtKB/TrEMBL
Pfam EF-hand_4 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  INTAP UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PF00168 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PH_13 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  RhoGEF UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SH3_1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SH3_2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SH3_9 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA29981 PharmGKB
PRINTS P67PHOX UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SH3DOMAIN UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SPECTRNALPHA UniProtKB/TrEMBL
PROSITE DH_1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  DH_2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  EF_HAND_1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  EF_HAND_2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PH_DOMAIN UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PS50004 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PS50031 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SH3 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART EFh UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  RhoGEF UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SH3 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SM00027 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SM00233 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SM00239 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP PH domain-like UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SSF47473 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SSF48065 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SSF49562 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SSF50044 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A0A2X0TVY8 ENTREZGENE, UniProtKB/TrEMBL
  A7XZY7 ENTREZGENE, UniProtKB/TrEMBL
  A7Y322 ENTREZGENE
  A8CTX8 ENTREZGENE
  A8CTY3 ENTREZGENE
  A8CTY7 ENTREZGENE
  A8CTZ0 ENTREZGENE, UniProtKB/TrEMBL
  A8D7D0 ENTREZGENE
  A8DCP3 ENTREZGENE
  A8W608_HUMAN UniProtKB/TrEMBL
  B4DTM2 ENTREZGENE
  C9J1A4_HUMAN UniProtKB/TrEMBL
  C9JQZ7_HUMAN UniProtKB/TrEMBL
  C9JXS9_HUMAN UniProtKB/TrEMBL
  D6PAV9_HUMAN UniProtKB/TrEMBL
  D6PAW0_HUMAN UniProtKB/TrEMBL
  D6PAW2_HUMAN UniProtKB/TrEMBL
  E7ERJ1 ENTREZGENE
  E9PD98 ENTREZGENE
  E9PE44 ENTREZGENE
  E9PG01 ENTREZGENE
  E9PHV2 ENTREZGENE
  F8W7U0 ENTREZGENE, UniProtKB/TrEMBL
  H0Y3G5_HUMAN UniProtKB/TrEMBL
  H0Y523_HUMAN UniProtKB/TrEMBL
  H0Y6W3_HUMAN UniProtKB/TrEMBL
  H0Y7J7_HUMAN UniProtKB/TrEMBL
  H7C3F1_HUMAN UniProtKB/TrEMBL
  H7C429_HUMAN UniProtKB/TrEMBL
  ITSN1_HUMAN UniProtKB/Swiss-Prot
  O95216 ENTREZGENE
  Q0PW94 ENTREZGENE
  Q0PW95 ENTREZGENE
  Q0PW96 ENTREZGENE, UniProtKB/TrEMBL
  Q0PW97 ENTREZGENE
  Q14BD3 ENTREZGENE
  Q14BD4 ENTREZGENE, UniProtKB/TrEMBL
  Q15811 ENTREZGENE
  Q1ED40 ENTREZGENE
  Q20BK3 ENTREZGENE
  Q2LAE2_HUMAN UniProtKB/TrEMBL
  Q6GMY7_HUMAN UniProtKB/TrEMBL
  Q6J1T1_HUMAN UniProtKB/TrEMBL
  Q6J1T2_HUMAN UniProtKB/TrEMBL
  Q6J333_HUMAN UniProtKB/TrEMBL
  Q6J334_HUMAN UniProtKB/TrEMBL
  Q6PD56_HUMAN UniProtKB/TrEMBL
  Q7Z452_HUMAN UniProtKB/TrEMBL
  Q7Z453_HUMAN UniProtKB/TrEMBL
  Q86VI9_HUMAN UniProtKB/TrEMBL
  Q9UET5 ENTREZGENE
  Q9UK60 ENTREZGENE
  Q9UNK1 ENTREZGENE
  Q9UNK2 ENTREZGENE
  Q9UQ92 ENTREZGENE
UniProt Secondary A7Y322 UniProtKB/Swiss-Prot
  A8CTX8 UniProtKB/Swiss-Prot
  A8CTY3 UniProtKB/Swiss-Prot
  A8CTY7 UniProtKB/Swiss-Prot
  A8D7D0 UniProtKB/Swiss-Prot
  A8DCP3 UniProtKB/Swiss-Prot
  B4DTM2 UniProtKB/Swiss-Prot
  E7ERJ1 UniProtKB/Swiss-Prot
  E9PD98 UniProtKB/TrEMBL
  E9PE44 UniProtKB/Swiss-Prot
  E9PG01 UniProtKB/Swiss-Prot
  E9PHV2 UniProtKB/Swiss-Prot
  O95216 UniProtKB/Swiss-Prot
  Q0PW94 UniProtKB/Swiss-Prot
  Q0PW95 UniProtKB/Swiss-Prot
  Q0PW97 UniProtKB/Swiss-Prot
  Q14BD3 UniProtKB/Swiss-Prot
  Q1ED40 UniProtKB/Swiss-Prot
  Q20BK3 UniProtKB/Swiss-Prot
  Q9UET5 UniProtKB/Swiss-Prot
  Q9UK60 UniProtKB/Swiss-Prot
  Q9UNK1 UniProtKB/Swiss-Prot
  Q9UNK2 UniProtKB/Swiss-Prot
  Q9UQ92 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2015-11-17 ITSN1  intersectin 1  ITSN1  intersectin 1 (SH3 domain protein)  Symbol and/or name change 5135510 APPROVED