IFNAR1 (interferon alpha and beta receptor subunit 1) - Rat Genome Database

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Gene: IFNAR1 (interferon alpha and beta receptor subunit 1) Homo sapiens
Analyze
Symbol: IFNAR1
Name: interferon alpha and beta receptor subunit 1
RGD ID: 1313408
HGNC Page HGNC:5432
Description: Enables JAK pathway signal transduction adaptor activity; cytokine binding activity; and type I interferon receptor activity. Involved in cell surface receptor signaling pathway via JAK-STAT; cellular response to cytokine stimulus; and positive regulation of cellular respiration. Located in plasma membrane. Implicated in hepatitis C and primary immunodeficiency disease.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: alpha-type antiviral protein; AVP; beta-type antiviral protein; CRF2-1; cytokine receptor class-II member 1; cytokine receptor family 2 member 1; IFN-alpha-REC; IFN-alpha/beta receptor 1; IFN-R-1; IFNalpha/beta receptor 1; IFNAR; IFNBR; IFRC; IMD106; interferon (alpha, beta and omega) receptor 1; interferon alpha/beta receptor 1; interferon receptor 1; interferon-alpha/beta receptor alpha chain; interferon-beta receptor 1; type I interferon receptor 1
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Orthologs
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
NCBI Annotation Information: Note: This gene has been reviewed for its involvement in coronavirus biology, and is involved in immune response or antiviral activity.
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh382133,324,395 - 33,359,864 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl2133,324,387 - 33,359,864 (+)EnsemblGRCh38hg38GRCh38
GRCh372134,696,700 - 34,732,170 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 362133,619,084 - 33,653,999 (+)NCBINCBI36Build 36hg18NCBI36
Build 342133,619,083 - 33,653,996NCBI
Celera2119,887,300 - 19,922,214 (+)NCBICelera
Cytogenetic Map21q22.11ENTREZGENE
HuRef2120,166,044 - 20,200,958 (+)NCBIHuRef
CHM1_12134,259,582 - 34,294,500 (+)NCBICHM1_1
T2T-CHM13v2.02131,696,639 - 31,732,109 (+)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Gene Ontology Annotations     Click to see Annotation Detail View

Cellular Component
endosome  (IEA)
late endosome  (IEA)
lysosome  (IEA)
membrane  (IEA)
plasma membrane  (IBA,IDA,IEA,IMP,TAS)

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. IFN-alpha/beta signaling is required for polarization of cytokine responses toward a protective type 1 pattern during experimental cryptococcosis. Biondo C, etal., J Immunol. 2008 Jul 1;181(1):566-73.
2. Mechanism of HCV's resistance to IFN-alpha in cell culture involves expression of functional IFN-alpha receptor 1. Datta S, etal., Virol J. 2011 Jul 14;8(1):351.
3. GOAs Human GO annotations GOA_HUMAN data from the GO Consortium
4. IRF9 Prevents CD8+ T Cell Exhaustion in an Extrinsic Manner during Acute Lymphocytic Choriomeningitis Virus Infection. Huber M, etal., J Virol. 2017 Oct 27;91(22). pii: JVI.01219-17. doi: 10.1128/JVI.01219-17. Print 2017 Nov 15.
5. Inflammatory monocytes require type I interferon receptor signaling to activate NK cells via IL-18 during a mucosal viral infection. Lee AJ, etal., J Exp Med. 2017 Apr 3;214(4):1153-1167. doi: 10.1084/jem.20160880. Epub 2017 Mar 6.
6. IRF7-dependent type I interferon production induces lethal immune-mediated disease in STAT1 knockout mice infected with lymphocytic choriomeningitis virus. Li W, etal., J Virol. 2014 Jul;88(13):7578-88. doi: 10.1128/JVI.03117-13. Epub 2014 Apr 23.
7. Staphylococcus aureus activates type I IFN signaling in mice and humans through the Xr repeated sequences of protein A. Martin FJ, etal., J Clin Invest. 2009 Jul;119(7):1931-9.
8. KEGG Annotation Import Pipeline Pipeline to import KEGG annotations from KEGG into RGD
9. A Critical Role for the Type I Interferon Receptor in Virus-Induced Autoimmune Diabetes in Rats. Qaisar N, etal., Diabetes. 2017 Jan;66(1):145-157. doi: 10.2337/db16-0462. Epub 2016 Oct 7.
10. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
11. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
12. Type I interferon signaling regulates Ly6C(hi) monocytes and neutrophils during acute viral pneumonia in mice. Seo SU, etal., PLoS Pathog. 2011 Feb;7(2):e1001304. Epub 2011 Feb 24.
13. Type I IFNs mediate development of postinfluenza bacterial pneumonia in mice. Shahangian A, etal., J Clin Invest. 2009 Jul;119(7):1910-20.
14. Heightened Innate Immune Responses in the Respiratory Tract of COVID-19 Patients. Zhou Z, etal., Cell Host Microbe. 2020 Jun 10;27(6):883-890.e2. doi: 10.1016/j.chom.2020.04.017. Epub 2020 May 4.
Additional References at PubMed
PMID:1350660   PMID:1370833   PMID:1834641   PMID:2148760   PMID:2153461   PMID:7526154   PMID:7559568   PMID:7657660   PMID:7665574   PMID:7813427   PMID:7932753   PMID:8125298  
PMID:8181059   PMID:8524272   PMID:8605876   PMID:8626489   PMID:9029147   PMID:9121453   PMID:9174595   PMID:9225992   PMID:9403695   PMID:9677371   PMID:9733772   PMID:10490982  
PMID:10542297   PMID:10830953   PMID:11167825   PMID:11301323   PMID:11694501   PMID:11786546   PMID:12220192   PMID:12477932   PMID:12554654   PMID:12618863   PMID:12620806   PMID:12697242  
PMID:12761564   PMID:12960323   PMID:14532120   PMID:14647450   PMID:14727154   PMID:15063762   PMID:15337770   PMID:15356134   PMID:15389589   PMID:15449939   PMID:15489334   PMID:15589821  
PMID:15885318   PMID:15946680   PMID:15990456   PMID:16171819   PMID:16338279   PMID:16624932   PMID:17001036   PMID:17027223   PMID:17125879   PMID:17310065   PMID:17517919   PMID:17667505  
PMID:17703412   PMID:17823081   PMID:17923090   PMID:18056411   PMID:18166147   PMID:18250407   PMID:18338947   PMID:18362156   PMID:18474601   PMID:18535656   PMID:18761606   PMID:18801736  
PMID:18937499   PMID:18953482   PMID:19103527   PMID:19124753   PMID:19220955   PMID:19258923   PMID:19299650   PMID:19434718   PMID:19453261   PMID:19501422   PMID:19559055   PMID:19561067  
PMID:19730683   PMID:19773451   PMID:19796549   PMID:19805514   PMID:19817957   PMID:19879773   PMID:19913121   PMID:19948722   PMID:19957332   PMID:20020050   PMID:20065083   PMID:20237496  
PMID:20331378   PMID:20378664   PMID:20503287   PMID:20565290   PMID:20588308   PMID:20628086   PMID:20811626   PMID:21173164   PMID:21540188   PMID:21690295   PMID:21695243   PMID:21716316  
PMID:21757742   PMID:21821707   PMID:21830897   PMID:21832278   PMID:21854986   PMID:21865166   PMID:21873635   PMID:22036215   PMID:22136495   PMID:22156349   PMID:22162633   PMID:22218495  
PMID:22258259   PMID:22786773   PMID:22824466   PMID:23128233   PMID:23129613   PMID:23201923   PMID:23209811   PMID:23663046   PMID:24075985   PMID:24334027   PMID:24460759   PMID:24704786  
PMID:25072284   PMID:25265476   PMID:25445652   PMID:25501140   PMID:25675103   PMID:25930096   PMID:25939635   PMID:26008745   PMID:26159719   PMID:26429320   PMID:26676772   PMID:26679744  
PMID:26679999   PMID:26787880   PMID:27346865   PMID:27569280   PMID:28122987   PMID:28196594   PMID:28282804   PMID:28514442   PMID:28576494   PMID:28583475   PMID:28656291   PMID:28842285  
PMID:29106381   PMID:29117863   PMID:29311663   PMID:29343571   PMID:29375208   PMID:29637882   PMID:29674694   PMID:29713327   PMID:30383464   PMID:30410131   PMID:30555157   PMID:30645975  
PMID:30936491   PMID:31270247   PMID:31298317   PMID:31512106   PMID:32296183   PMID:32960813   PMID:33252644   PMID:33583067   PMID:33746965   PMID:33807175   PMID:33811647   PMID:33961781  
PMID:34328599   PMID:34713375   PMID:34794508   PMID:34813358   PMID:34899713   PMID:35048182   PMID:35271311   PMID:35288721   PMID:35339044   PMID:35442418   PMID:35708626   PMID:35816776  
PMID:35985475   PMID:36063748   PMID:37028439   PMID:37973454  


Genomics

Comparative Map Data
IFNAR1
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh382133,324,395 - 33,359,864 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl2133,324,387 - 33,359,864 (+)EnsemblGRCh38hg38GRCh38
GRCh372134,696,700 - 34,732,170 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 362133,619,084 - 33,653,999 (+)NCBINCBI36Build 36hg18NCBI36
Build 342133,619,083 - 33,653,996NCBI
Celera2119,887,300 - 19,922,214 (+)NCBICelera
Cytogenetic Map21q22.11ENTREZGENE
HuRef2120,166,044 - 20,200,958 (+)NCBIHuRef
CHM1_12134,259,582 - 34,294,500 (+)NCBICHM1_1
T2T-CHM13v2.02131,696,639 - 31,732,109 (+)NCBIT2T-CHM13v2.0
Ifnar1
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391691,281,016 - 91,307,411 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl1691,282,126 - 91,304,329 (+)EnsemblGRCm39 Ensembl
GRCm381691,485,032 - 91,510,523 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1691,485,238 - 91,507,441 (+)EnsemblGRCm38mm10GRCm38
MGSCv371691,485,460 - 91,510,768 (+)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv361691,374,108 - 91,396,296 (+)NCBIMGSCv36mm8
Celera1692,562,831 - 92,587,086 (+)NCBICelera
Cytogenetic Map16C3.3NCBI
cM Map1652.98NCBI
Ifnar1
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr81144,211,769 - 44,238,206 (+)NCBIGRCr8
mRatBN7.21130,725,774 - 30,752,227 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl1130,725,790 - 30,749,979 (+)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx1139,420,142 - 39,442,802 (+)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.01132,091,572 - 32,114,232 (+)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.01131,257,245 - 31,279,947 (+)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.01131,640,407 - 31,666,839 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl1131,640,407 - 31,664,061 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.01135,248,575 - 35,272,235 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41131,454,789 - 31,478,449 (+)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.11131,494,121 - 31,518,864 (+)NCBI
Celera1130,393,241 - 30,416,960 (+)NCBICelera
Cytogenetic Map11q11NCBI
Ifnar1
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_00495540732,730,953 - 32,754,651 (+)EnsemblChiLan1.0
ChiLan1.0NW_00495540732,730,973 - 32,755,404 (+)NCBIChiLan1.0ChiLan1.0
IFNAR1
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v22229,433,955 - 29,471,654 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan12124,293,349 - 24,331,230 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v02119,683,496 - 19,719,034 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.12133,058,410 - 33,093,824 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl2133,058,396 - 33,093,824 (+)Ensemblpanpan1.1panPan2
IFNAR1
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.13128,854,765 - 28,876,399 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha3127,950,128 - 27,972,344 (+)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.03128,160,372 - 28,182,033 (+)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl3128,160,333 - 28,195,529 (+)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.13128,027,680 - 28,049,300 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.03128,037,690 - 28,059,324 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.03128,540,987 - 28,562,614 (+)NCBIUU_Cfam_GSD_1.0
Ifnar1
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440497128,493,890 - 28,514,014 (+)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_0049365008,953,049 - 8,973,978 (-)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_0049365008,953,809 - 8,975,261 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
IFNAR1
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl13196,925,734 - 196,952,239 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.113196,925,731 - 196,951,398 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
IFNAR1
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.1258,824,600 - 58,854,519 (-)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl258,825,916 - 58,854,568 (-)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_0236660711,327,549 - 1,360,671 (-)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Ifnar1
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_00462474521,546,007 - 21,572,776 (+)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_00462474521,545,846 - 21,569,719 (+)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in IFNAR1
246 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 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_000629.2(IFNAR1):c.1492C>A (p.Gln498Lys) single nucleotide variant Malignant melanoma [RCV000063820] Chr21:33355367 [GRCh38]
Chr21:34727673 [GRCh37]
Chr21:33649543 [NCBI36]
Chr21:21q22.11		 not provided
NM_000629.3(IFNAR1):c.115G>A (p.Asp39Asn) single nucleotide variant IFNAR1-related disorder [RCV003963202]|not provided [RCV001303454] Chr21:33335562 [GRCh38]
Chr21:34707868 [GRCh37]
Chr21:21q22.11		 likely benign|conflicting interpretations of pathogenicity|uncertain significance
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
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 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
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
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
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
GRCh37/hg19 21q22.11(chr21:34117564-34917877)x3 copy number gain not provided [RCV000684151] Chr21:34117564..34917877 [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 21q21.3-22.11(chr21:30214872-34896962)x3 copy number gain not provided [RCV000741530] Chr21:30214872..34896962 [GRCh37]
Chr21:21q21.3-22.11		 pathogenic
GRCh37/hg19 21q22.11(chr21:34708140-34723661)x1 copy number loss not provided [RCV000741539] Chr21:34708140..34723661 [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
GRCh37/hg19 21q22.11(chr21:32589903-35359935) copy number loss not provided [RCV000767744] Chr21:32589903..35359935 [GRCh37]
Chr21:21q22.11		 pathogenic
NM_000629.3(IFNAR1):c.213T>C (p.Asp71=) single nucleotide variant not provided [RCV000959638] Chr21:33341011 [GRCh38]
Chr21:34713317 [GRCh37]
Chr21:21q22.11		 benign
NM_000629.3(IFNAR1):c.1371G>A (p.Ala457=) single nucleotide variant not provided [RCV000894346] Chr21:33353714 [GRCh38]
Chr21:34726020 [GRCh37]
Chr21:21q22.11		 benign
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.(?_34713285)_(34713500_?)del deletion not provided [RCV003105269] Chr21:34713285..34713500 [GRCh37]
Chr21:21q22.11		 pathogenic
NM_000629.3(IFNAR1):c.674-2A>G single nucleotide variant Immunodeficiency 106, susceptibility to viral infections [RCV002260519] Chr21:33345244 [GRCh38]
Chr21:34717550 [GRCh37]
Chr21:21q22.11		 risk factor|uncertain significance
NM_000629.3(IFNAR1):c.189C>T (p.Phe63=) single nucleotide variant not provided [RCV000888264] Chr21:33335636 [GRCh38]
Chr21:34707942 [GRCh37]
Chr21:21q22.11		 benign
NM_000629.3(IFNAR1):c.867C>A (p.Thr289=) single nucleotide variant not provided [RCV000880485] Chr21:33349169 [GRCh38]
Chr21:34721475 [GRCh37]
Chr21:21q22.11		 benign|likely benign
NM_000629.3(IFNAR1):c.272C>T (p.Ser91Leu) single nucleotide variant not specified [RCV004310638] Chr21:33341070 [GRCh38]
Chr21:34713376 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.830G>A (p.Trp277Ter) single nucleotide variant not provided [RCV001093462] Chr21:33349132 [GRCh38]
Chr21:34721438 [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
GRCh37/hg19 21q22.11(chr21:34379096-35572731)x1 copy number loss not provided [RCV001259407] Chr21:34379096..35572731 [GRCh37]
Chr21:21q22.11		 pathogenic
GRCh37/hg19 21q11.2-22.3(chr21:14420615-48080926)x3 copy number gain Down syndrome [RCV002284306] Chr21:14420615..48080926 [GRCh37]
Chr21:21q11.2-22.3		 pathogenic
NM_000629.3(IFNAR1):c.919G>A (p.Val307Ile) single nucleotide variant IFNAR1-related disorder [RCV003918855]|not provided [RCV001324701] Chr21:33349221 [GRCh38]
Chr21:34721527 [GRCh37]
Chr21:21q22.11		 likely benign|uncertain significance
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
NM_000629.3(IFNAR1):c.100C>T (p.Gln34Ter) single nucleotide variant not provided [RCV003852712] Chr21:33335547 [GRCh38]
Chr21:34707853 [GRCh37]
Chr21:21q22.11		 pathogenic
NM_000629.3(IFNAR1):c.284A>G (p.Asn95Ser) single nucleotide variant not provided [RCV001371005]|not specified [RCV004037492] Chr21:33341082 [GRCh38]
Chr21:34713388 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.1270G>A (p.Ala424Thr) single nucleotide variant not provided [RCV001308616]|not specified [RCV004034174] Chr21:33352884 [GRCh38]
Chr21:34725190 [GRCh37]
Chr21:21q22.11		 likely benign|uncertain significance
NM_000629.3(IFNAR1):c.1175C>T (p.Thr392Ile) single nucleotide variant not provided [RCV001371471] Chr21:33352789 [GRCh38]
Chr21:34725095 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.1076C>T (p.Thr359Met) single nucleotide variant not provided [RCV001510831] Chr21:33349476 [GRCh38]
Chr21:34721782 [GRCh37]
Chr21:21q22.11		 benign
NC_000021.8:g.(?_34540717)_(35013574_?)del deletion not provided [RCV001385476] Chr21:34540717..35013574 [GRCh37]
Chr21:21q22.11		 pathogenic
NM_000629.3(IFNAR1):c.36G>A (p.Val12=) single nucleotide variant not provided [RCV001463407] Chr21:33325091 [GRCh38]
Chr21:34697396 [GRCh37]
Chr21:21q22.11		 likely benign
NM_000629.3(IFNAR1):c.502G>C (p.Val168Leu) single nucleotide variant not provided [RCV001523496]|not specified [RCV003487419] Chr21:33343393 [GRCh38]
Chr21:33343393..33343394 [GRCh38]
Chr21:34715699 [GRCh37]
Chr21:34715699..34715700 [GRCh37]
Chr21:21q22.11		 benign
NM_000629.3(IFNAR1):c.1587C>T (p.Ser529=) single nucleotide variant not provided [RCV001520578] Chr21:33355462 [GRCh38]
Chr21:34727768 [GRCh37]
Chr21:21q22.11		 benign
NM_000629.3(IFNAR1):c.624G>A (p.Thr208=) single nucleotide variant not provided [RCV001520724] Chr21:33343627 [GRCh38]
Chr21:34715933 [GRCh37]
Chr21:21q22.11		 benign|likely benign
NM_000629.3(IFNAR1):c.504T>C (p.Val168=) single nucleotide variant not provided [RCV001514127] Chr21:33343395 [GRCh38]
Chr21:34715701 [GRCh37]
Chr21:21q22.11		 benign
NM_000629.3(IFNAR1):c.916C>T (p.Arg306Cys) single nucleotide variant not provided [RCV001514954] Chr21:33349218 [GRCh38]
Chr21:34721524 [GRCh37]
Chr21:21q22.11		 benign
NM_000629.3(IFNAR1):c.1458A>G (p.Pro486=) single nucleotide variant not provided [RCV001515276] Chr21:33355333 [GRCh38]
Chr21:34727639 [GRCh37]
Chr21:21q22.11		 benign
NM_000629.3(IFNAR1):c.190G>A (p.Asp64Asn) single nucleotide variant not provided [RCV001915001] Chr21:33335637 [GRCh38]
Chr21:34707943 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.1627G>A (p.Glu543Lys) single nucleotide variant not provided [RCV001988713] Chr21:33355502 [GRCh38]
Chr21:34727808 [GRCh37]
Chr21:21q22.11		 uncertain significance
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
NM_000629.3(IFNAR1):c.1571A>C (p.His524Pro) single nucleotide variant not provided [RCV001896588]|not specified [RCV004041727] Chr21:33355446 [GRCh38]
Chr21:34727752 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.547A>G (p.Ile183Val) single nucleotide variant not provided [RCV001914716] Chr21:33343550 [GRCh38]
Chr21:34715856 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.317C>T (p.Ala106Val) single nucleotide variant not provided [RCV001894185] Chr21:33341115 [GRCh38]
Chr21:34713421 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.1414C>T (p.Leu472Phe) single nucleotide variant not provided [RCV001874406] Chr21:33353757 [GRCh38]
Chr21:34726063 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.286G>T (p.Val96Phe) single nucleotide variant not provided [RCV002045384] Chr21:33341084 [GRCh38]
Chr21:34713390 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.1060A>G (p.Lys354Glu) single nucleotide variant not provided [RCV001864351] Chr21:33349460 [GRCh38]
Chr21:34721766 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.1650A>C (p.Glu550Asp) single nucleotide variant not provided [RCV001988539] Chr21:33355525 [GRCh38]
Chr21:34727831 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.397G>T (p.Val133Leu) single nucleotide variant not provided [RCV002008676] Chr21:33343288 [GRCh38]
Chr21:34715594 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.623C>T (p.Thr208Met) single nucleotide variant not provided [RCV001983105]|not specified [RCV004044401] Chr21:33343626 [GRCh38]
Chr21:34715932 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.460G>T (p.Val154Phe) single nucleotide variant not provided [RCV002020575] Chr21:33343351 [GRCh38]
Chr21:34715657 [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
NM_000629.3(IFNAR1):c.1670T>C (p.Val557Ala) single nucleotide variant not provided [RCV001894522] Chr21:33355545 [GRCh38]
Chr21:34727851 [GRCh37]
Chr21:21q22.11		 conflicting interpretations of pathogenicity|uncertain significance
NM_000629.3(IFNAR1):c.1366G>A (p.Ala456Thr) single nucleotide variant not provided [RCV001985865] Chr21:33353709 [GRCh38]
Chr21:34726015 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.637G>A (p.Gly213Ser) single nucleotide variant not provided [RCV002007813] Chr21:33343640 [GRCh38]
Chr21:34715946 [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_000629.3(IFNAR1):c.86A>G (p.Asn29Ser) single nucleotide variant not provided [RCV001966532] Chr21:33335533 [GRCh38]
Chr21:34707839 [GRCh37]
Chr21:21q22.11		 uncertain significance
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
NM_000629.3(IFNAR1):c.1155C>G (p.Ile385Met) single nucleotide variant not provided [RCV002005252]|not specified [RCV004042231] Chr21:33352769 [GRCh38]
Chr21:34725075 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.1436A>G (p.Asp479Gly) single nucleotide variant not provided [RCV002044173] Chr21:33353779 [GRCh38]
Chr21:34726085 [GRCh37]
Chr21:21q22.11		 uncertain significance
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
NM_000629.3(IFNAR1):c.1156G>T (p.Glu386Ter) single nucleotide variant Immunodeficiency 106, susceptibility to viral infections [RCV002260524]|not provided [RCV001948683] Chr21:33352770 [GRCh38]
Chr21:34725076 [GRCh37]
Chr21:21q22.11		 pathogenic|risk factor|uncertain significance
NM_000629.3(IFNAR1):c.788A>C (p.His263Pro) single nucleotide variant not provided [RCV002006441] Chr21:33345360 [GRCh38]
Chr21:34717666 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.1038C>G (p.Phe346Leu) single nucleotide variant not provided [RCV001983700] Chr21:33349438 [GRCh38]
Chr21:34721744 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.310A>G (p.Ile104Val) single nucleotide variant not provided [RCV002036997]|not specified [RCV004044903] Chr21:33341108 [GRCh38]
Chr21:34713414 [GRCh37]
Chr21:21q22.11		 likely benign|uncertain significance
NM_000629.3(IFNAR1):c.1619A>T (p.Asn540Ile) single nucleotide variant not provided [RCV001887640] Chr21:33355494 [GRCh38]
Chr21:34727800 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.190G>T (p.Asp64Tyr) single nucleotide variant not provided [RCV001907300]|not specified [RCV004039756] Chr21:33335637 [GRCh38]
Chr21:34707943 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.603A>C (p.Lys201Asn) single nucleotide variant not provided [RCV001888048] Chr21:33343606 [GRCh38]
Chr21:34715912 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.278A>G (p.Lys93Arg) single nucleotide variant not provided [RCV002032328] Chr21:33341076 [GRCh38]
Chr21:34713382 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.925G>T (p.Ala309Ser) single nucleotide variant not provided [RCV001975368] Chr21:33349227 [GRCh38]
Chr21:34721533 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.1282A>C (p.Lys428Gln) single nucleotide variant not provided [RCV001941024] Chr21:33352896 [GRCh38]
Chr21:34725202 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.235T>C (p.Cys79Arg) single nucleotide variant not provided [RCV001905942] Chr21:33341033 [GRCh38]
Chr21:34713339 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.1647_1651del (p.Ser549fs) deletion not provided [RCV001944270] Chr21:33355519..33355523 [GRCh38]
Chr21:34727825..34727829 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.644A>G (p.Tyr215Cys) single nucleotide variant not provided [RCV001924584] Chr21:33343647 [GRCh38]
Chr21:34715953 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.31C>G (p.Leu11Val) single nucleotide variant not provided [RCV001940863] Chr21:33325086 [GRCh38]
Chr21:34697391 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.934G>T (p.Gly312Ter) single nucleotide variant not provided [RCV002000009] Chr21:33349236 [GRCh38]
Chr21:34721542 [GRCh37]
Chr21:21q22.11		 pathogenic
NM_000629.3(IFNAR1):c.897A>G (p.Gln299=) single nucleotide variant not provided [RCV001938116] Chr21:33349199 [GRCh38]
Chr21:34721505 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.1429A>G (p.Ser477Gly) single nucleotide variant not provided [RCV001940051] Chr21:33353772 [GRCh38]
Chr21:34726078 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.1018A>G (p.Arg340Gly) single nucleotide variant not provided [RCV001883703]|not specified [RCV004041154] Chr21:33349418 [GRCh38]
Chr21:34721724 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.17T>C (p.Leu6Pro) single nucleotide variant not provided [RCV002033813] Chr21:33325072 [GRCh38]
Chr21:34697377 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.501_503del (p.Leu167_Val168delinsPhe) deletion not provided [RCV001930717] Chr21:33343391..33343393 [GRCh38]
Chr21:34715697..34715699 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.910C>T (p.Leu304Phe) single nucleotide variant not provided [RCV001906490] Chr21:33349212 [GRCh38]
Chr21:34721518 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.1632C>T (p.Ser544=) single nucleotide variant not provided [RCV001954147] Chr21:33355507 [GRCh38]
Chr21:34727813 [GRCh37]
Chr21:21q22.11		 likely benign
NM_000629.3(IFNAR1):c.130A>C (p.Asn44His) single nucleotide variant not provided [RCV001901707]|not specified [RCV004042624] Chr21:33335577 [GRCh38]
Chr21:34707883 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.377-2A>G single nucleotide variant not provided [RCV002010249] Chr21:33343266 [GRCh38]
Chr21:34715572 [GRCh37]
Chr21:21q22.11		 likely pathogenic|uncertain significance
NM_000629.3(IFNAR1):c.1024C>T (p.Leu342Phe) single nucleotide variant not provided [RCV002026860] Chr21:33349424 [GRCh38]
Chr21:34721730 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.157G>A (p.Asp53Asn) single nucleotide variant not provided [RCV001919178] Chr21:33335604 [GRCh38]
Chr21:34707910 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.55T>G (p.Trp19Gly) single nucleotide variant not provided [RCV001876300] Chr21:33325110 [GRCh38]
Chr21:34697415 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.65CCGCAG[1] (p.Ala24_Ala25del) microsatellite not provided [RCV001916620] Chr21:33325120..33325125 [GRCh38]
Chr21:34697425..34697430 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.866C>T (p.Thr289Ile) single nucleotide variant not provided [RCV001879048]|not specified [RCV004040526] Chr21:33349168 [GRCh38]
Chr21:34721474 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.1294+1G>A single nucleotide variant not provided [RCV002048225] Chr21:33352909 [GRCh38]
Chr21:34725215 [GRCh37]
Chr21:21q22.11		 likely pathogenic|uncertain significance
NM_000629.3(IFNAR1):c.673+6G>A single nucleotide variant not provided [RCV001880373] Chr21:33343682 [GRCh38]
Chr21:34715988 [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]|Hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX1 [RCV004579580]|Immunodeficiency 28 [RCV004579581] Chr21:32439271..39212984 [GRCh37]
Chr21:21q22.11-22.13		 uncertain significance
NM_000629.3(IFNAR1):c.370C>T (p.Arg124Cys) single nucleotide variant not provided [RCV001989303] Chr21:33341168 [GRCh38]
Chr21:33341168..33341169 [GRCh38]
Chr21:34713474 [GRCh37]
Chr21:34713474..34713475 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.1028G>C (p.Ser343Thr) single nucleotide variant not provided [RCV002011325] Chr21:33349428 [GRCh38]
Chr21:34721734 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.131A>G (p.Asn44Ser) single nucleotide variant not provided [RCV002016058] Chr21:33335578 [GRCh38]
Chr21:34707884 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.506del (p.Ile169fs) deletion not provided [RCV001901678] Chr21:33343397 [GRCh38]
Chr21:34715703 [GRCh37]
Chr21:21q22.11		 pathogenic|uncertain significance
NM_000629.3(IFNAR1):c.358T>C (p.Phe120Leu) single nucleotide variant not provided [RCV002018772] Chr21:33341156 [GRCh38]
Chr21:34713462 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.817C>A (p.His273Asn) single nucleotide variant not provided [RCV002030948] Chr21:33349119 [GRCh38]
Chr21:34721425 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.1210G>T (p.Val404Leu) single nucleotide variant not provided [RCV002036213] Chr21:33352824 [GRCh38]
Chr21:34725130 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.169G>A (p.Gly57Arg) single nucleotide variant not provided [RCV001940852] Chr21:33335616 [GRCh38]
Chr21:34707922 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.102A>G (p.Gln34=) single nucleotide variant not provided [RCV002019016] Chr21:33335549 [GRCh38]
Chr21:34707855 [GRCh37]
Chr21:21q22.11		 likely benign|uncertain significance
NM_000629.3(IFNAR1):c.1111A>G (p.Ile371Val) single nucleotide variant not provided [RCV001938053]|not specified [RCV004616862] Chr21:33349511 [GRCh38]
Chr21:34721817 [GRCh37]
Chr21:21q22.11		 likely benign|uncertain significance
NM_000629.3(IFNAR1):c.1543G>A (p.Glu515Lys) single nucleotide variant not provided [RCV001999001] Chr21:33355418 [GRCh38]
Chr21:34727724 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.917G>A (p.Arg306His) single nucleotide variant not provided [RCV001971889] Chr21:33349219 [GRCh38]
Chr21:34721525 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.1144-3T>C single nucleotide variant not provided [RCV002027606] Chr21:33352755 [GRCh38]
Chr21:34725061 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.200+2del deletion not provided [RCV001994330] Chr21:33335649 [GRCh38]
Chr21:34707955 [GRCh37]
Chr21:21q22.11		 likely pathogenic
NM_000629.3(IFNAR1):c.360del (p.Phe120fs) deletion not provided [RCV002019893] Chr21:33341156 [GRCh38]
Chr21:34713462 [GRCh37]
Chr21:21q22.11		 pathogenic|uncertain significance
NM_000629.3(IFNAR1):c.731A>G (p.Tyr244Cys) single nucleotide variant not provided [RCV001938294]|not specified [RCV004043573] Chr21:33345303 [GRCh38]
Chr21:34717609 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.211G>T (p.Asp71Tyr) single nucleotide variant not provided [RCV001916536] Chr21:33341009 [GRCh38]
Chr21:34713315 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.1321G>A (p.Val441Ile) single nucleotide variant not provided [RCV001997314] Chr21:33353664 [GRCh38]
Chr21:34725970 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.28A>G (p.Thr10Ala) single nucleotide variant not provided [RCV001920296]|not specified [RCV004043304] Chr21:33325083 [GRCh38]
Chr21:34697388 [GRCh37]
Chr21:21q22.11		 likely benign|uncertain significance
NM_000629.3(IFNAR1):c.46G>A (p.Val16Met) single nucleotide variant not provided [RCV001989289] Chr21:33325101 [GRCh38]
Chr21:34697406 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.1301C>G (p.Thr434Ser) single nucleotide variant not provided [RCV001994017] Chr21:33353644 [GRCh38]
Chr21:34725950 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.1110A>G (p.Glu370=) single nucleotide variant not provided [RCV002075510] Chr21:33349510 [GRCh38]
Chr21:34721816 [GRCh37]
Chr21:21q22.11		 likely benign
NM_000629.3(IFNAR1):c.36G>C (p.Val12=) single nucleotide variant not provided [RCV002107330] Chr21:33325091 [GRCh38]
Chr21:34697396 [GRCh37]
Chr21:21q22.11		 likely benign
NM_000629.3(IFNAR1):c.377-13G>C single nucleotide variant not provided [RCV002146375] Chr21:33343255 [GRCh38]
Chr21:34715561 [GRCh37]
Chr21:21q22.11		 likely benign
NM_000629.3(IFNAR1):c.1269C>T (p.Asp423=) single nucleotide variant not provided [RCV002075322] Chr21:33352883 [GRCh38]
Chr21:34725189 [GRCh37]
Chr21:21q22.11		 likely benign
NM_000629.3(IFNAR1):c.750T>C (p.Tyr250=) single nucleotide variant not provided [RCV002187651] Chr21:33345322 [GRCh38]
Chr21:34717628 [GRCh37]
Chr21:21q22.11		 likely benign
NM_000629.3(IFNAR1):c.999TCC[1] (p.Pro335del) microsatellite not provided [RCV002090878] Chr21:33349399..33349401 [GRCh38]
Chr21:34721705..34721707 [GRCh37]
Chr21:21q22.11		 likely benign
NM_000629.3(IFNAR1):c.1437_1439dup (p.Asp479dup) duplication IFNAR1-related disorder [RCV003958828]|not provided [RCV002110328] Chr21:33353777..33353778 [GRCh38]
Chr21:34726083..34726084 [GRCh37]
Chr21:21q22.11		 likely benign
NM_000629.3(IFNAR1):c.756T>C (p.Tyr252=) single nucleotide variant not provided [RCV002191380] Chr21:33345328 [GRCh38]
Chr21:34717634 [GRCh37]
Chr21:21q22.11		 likely benign
NM_000629.3(IFNAR1):c.516C>G (p.Asn172Lys) single nucleotide variant not provided [RCV002108274] Chr21:33343407 [GRCh38]
Chr21:34715713 [GRCh37]
Chr21:21q22.11		 likely benign
NM_000629.3(IFNAR1):c.1295-15C>T single nucleotide variant not provided [RCV002089562] Chr21:33353623 [GRCh38]
Chr21:34725929 [GRCh37]
Chr21:21q22.11		 likely benign
NM_000629.3(IFNAR1):c.1170T>C (p.Asp390=) single nucleotide variant not provided [RCV002091185] Chr21:33352784 [GRCh38]
Chr21:34725090 [GRCh37]
Chr21:21q22.11		 likely benign
NM_000629.3(IFNAR1):c.1143+12G>A single nucleotide variant not provided [RCV002124427] Chr21:33349555 [GRCh38]
Chr21:34721861 [GRCh37]
Chr21:21q22.11		 likely benign
NM_000629.3(IFNAR1):c.377-11T>C single nucleotide variant not provided [RCV002149994] Chr21:33343257 [GRCh38]
Chr21:34715563 [GRCh37]
Chr21:21q22.11		 benign
NM_000629.3(IFNAR1):c.1470T>C (p.Leu490=) single nucleotide variant not provided [RCV002195104] Chr21:33355345 [GRCh38]
Chr21:34727651 [GRCh37]
Chr21:21q22.11		 likely benign
NM_000629.3(IFNAR1):c.168C>T (p.Val56=) single nucleotide variant not provided [RCV002215012] Chr21:33335615 [GRCh38]
Chr21:34707921 [GRCh37]
Chr21:21q22.11		 likely benign
NM_000629.3(IFNAR1):c.1393A>T (p.Asn465Tyr) single nucleotide variant not provided [RCV002117307] Chr21:33353736 [GRCh38]
Chr21:34726042 [GRCh37]
Chr21:21q22.11		 likely benign
NM_000629.3(IFNAR1):c.1176A>G (p.Thr392=) single nucleotide variant not provided [RCV002071608] Chr21:33352790 [GRCh38]
Chr21:34725096 [GRCh37]
Chr21:21q22.11		 likely benign
NM_000629.3(IFNAR1):c.789-17_789-14del deletion not provided [RCV002145501] Chr21:33349073..33349076 [GRCh38]
Chr21:34721379..34721382 [GRCh37]
Chr21:21q22.11		 likely benign
NM_000629.3(IFNAR1):c.200+11C>G single nucleotide variant not provided [RCV002194916] Chr21:33335658 [GRCh38]
Chr21:34707964 [GRCh37]
Chr21:21q22.11		 likely benign
NM_000629.3(IFNAR1):c.318A>T (p.Ala106=) single nucleotide variant not provided [RCV002186233] Chr21:33341116 [GRCh38]
Chr21:34713422 [GRCh37]
Chr21:21q22.11		 likely benign
NM_000629.3(IFNAR1):c.674-20A>G single nucleotide variant not provided [RCV002131452] Chr21:33345226 [GRCh38]
Chr21:34717532 [GRCh37]
Chr21:21q22.11		 likely benign
NM_000629.3(IFNAR1):c.990T>C (p.Ala330=) single nucleotide variant not provided [RCV002126535] Chr21:33349390 [GRCh38]
Chr21:34721696 [GRCh37]
Chr21:21q22.11		 likely benign
NM_000629.3(IFNAR1):c.989-13A>C single nucleotide variant not provided [RCV002131565] Chr21:33349376 [GRCh38]
Chr21:34721682 [GRCh37]
Chr21:21q22.11		 likely benign
NM_000629.3(IFNAR1):c.132C>T (p.Asn44=) single nucleotide variant not provided [RCV002195709] Chr21:33335579 [GRCh38]
Chr21:34707885 [GRCh37]
Chr21:21q22.11		 likely benign
NM_000629.3(IFNAR1):c.651A>G (p.Pro217=) single nucleotide variant not provided [RCV002152532] Chr21:33343654 [GRCh38]
Chr21:34715960 [GRCh37]
Chr21:21q22.11		 likely benign
NM_000629.3(IFNAR1):c.498C>T (p.Ser166=) single nucleotide variant not provided [RCV002131547] Chr21:33343389 [GRCh38]
Chr21:34715695 [GRCh37]
Chr21:21q22.11		 likely benign
NM_000629.3(IFNAR1):c.1295-7T>A single nucleotide variant not provided [RCV002114360] Chr21:33353631 [GRCh38]
Chr21:34725937 [GRCh37]
Chr21:21q22.11		 likely benign
NM_000629.3(IFNAR1):c.16C>T (p.Leu6=) single nucleotide variant not provided [RCV002119295] Chr21:33325071 [GRCh38]
Chr21:34697376 [GRCh37]
Chr21:21q22.11		 likely benign
NM_000629.3(IFNAR1):c.1440+19T>C single nucleotide variant not provided [RCV002175688] Chr21:33353802 [GRCh38]
Chr21:34726108 [GRCh37]
Chr21:21q22.11		 likely benign
NM_000629.3(IFNAR1):c.76+7G>A single nucleotide variant not provided [RCV002160571] Chr21:33325138 [GRCh38]
Chr21:34697443 [GRCh37]
Chr21:21q22.11		 likely benign
NM_000629.3(IFNAR1):c.789-14A>T single nucleotide variant not provided [RCV002160825] Chr21:33349077 [GRCh38]
Chr21:34721383 [GRCh37]
Chr21:21q22.11		 likely benign
NM_000629.3(IFNAR1):c.376+15C>G single nucleotide variant not provided [RCV002161522] Chr21:33341189 [GRCh38]
Chr21:34713495 [GRCh37]
Chr21:21q22.11		 likely benign
NM_000629.3(IFNAR1):c.201-22_201-19del deletion not provided [RCV002156107] Chr21:33340977..33340980 [GRCh38]
Chr21:34713283..34713286 [GRCh37]
Chr21:21q22.11		 benign
NM_000629.3(IFNAR1):c.1143+17_1143+21del microsatellite not provided [RCV002121710] Chr21:33349555..33349559 [GRCh38]
Chr21:34721861..34721865 [GRCh37]
Chr21:21q22.11		 likely benign
NM_000629.3(IFNAR1):c.1143+16A>C single nucleotide variant not provided [RCV002204601] Chr21:33349559 [GRCh38]
Chr21:34721865 [GRCh37]
Chr21:21q22.11		 likely benign
NM_000629.3(IFNAR1):c.1295-14_1295-13del deletion not provided [RCV002164249] Chr21:33353624..33353625 [GRCh38]
Chr21:34725930..34725931 [GRCh37]
Chr21:21q22.11		 likely benign
NM_000629.3(IFNAR1):c.1353G>A (p.Pro451=) single nucleotide variant not provided [RCV002142233]|not specified [RCV004631963] Chr21:33353696 [GRCh38]
Chr21:34726002 [GRCh37]
Chr21:21q22.11		 likely benign
NM_000629.3(IFNAR1):c.531+12T>G single nucleotide variant not provided [RCV002142578] Chr21:33343434 [GRCh38]
Chr21:34715740 [GRCh37]
Chr21:21q22.11		 likely benign
NM_000629.3(IFNAR1):c.201-10dup duplication not provided [RCV002175738] Chr21:33340981..33340982 [GRCh38]
Chr21:34713287..34713288 [GRCh37]
Chr21:21q22.11		 benign
NM_000629.3(IFNAR1):c.201-18del deletion not provided [RCV002162198] Chr21:33340981 [GRCh38]
Chr21:34713287 [GRCh37]
Chr21:21q22.11		 likely benign
NM_000629.3(IFNAR1):c.1241del (p.Lys414fs) deletion not provided [RCV003114843] Chr21:33352852 [GRCh38]
Chr21:34725158 [GRCh37]
Chr21:21q22.11		 pathogenic
NM_000629.3(IFNAR1):c.341G>C (p.Trp114Ser) single nucleotide variant Susceptibility to severe COVID-19 [RCV003120380] Chr21:33341139 [GRCh38]
Chr21:34713445 [GRCh37]
Chr21:21q22.11		 likely risk allele
NM_000629.3(IFNAR1):c.131A>C (p.Asn44Thr) single nucleotide variant Susceptibility to severe COVID-19 [RCV003120381] Chr21:33335578 [GRCh38]
Chr21:34707884 [GRCh37]
Chr21:21q22.11		 likely risk allele
Single allele deletion ZTTK syndrome [RCV002247722] Chr21:32213458..34373118 [GRCh38]
Chr21:21q22.11		 pathogenic
NM_000629.3(IFNAR1):c.922C>T (p.Gln308Ter) single nucleotide variant Immunodeficiency 106, susceptibility to viral infections [RCV002260525] Chr21:33349224 [GRCh38]
Chr21:34721530 [GRCh37]
Chr21:21q22.11		 risk factor
NM_000629.3(IFNAR1):c.1440+331_*239del deletion Immunodeficiency 106, susceptibility to viral infections [RCV002260526] Chr21:33354082..33355756 [GRCh38]
Chr21:34726388..34728062 [GRCh37]
Chr21:21q22.11		 risk factor
NM_000629.3(IFNAR1):c.788+1636_1144-1368del deletion Immunodeficiency 106, susceptibility to viral infections [RCV002260527] Chr21:33346995..33351389 [GRCh38]
Chr21:34719301..34723695 [GRCh37]
Chr21:21q22.11		 risk factor
GRCh37/hg19 21q22.11(chr21:33032083-34809269)x3 copy number gain not provided [RCV002293062] Chr21:33032083..34809269 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.392C>T (p.Pro131Leu) single nucleotide variant not specified [RCV004314164] Chr21:33343283 [GRCh38]
Chr21:34715589 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.531+2T>G single nucleotide variant not provided [RCV002750443] Chr21:33343424 [GRCh38]
Chr21:34715730 [GRCh37]
Chr21:21q22.11		 likely pathogenic
NM_000629.3(IFNAR1):c.206G>A (p.Gly69Glu) single nucleotide variant not provided [RCV002304282] Chr21:33341004 [GRCh38]
Chr21:34713310 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.688C>G (p.Pro230Ala) single nucleotide variant not provided [RCV002296502] Chr21:33345260 [GRCh38]
Chr21:34717566 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.464T>G (p.Met155Arg) single nucleotide variant not provided [RCV002298035] Chr21:33343355 [GRCh38]
Chr21:34715661 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.1643C>T (p.Thr548Ile) single nucleotide variant not provided [RCV002731612] Chr21:33355518 [GRCh38]
Chr21:34727824 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.27del (p.Thr10fs) deletion not provided [RCV002904554] Chr21:33325082 [GRCh38]
Chr21:34697387 [GRCh37]
Chr21:21q22.11		 pathogenic
NM_000629.3(IFNAR1):c.50C>T (p.Ala17Val) single nucleotide variant not provided [RCV002862365]|not specified [RCV004064980] Chr21:33325105 [GRCh38]
Chr21:34697410 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.646A>G (p.Ser216Gly) single nucleotide variant not provided [RCV002816178] Chr21:33343649 [GRCh38]
Chr21:34715955 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.1441-1G>A single nucleotide variant not provided [RCV002971462] Chr21:33355315 [GRCh38]
Chr21:34727621 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.219G>C (p.Trp73Cys) single nucleotide variant not provided [RCV002618762] Chr21:33341017 [GRCh38]
Chr21:34713323 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.1570C>A (p.His524Asn) single nucleotide variant not provided [RCV002731559] Chr21:33355445 [GRCh38]
Chr21:34727751 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.752C>T (p.Thr251Ile) single nucleotide variant not provided [RCV002616211] Chr21:33345324 [GRCh38]
Chr21:34717630 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.76+9C>A single nucleotide variant not provided [RCV003014445] Chr21:33325140 [GRCh38]
Chr21:34697445 [GRCh37]
Chr21:21q22.11		 likely benign
NM_000629.3(IFNAR1):c.940A>G (p.Asn314Asp) single nucleotide variant not specified [RCV004119373] Chr21:33349242 [GRCh38]
Chr21:34721548 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.1523T>C (p.Ile508Thr) single nucleotide variant not provided [RCV003013571] Chr21:33355398 [GRCh38]
Chr21:34727704 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.1089G>C (p.Gln363His) single nucleotide variant not specified [RCV004205700] Chr21:33349489 [GRCh38]
Chr21:34721795 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.1608A>G (p.Gly536=) single nucleotide variant not provided [RCV002996485] Chr21:33355483 [GRCh38]
Chr21:34727789 [GRCh37]
Chr21:21q22.11		 likely benign
NM_000629.3(IFNAR1):c.1143+9A>G single nucleotide variant not provided [RCV002947618] Chr21:33349552 [GRCh38]
Chr21:34721858 [GRCh37]
Chr21:21q22.11		 likely benign
NM_000629.3(IFNAR1):c.1440+7T>C single nucleotide variant not provided [RCV002881582] Chr21:33353790 [GRCh38]
Chr21:34726096 [GRCh37]
Chr21:21q22.11		 likely benign
NM_000629.3(IFNAR1):c.1486del (p.Glu496fs) deletion not provided [RCV002843135] Chr21:33355361 [GRCh38]
Chr21:34727667 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.1611T>A (p.Asn537Lys) single nucleotide variant not specified [RCV004140598] Chr21:33355486 [GRCh38]
Chr21:34727792 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.1372A>G (p.Lys458Glu) single nucleotide variant not provided [RCV002755764] Chr21:33353715 [GRCh38]
Chr21:34726021 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.1497C>T (p.Ile499=) single nucleotide variant not provided [RCV002842429] Chr21:33355372 [GRCh38]
Chr21:34727678 [GRCh37]
Chr21:21q22.11		 likely benign
NM_000629.3(IFNAR1):c.673+11T>A single nucleotide variant not provided [RCV002867249] Chr21:33343687 [GRCh38]
Chr21:34715993 [GRCh37]
Chr21:21q22.11		 likely benign
NM_000629.3(IFNAR1):c.1062A>C (p.Lys354Asn) single nucleotide variant not provided [RCV003079378] Chr21:33349462 [GRCh38]
Chr21:34721768 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.1587C>G (p.Ser529=) single nucleotide variant not provided [RCV002705549] Chr21:33355462 [GRCh38]
Chr21:34727768 [GRCh37]
Chr21:21q22.11		 likely benign
NM_000629.3(IFNAR1):c.335C>A (p.Ser112Tyr) single nucleotide variant not provided [RCV002824135] Chr21:33341133 [GRCh38]
Chr21:34713439 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.913C>A (p.Leu305Ile) single nucleotide variant not provided [RCV002590755] Chr21:33349215 [GRCh38]
Chr21:34721521 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.84A>G (p.Lys28=) single nucleotide variant not provided [RCV003035629] Chr21:33335531 [GRCh38]
Chr21:34707837 [GRCh37]
Chr21:21q22.11		 likely benign
NM_000629.3(IFNAR1):c.1042A>G (p.Ile348Val) single nucleotide variant not provided [RCV002736057] Chr21:33349442 [GRCh38]
Chr21:34721748 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.945A>T (p.Thr315=) single nucleotide variant not provided [RCV002735118] Chr21:33349247 [GRCh38]
Chr21:34721553 [GRCh37]
Chr21:21q22.11		 likely benign
NM_000629.3(IFNAR1):c.1440+24dup duplication not provided [RCV002590799] Chr21:33353800..33353801 [GRCh38]
Chr21:34726106..34726107 [GRCh37]
Chr21:21q22.11		 benign
NM_000629.3(IFNAR1):c.201-12T>A single nucleotide variant not provided [RCV002848130] Chr21:33340987 [GRCh38]
Chr21:34713293 [GRCh37]
Chr21:21q22.11		 likely benign
NM_000629.3(IFNAR1):c.889G>A (p.Val297Ile) single nucleotide variant not specified [RCV004220559] Chr21:33349191 [GRCh38]
Chr21:34721497 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.1390A>G (p.Ile464Val) single nucleotide variant not provided [RCV002909517] Chr21:33353733 [GRCh38]
Chr21:34726039 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.205G>C (p.Gly69Arg) single nucleotide variant not provided [RCV002570232] Chr21:33341003 [GRCh38]
Chr21:34713309 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.1350C>G (p.Leu450=) single nucleotide variant not provided [RCV002700696] Chr21:33353693 [GRCh38]
Chr21:34725999 [GRCh37]
Chr21:21q22.11		 likely benign
NM_000629.3(IFNAR1):c.518C>T (p.Ser173Phe) single nucleotide variant not provided [RCV002745670] Chr21:33343409 [GRCh38]
Chr21:34715715 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.200+5G>T single nucleotide variant not provided [RCV002576404] Chr21:33335652 [GRCh38]
Chr21:34707958 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.1427C>T (p.Ser476Phe) single nucleotide variant not provided [RCV002933462] Chr21:33353770 [GRCh38]
Chr21:34726076 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.193T>C (p.Tyr65His) single nucleotide variant not provided [RCV003043015] Chr21:33335640 [GRCh38]
Chr21:34707946 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.1440+16T>A single nucleotide variant not provided [RCV002790997] Chr21:33353799 [GRCh38]
Chr21:34726105 [GRCh37]
Chr21:21q22.11		 likely benign
NM_000629.3(IFNAR1):c.988+12G>T single nucleotide variant not provided [RCV002700302] Chr21:33349302 [GRCh38]
Chr21:34721608 [GRCh37]
Chr21:21q22.11		 likely benign
NM_000629.3(IFNAR1):c.21C>T (p.Gly7=) single nucleotide variant not provided [RCV002766176] Chr21:33325076 [GRCh38]
Chr21:34697381 [GRCh37]
Chr21:21q22.11		 likely benign
NM_000629.3(IFNAR1):c.988+2_988+6del deletion not provided [RCV002740827] Chr21:33349288..33349292 [GRCh38]
Chr21:34721594..34721598 [GRCh37]
Chr21:21q22.11		 likely pathogenic
NM_000629.3(IFNAR1):c.1570C>T (p.His524Tyr) single nucleotide variant not provided [RCV002594913] Chr21:33355445 [GRCh38]
Chr21:34727751 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.789-12T>C single nucleotide variant not provided [RCV002573649] Chr21:33349079 [GRCh38]
Chr21:34721385 [GRCh37]
Chr21:21q22.11		 likely benign
NM_000629.3(IFNAR1):c.1143+1G>A single nucleotide variant not provided [RCV002626676] Chr21:33349544 [GRCh38]
Chr21:34721850 [GRCh37]
Chr21:21q22.11		 likely pathogenic
NM_000629.3(IFNAR1):c.252dup (p.Thr85fs) duplication not provided [RCV002853459] Chr21:33341049..33341050 [GRCh38]
Chr21:34713355..34713356 [GRCh37]
Chr21:21q22.11		 pathogenic
NM_000629.3(IFNAR1):c.24G>A (p.Ala8=) single nucleotide variant not provided [RCV002829549] Chr21:33325079 [GRCh38]
Chr21:34697384 [GRCh37]
Chr21:21q22.11		 likely benign
NM_000629.3(IFNAR1):c.1370C>T (p.Ala457Val) single nucleotide variant not provided [RCV003059024]|not specified [RCV004070273] Chr21:33353713 [GRCh38]
Chr21:34726019 [GRCh37]
Chr21:21q22.11		 likely benign|uncertain significance
NM_000629.3(IFNAR1):c.1077G>A (p.Thr359=) single nucleotide variant not provided [RCV003083281] Chr21:33349477 [GRCh38]
Chr21:34721783 [GRCh37]
Chr21:21q22.11		 likely benign
NM_000629.3(IFNAR1):c.560A>G (p.His187Arg) single nucleotide variant not specified [RCV004132441] Chr21:33343563 [GRCh38]
Chr21:34715869 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.308G>A (p.Arg103His) single nucleotide variant not provided [RCV002982505] Chr21:33341106 [GRCh38]
Chr21:34713412 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.10G>A (p.Val4Ile) single nucleotide variant not provided [RCV003040244] Chr21:33325065 [GRCh38]
Chr21:34697370 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.291T>A (p.Tyr97Ter) single nucleotide variant not provided [RCV002811728] Chr21:33341089 [GRCh38]
Chr21:34713395 [GRCh37]
Chr21:21q22.11		 pathogenic
NM_000629.3(IFNAR1):c.181T>G (p.Phe61Val) single nucleotide variant not provided [RCV002966804] Chr21:33335628 [GRCh38]
Chr21:34707934 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.444T>C (p.Pro148=) single nucleotide variant not provided [RCV002962430] Chr21:33343335 [GRCh38]
Chr21:34715641 [GRCh37]
Chr21:21q22.11		 likely benign
NM_000629.3(IFNAR1):c.371G>A (p.Arg124His) single nucleotide variant not provided [RCV002632906] Chr21:33341169 [GRCh38]
Chr21:34713475 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.1484C>T (p.Ser495Phe) single nucleotide variant not provided [RCV003044469] Chr21:33355359 [GRCh38]
Chr21:34727665 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.518C>G (p.Ser173Cys) single nucleotide variant not provided [RCV003669343]|not specified [RCV004165102] Chr21:33343409 [GRCh38]
Chr21:34715715 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.14T>G (p.Leu5Arg) single nucleotide variant not provided [RCV002598495] Chr21:33325069 [GRCh38]
Chr21:34697374 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.996A>G (p.Leu332=) single nucleotide variant not provided [RCV002720036] Chr21:33349396 [GRCh38]
Chr21:34721702 [GRCh37]
Chr21:21q22.11		 likely benign
NM_000629.3(IFNAR1):c.872G>T (p.Cys291Phe) single nucleotide variant not provided [RCV003029639] Chr21:33349174 [GRCh38]
Chr21:34721480 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.1156G>A (p.Glu386Lys) single nucleotide variant not provided [RCV002579902] Chr21:33352770 [GRCh38]
Chr21:34725076 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.1295-14G>A single nucleotide variant not provided [RCV002650848] Chr21:33353624 [GRCh38]
Chr21:34725930 [GRCh37]
Chr21:21q22.11		 likely benign
NM_000629.3(IFNAR1):c.201-19T>C single nucleotide variant not provided [RCV002807199] Chr21:33340980 [GRCh38]
Chr21:34713286 [GRCh37]
Chr21:21q22.11		 likely benign
NM_000629.3(IFNAR1):c.790G>A (p.Ala264Thr) single nucleotide variant not specified [RCV004077921] Chr21:33349092 [GRCh38]
Chr21:34721398 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.958G>A (p.Glu320Lys) single nucleotide variant not specified [RCV004144457] Chr21:33349260 [GRCh38]
Chr21:34721566 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.93A>C (p.Lys31Asn) single nucleotide variant not provided [RCV002649343] Chr21:33335540 [GRCh38]
Chr21:34707846 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.128A>G (p.Asp43Gly) single nucleotide variant not specified [RCV004096351] Chr21:33335575 [GRCh38]
Chr21:34707881 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.976A>G (p.Thr326Ala) single nucleotide variant not specified [RCV004077651] Chr21:33349278 [GRCh38]
Chr21:34721584 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.954G>C (p.Trp318Cys) single nucleotide variant not provided [RCV002608333] Chr21:33349256 [GRCh38]
Chr21:34721562 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.1264A>C (p.Ser422Arg) single nucleotide variant not provided [RCV002608493] Chr21:33352878 [GRCh38]
Chr21:34725184 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.989-13A>G single nucleotide variant not provided [RCV002586357] Chr21:33349376 [GRCh38]
Chr21:34721682 [GRCh37]
Chr21:21q22.11		 likely benign
NM_000629.3(IFNAR1):c.285T>C (p.Asn95=) single nucleotide variant not provided [RCV002654311] Chr21:33341083 [GRCh38]
Chr21:34713389 [GRCh37]
Chr21:21q22.11		 likely benign
NM_000629.3(IFNAR1):c.69A>G (p.Ala23=) single nucleotide variant not provided [RCV002607825] Chr21:33325124 [GRCh38]
Chr21:34697429 [GRCh37]
Chr21:21q22.11		 likely benign
NM_000629.3(IFNAR1):c.831G>A (p.Trp277Ter) single nucleotide variant not provided [RCV002589655] Chr21:33349133 [GRCh38]
Chr21:34721439 [GRCh37]
Chr21:21q22.11		 pathogenic
NM_000629.3(IFNAR1):c.516C>T (p.Asn172=) single nucleotide variant not provided [RCV002603027] Chr21:33343407 [GRCh38]
Chr21:34715713 [GRCh37]
Chr21:21q22.11		 likely benign
NM_000629.3(IFNAR1):c.548T>G (p.Ile183Ser) single nucleotide variant not specified [RCV004265430] Chr21:33343551 [GRCh38]
Chr21:34715857 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.299T>C (p.Ile100Thr) single nucleotide variant not specified [RCV004314308] Chr21:33341097 [GRCh38]
Chr21:34713403 [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_000629.3(IFNAR1):c.835C>A (p.Gln279Lys) single nucleotide variant not provided [RCV003440542] Chr21:33349137 [GRCh38]
Chr21:34721443 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.1050C>T (p.Ile350=) single nucleotide variant not provided [RCV003739431] Chr21:33349450 [GRCh38]
Chr21:34721756 [GRCh37]
Chr21:21q22.11		 likely benign
NM_000629.3(IFNAR1):c.472T>C (p.Leu158=) single nucleotide variant not provided [RCV003876976] Chr21:33343363 [GRCh38]
Chr21:34715669 [GRCh37]
Chr21:21q22.11		 likely benign
NM_000629.3(IFNAR1):c.227dup (p.Leu76fs) duplication not provided [RCV003573778] Chr21:33341023..33341024 [GRCh38]
Chr21:34713329..34713330 [GRCh37]
Chr21:21q22.11		 pathogenic
NM_000629.3(IFNAR1):c.1440+38T>A single nucleotide variant not specified [RCV003488843] Chr21:33353821 [GRCh38]
Chr21:34726127 [GRCh37]
Chr21:21q22.11		 benign
NM_000629.3(IFNAR1):c.77-22T>G single nucleotide variant not specified [RCV003488982] Chr21:33335502 [GRCh38]
Chr21:34707808 [GRCh37]
Chr21:21q22.11		 benign
NM_000629.3(IFNAR1):c.200+108A>G single nucleotide variant not specified [RCV003489164] Chr21:33335755 [GRCh38]
Chr21:34708061 [GRCh37]
Chr21:21q22.11		 benign
NM_000629.3(IFNAR1):c.789-49A>G single nucleotide variant not specified [RCV003489145] Chr21:33349042 [GRCh38]
Chr21:34721348 [GRCh37]
Chr21:21q22.11		 benign
NM_000629.3(IFNAR1):c.64T>G (p.Ser22Ala) single nucleotide variant not provided [RCV003547199] Chr21:33325119 [GRCh38]
Chr21:34697424 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.687A>G (p.Leu229=) single nucleotide variant not provided [RCV003661359] Chr21:33345259 [GRCh38]
Chr21:34717565 [GRCh37]
Chr21:21q22.11		 likely benign
NM_000629.3(IFNAR1):c.1165del (p.Thr389fs) deletion not provided [RCV003545777] Chr21:33352773 [GRCh38]
Chr21:34725079 [GRCh37]
Chr21:21q22.11		 pathogenic
NM_000629.3(IFNAR1):c.1440+9C>T single nucleotide variant not provided [RCV003881599] Chr21:33353792 [GRCh38]
Chr21:34726098 [GRCh37]
Chr21:21q22.11		 likely benign
NM_000629.3(IFNAR1):c.532-15A>T single nucleotide variant not provided [RCV003882133] Chr21:33343520 [GRCh38]
Chr21:34715826 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.846C>T (p.Asp282=) single nucleotide variant not provided [RCV003691898] Chr21:33349148 [GRCh38]
Chr21:34721454 [GRCh37]
Chr21:21q22.11		 likely benign
NM_000629.3(IFNAR1):c.333T>G (p.Thr111=) single nucleotide variant not provided [RCV003547935] Chr21:33341131 [GRCh38]
Chr21:34713437 [GRCh37]
Chr21:21q22.11		 likely benign
NM_000629.3(IFNAR1):c.959A>C (p.Glu320Ala) single nucleotide variant not provided [RCV003543991] Chr21:33349261 [GRCh38]
Chr21:34721567 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.354C>T (p.Asp118=) single nucleotide variant not provided [RCV003664293] Chr21:33341152 [GRCh38]
Chr21:34713458 [GRCh37]
Chr21:21q22.11		 likely benign
NM_000629.3(IFNAR1):c.789-2A>G single nucleotide variant not provided [RCV003855489] Chr21:33349089 [GRCh38]
Chr21:34721395 [GRCh37]
Chr21:21q22.11		 likely pathogenic
NM_000629.3(IFNAR1):c.1143+19A>T single nucleotide variant not provided [RCV003674191] Chr21:33349562 [GRCh38]
Chr21:34721868 [GRCh37]
Chr21:21q22.11		 likely benign
NM_000629.3(IFNAR1):c.377-12A>T single nucleotide variant not provided [RCV003666679] Chr21:33343256 [GRCh38]
Chr21:34715562 [GRCh37]
Chr21:21q22.11		 likely benign
NM_000629.3(IFNAR1):c.76+10G>A single nucleotide variant not provided [RCV003703578] Chr21:33325141 [GRCh38]
Chr21:34697446 [GRCh37]
Chr21:21q22.11		 likely benign
NM_000629.3(IFNAR1):c.77-9C>T single nucleotide variant not provided [RCV003548280] Chr21:33335515 [GRCh38]
Chr21:34707821 [GRCh37]
Chr21:21q22.11		 likely benign
NM_000629.3(IFNAR1):c.660T>C (p.Cys220=) single nucleotide variant not provided [RCV003666985] Chr21:33343663 [GRCh38]
Chr21:34715969 [GRCh37]
Chr21:21q22.11		 likely benign
NM_000629.3(IFNAR1):c.1143+16A>G single nucleotide variant not provided [RCV003837963] Chr21:33349559 [GRCh38]
Chr21:34721865 [GRCh37]
Chr21:21q22.11		 likely benign
NM_000629.3(IFNAR1):c.639T>C (p.Gly213=) single nucleotide variant not provided [RCV003856019] Chr21:33343642 [GRCh38]
Chr21:34715948 [GRCh37]
Chr21:21q22.11		 likely benign
NM_000629.3(IFNAR1):c.15C>A (p.Leu5=) single nucleotide variant not provided [RCV003668977] Chr21:33325070 [GRCh38]
Chr21:34697375 [GRCh37]
Chr21:21q22.11		 likely benign
NM_000629.3(IFNAR1):c.72C>T (p.Ala24=) single nucleotide variant not provided [RCV003558070] Chr21:33325127 [GRCh38]
Chr21:34697432 [GRCh37]
Chr21:21q22.11		 likely benign
NM_000629.3(IFNAR1):c.1633G>A (p.Glu545Lys) single nucleotide variant not provided [RCV003823524] Chr21:33355508 [GRCh38]
Chr21:34727814 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.18G>A (p.Leu6=) single nucleotide variant not provided [RCV003848181] Chr21:33325073 [GRCh38]
Chr21:34697378 [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_000629.3(IFNAR1):c.750T>G (p.Tyr250Ter) single nucleotide variant not provided [RCV003859797] Chr21:33345322 [GRCh38]
Chr21:34717628 [GRCh37]
Chr21:21q22.11		 pathogenic
NM_000629.3(IFNAR1):c.222A>C (p.Ile74=) single nucleotide variant not provided [RCV003554264] Chr21:33341020 [GRCh38]
Chr21:34713326 [GRCh37]
Chr21:21q22.11		 likely 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
NM_000629.3(IFNAR1):c.1130_1134del (p.Thr377fs) deletion not provided [RCV003858982] Chr21:33349528..33349532 [GRCh38]
Chr21:34721834..34721838 [GRCh37]
Chr21:21q22.11		 pathogenic
NM_000629.3(IFNAR1):c.1144-9A>G single nucleotide variant not provided [RCV003677955] Chr21:33352749 [GRCh38]
Chr21:34725055 [GRCh37]
Chr21:21q22.11		 likely benign
NM_000629.3(IFNAR1):c.989-11A>T single nucleotide variant not provided [RCV003683518] Chr21:33349378 [GRCh38]
Chr21:34721684 [GRCh37]
Chr21:21q22.11		 likely benign
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_000629.3(IFNAR1):c.908A>G (p.Tyr303Cys) single nucleotide variant not provided [RCV003864907] Chr21:33349210 [GRCh38]
Chr21:34721516 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.141G>C (p.Leu47=) single nucleotide variant not provided [RCV003557341] Chr21:33335588 [GRCh38]
Chr21:34707894 [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
NM_000629.3(IFNAR1):c.473T>C (p.Leu158Ser) single nucleotide variant not provided [RCV003705819] Chr21:33343364 [GRCh38]
Chr21:34715670 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.114C>T (p.Val38=) single nucleotide variant not provided [RCV003821474] Chr21:33335561 [GRCh38]
Chr21:34707867 [GRCh37]
Chr21:21q22.11		 likely benign
NM_000629.3(IFNAR1):c.*2205_*2213del deletion Immunodeficiency 106, susceptibility to viral infections [RCV003990193] Chr21:33357754..33357762 [GRCh38]
Chr21:34730060..34730068 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.1671_*1821del (p.Ter558AlaextTer?) deletion Immunodeficiency 106, susceptibility to viral infections [RCV003988960] Chr21:33355546..33357370 [GRCh38]
Chr21:34727852..34729676 [GRCh37]
Chr21:21q22.11		 uncertain significance
GRCh37/hg19 21q11.2-22.3(chr21:15380398-48100790)x3 copy number gain not provided [RCV004577449] Chr21:15380398..48100790 [GRCh37]
Chr21:21q11.2-22.3		 pathogenic
NM_000629.3(IFNAR1):c.470C>T (p.Ala157Val) single nucleotide variant not specified [RCV004400184] Chr21:33343361 [GRCh38]
Chr21:34715667 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.478G>A (p.Gly160Ser) single nucleotide variant not specified [RCV004400185] Chr21:33343369 [GRCh38]
Chr21:34715675 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.688C>T (p.Pro230Ser) single nucleotide variant not specified [RCV004400186] Chr21:33345260 [GRCh38]
Chr21:34717566 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.812G>A (p.Gly271Glu) single nucleotide variant not specified [RCV004400187] Chr21:33349114 [GRCh38]
Chr21:34721420 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.1046A>G (p.Tyr349Cys) single nucleotide variant not specified [RCV004400181] Chr21:33349446 [GRCh38]
Chr21:34721752 [GRCh37]
Chr21:21q22.11		 uncertain significance
NC_000021.8:g.(?_34720267)_(34721595_?)del deletion not provided [RCV004579346] Chr21:34720267..34721595 [GRCh37]
Chr21:21q22.11		 likely pathogenic
NM_000629.3(IFNAR1):c.1529C>T (p.Thr510Ile) single nucleotide variant not specified [RCV004635601] Chr21:33355404 [GRCh38]
Chr21:34727710 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.380A>C (p.Gln127Pro) single nucleotide variant not specified [RCV004400183] Chr21:33343271 [GRCh38]
Chr21:34715577 [GRCh37]
Chr21:21q22.11		 uncertain significance
NC_000021.8:g.(?_34638751)_(34809289_?)dup duplication Immunodeficiency 28 [RCV000652134] Chr21:34638751..34809289 [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
NM_000629.3(IFNAR1):c.674-1G>A single nucleotide variant Immunodeficiency 106, susceptibility to viral infections [RCV002260520] Chr21:33345245 [GRCh38]
Chr21:34717551 [GRCh37]
Chr21:21q22.11		 risk factor|uncertain significance
NM_000629.3(IFNAR1):c.783G>A (p.Trp261Ter) single nucleotide variant Immunodeficiency 106, susceptibility to viral infections [RCV002260521] Chr21:33345355 [GRCh38]
Chr21:34717661 [GRCh37]
Chr21:21q22.11		 risk factor|uncertain significance
NM_000629.3(IFNAR1):c.728A>C (p.Asn243Thr) single nucleotide variant not provided [RCV001493071] Chr21:33345300 [GRCh38]
Chr21:34717606 [GRCh37]
Chr21:21q22.11		 benign|likely benign
NM_000629.3(IFNAR1):c.1672_*3del (p.Ter558del) deletion IMMUNODEFICIENCY 106, SUSCEPTIBILITY TO VIRAL INFECTIONS/IMMUNODEFICIENCY 28, DIGENIC [RCV002260522]|Immunodeficiency 106, susceptibility to viral infections [RCV003989703] Chr21:33355546..33355551 [GRCh38]
Chr21:34727852..34727857 [GRCh37]
Chr21:21q22.11		 risk factor|uncertain significance
GRCh37/hg19 21p13-q22.3(chr21:1-48129895)x3 copy number gain See cases [RCV001780078] Chr21:1..48129895 [GRCh37]
Chr21:21p13-q22.3		 pathogenic
NM_000629.3(IFNAR1):c.1223C>T (p.Ala408Val) single nucleotide variant not provided [RCV002001965] Chr21:33352837 [GRCh38]
Chr21:34725143 [GRCh37]
Chr21:21q22.11		 uncertain significance
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
NM_000629.3(IFNAR1):c.1083G>T (p.Val361=) single nucleotide variant not provided [RCV002088084] Chr21:33349483 [GRCh38]
Chr21:34721789 [GRCh37]
Chr21:21q22.11		 likely benign
NC_000021.9:g.(33336874_33344911)del deletion Immunodeficiency 106, susceptibility to viral infections [RCV003140469]   pathogenic
NM_000629.3(IFNAR1):c.1356del (p.Phe452fs) deletion Immunodeficiency 106, susceptibility to viral infections [RCV003331968] Chr21:33353697 [GRCh38]
Chr21:34726003 [GRCh37]
Chr21:21q22.11		 likely pathogenic
NM_000629.3(IFNAR1):c.1672T>C (p.Ter558Arg) single nucleotide variant Immunodeficiency 106, susceptibility to viral infections [RCV003990929] Chr21:33355547 [GRCh38]
Chr21:34727853 [GRCh37]
Chr21:21q22.11		 uncertain significance
NM_000629.3(IFNAR1):c.218G>C (p.Trp73Ser) single nucleotide variant not specified [RCV004400182] Chr21:33341016 [GRCh38]
Chr21:34713322 [GRCh37]
Chr21:21q22.11		 uncertain significance
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:2123
Count of miRNA genes:1034
Interacting mature miRNAs:1242
Transcripts:ENST00000270139, ENST00000416947, ENST00000442071, ENST00000442357, ENST00000493503
Prediction methods:Miranda, Rnahybrid, Targetscan
Result types:miRGate_prediction

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

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


QTLs in Region (GRCh38)
The following QTLs overlap with this region.    Full Report CSV TAB Printer Gviewer
RGD IDSymbolNameLODP ValueTraitSub TraitChrStartStopSpecies
407258866GWAS907842_Hinterferon alpha/beta receptor 1 measurement QTL GWAS907842 (human)1e-51interferon alpha/beta receptor 1 measurement213332567633325677Human
407293170GWAS942146_Hinterferon alpha/beta receptor 1 measurement QTL GWAS942146 (human)8e-13interferon alpha/beta receptor 1 measurement213332820033328201Human
406893060GWAS542036_Hinterferon alpha/beta receptor 1 measurement QTL GWAS542036 (human)1e-15interferon alpha/beta receptor 1 measurement213334339333343394Human
407280753GWAS929729_Hinterferon alpha/beta receptor 1 measurement QTL GWAS929729 (human)5e-58interferon alpha/beta receptor 1 measurement213334339333343394Human
407293166GWAS942142_Hinterferon alpha/beta receptor 1 measurement QTL GWAS942142 (human)2e-123interferon alpha/beta receptor 1 measurement213334339333343394Human
406939209GWAS588185_Hinterferon alpha/beta receptor 1 measurement QTL GWAS588185 (human)3e-328interferon alpha/beta receptor 1 measurement213334339333343394Human
407293167GWAS942143_Hinterferon alpha/beta receptor 1 measurement QTL GWAS942143 (human)2e-28interferon alpha/beta receptor 1 measurement213335864833358649Human
2303081MAMTS49_HMammary tumor susceptibility QTL 49 (human)1.72Mammary tumor susceptibility211795044843950448Human
407036712GWAS685688_Hblood protein measurement QTL GWAS685688 (human)3e-32blood protein measurementblood protein measurement (CMO:0000028)213334339333343394Human
407199577GWAS848553_Hblood protein measurement QTL GWAS848553 (human)1e-41blood protein measurementblood protein measurement (CMO:0000028)213334116833341169Human
407199578GWAS848554_Hblood protein measurement QTL GWAS848554 (human)1e-53blood protein measurementblood protein measurement (CMO:0000028)213334339333343394Human

Markers in Region
G34659  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,728,630 - 34,728,805UniSTSGRCh37
Build 362133,650,500 - 33,650,675RGDNCBI36
Celera2119,918,715 - 19,918,890RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,197,460 - 20,197,635UniSTS
SHGC-87597  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,721,825 - 34,721,945UniSTSGRCh37
Build 362133,643,695 - 33,643,815RGDNCBI36
Celera2119,911,910 - 19,912,030RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,190,655 - 20,190,775UniSTS
TNG Radiation Hybrid Map2111423.0UniSTS
GeneMap99-GB4 RH Map21170.1UniSTS
NCBI RH Map21250.3UniSTS
SHGC-19221  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,731,990 - 34,732,129UniSTSGRCh37
Build 362133,653,860 - 33,653,999RGDNCBI36
Celera2119,922,075 - 19,922,214RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,200,819 - 20,200,958UniSTS
TNG Radiation Hybrid Map2111427.0UniSTS
STS-J03171  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,727,885 - 34,728,009UniSTSGRCh37
Build 362133,649,755 - 33,649,879RGDNCBI36
Celera2119,917,970 - 19,918,094RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,196,715 - 20,196,839UniSTS
GeneMap99-GB4 RH Map21152.54UniSTS
D20S588E  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,730,140 - 34,730,246UniSTSGRCh37
Build 362133,652,010 - 33,652,116RGDNCBI36
Celera2119,920,225 - 19,920,331RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,198,969 - 20,199,075UniSTS
GDB:182417  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,716,968 - 34,717,432UniSTSGRCh37
Build 362133,638,838 - 33,639,302RGDNCBI36
Celera2119,907,054 - 19,907,518RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,185,795 - 20,186,263UniSTS
GDB:185153  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,728,342 - 34,728,583UniSTSGRCh37
Build 362133,650,212 - 33,650,453RGDNCBI36
Celera2119,918,427 - 19,918,668RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,197,172 - 20,197,413UniSTS
GDB:185155  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,727,854 - 34,728,122UniSTSGRCh37
Build 362133,649,724 - 33,649,992RGDNCBI36
Celera2119,917,939 - 19,918,207RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,196,684 - 20,196,952UniSTS
ECD04183  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,725,567 - 34,726,339UniSTSGRCh37
Build 362133,647,437 - 33,648,209RGDNCBI36
Celera2119,915,652 - 19,916,424RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,194,397 - 20,195,169UniSTS
ECD04816  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,697,096 - 34,697,849UniSTSGRCh37
Build 362133,618,966 - 33,619,719RGDNCBI36
Celera2119,887,182 - 19,887,935RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,165,926 - 20,166,679UniSTS
ECD04919  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,701,381 - 34,702,131UniSTSGRCh37
Build 362133,623,251 - 33,624,001RGDNCBI36
Celera2119,891,467 - 19,892,217RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,170,209 - 20,170,959UniSTS
ECD05456  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,707,484 - 34,708,219UniSTSGRCh37
Build 362133,629,354 - 33,630,089RGDNCBI36
Celera2119,897,570 - 19,898,305RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,176,313 - 20,177,048UniSTS
ECD07519  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,729,111 - 34,729,790UniSTSGRCh37
Build 362133,650,981 - 33,651,660RGDNCBI36
Celera2119,919,196 - 19,919,875RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,197,941 - 20,198,620UniSTS
ECD07559  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,728,377 - 34,729,055UniSTSGRCh37
Build 362133,650,247 - 33,650,925RGDNCBI36
Celera2119,918,462 - 19,919,140RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,197,207 - 20,197,885UniSTS
ECD09740  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,718,513 - 34,719,134UniSTSGRCh37
Build 362133,640,383 - 33,641,004RGDNCBI36
Celera2119,908,599 - 19,909,220RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,187,344 - 20,187,965UniSTS
ECD10724  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,696,476 - 34,697,069UniSTSGRCh37
Build 362133,618,346 - 33,618,939RGDNCBI36
Celera2119,886,562 - 19,887,155RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,165,306 - 20,165,899UniSTS
ECD11881  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,726,958 - 34,727,517UniSTSGRCh37
Build 362133,648,828 - 33,649,387RGDNCBI36
Celera2119,917,043 - 19,917,602RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,195,788 - 20,196,347UniSTS
ECD12012  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,712,994 - 34,713,549UniSTSGRCh37
Build 362133,634,864 - 33,635,419RGDNCBI36
Celera2119,903,080 - 19,903,635RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,181,821 - 20,182,376UniSTS
ECD13186  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,716,522 - 34,717,046UniSTSGRCh37
Build 362133,638,392 - 33,638,916RGDNCBI36
Celera2119,906,608 - 19,907,132RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,185,349 - 20,185,873UniSTS
ECD13225  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,721,411 - 34,721,934UniSTSGRCh37
Build 362133,643,281 - 33,643,804RGDNCBI36
Celera2119,911,496 - 19,912,019RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,190,241 - 20,190,764UniSTS
ECD13536  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,730,138 - 34,730,653UniSTSGRCh37
Build 362133,652,008 - 33,652,523RGDNCBI36
Celera2119,920,223 - 19,920,738RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,198,967 - 20,199,482UniSTS
ECD14456  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,731,454 - 34,731,947UniSTSGRCh37
Build 362133,653,324 - 33,653,817RGDNCBI36
Celera2119,921,539 - 19,922,032RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,200,283 - 20,200,776UniSTS
ECD14769  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,699,127 - 34,699,613UniSTSGRCh37
Build 362133,620,997 - 33,621,483RGDNCBI36
Celera2119,889,213 - 19,889,699RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,167,956 - 20,168,442UniSTS
ECD14770  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,715,573 - 34,716,059UniSTSGRCh37
Build 362133,637,443 - 33,637,929RGDNCBI36
Celera2119,905,659 - 19,906,145RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,184,400 - 20,184,886UniSTS
ECD14850  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,731,980 - 34,732,464UniSTSGRCh37
Build 362133,653,850 - 33,654,334RGDNCBI36
Celera2119,922,065 - 19,922,549RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,200,809 - 20,201,293UniSTS
ECD14982  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,706,921 - 34,707,402UniSTSGRCh37
GRCh371161,011,123 - 161,012,646UniSTSGRCh37
Build 362133,628,791 - 33,629,272RGDNCBI36
Celera1134,078,391 - 134,079,914UniSTS
Celera2119,897,007 - 19,897,488RGD
Cytogenetic Map21q22.11UniSTS
Cytogenetic Map1q22-q23UniSTS
HuRef1132,369,058 - 132,370,581UniSTS
HuRef2120,175,750 - 20,176,231UniSTS
ECD14983  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,724,944 - 34,725,425UniSTSGRCh37
Build 362133,646,814 - 33,647,295RGDNCBI36
Celera2119,915,029 - 19,915,510RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,193,774 - 20,194,255UniSTS
ECD17703  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,727,626 - 34,728,013UniSTSGRCh37
Build 362133,649,496 - 33,649,883RGDNCBI36
Celera2119,917,711 - 19,918,098RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,196,456 - 20,196,843UniSTS
ECD18252  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,712,284 - 34,712,651UniSTSGRCh37
Build 362133,634,154 - 33,634,521RGDNCBI36
Celera2119,902,370 - 19,902,737RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,181,111 - 20,181,478UniSTS
ECD19003  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,717,397 - 34,717,735UniSTSGRCh37
Build 362133,639,267 - 33,639,605RGDNCBI36
Celera2119,907,483 - 19,907,821RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,186,228 - 20,186,566UniSTS
ECD19158  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,709,570 - 34,709,902UniSTSGRCh37
Build 362133,631,440 - 33,631,772RGDNCBI36
Celera2119,899,656 - 19,899,988RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,178,399 - 20,178,731UniSTS
ECD19620  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,723,499 - 34,723,814UniSTSGRCh37
Build 362133,645,369 - 33,645,684RGDNCBI36
Celera2119,913,584 - 19,913,899RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,192,329 - 20,192,644UniSTS
ECD20408  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,711,466 - 34,711,751UniSTSGRCh37
Build 362133,633,336 - 33,633,621RGDNCBI36
Celera2119,901,552 - 19,901,837RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,180,293 - 20,180,578UniSTS
ECD20662  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,722,855 - 34,723,131UniSTSGRCh37
Build 362133,644,725 - 33,645,001RGDNCBI36
Celera2119,912,940 - 19,913,216RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,191,685 - 20,191,961UniSTS
ECD21407  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,720,129 - 34,720,379UniSTSGRCh37
Build 362133,641,999 - 33,642,249RGDNCBI36
Celera2119,910,214 - 19,910,464RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,188,959 - 20,189,209UniSTS
ECD21448  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,717,971 - 34,718,220UniSTSGRCh37
Build 362133,639,841 - 33,640,090RGDNCBI36
Celera2119,908,057 - 19,908,306RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,186,802 - 20,187,051UniSTS
ECD24140  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,730,803 - 34,730,961UniSTSGRCh37
Build 362133,652,673 - 33,652,831RGDNCBI36
Celera2119,920,888 - 19,921,046RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,199,632 - 20,199,790UniSTS
RH18397  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,731,842 - 34,731,976UniSTSGRCh37
Build 362133,653,712 - 33,653,846RGDNCBI36
Celera2119,921,927 - 19,922,061RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,200,671 - 20,200,805UniSTS
GeneMap99-GB4 RH Map21158.76UniSTS
NCBI RH Map21248.3UniSTS
REN84794  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,696,427 - 34,696,651UniSTSGRCh37
Build 362133,618,297 - 33,618,521RGDNCBI36
Celera2119,886,513 - 19,886,737RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,165,257 - 20,165,481UniSTS
REN84795  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,696,626 - 34,696,852UniSTSGRCh37
Build 362133,618,496 - 33,618,722RGDNCBI36
Celera2119,886,712 - 19,886,938RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,165,456 - 20,165,682UniSTS
REN84796  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,696,832 - 34,697,072UniSTSGRCh37
Build 362133,618,702 - 33,618,942RGDNCBI36
Celera2119,886,918 - 19,887,158RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,165,662 - 20,165,902UniSTS
REN84797  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,697,063 - 34,697,297UniSTSGRCh37
Build 362133,618,933 - 33,619,167RGDNCBI36
Celera2119,887,149 - 19,887,383RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,165,893 - 20,166,127UniSTS
REN84798  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,697,227 - 34,697,467UniSTSGRCh37
Build 362133,619,097 - 33,619,337RGDNCBI36
Celera2119,887,313 - 19,887,553RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,166,057 - 20,166,297UniSTS
REN84799  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,697,442 - 34,697,667UniSTSGRCh37
Build 362133,619,312 - 33,619,537RGDNCBI36
Celera2119,887,528 - 19,887,753RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,166,272 - 20,166,497UniSTS
REN84800  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,697,609 - 34,697,876UniSTSGRCh37
Build 362133,619,479 - 33,619,746RGDNCBI36
Celera2119,887,695 - 19,887,962RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,166,439 - 20,166,706UniSTS
REN84801  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,697,857 - 34,698,092UniSTSGRCh37
Build 362133,619,727 - 33,619,962RGDNCBI36
Celera2119,887,943 - 19,888,178RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,166,687 - 20,166,922UniSTS
REN84802  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,698,027 - 34,698,284UniSTSGRCh37
Build 362133,619,897 - 33,620,154RGDNCBI36
Celera2119,888,113 - 19,888,370RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,166,857 - 20,167,114UniSTS
REN84803  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,698,245 - 34,698,504UniSTSGRCh37
Build 362133,620,115 - 33,620,374RGDNCBI36
Celera2119,888,331 - 19,888,590RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,167,075 - 20,167,334UniSTS
REN84804  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,698,339 - 34,698,578UniSTSGRCh37
Build 362133,620,209 - 33,620,448RGDNCBI36
Celera2119,888,425 - 19,888,664RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,167,169 - 20,167,408UniSTS
REN84805  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,698,736 - 34,698,975UniSTSGRCh37
Build 362133,620,606 - 33,620,845RGDNCBI36
Celera2119,888,822 - 19,889,061RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,167,566 - 20,167,805UniSTS
REN84806  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,698,933 - 34,699,191UniSTSGRCh37
Build 362133,620,803 - 33,621,061RGDNCBI36
Celera2119,889,019 - 19,889,277RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,167,763 - 20,168,020UniSTS
REN84807  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,699,168 - 34,699,439UniSTSGRCh37
Build 362133,621,038 - 33,621,309RGDNCBI36
Celera2119,889,254 - 19,889,525RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,167,997 - 20,168,268UniSTS
REN84808  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,699,416 - 34,699,665UniSTSGRCh37
Build 362133,621,286 - 33,621,535RGDNCBI36
Celera2119,889,502 - 19,889,751RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,168,245 - 20,168,494UniSTS
REN84809  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,699,658 - 34,699,887UniSTSGRCh37
Build 362133,621,528 - 33,621,757RGDNCBI36
Celera2119,889,744 - 19,889,973RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,168,487 - 20,168,716UniSTS
REN84810  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,699,861 - 34,700,104UniSTSGRCh37
Build 362133,621,731 - 33,621,974RGDNCBI36
Celera2119,889,947 - 19,890,190RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,168,690 - 20,168,933UniSTS
REN84811  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,700,074 - 34,700,315UniSTSGRCh37
Build 362133,621,944 - 33,622,185RGDNCBI36
Celera2119,890,160 - 19,890,401RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,168,903 - 20,169,144UniSTS
REN84812  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,700,244 - 34,700,485UniSTSGRCh37
Build 362133,622,114 - 33,622,355RGDNCBI36
Celera2119,890,330 - 19,890,571RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,169,073 - 20,169,314UniSTS
REN84813  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,700,379 - 34,700,634UniSTSGRCh37
Build 362133,622,249 - 33,622,504RGDNCBI36
Celera2119,890,465 - 19,890,720RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,169,208 - 20,169,462UniSTS
REN84814  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,700,611 - 34,700,856UniSTSGRCh37
Build 362133,622,481 - 33,622,726RGDNCBI36
Celera2119,890,697 - 19,890,942RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,169,439 - 20,169,684UniSTS
REN84815  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,700,754 - 34,701,007UniSTSGRCh37
Build 362133,622,624 - 33,622,877RGDNCBI36
Celera2119,890,840 - 19,891,093RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,169,582 - 20,169,835UniSTS
REN84816  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,700,905 - 34,701,129UniSTSGRCh37
Build 362133,622,775 - 33,622,999RGDNCBI36
Celera2119,890,991 - 19,891,215RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,169,733 - 20,169,957UniSTS
REN84817  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,701,089 - 34,701,357UniSTSGRCh37
Build 362133,622,959 - 33,623,227RGDNCBI36
Celera2119,891,175 - 19,891,443RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,169,917 - 20,170,185UniSTS
REN84818  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,701,350 - 34,701,604UniSTSGRCh37
Build 362133,623,220 - 33,623,474RGDNCBI36
Celera2119,891,436 - 19,891,690RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,170,178 - 20,170,432UniSTS
REN84819  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,701,598 - 34,701,859UniSTSGRCh37
Build 362133,623,468 - 33,623,729RGDNCBI36
Celera2119,891,684 - 19,891,945RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,170,426 - 20,170,687UniSTS
REN84820  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,701,806 - 34,702,065UniSTSGRCh37
Build 362133,623,676 - 33,623,935RGDNCBI36
Celera2119,891,892 - 19,892,151RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,170,634 - 20,170,893UniSTS
REN84821  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,702,055 - 34,702,311UniSTSGRCh37
Build 362133,623,925 - 33,624,181RGDNCBI36
Celera2119,892,141 - 19,892,397RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,170,883 - 20,171,139UniSTS
REN84822  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,702,281 - 34,702,528UniSTSGRCh37
Build 362133,624,151 - 33,624,398RGDNCBI36
Celera2119,892,367 - 19,892,614RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,171,109 - 20,171,356UniSTS
REN84823  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,702,504 - 34,702,771UniSTSGRCh37
Build 362133,624,374 - 33,624,641RGDNCBI36
Celera2119,892,590 - 19,892,857RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,171,332 - 20,171,599UniSTS
REN84824  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,702,748 - 34,703,003UniSTSGRCh37
Build 362133,624,618 - 33,624,873RGDNCBI36
Celera2119,892,834 - 19,893,089RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,171,576 - 20,171,831UniSTS
REN84825  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,702,979 - 34,703,219UniSTSGRCh37
Build 362133,624,849 - 33,625,089RGDNCBI36
Celera2119,893,065 - 19,893,305RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,171,807 - 20,172,047UniSTS
REN84826  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,703,209 - 34,703,473UniSTSGRCh37
Build 362133,625,079 - 33,625,343RGDNCBI36
Celera2119,893,295 - 19,893,559RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,172,037 - 20,172,301UniSTS
REN84827  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,703,471 - 34,703,718UniSTSGRCh37
Build 362133,625,341 - 33,625,588RGDNCBI36
Celera2119,893,557 - 19,893,804RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,172,299 - 20,172,546UniSTS
REN84828  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,703,667 - 34,703,941UniSTSGRCh37
Build 362133,625,537 - 33,625,811RGDNCBI36
Celera2119,893,753 - 19,894,027RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,172,495 - 20,172,769UniSTS
REN84829  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,703,919 - 34,704,165UniSTSGRCh37
Build 362133,625,789 - 33,626,035RGDNCBI36
Celera2119,894,005 - 19,894,251RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,172,747 - 20,172,993UniSTS
REN84830  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,704,136 - 34,704,385UniSTSGRCh37
Build 362133,626,006 - 33,626,255RGDNCBI36
Celera2119,894,222 - 19,894,471RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,172,964 - 20,173,213UniSTS
REN84831  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,704,362 - 34,704,611UniSTSGRCh37
Build 362133,626,232 - 33,626,481RGDNCBI36
Celera2119,894,448 - 19,894,697RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,173,190 - 20,173,439UniSTS
REN84832  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,704,571 - 34,704,831UniSTSGRCh37
Build 362133,626,441 - 33,626,701RGDNCBI36
Celera2119,894,657 - 19,894,917RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,173,399 - 20,173,659UniSTS
REN84833  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,704,829 - 34,705,076UniSTSGRCh37
Build 362133,626,699 - 33,626,946RGDNCBI36
Celera2119,894,915 - 19,895,162RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,173,657 - 20,173,904UniSTS
REN84834  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,705,051 - 34,705,308UniSTSGRCh37
Build 362133,626,921 - 33,627,178RGDNCBI36
Celera2119,895,137 - 19,895,394RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,173,879 - 20,174,136UniSTS
REN84835  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,705,301 - 34,705,547UniSTSGRCh37
Build 362133,627,171 - 33,627,417RGDNCBI36
Celera2119,895,387 - 19,895,633RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,174,129 - 20,174,375UniSTS
REN84836  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,705,524 - 34,705,776UniSTSGRCh37
Build 362133,627,394 - 33,627,646RGDNCBI36
Celera2119,895,610 - 19,895,862RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,174,352 - 20,174,604UniSTS
REN84837  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,705,671 - 34,705,918UniSTSGRCh37
Build 362133,627,541 - 33,627,788RGDNCBI36
Celera2119,895,757 - 19,896,004RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,174,499 - 20,174,746UniSTS
REN84838  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,706,224 - 34,706,469UniSTSGRCh37
Build 362133,628,094 - 33,628,339RGDNCBI36
Celera2119,896,310 - 19,896,555RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,175,053 - 20,175,298UniSTS
REN84839  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,706,445 - 34,706,708UniSTSGRCh37
Build 362133,628,315 - 33,628,578RGDNCBI36
Celera2119,896,531 - 19,896,794RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,175,274 - 20,175,537UniSTS
REN84840  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,706,701 - 34,706,934UniSTSGRCh37
Build 362133,628,571 - 33,628,804RGDNCBI36
Celera2119,896,787 - 19,897,020RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,175,530 - 20,175,763UniSTS
REN84841  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,706,926 - 34,707,182UniSTSGRCh37
Build 362133,628,796 - 33,629,052RGDNCBI36
Celera2119,897,012 - 19,897,268RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,175,755 - 20,176,011UniSTS
REN84842  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,707,179 - 34,707,435UniSTSGRCh37
Build 362133,629,049 - 33,629,305RGDNCBI36
Celera2119,897,265 - 19,897,521RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,176,008 - 20,176,264UniSTS
REN84843  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,707,412 - 34,707,656UniSTSGRCh37
Build 362133,629,282 - 33,629,526RGDNCBI36
Celera2119,897,498 - 19,897,742RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,176,241 - 20,176,485UniSTS
REN84844  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,707,654 - 34,707,902UniSTSGRCh37
Build 362133,629,524 - 33,629,772RGDNCBI36
Celera2119,897,740 - 19,897,988RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,176,483 - 20,176,731UniSTS
REN84845  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,707,883 - 34,708,144UniSTSGRCh37
Build 362133,629,753 - 33,630,014RGDNCBI36
Celera2119,897,969 - 19,898,230RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,176,712 - 20,176,973UniSTS
REN84846  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,707,970 - 34,708,213UniSTSGRCh37
Build 362133,629,840 - 33,630,083RGDNCBI36
Celera2119,898,056 - 19,898,299RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,176,799 - 20,177,042UniSTS
REN84847  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,709,348 - 34,709,591UniSTSGRCh37
Build 362133,631,218 - 33,631,461RGDNCBI36
Celera2119,899,434 - 19,899,677RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,178,177 - 20,178,420UniSTS
REN84848  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,709,568 - 34,709,799UniSTSGRCh37
Build 362133,631,438 - 33,631,669RGDNCBI36
Celera2119,899,654 - 19,899,885RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,178,397 - 20,178,628UniSTS
REN84849  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,709,679 - 34,709,903UniSTSGRCh37
Build 362133,631,549 - 33,631,773RGDNCBI36
Celera2119,899,765 - 19,899,989RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,178,508 - 20,178,732UniSTS
REN84850  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,710,167 - 34,710,391UniSTSGRCh37
Build 362133,632,037 - 33,632,261RGDNCBI36
Celera2119,900,253 - 19,900,477RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,178,996 - 20,179,220UniSTS
REN84851  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,710,309 - 34,710,533UniSTSGRCh37
Build 362133,632,179 - 33,632,403RGDNCBI36
Celera2119,900,395 - 19,900,619RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,179,138 - 20,179,362UniSTS
REN84852  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,710,490 - 34,710,734UniSTSGRCh37
Build 362133,632,360 - 33,632,604RGDNCBI36
Celera2119,900,576 - 19,900,820RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,179,319 - 20,179,561UniSTS
REN84853  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,711,001 - 34,711,264UniSTSGRCh37
Build 362133,632,871 - 33,633,134RGDNCBI36
Celera2119,901,087 - 19,901,350RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,179,828 - 20,180,091UniSTS
REN84854  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,711,247 - 34,711,488UniSTSGRCh37
Build 362133,633,117 - 33,633,358RGDNCBI36
Celera2119,901,333 - 19,901,574RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,180,074 - 20,180,315UniSTS
REN84855  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,711,447 - 34,711,671UniSTSGRCh37
Build 362133,633,317 - 33,633,541RGDNCBI36
Celera2119,901,533 - 19,901,757RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,180,274 - 20,180,498UniSTS
REN84856  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,711,643 - 34,711,909UniSTSGRCh37
Build 362133,633,513 - 33,633,779RGDNCBI36
Celera2119,901,729 - 19,901,995RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,180,470 - 20,180,736UniSTS
REN84857  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,711,890 - 34,712,136UniSTSGRCh37
Build 362133,633,760 - 33,634,006RGDNCBI36
Celera2119,901,976 - 19,902,222RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,180,717 - 20,180,963UniSTS
REN84858  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,712,263 - 34,712,489UniSTSGRCh37
Build 362133,634,133 - 33,634,359RGDNCBI36
Celera2119,902,349 - 19,902,575RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,181,090 - 20,181,316UniSTS
REN84859  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,712,399 - 34,712,646UniSTSGRCh37
Build 362133,634,269 - 33,634,516RGDNCBI36
Celera2119,902,485 - 19,902,732RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,181,226 - 20,181,473UniSTS
REN84860  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,712,637 - 34,712,902UniSTSGRCh37
Build 362133,634,507 - 33,634,772RGDNCBI36
Celera2119,902,723 - 19,902,988RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,181,464 - 20,181,729UniSTS
REN84861  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,712,879 - 34,713,129UniSTSGRCh37
Build 362133,634,749 - 33,634,999RGDNCBI36
Celera2119,902,965 - 19,903,215RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,181,706 - 20,181,956UniSTS
REN84862  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,713,107 - 34,713,381UniSTSGRCh37
Build 362133,634,977 - 33,635,251RGDNCBI36
Celera2119,903,193 - 19,903,467RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,181,934 - 20,182,208UniSTS
REN84863  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,713,369 - 34,713,635UniSTSGRCh37
Build 362133,635,239 - 33,635,505RGDNCBI36
Celera2119,903,455 - 19,903,721RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,182,196 - 20,182,462UniSTS
REN84864  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,713,624 - 34,713,869UniSTSGRCh37
Build 362133,635,494 - 33,635,739RGDNCBI36
Celera2119,903,710 - 19,903,955RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,182,451 - 20,182,696UniSTS
REN84865  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,713,695 - 34,713,953UniSTSGRCh37
Build 362133,635,565 - 33,635,823RGDNCBI36
Celera2119,903,781 - 19,904,039RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,182,522 - 20,182,780UniSTS
REN84866  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,713,910 - 34,714,136UniSTSGRCh37
Build 362133,635,780 - 33,636,006RGDNCBI36
Celera2119,903,996 - 19,904,222RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,182,737 - 20,182,963UniSTS
REN84867  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,715,180 - 34,715,411UniSTSGRCh37
Build 362133,637,050 - 33,637,281RGDNCBI36
Celera2119,905,266 - 19,905,497RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,184,007 - 20,184,238UniSTS
REN84868  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,715,406 - 34,715,649UniSTSGRCh37
Build 362133,637,276 - 33,637,519RGDNCBI36
Celera2119,905,492 - 19,905,735RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,184,233 - 20,184,476UniSTS
REN84869  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,715,629 - 34,715,867UniSTSGRCh37
Build 362133,637,499 - 33,637,737RGDNCBI36
Celera2119,905,715 - 19,905,953RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,184,456 - 20,184,694UniSTS
REN84870  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,715,841 - 34,716,079UniSTSGRCh37
Build 362133,637,711 - 33,637,949RGDNCBI36
Celera2119,905,927 - 19,906,165RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,184,668 - 20,184,906UniSTS
REN84871  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,716,045 - 34,716,271UniSTSGRCh37
Build 362133,637,915 - 33,638,141RGDNCBI36
Celera2119,906,131 - 19,906,357RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,184,872 - 20,185,098UniSTS
REN84872  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,716,228 - 34,716,465UniSTSGRCh37
Build 362133,638,098 - 33,638,335RGDNCBI36
Celera2119,906,314 - 19,906,551RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,185,055 - 20,185,292UniSTS
REN84873  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,716,445 - 34,716,704UniSTSGRCh37
Build 362133,638,315 - 33,638,574RGDNCBI36
Celera2119,906,531 - 19,906,790RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,185,272 - 20,185,531UniSTS
REN84874  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,716,683 - 34,716,924UniSTSGRCh37
Build 362133,638,553 - 33,638,794RGDNCBI36
Celera2119,906,769 - 19,907,010RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,185,510 - 20,185,751UniSTS
REN84875  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,716,841 - 34,717,065UniSTSGRCh37
Build 362133,638,711 - 33,638,935RGDNCBI36
Celera2119,906,927 - 19,907,151RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,185,668 - 20,185,892UniSTS
REN84876  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,717,394 - 34,717,644UniSTSGRCh37
Build 362133,639,264 - 33,639,514RGDNCBI36
Celera2119,907,480 - 19,907,730RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,186,225 - 20,186,475UniSTS
REN84877  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,717,629 - 34,717,866UniSTSGRCh37
Build 362133,639,499 - 33,639,736RGDNCBI36
Celera2119,907,715 - 19,907,952RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,186,460 - 20,186,697UniSTS
REN84878  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,717,849 - 34,718,076UniSTSGRCh37
Build 362133,639,719 - 33,639,946RGDNCBI36
Celera2119,907,935 - 19,908,162RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,186,680 - 20,186,907UniSTS
REN84879  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,718,018 - 34,718,249UniSTSGRCh37
Build 362133,639,888 - 33,640,119RGDNCBI36
Celera2119,908,104 - 19,908,335RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,186,849 - 20,187,080UniSTS
REN84880  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,718,230 - 34,718,479UniSTSGRCh37
Build 362133,640,100 - 33,640,349RGDNCBI36
Celera2119,908,316 - 19,908,565RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,187,061 - 20,187,310UniSTS
REN84881  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,718,455 - 34,718,721UniSTSGRCh37
Build 362133,640,325 - 33,640,591RGDNCBI36
Celera2119,908,541 - 19,908,807RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,187,286 - 20,187,552UniSTS
REN84882  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,718,714 - 34,718,964UniSTSGRCh37
Build 362133,640,584 - 33,640,834RGDNCBI36
Celera2119,908,800 - 19,909,050RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,187,545 - 20,187,795UniSTS
REN84883  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,718,944 - 34,719,211UniSTSGRCh37
Build 362133,640,814 - 33,641,081RGDNCBI36
Celera2119,909,030 - 19,909,297RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,187,775 - 20,188,042UniSTS
REN84884  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,719,207 - 34,719,434UniSTSGRCh37
Build 362133,641,077 - 33,641,304RGDNCBI36
Celera2119,909,293 - 19,909,520RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,188,038 - 20,188,265UniSTS
REN84885  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,719,773 - 34,720,021UniSTSGRCh37
Build 362133,641,643 - 33,641,891RGDNCBI36
Celera2119,909,858 - 19,910,106RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,188,603 - 20,188,851UniSTS
REN84886  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,720,017 - 34,720,264UniSTSGRCh37
Build 362133,641,887 - 33,642,134RGDNCBI36
Celera2119,910,102 - 19,910,349RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,188,847 - 20,189,094UniSTS
REN84887  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,720,253 - 34,720,496UniSTSGRCh37
Build 362133,642,123 - 33,642,366RGDNCBI36
Celera2119,910,338 - 19,910,581RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,189,083 - 20,189,326UniSTS
REN84888  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,720,471 - 34,720,731UniSTSGRCh37
Build 362133,642,341 - 33,642,601RGDNCBI36
Celera2119,910,556 - 19,910,816RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,189,301 - 20,189,561UniSTS
REN84889  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,720,637 - 34,720,882UniSTSGRCh37
Build 362133,642,507 - 33,642,752RGDNCBI36
Celera2119,910,722 - 19,910,967RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,189,467 - 20,189,712UniSTS
REN84890  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,721,054 - 34,721,281UniSTSGRCh37
Build 362133,642,924 - 33,643,151RGDNCBI36
Celera2119,911,139 - 19,911,366RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,189,884 - 20,190,111UniSTS
REN84891  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,721,269 - 34,721,499UniSTSGRCh37
Build 362133,643,139 - 33,643,369RGDNCBI36
Celera2119,911,354 - 19,911,584RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,190,099 - 20,190,329UniSTS
REN84892  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,721,472 - 34,721,717UniSTSGRCh37
Build 362133,643,342 - 33,643,587RGDNCBI36
Celera2119,911,557 - 19,911,802RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,190,302 - 20,190,547UniSTS
REN84893  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,721,694 - 34,721,921UniSTSGRCh37
Build 362133,643,564 - 33,643,791RGDNCBI36
Celera2119,911,779 - 19,912,006RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,190,524 - 20,190,751UniSTS
REN84894  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,721,785 - 34,722,034UniSTSGRCh37
Build 362133,643,655 - 33,643,904RGDNCBI36
Celera2119,911,870 - 19,912,119RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,190,615 - 20,190,864UniSTS
REN84895  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,722,008 - 34,722,232UniSTSGRCh37
Build 362133,643,878 - 33,644,102RGDNCBI36
Celera2119,912,093 - 19,912,317RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,190,838 - 20,191,062UniSTS
REN84896  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,722,203 - 34,722,459UniSTSGRCh37
Build 362133,644,073 - 33,644,329RGDNCBI36
Celera2119,912,288 - 19,912,544RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,191,033 - 20,191,289UniSTS
REN84897  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,722,458 - 34,722,703UniSTSGRCh37
Build 362133,644,328 - 33,644,573RGDNCBI36
Celera2119,912,543 - 19,912,788RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,191,288 - 20,191,533UniSTS
REN84898  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,722,676 - 34,722,928UniSTSGRCh37
Build 362133,644,546 - 33,644,798RGDNCBI36
Celera2119,912,761 - 19,913,013RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,191,506 - 20,191,758UniSTS
REN84899  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,722,905 - 34,723,133UniSTSGRCh37
Build 362133,644,775 - 33,645,003RGDNCBI36
Celera2119,912,990 - 19,913,218RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,191,735 - 20,191,963UniSTS
REN84900  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,723,122 - 34,723,376UniSTSGRCh37
Build 362133,644,992 - 33,645,246RGDNCBI36
Celera2119,913,207 - 19,913,461RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,191,952 - 20,192,206UniSTS
REN84901  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,723,317 - 34,723,586UniSTSGRCh37
Build 362133,645,187 - 33,645,456RGDNCBI36
Celera2119,913,402 - 19,913,671RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,192,147 - 20,192,416UniSTS
REN84902  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,723,563 - 34,723,810UniSTSGRCh37
Build 362133,645,433 - 33,645,680RGDNCBI36
Celera2119,913,648 - 19,913,895RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,192,393 - 20,192,640UniSTS
REN84903  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,723,804 - 34,724,057UniSTSGRCh37
Build 362133,645,674 - 33,645,927RGDNCBI36
Celera2119,913,889 - 19,914,142RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,192,634 - 20,192,887UniSTS
REN84904  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,723,906 - 34,724,153UniSTSGRCh37
Build 362133,645,776 - 33,646,023RGDNCBI36
Celera2119,913,991 - 19,914,238RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,192,736 - 20,192,983UniSTS
REN84905  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,724,088 - 34,724,316UniSTSGRCh37
Build 362133,645,958 - 33,646,186RGDNCBI36
Celera2119,914,173 - 19,914,401RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,192,918 - 20,193,146UniSTS
REN84906  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,724,307 - 34,724,534UniSTSGRCh37
Build 362133,646,177 - 33,646,404RGDNCBI36
Celera2119,914,392 - 19,914,619RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,193,137 - 20,193,364UniSTS
REN84907  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,724,401 - 34,724,668UniSTSGRCh37
Build 362133,646,271 - 33,646,538RGDNCBI36
Celera2119,914,486 - 19,914,753RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,193,231 - 20,193,498UniSTS
REN84908  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,724,758 - 34,724,985UniSTSGRCh37
Build 362133,646,628 - 33,646,855RGDNCBI36
Celera2119,914,843 - 19,915,070RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,193,588 - 20,193,815UniSTS
REN84909  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,724,961 - 34,725,209UniSTSGRCh37
Build 362133,646,831 - 33,647,079RGDNCBI36
Celera2119,915,046 - 19,915,294RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,193,791 - 20,194,039UniSTS
REN84910  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,725,207 - 34,725,432UniSTSGRCh37
Build 362133,647,077 - 33,647,302RGDNCBI36
Celera2119,915,292 - 19,915,517RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,194,037 - 20,194,262UniSTS
REN84911  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,725,430 - 34,725,695UniSTSGRCh37
Build 362133,647,300 - 33,647,565RGDNCBI36
Celera2119,915,515 - 19,915,780RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,194,260 - 20,194,525UniSTS
REN84912  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,725,687 - 34,725,919UniSTSGRCh37
Build 362133,647,557 - 33,647,789RGDNCBI36
Celera2119,915,772 - 19,916,004RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,194,517 - 20,194,749UniSTS
REN84913  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,725,887 - 34,726,154UniSTSGRCh37
Build 362133,647,757 - 33,648,024RGDNCBI36
Celera2119,915,972 - 19,916,239RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,194,717 - 20,194,984UniSTS
REN84914  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,726,113 - 34,726,361UniSTSGRCh37
Build 362133,647,983 - 33,648,231RGDNCBI36
Celera2119,916,198 - 19,916,446RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,194,943 - 20,195,191UniSTS
REN84915  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,726,685 - 34,726,909UniSTSGRCh37
Build 362133,648,555 - 33,648,779RGDNCBI36
Celera2119,916,770 - 19,916,994RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,195,515 - 20,195,739UniSTS
REN84916  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,726,887 - 34,727,111UniSTSGRCh37
Build 362133,648,757 - 33,648,981RGDNCBI36
Celera2119,916,972 - 19,917,196RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,195,717 - 20,195,941UniSTS
REN84917  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,727,060 - 34,727,326UniSTSGRCh37
Build 362133,648,930 - 33,649,196RGDNCBI36
Celera2119,917,145 - 19,917,411RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,195,890 - 20,196,156UniSTS
REN84918  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,727,248 - 34,727,520UniSTSGRCh37
Build 362133,649,118 - 33,649,390RGDNCBI36
Celera2119,917,333 - 19,917,605RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,196,078 - 20,196,350UniSTS
REN84919  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,727,516 - 34,727,780UniSTSGRCh37
Build 362133,649,386 - 33,649,650RGDNCBI36
Celera2119,917,601 - 19,917,865RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,196,346 - 20,196,610UniSTS
REN84920  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,727,768 - 34,728,027UniSTSGRCh37
Build 362133,649,638 - 33,649,897RGDNCBI36
Celera2119,917,853 - 19,918,112RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,196,598 - 20,196,857UniSTS
REN84921  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,727,999 - 34,728,253UniSTSGRCh37
Build 362133,649,869 - 33,650,123RGDNCBI36
Celera2119,918,084 - 19,918,338RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,196,829 - 20,197,083UniSTS
REN84922  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,728,231 - 34,728,467UniSTSGRCh37
Build 362133,650,101 - 33,650,337RGDNCBI36
Celera2119,918,316 - 19,918,552RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,197,061 - 20,197,297UniSTS
REN84923  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,728,444 - 34,728,701UniSTSGRCh37
Build 362133,650,314 - 33,650,571RGDNCBI36
Celera2119,918,529 - 19,918,786RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,197,274 - 20,197,531UniSTS
REN84924  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,728,676 - 34,728,926UniSTSGRCh37
Build 362133,650,546 - 33,650,796RGDNCBI36
Celera2119,918,761 - 19,919,011RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,197,506 - 20,197,756UniSTS
REN84925  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,728,887 - 34,729,135UniSTSGRCh37
Build 362133,650,757 - 33,651,005RGDNCBI36
Celera2119,918,972 - 19,919,220RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,197,717 - 20,197,965UniSTS
REN84926  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,729,112 - 34,729,370UniSTSGRCh37
Build 362133,650,982 - 33,651,240RGDNCBI36
Celera2119,919,197 - 19,919,455RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,197,942 - 20,198,200UniSTS
REN84927  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,729,347 - 34,729,601UniSTSGRCh37
Build 362133,651,217 - 33,651,471RGDNCBI36
Celera2119,919,432 - 19,919,686RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,198,177 - 20,198,431UniSTS
REN84928  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,729,585 - 34,729,834UniSTSGRCh37
Build 362133,651,455 - 33,651,704RGDNCBI36
Celera2119,919,670 - 19,919,919RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,198,415 - 20,198,664UniSTS
REN84929  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,730,140 - 34,730,364UniSTSGRCh37
Build 362133,652,010 - 33,652,234RGDNCBI36
Celera2119,920,225 - 19,920,449RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,198,969 - 20,199,193UniSTS
REN84930  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,730,356 - 34,730,592UniSTSGRCh37
Build 362133,652,226 - 33,652,462RGDNCBI36
Celera2119,920,441 - 19,920,677RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,199,185 - 20,199,421UniSTS
REN84931  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,730,565 - 34,730,824UniSTSGRCh37
Build 362133,652,435 - 33,652,694RGDNCBI36
Celera2119,920,650 - 19,920,909RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,199,394 - 20,199,653UniSTS
REN84932  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,730,806 - 34,731,037UniSTSGRCh37
Build 362133,652,676 - 33,652,907RGDNCBI36
Celera2119,920,891 - 19,921,122RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,199,635 - 20,199,866UniSTS
REN84933  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,731,009 - 34,731,238UniSTSGRCh37
Build 362133,652,879 - 33,653,108RGDNCBI36
Celera2119,921,094 - 19,921,323RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,199,838 - 20,200,067UniSTS
REN84934  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,731,235 - 34,731,483UniSTSGRCh37
Build 362133,653,105 - 33,653,353RGDNCBI36
Celera2119,921,320 - 19,921,568RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,200,064 - 20,200,312UniSTS
REN84935  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,731,459 - 34,731,703UniSTSGRCh37
Build 362133,653,329 - 33,653,573RGDNCBI36
Celera2119,921,544 - 19,921,788RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,200,288 - 20,200,532UniSTS
REN84936  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,731,678 - 34,731,921UniSTSGRCh37
Build 362133,653,548 - 33,653,791RGDNCBI36
Celera2119,921,763 - 19,922,006RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,200,507 - 20,200,750UniSTS
REN84937  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,731,887 - 34,732,127UniSTSGRCh37
Build 362133,653,757 - 33,653,997RGDNCBI36
Celera2119,921,972 - 19,922,212RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,200,716 - 20,200,956UniSTS
REN84938  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,732,122 - 34,732,370UniSTSGRCh37
Build 362133,653,992 - 33,654,240RGDNCBI36
Celera2119,922,207 - 19,922,455RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,200,951 - 20,201,199UniSTS
REN84939  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,732,247 - 34,732,471UniSTSGRCh37
Build 362133,654,117 - 33,654,341RGDNCBI36
Celera2119,922,332 - 19,922,556RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,201,076 - 20,201,300UniSTS
stSG607080  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,696,525 - 34,697,587UniSTSGRCh37
Build 362133,618,395 - 33,619,457RGDNCBI36
Celera2119,886,611 - 19,887,673RGD
HuRef2120,165,355 - 20,166,417UniSTS
stSG607081  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,697,568 - 34,697,817UniSTSGRCh37
Build 362133,619,438 - 33,619,687RGDNCBI36
Celera2119,887,654 - 19,887,903RGD
HuRef2120,166,398 - 20,166,647UniSTS
stSG607082  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,697,827 - 34,699,160UniSTSGRCh37
Build 362133,619,697 - 33,621,030RGDNCBI36
Celera2119,887,913 - 19,889,246RGD
HuRef2120,166,657 - 20,167,989UniSTS
stSG607083  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,699,244 - 34,699,613UniSTSGRCh37
Build 362133,621,114 - 33,621,483RGDNCBI36
Celera2119,889,330 - 19,889,699RGD
HuRef2120,168,073 - 20,168,442UniSTS
stSG607085  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,701,095 - 34,702,132UniSTSGRCh37
Build 362133,622,965 - 33,624,002RGDNCBI36
Celera2119,891,181 - 19,892,218RGD
HuRef2120,169,923 - 20,170,960UniSTS
stSG607086  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,706,921 - 34,707,931UniSTSGRCh37
Build 362133,628,791 - 33,629,801RGDNCBI36
Celera2119,897,007 - 19,898,017RGD
HuRef2120,175,750 - 20,176,760UniSTS
stSG607087  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,707,912 - 34,708,997UniSTSGRCh37
Build 362133,629,782 - 33,630,867RGDNCBI36
Celera2119,897,998 - 19,899,083RGD
HuRef2120,176,741 - 20,177,826UniSTS
stSG607088  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,708,993 - 34,709,666UniSTSGRCh37
Build 362133,630,863 - 33,631,536RGDNCBI36
Celera2119,899,079 - 19,899,752RGD
HuRef2120,177,822 - 20,178,495UniSTS
stSG607089  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,709,712 - 34,710,895UniSTSGRCh37
Build 362133,631,582 - 33,632,765RGDNCBI36
Celera2119,899,798 - 19,900,981RGD
HuRef2120,178,541 - 20,179,722UniSTS
stSG607090  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,710,907 - 34,712,362UniSTSGRCh37
Build 362133,632,777 - 33,634,232RGDNCBI36
Celera2119,900,993 - 19,902,448RGD
HuRef2120,179,734 - 20,181,189UniSTS
stSG607091  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,712,343 - 34,713,565UniSTSGRCh37
Build 362133,634,213 - 33,635,435RGDNCBI36
Celera2119,902,429 - 19,903,651RGD
HuRef2120,181,170 - 20,182,392UniSTS
stSG607092  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,715,572 - 34,716,577UniSTSGRCh37
Build 362133,637,442 - 33,638,447RGDNCBI36
Celera2119,905,658 - 19,906,663RGD
HuRef2120,184,399 - 20,185,404UniSTS
stSG607093  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,716,558 - 34,717,751UniSTSGRCh37
Build 362133,638,428 - 33,639,621RGDNCBI36
Celera2119,906,644 - 19,907,837RGD
HuRef2120,185,385 - 20,186,582UniSTS
stSG607094  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,717,732 - 34,718,972UniSTSGRCh37
Build 362133,639,602 - 33,640,842RGDNCBI36
Celera2119,907,818 - 19,909,058RGD
HuRef2120,186,563 - 20,187,803UniSTS
stSG607095  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,718,953 - 34,720,248UniSTSGRCh37
Build 362133,640,823 - 33,642,118RGDNCBI36
Celera2119,909,039 - 19,910,333RGD
HuRef2120,187,784 - 20,189,078UniSTS
stSG607096  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,720,233 - 34,721,544UniSTSGRCh37
Build 362133,642,103 - 33,643,414RGDNCBI36
Celera2119,910,318 - 19,911,629RGD
HuRef2120,189,063 - 20,190,374UniSTS
stSG607097  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,721,525 - 34,722,929UniSTSGRCh37
Build 362133,643,395 - 33,644,799RGDNCBI36
Celera2119,911,610 - 19,913,014RGD
HuRef2120,190,355 - 20,191,759UniSTS
stSG607098  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,722,910 - 34,724,327UniSTSGRCh37
Build 362133,644,780 - 33,646,197RGDNCBI36
Celera2119,912,995 - 19,914,412RGD
HuRef2120,191,740 - 20,193,157UniSTS
stSG607099  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,724,308 - 34,725,420UniSTSGRCh37
Build 362133,646,178 - 33,647,290RGDNCBI36
Celera2119,914,393 - 19,915,505RGD
HuRef2120,193,138 - 20,194,250UniSTS
stSG607100  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,725,401 - 34,725,710UniSTSGRCh37
Build 362133,647,271 - 33,647,580RGDNCBI36
Celera2119,915,486 - 19,915,795RGD
HuRef2120,194,231 - 20,194,540UniSTS
stSG607101  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,725,737 - 34,726,909UniSTSGRCh37
Build 362133,647,607 - 33,648,779RGDNCBI36
Celera2119,915,822 - 19,916,994RGD
HuRef2120,194,567 - 20,195,739UniSTS
stSG607102  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,726,958 - 34,727,959UniSTSGRCh37
Build 362133,648,828 - 33,649,829RGDNCBI36
Celera2119,917,043 - 19,918,044RGD
HuRef2120,195,788 - 20,196,789UniSTS
stSG607103  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,727,994 - 34,729,442UniSTSGRCh37
Build 362133,649,864 - 33,651,312RGDNCBI36
Celera2119,918,079 - 19,919,527RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,196,824 - 20,198,272UniSTS
stSG607104  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,729,459 - 34,730,487UniSTSGRCh37
Build 362133,651,329 - 33,652,357RGDNCBI36
Celera2119,919,544 - 19,920,572RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,198,289 - 20,199,316UniSTS
stSG607105  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,730,468 - 34,731,795UniSTSGRCh37
Build 362133,652,338 - 33,653,665RGDNCBI36
Celera2119,920,553 - 19,921,880RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,199,297 - 20,200,624UniSTS
D21S2039  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,717,022 - 34,717,256UniSTSGRCh37
Build 362133,638,892 - 33,639,126RGDNCBI36
Celera2119,907,108 - 19,907,342RGD
HuRef2120,185,849 - 20,186,087UniSTS
SHGC-5963  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,728,103 - 34,728,361UniSTSGRCh37
Build 362133,649,973 - 33,650,231RGDNCBI36
Celera2119,918,188 - 19,918,446RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,196,933 - 20,197,191UniSTS
TNG Radiation Hybrid Map2111423.0UniSTS
GeneMap99-G3 RH Map21891.0UniSTS
D21S1827  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,731,337 - 34,731,611UniSTSGRCh37
Build 362133,653,207 - 33,653,481RGDNCBI36
Celera2119,921,422 - 19,921,696RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,200,166 - 20,200,440UniSTS
TNG Radiation Hybrid Map2111430.0UniSTS
GeneMap99-GB4 RH Map21149.67UniSTS
Whitehead-RH Map21159.1UniSTS
Whitehead-YAC Contig Map21 UniSTS
SHGC-52130  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,731,824 - 34,732,041UniSTSGRCh37
Build 362133,653,694 - 33,653,911RGDNCBI36
Celera2119,921,909 - 19,922,126RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,200,653 - 20,200,870UniSTS
TNG Radiation Hybrid Map2111430.0UniSTS
SHGC-35315  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,727,853 - 34,728,028UniSTSGRCh37
Build 362133,649,723 - 33,649,898RGDNCBI36
Celera2119,917,938 - 19,918,113RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,196,683 - 20,196,858UniSTS
TNG Radiation Hybrid Map2111427.0UniSTS
Stanford-G3 RH Map21888.0UniSTS
GeneMap99-GB4 RH Map21157.0UniSTS
Whitehead-RH Map21156.3UniSTS
NCBI RH Map21250.3UniSTS
GeneMap99-G3 RH Map21888.0UniSTS
IFNAR1_4106  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,731,481 - 34,732,175UniSTSGRCh37
Build 362133,653,351 - 33,654,045RGDNCBI36
Celera2119,921,566 - 19,922,260RGD
HuRef2120,200,310 - 20,201,004UniSTS
D11S2560  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map10p12.1-p11.2UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map12p13.3UniSTS
Cytogenetic Map20q13.3UniSTS
Cytogenetic Map19p13.12UniSTS
Cytogenetic Map8q21.13UniSTS
Cytogenetic Map18p11.22UniSTS
Cytogenetic Map9p13.3-p12UniSTS
Cytogenetic Map10p12.1UniSTS
Cytogenetic Map19q13.11UniSTS
Cytogenetic Map22q11.23UniSTS
Cytogenetic Map5q23.3UniSTS
Cytogenetic Map15q21.1UniSTS
Cytogenetic Map14q24.2UniSTS
Cytogenetic Map15q13UniSTS
Cytogenetic Map6q25.3UniSTS
Cytogenetic Map8p22-p21UniSTS
Cytogenetic Map1p34.1UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map15q21.3UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map2p13.1UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map10q24.2UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map6q16.2UniSTS
Cytogenetic MapXq26.3UniSTS
Cytogenetic Map9q22.33UniSTS
Cytogenetic Map7q21.2UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map8q24.13UniSTS
Cytogenetic Map4q25UniSTS
Cytogenetic Map12p13.33UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map5q23UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map3p21.2UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map1p13.2UniSTS
Cytogenetic Map6q27UniSTS
Cytogenetic Map2p13.3UniSTS
Cytogenetic Map2p25.1UniSTS
Cytogenetic Map16q24.1UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map2q12.1UniSTS
Cytogenetic Map9q13-q21UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map2p15UniSTS
Cytogenetic Map8q11.21UniSTS
Cytogenetic Map15q15UniSTS
Cytogenetic Map1p36.21UniSTS
Cytogenetic Map12q23-q24.1UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map10q23.2UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map15q21UniSTS
Cytogenetic Map9q34.2UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map2q35UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map22q12.2UniSTS
Cytogenetic Map1p32UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map7p15.2UniSTS
Cytogenetic Map12p13.2UniSTS
Cytogenetic Map16q12.2UniSTS
Cytogenetic Map3q26.2-q27UniSTS
Cytogenetic Map2p21UniSTS
Cytogenetic Map8p23.1UniSTS
Cytogenetic Map17p11.2UniSTS
Cytogenetic MapXp11.2UniSTS
Cytogenetic Map20q11.2UniSTS
Cytogenetic Map3q26.2UniSTS
Cytogenetic Map4q22.1UniSTS
Cytogenetic Map4p15.32UniSTS
Cytogenetic Map7q36.3UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map10p13UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map1p36.11-p34.2UniSTS
Cytogenetic Map1q21.3UniSTS
Cytogenetic Map8p21.3UniSTS
Cytogenetic Map18p11.32UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map8q22.1UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map3p21UniSTS
Cytogenetic Map14q13.2UniSTS
Cytogenetic Map8q12.1UniSTS
Cytogenetic Map3p22.3UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map13q12.11UniSTS
Cytogenetic Map12p12UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map14q31.1UniSTS
Cytogenetic Map21q22.2UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map18q12.3UniSTS
Cytogenetic Map12q13.3UniSTS
Cytogenetic Map2p16.1UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map8q24.21UniSTS
Cytogenetic Map12q22-q23.1UniSTS
Cytogenetic Map3q26.33UniSTS
Cytogenetic Map1q23UniSTS
Cytogenetic Map11p15.1UniSTS
Cytogenetic Map7q32UniSTS
Cytogenetic Map11p13UniSTS
Cytogenetic Map5p13.1UniSTS
Cytogenetic Map18q21UniSTS
Cytogenetic Map7p14-p13UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map11q22-q23UniSTS
Cytogenetic Map19p13.3-p13.2UniSTS
Cytogenetic Map6q22-q23UniSTS
Cytogenetic Map7p14.3UniSTS
Cytogenetic Map1q21.1UniSTS
Cytogenetic Map14q32.31UniSTS
Cytogenetic Map11q13.1-q13.3UniSTS
Cytogenetic Map1q32UniSTS
Cytogenetic Map6p24UniSTS
Cytogenetic Map10q25UniSTS
Cytogenetic Map8q22.3UniSTS
Cytogenetic Map2p14UniSTS
Cytogenetic Map1p36.31UniSTS
Cytogenetic Map6q13UniSTS
Cytogenetic Map2p25.2UniSTS
Cytogenetic Map1p31.1UniSTS
Cytogenetic Map15q14-q15UniSTS
Cytogenetic Map9q31.1UniSTS
Cytogenetic Map21q22.11UniSTS
Cytogenetic Map7p15.3UniSTS
Cytogenetic Map5q35.3UniSTS
Cytogenetic Map1p36.32UniSTS
Cytogenetic Map15q11.2UniSTS
Cytogenetic Map12p12.1UniSTS
Cytogenetic MapXq25UniSTS
Cytogenetic MapXq28UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map8p21.1UniSTS
Cytogenetic Map3p26.1-p25.1UniSTS
Cytogenetic Map6q16.3UniSTS
Cytogenetic Map3q21.3UniSTS
Cytogenetic MapXq27.1UniSTS
Cytogenetic Map3q12.3UniSTS
Cytogenetic Map3q25.31UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map11q12.3UniSTS
Cytogenetic Map11q13.4UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic Map1q42.3UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map12q13.12UniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic Map4q31.1UniSTS
Cytogenetic Map14q32.33UniSTS
Cytogenetic Map9q33.2UniSTS
Cytogenetic Map5q13UniSTS
Cytogenetic Map8q12UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic Map17q24.3UniSTS
Cytogenetic Map5q12.3UniSTS
Cytogenetic Map1p32.3UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map10q24.32UniSTS
Cytogenetic Map19q13UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map14q32.32UniSTS
Cytogenetic Map16p13.2UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map10q11.22UniSTS
Cytogenetic Map1p34UniSTS
Cytogenetic Map6q14.1UniSTS
Cytogenetic Map14q32UniSTS
Cytogenetic Map1p36.3-p36.2UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic Map1p32-p31UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic Map5q33.1UniSTS
Cytogenetic Map2q21.1UniSTS
Cytogenetic Map19q13.41UniSTS
Cytogenetic Map18p11.21UniSTS
Cytogenetic Map10q26.11UniSTS
Cytogenetic Map12q14.3UniSTS
Cytogenetic Map5q34UniSTS
Cytogenetic Map2q36.1UniSTS
Cytogenetic Map15q25.2UniSTS
Cytogenetic Map1q21UniSTS
Cytogenetic Map4p16.1UniSTS
Cytogenetic Map9q32UniSTS
Cytogenetic Map15q24UniSTS
Cytogenetic Map1p34.3UniSTS
Cytogenetic Map12q21UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map1p35-p34UniSTS
Cytogenetic Map9q34.1UniSTS
Cytogenetic Map9q22.2UniSTS
Cytogenetic MapXp22UniSTS
Cytogenetic Map13q14UniSTS
Cytogenetic Map2q33UniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map10q11.23UniSTS
Cytogenetic Map20q13.31UniSTS
Cytogenetic Map3p25.2UniSTS
Cytogenetic Map5q11UniSTS
D8S2279  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map21q22.12UniSTS
Cytogenetic Map15q13UniSTS
Cytogenetic Map9q32UniSTS
Cytogenetic Map15q22.3UniSTS
Cytogenetic Map17p12UniSTS
Cytogenetic Map21q21.3UniSTS
Cytogenetic Map3p22-p21.3UniSTS
Cytogenetic Map1q21.1UniSTS
Cytogenetic Map2q24.2UniSTS
Cytogenetic Map17q24.2UniSTS
Cytogenetic Map1q32UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map20q13.3UniSTS
Cytogenetic Map2q31.1UniSTS
Cytogenetic Map1q21UniSTS
Cytogenetic Map3p14.1UniSTS
Cytogenetic Map2q37.3UniSTS
Cytogenetic Map7p14.1UniSTS
Cytogenetic Map2q22.3UniSTS
Cytogenetic Map15q13.2UniSTS
Cytogenetic Map12q24.1UniSTS
Cytogenetic Map7p15.2UniSTS
Cytogenetic Map5q31.2UniSTS
Cytogenetic Map2p25.2UniSTS
Cytogenetic Map3p24.3UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic Map5q14UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map1p36.32UniSTS
Cytogenetic Map1q42.12UniSTS
Cytogenetic Map7q21.11UniSTS
Cytogenetic Map9q34.2UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map8q22.3UniSTS
Cytogenetic Map6p21.1-p12UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map7q36.3UniSTS
Cytogenetic Map2p25.1UniSTS
Cytogenetic Map7p21.3UniSTS
Cytogenetic Map4q12UniSTS
Cytogenetic Map22q11.22UniSTS
Cytogenetic Map11p13UniSTS
Cytogenetic Map1q12UniSTS
Cytogenetic Map8p23UniSTS
Cytogenetic Map11q13.2-q13.3UniSTS
Cytogenetic Map13q14.1-q14.3UniSTS
Cytogenetic Map3q22-q24UniSTS
Cytogenetic Map3q13.1-q13.2UniSTS
Cytogenetic Map16q24UniSTS
Cytogenetic Map5q23.3-q31.1UniSTS
Cytogenetic Map8p21.3UniSTS
Cytogenetic Map14q32.3UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map7q32UniSTS
Cytogenetic Map14q32.33UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map1p32.3UniSTS
Cytogenetic Map17q11UniSTS
Cytogenetic Map17p13.1-p12UniSTS
Cytogenetic Map18q21.33UniSTS
Cytogenetic Map19p13.12UniSTS
Cytogenetic Map5q14.1UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map1q21-q23UniSTS
Cytogenetic MapXp11.23UniSTS
Cytogenetic Map4q21.1UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map14q23.3UniSTS
Cytogenetic Map17p12-p11.2UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map1q24UniSTS
Cytogenetic Map1q43UniSTS
Cytogenetic Map9q34.13UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map2q32UniSTS
Cytogenetic MapXp22.2UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map2q33UniSTS
Cytogenetic Map10p13UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic Map3q27UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map4p16.1UniSTS
Cytogenetic Map14q22.3UniSTS
Cytogenetic Map10q23-q24UniSTS
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map14q31-q32UniSTS
Cytogenetic Map5p15.33UniSTS
Cytogenetic Map1q23.2UniSTS
Cytogenetic Map16q24.3UniSTS
Cytogenetic Map4p14UniSTS
Cytogenetic Map2q32.3UniSTS
Cytogenetic Map15q21.1UniSTS
Cytogenetic Map4q32.2UniSTS
Cytogenetic Map10q23UniSTS
Cytogenetic Map5q14.2UniSTS
Cytogenetic Map4q32.1UniSTS
Cytogenetic Map1q25.1UniSTS
Cytogenetic Map11q14.1UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map11q23.1UniSTS
Cytogenetic Map3p21.1UniSTS
Cytogenetic Map16q22.2UniSTS
Cytogenetic Map14q32.31UniSTS
Cytogenetic Map16q11.2UniSTS
Cytogenetic Map6q22UniSTS
Cytogenetic Map10p15.3UniSTS
Cytogenetic Map11q23UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map12q12UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map19q13.11UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map15q15UniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map22q12.3UniSTS
Cytogenetic Map20q11UniSTS
Cytogenetic Map22q11.23UniSTS
Cytogenetic Map17q25UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map3p22.1UniSTS
Cytogenetic Map8q22.1UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map18p11.31UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map2p22.1UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map1p35.2UniSTS
Cytogenetic MapYp11.2UniSTS
Cytogenetic Map13q13.1UniSTS
Cytogenetic Map20q11.22UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map18q12UniSTS
Cytogenetic Map17q21.33UniSTS
Cytogenetic Map15q15.1UniSTS
Cytogenetic Map3q27.2UniSTS
Cytogenetic Map3q21.3UniSTS
Cytogenetic Map5p15.2UniSTS
Cytogenetic Map20q13.12UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map1q42UniSTS
Cytogenetic Map14q32.11UniSTS
Cytogenetic Map17q21.2-q21.3UniSTS
Cytogenetic Map5q32-q34UniSTS
Cytogenetic Map15q14UniSTS
Cytogenetic Map16q13UniSTS
Cytogenetic Map3q21.2UniSTS
Cytogenetic Map3p21.3UniSTS
Cytogenetic Map14q24.2UniSTS
Cytogenetic Map12q24.13UniSTS
Cytogenetic Map13q14.11UniSTS
Cytogenetic Map3q27.3UniSTS
Cytogenetic Map1q32.3UniSTS
Cytogenetic Map6p22.1UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map6q25.3UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map13q14.3UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map10p12UniSTS
Cytogenetic Map2q33.3UniSTS
Cytogenetic Map14q21.3UniSTS
Cytogenetic Map8p22-p21UniSTS
Cytogenetic Map18q11.2UniSTS
Cytogenetic Map2p15UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map12q21.33UniSTS
Cytogenetic Map20q13.32UniSTS
Cytogenetic Map1p34.1UniSTS
Cytogenetic Map10q26UniSTS
Cytogenetic Map8p23.1UniSTS
Cytogenetic Map19p13UniSTS
Cytogenetic Map7q21.13UniSTS
Cytogenetic Map7q31.1UniSTS
Cytogenetic Map1p33UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map22q12.2UniSTS
Cytogenetic Map9q22.3UniSTS
Cytogenetic Map8q13.1UniSTS
Cytogenetic Map3q25UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map20q13.33UniSTS
Cytogenetic Map1p31.3UniSTS
Cytogenetic Map14q31.1UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map12q13.2UniSTS
Cytogenetic Map22q13.31-q13.33UniSTS
Cytogenetic Map20q13.31UniSTS
Cytogenetic Map11p11.2UniSTS
Cytogenetic Map1q41UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map15q25.2UniSTS
Cytogenetic Map14q11.2UniSTS
Cytogenetic Map17q23.2UniSTS
Cytogenetic Map7q32.2UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map6q25.1UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map9p13.3UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map2p13.1UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map3q29UniSTS
Cytogenetic Map7p13UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic Map14q31-q32.1UniSTS
Cytogenetic Map1q42.11UniSTS
Cytogenetic Map4q35.1UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic Map2p13.3UniSTS
Cytogenetic MapXp11.3UniSTS
Cytogenetic Map2q11.2-q12.1UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map1p22UniSTS
Cytogenetic Map6q16.2UniSTS
Cytogenetic Map18q23UniSTS
Cytogenetic Map2q14UniSTS
Cytogenetic Map20p11.23-p11.21UniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map8p11.23UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic Map19q13UniSTS
Cytogenetic Map8p11.21UniSTS
Cytogenetic Map12q14.3UniSTS
Cytogenetic MapXq26.3UniSTS
Cytogenetic Map8q24.11UniSTS
Cytogenetic Map10q23.1UniSTS
Cytogenetic Map1q44UniSTS
Cytogenetic Map9q22.33UniSTS
Cytogenetic Map3p21.31UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map9q21.32UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic Map9q33.3UniSTS
Cytogenetic Map1p36.1UniSTS
Cytogenetic Map20q12UniSTS
Cytogenetic Map4q21.23UniSTS
Cytogenetic Map5q13.2UniSTS
Cytogenetic Map22q12.1UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic Map2q21.3UniSTS
Cytogenetic Map7q21.2UniSTS
Cytogenetic Map17q22.2UniSTS
Cytogenetic Map17p13UniSTS
Cytogenetic Map12q24.11UniSTS
Cytogenetic Map18q21UniSTS
Cytogenetic Map10q11.1UniSTS
Cytogenetic Map22q11.2UniSTS
Cytogenetic Map19q12UniSTS
Cytogenetic Map7q34-q35UniSTS
Cytogenetic Map15q24.1UniSTS
Cytogenetic Map18p11.21UniSTS
Cytogenetic Map1q23.1UniSTS
Cytogenetic Map19q13.41UniSTS
Cytogenetic Map6p25.1-p23UniSTS
Cytogenetic Map11p15.4UniSTS
Cytogenetic Map10q22UniSTS
Cytogenetic Map5q35.3UniSTS
Cytogenetic Map18q12.1-q21.1UniSTS
Cytogenetic Map12p13.1UniSTS
Cytogenetic Map13q12.1UniSTS
Cytogenetic Map12q15UniSTS
Cytogenetic Map6p21.32UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map10p14UniSTS
Cytogenetic Map12p13.1-p12.3UniSTS
Cytogenetic Map3p25.2UniSTS
Cytogenetic Map6p21.33UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map3p21.2UniSTS
Cytogenetic Map10q26.3UniSTS
Cytogenetic Map1q21.3UniSTS
Cytogenetic MapXp21.2UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map14q12UniSTS
Cytogenetic Map8p11.22UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map2q21.1UniSTS
Cytogenetic Map9q21.12UniSTS
Cytogenetic Map15q23UniSTS
Cytogenetic Map7p22.2UniSTS
Cytogenetic Map8p21.2UniSTS
Cytogenetic Map7q33UniSTS
Cytogenetic Map15q15.3UniSTS
Cytogenetic Map4q21.22UniSTS
Cytogenetic Map12q13.12UniSTS
Cytogenetic Map10q24.31UniSTS
Cytogenetic Map12p13.31UniSTS
Cytogenetic Map14q32.12UniSTS
Cytogenetic Map10q24.32UniSTS
Cytogenetic Map11q12.3UniSTS
Cytogenetic Map16p12.3UniSTS
Cytogenetic Map1p34.3UniSTS
Cytogenetic Map1p36.21UniSTS
Cytogenetic Map2q24.3UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map16q24.1UniSTS
Cytogenetic Map1p31.1UniSTS
Cytogenetic Map19q13.33UniSTS
Cytogenetic Map1p36.31UniSTS
Cytogenetic Map3q13.31UniSTS
Cytogenetic Map15q22.2UniSTS
Cytogenetic Map5q32UniSTS
Cytogenetic Map6q13UniSTS
Cytogenetic MapXq24UniSTS
Cytogenetic Map6q25UniSTS
Cytogenetic Map6p21UniSTS
Cytogenetic Map2q35UniSTS
Cytogenetic Map12p13-p12UniSTS
Cytogenetic Map9p13.2UniSTS
Cytogenetic Map6p22UniSTS
Cytogenetic Map2q12.1UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map9q22.2UniSTS
Cytogenetic Map1q22UniSTS
Cytogenetic Map1p22.1UniSTS
Cytogenetic Map1p36UniSTS
Cytogenetic Map9q13-q21UniSTS
Cytogenetic Map11p15.5UniSTS
Cytogenetic MapXp11.2UniSTS
Cytogenetic Map19pUniSTS
Cytogenetic Map19p13.1-p12UniSTS
Cytogenetic Map7q22UniSTS
Cytogenetic Map12q24.33UniSTS
Cytogenetic Map3q21UniSTS
Cytogenetic Map8q24UniSTS
Cytogenetic Map18p11.31-p11.21UniSTS
Cytogenetic Map11p15.3-p15.1UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map8q22UniSTS
Cytogenetic Map4p15.1UniSTS
Cytogenetic Map1q25.2UniSTS
Cytogenetic Map2p16.3UniSTS
Cytogenetic Map16p13.12UniSTS
Cytogenetic Map7p21.2UniSTS
Cytogenetic Map12q21.1UniSTS
Cytogenetic Map2p14UniSTS
Cytogenetic Map6q24.3UniSTS
Cytogenetic Map10q22.2UniSTS
Cytogenetic Map5q23.1UniSTS
Cytogenetic Map10q23.2UniSTS
Cytogenetic Map7p22.3UniSTS
Cytogenetic Map21q22.2UniSTS
Cytogenetic Map6q22.1UniSTS
Cytogenetic Map1q42.1UniSTS
Cytogenetic Map1q25UniSTS
Cytogenetic Map6p22.3UniSTS
Cytogenetic Map1q21.2UniSTS
Cytogenetic Map15q22.1UniSTS
Cytogenetic Map12p13.2UniSTS
Cytogenetic Map12q22UniSTS
Cytogenetic Map3p21-p12UniSTS
Cytogenetic Map4q35UniSTS
Cytogenetic Map1p34-p33UniSTS
Cytogenetic Map21q22.11UniSTS
Cytogenetic Map3p22-p21.33UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map3q22.1UniSTS
Cytogenetic Map8q21.11UniSTS
Cytogenetic MapXq22.3UniSTS
Cytogenetic Map7p14UniSTS
Cytogenetic Map17q21.1UniSTS
Cytogenetic Map15q21UniSTS
Cytogenetic Map1q42.3UniSTS
Cytogenetic Map9q22UniSTS
Cytogenetic Map2q12.3UniSTS
Cytogenetic Map20q11.2-q13.2UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map17q24UniSTS
Cytogenetic Map3q25.31UniSTS
Cytogenetic Map6p24.3UniSTS
Cytogenetic Map2q31.3UniSTS
Cytogenetic Map1q31UniSTS
Cytogenetic Map7q32-q33UniSTS
Cytogenetic Map7q21.1UniSTS
Cytogenetic Map14q23-q24.2UniSTS
Cytogenetic Map19q13.3-q13.4UniSTS
Cytogenetic Map2p24-p21UniSTS
Cytogenetic Map15q11.2UniSTS
Cytogenetic Map15q26.3UniSTS
Cytogenetic Map7p22UniSTS
Cytogenetic Map12p11UniSTS
Cytogenetic Map1p35.3UniSTS
Cytogenetic Map1p12UniSTS
Cytogenetic Map13q32.3UniSTS
Cytogenetic Map5q23.3UniSTS
Cytogenetic Map20q13UniSTS
Cytogenetic Map17q25.2UniSTS
Cytogenetic Map7q36.1UniSTS
Cytogenetic Map10p12.33UniSTS
Cytogenetic Map17q21.32UniSTS
Cytogenetic MapXp11.22UniSTS
Cytogenetic Map12p13.3UniSTS
Cytogenetic MapXq25-q26UniSTS
Cytogenetic Map2q36.1UniSTS
Cytogenetic Map5p13UniSTS
Cytogenetic Map15q25UniSTS
Cytogenetic Map5q12.1UniSTS
Cytogenetic Map5p12UniSTS
Cytogenetic Map1p36.22UniSTS
Cytogenetic Map3q26.31UniSTS
Cytogenetic Map17q22-q23UniSTS
Cytogenetic MapXp22.33UniSTS
Cytogenetic MapYp11.3UniSTS
Cytogenetic Map17p11.2UniSTS
Cytogenetic MapXq13.2UniSTS
Cytogenetic Map12q23.1UniSTS
Cytogenetic Map16q12.2UniSTS
Cytogenetic Map3q26.32UniSTS
Cytogenetic Map6q22.31UniSTS
Cytogenetic Map3q26.2-q27UniSTS
Cytogenetic Map1q25.1-q25.2UniSTS
Cytogenetic Map14q24UniSTS
Cytogenetic Map9q21.13UniSTS
Cytogenetic Map10q11.22UniSTS
Cytogenetic Map22q13.31UniSTS
Cytogenetic Map3p25.1UniSTS
Cytogenetic Map5q21.3UniSTS
Cytogenetic Map5p13.3UniSTS
Cytogenetic Map10q22.1UniSTS
Cytogenetic Map14q12-q13UniSTS
Cytogenetic MapXp22UniSTS
Cytogenetic MapXq23UniSTS
Cytogenetic Map20p12.3-p11.21UniSTS
Cytogenetic Map2p21UniSTS
Cytogenetic Map17q11.2-q12UniSTS
Cytogenetic Map4q32-q34UniSTS
Cytogenetic MapXq25-q26.1UniSTS
Cytogenetic Map2p25-p24UniSTS
Cytogenetic Map2p25UniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic MapXp22.2-p22.1UniSTS
Cytogenetic MapXq22.1UniSTS
Cytogenetic Map4q25UniSTS
Cytogenetic Map3p24.2UniSTS
Cytogenetic Map22q13UniSTS
Cytogenetic Map20q11.22-q12UniSTS
Cytogenetic Map4q34.2UniSTS
Cytogenetic Map20p13UniSTS
Cytogenetic Map22q13.1-q13.2UniSTS
Cytogenetic MapXq28UniSTS
Cytogenetic Map12q13-q14UniSTS
Cytogenetic Map6q14.1UniSTS
Cytogenetic Map12q13.3UniSTS
Cytogenetic Map9q31.2UniSTS
Cytogenetic Map11q13.1-q13.2UniSTS
Cytogenetic Map12q13UniSTS
Cytogenetic Map1p32-p31UniSTS
Cytogenetic Map21q21.2UniSTS
Cytogenetic Map10q24.3UniSTS
Cytogenetic Map16q21UniSTS
Cytogenetic Map8q21.1UniSTS
Cytogenetic Map5p13.2UniSTS
Cytogenetic Map1p34UniSTS
Cytogenetic Map1q32.2UniSTS
Cytogenetic Map4q21.3UniSTS
Cytogenetic Map7q21-q22UniSTS
Cytogenetic Map3q26.2UniSTS
Cytogenetic Map2q36.3UniSTS
Cytogenetic Map8p22UniSTS
Cytogenetic Map11q22.1UniSTS
Cytogenetic Map3q25.33UniSTS
Cytogenetic Map10q23.31UniSTS
Cytogenetic Map4p15.32UniSTS
Cytogenetic Map18q12.2UniSTS
Cytogenetic Map15q15.2UniSTS
Cytogenetic Map5q12.3UniSTS
Cytogenetic Map14q24.1UniSTS
Cytogenetic Map12q14.1UniSTS
Cytogenetic Map6p22.3-p22.1UniSTS
Cytogenetic Map7p11.2UniSTS
Cytogenetic Map6q15UniSTS
Cytogenetic Map6q23.3UniSTS
Cytogenetic Map13q14UniSTS
Cytogenetic Map5q35.2UniSTS
Cytogenetic Map10q22.3UniSTS
Cytogenetic Map1p35UniSTS
Cytogenetic Map3q12.3UniSTS
Cytogenetic Map19q13.31UniSTS
Cytogenetic Map8q23.1UniSTS
Cytogenetic Map6q27UniSTS
Cytogenetic Map2q14.3UniSTS
Cytogenetic MapXp11UniSTS
Cytogenetic Map11p15.3UniSTS
Cytogenetic Map20p12UniSTS
Cytogenetic Map15q13.1UniSTS
Cytogenetic MapXp22.3UniSTS
Cytogenetic Map11q13.5UniSTS
Cytogenetic Map19p13.3-p13.2UniSTS
Cytogenetic Map1p36.11-p34.2UniSTS
Cytogenetic Map4q22.1-q23UniSTS
Cytogenetic Map7q22.3UniSTS
Cytogenetic Map9p22UniSTS
Cytogenetic Map17q23.3UniSTS
Cytogenetic Map16q23.2UniSTS
Cytogenetic Map2p16.1UniSTS
Cytogenetic Map3q27.1UniSTS
Cytogenetic Map2p22.3UniSTS
Cytogenetic MapXq26.1UniSTS
Cytogenetic Map4q21.21UniSTS
Cytogenetic Map22q13.3UniSTS
Cytogenetic Map2q32.1UniSTS
Cytogenetic MapYp11.32UniSTS
Cytogenetic Map11p14UniSTS
Cytogenetic Map1p32.1UniSTS
Cytogenetic Map2p25.3UniSTS
Cytogenetic Map4q34.3UniSTS
Cytogenetic Map9p12UniSTS
Cytogenetic Map3q13.13UniSTS
Cytogenetic Map13q34UniSTS
Cytogenetic Map3p21UniSTS
Cytogenetic Map11q23.2UniSTS
Cytogenetic Map20p11.23UniSTS
Cytogenetic Map3p13UniSTS
Cytogenetic Map4p13UniSTS
Cytogenetic Map16q23.1UniSTS
Cytogenetic Map10p11.23UniSTS
Cytogenetic Map8p21.1UniSTS
Cytogenetic Map15q22-q24UniSTS
Cytogenetic Map8q23UniSTS
Cytogenetic Map16q12.1UniSTS
Cytogenetic Map14q13.2UniSTS
Cytogenetic Map18q12.1UniSTS
Cytogenetic Map5q31.3UniSTS
Cytogenetic Map11q14UniSTS
Cytogenetic Map13q33.1UniSTS
Cytogenetic Map14q21.2UniSTS
Cytogenetic Map4q31.3UniSTS
Cytogenetic Map15q21-q22UniSTS
Cytogenetic Map3p14.3UniSTS
Cytogenetic Map17p13.1UniSTS
Cytogenetic Map13q12.11UniSTS
Cytogenetic Map6p21.2UniSTS
Cytogenetic Map15q21.3UniSTS
Cytogenetic Map3q21.1UniSTS
Cytogenetic Map6p21.31UniSTS
Cytogenetic Map10p15.1UniSTS
Cytogenetic Map1q24.2UniSTS
Cytogenetic Map12p12UniSTS
Cytogenetic Map7p22.1UniSTS
Cytogenetic Map11q24UniSTS
Cytogenetic Map21q22.13UniSTS
Cytogenetic Map15q22.1-q22.31UniSTS
Cytogenetic Map15q22UniSTS
Cytogenetic MapXq13UniSTS
Cytogenetic Map1q31-q41UniSTS
Cytogenetic Map6p25UniSTS
Cytogenetic Map14q32.1UniSTS
Cytogenetic Map16q12-q13UniSTS
Cytogenetic MapXq12-q13UniSTS
Cytogenetic Map14q23UniSTS
Cytogenetic Map12q11-q12UniSTS
Cytogenetic Map1q42.1-q43UniSTS
Cytogenetic Map3q13.33UniSTS
Cytogenetic Map7q31UniSTS
Cytogenetic Map12q24UniSTS
Cytogenetic MapXp22.11UniSTS
Cytogenetic Map11q13.4UniSTS
Cytogenetic Map2p25.1-p24.1UniSTS
Cytogenetic Map8q24.21UniSTS
Cytogenetic Map12q13.1UniSTS
Cytogenetic Map12q22-q23.1UniSTS
Cytogenetic Map11q12.2UniSTS
Cytogenetic Map1p13.2UniSTS
Cytogenetic Map5q31.2-q34UniSTS
Cytogenetic Map11p15.1UniSTS
Cytogenetic Map6q24.2UniSTS
Cytogenetic Map22qUniSTS
Cytogenetic Map12q13.11-q14.3UniSTS
Cytogenetic Map7p11UniSTS
Cytogenetic MapXp22.12-p22.11UniSTS
Cytogenetic Map7q11.21UniSTS
Cytogenetic Map20q11.22-q11.23UniSTS
Cytogenetic Map8q24.22UniSTS
Cytogenetic Map8p22-p21.3UniSTS
Cytogenetic Map10q24UniSTS
Cytogenetic Map1q21.2-q21.3UniSTS
Cytogenetic Map1p36.12UniSTS
Cytogenetic Map9p24.1UniSTS
Cytogenetic Map6q25.2-q27UniSTS
Cytogenetic Map9q34UniSTS
Cytogenetic Map5p13.1UniSTS
Cytogenetic Map8q11.2UniSTS
Cytogenetic Map3q28-q29UniSTS
Cytogenetic Map7p14-p13UniSTS
Cytogenetic Map12q24.2UniSTS
Cytogenetic Map6p22.2UniSTS
Cytogenetic Map7q22-qterUniSTS
Cytogenetic Map12q24.2-q24.31UniSTS
Cytogenetic MapXq13.1UniSTS
Cytogenetic Map6p25.2UniSTS
Cytogenetic Map1p21UniSTS
Cytogenetic Map1q32.2-q41UniSTS
Cytogenetic Map11q22-q23UniSTS
Cytogenetic Map3q26.33UniSTS
Cytogenetic Map12q23-q24.1UniSTS
Cytogenetic Map5p15.1-p14.3UniSTS
Cytogenetic Map16p13.11UniSTS
Cytogenetic Map6q22-q23UniSTS
Cytogenetic Map9p21UniSTS
Cytogenetic Map6p12.3UniSTS
Cytogenetic Map3p12.1UniSTS
Cytogenetic Map9q21.11UniSTS
Cytogenetic Map17q24.1UniSTS
Cytogenetic Map10q11.21UniSTS
Cytogenetic Map14q21UniSTS
Cytogenetic Map11p15UniSTS
Cytogenetic Map16q22UniSTS
Cytogenetic Map15q11-q13UniSTS
Cytogenetic Map13q12-q14UniSTS
Cytogenetic Map18q21.1UniSTS
Cytogenetic Map2q24UniSTS
Cytogenetic Map12p13UniSTS
Cytogenetic Map3q28UniSTS
Cytogenetic Map7q32.1UniSTS
Cytogenetic MapXq22.2UniSTS
Cytogenetic Map7p12.3UniSTS
Cytogenetic Map7p15.1UniSTS
Cytogenetic Map2q37.2UniSTS
Cytogenetic Map18q22.3UniSTS
Cytogenetic Map14q32.13UniSTS
Cytogenetic Map14q22.1UniSTS
Cytogenetic Map16p13.1UniSTS
Cytogenetic Map7q31.3UniSTS
Cytogenetic Map20q13.2-q13.3UniSTS
Cytogenetic Map1p21.2UniSTS
Cytogenetic Map9q21.33UniSTS
Cytogenetic Map14q32.2UniSTS
Cytogenetic Map13q13.3UniSTS
Cytogenetic Map10p12.31UniSTS
Cytogenetic Map22q11.1UniSTS
Cytogenetic Map5q33.2UniSTS
Cytogenetic Map13q32.2UniSTS
Cytogenetic Map14q23.1UniSTS
Cytogenetic Map8q21.2UniSTS
Cytogenetic Map2q24.1UniSTS
Cytogenetic Map10q26.13UniSTS
Cytogenetic Map2q23.3UniSTS
Cytogenetic Map19p13.1UniSTS
Cytogenetic Map15q14-q15UniSTS
Cytogenetic Map1q42.13UniSTS
Cytogenetic Map14q31UniSTS
Cytogenetic Map7p21.1UniSTS
Cytogenetic Map8p12-p11UniSTS
Cytogenetic Map18p11.2UniSTS
Cytogenetic Map7p11.1UniSTS
Cytogenetic Map1q31-q32UniSTS
Cytogenetic Map2q12UniSTS
Cytogenetic Map3p21.32UniSTS
Cytogenetic Map2p24.2UniSTS
Cytogenetic Map2q33-q34UniSTS
Cytogenetic Map6q24.1UniSTS
Cytogenetic Map4q22.1UniSTS
Cytogenetic Map15q13.3UniSTS
Cytogenetic Map10q26.11UniSTS
Cytogenetic Map7p15.3UniSTS
Cytogenetic Map10q23.33UniSTS
Cytogenetic Map12p12.1UniSTS
Cytogenetic Map7p13-p12UniSTS
Cytogenetic MapXq25UniSTS
Cytogenetic Map17q11-q21UniSTS
Cytogenetic Map12q23UniSTS
Cytogenetic Map6p24-p22.3UniSTS
Cytogenetic Map14q23.2UniSTS
Cytogenetic Map7q31.1-q31.2UniSTS
Cytogenetic Map8q22.2UniSTS
Cytogenetic Map15q21.2UniSTS
Cytogenetic Map3p26.1-p25.1UniSTS
Cytogenetic Map5q35UniSTS
Cytogenetic Map3q13.2UniSTS
Cytogenetic Map4p15.2UniSTS
Cytogenetic Map6q16.3UniSTS
Cytogenetic Map17q24-q25UniSTS
Cytogenetic MapXq12UniSTS
Cytogenetic MapXq27.1UniSTS
Cytogenetic Map8q12.3UniSTS
Cytogenetic Map5q21.2UniSTS
Cytogenetic Map5q15UniSTS
Cytogenetic Map5q35.1UniSTS
Cytogenetic Map4q13.3UniSTS
Cytogenetic Map4q35.2UniSTS
Cytogenetic Map3p26.1UniSTS
Cytogenetic Map3p11.1UniSTS
Cytogenetic Map17q21.2UniSTS
Cytogenetic Map2q21.2UniSTS
Cytogenetic Map19p13.13UniSTS
Cytogenetic Map18q12.3UniSTS
Cytogenetic Map18p11.3UniSTS
Cytogenetic Map17q11.1UniSTS
Cytogenetic Map15q25.1UniSTS
Cytogenetic Map13q12.3UniSTS
Cytogenetic Map12q23.2UniSTS
Cytogenetic Map12q12-q13UniSTS
Cytogenetic Map12q14UniSTS
Cytogenetic Map5q33.1UniSTS
Cytogenetic Map2q32-q34UniSTS
Cytogenetic Map16q22.3UniSTS
Cytogenetic Map2p15-p13UniSTS
Cytogenetic MapXp11.4UniSTS
Cytogenetic Map19q13.33-q13.41UniSTS
Cytogenetic Map20p11UniSTS
Cytogenetic Map6q23-q24UniSTS
Cytogenetic Map2p12UniSTS
Cytogenetic Map2p13UniSTS
Cytogenetic Map13q11-q12UniSTS
Cytogenetic Map6p12.3-p11.2UniSTS
Cytogenetic Map6q16.1-q16.3UniSTS
Cytogenetic Map22q11UniSTS
Cytogenetic Map7q31.2UniSTS
Cytogenetic Map10q21.3UniSTS
Cytogenetic Map3q25.2UniSTS
Cytogenetic Map3p21.1-p14.3UniSTS
Cytogenetic Map6p12.1UniSTS
Cytogenetic Map3q23-q24UniSTS
Cytogenetic Map3q12UniSTS
Cytogenetic Map7q11.1UniSTS
Cytogenetic Map3q22.3UniSTS
Cytogenetic Map7q21.3UniSTS
Cytogenetic Map4q31.1UniSTS
Cytogenetic Map22q12-q13UniSTS
Cytogenetic Map4q23UniSTS
Cytogenetic MapXp22.12UniSTS
Cytogenetic Map6q16.1UniSTS
Cytogenetic Map13q14.13UniSTS
Cytogenetic Map18q21.3UniSTS
Cytogenetic Map9q33.2UniSTS
Cytogenetic Map11q21UniSTS
Cytogenetic Map8q12UniSTS
Cytogenetic Map4q28-q32UniSTS
Cytogenetic Map17q24.3UniSTS
Cytogenetic Map6p23UniSTS
Cytogenetic Map8p11UniSTS
Cytogenetic Map5q34UniSTS
Cytogenetic Map1q24.3UniSTS
Cytogenetic Map9q33.1UniSTS
Cytogenetic Map1q23.3UniSTS
Cytogenetic Map2p16.2UniSTS
Cytogenetic Map9q22.31UniSTS
Cytogenetic Map9p24.3UniSTS
Cytogenetic Map7q35UniSTS
Cytogenetic Map1p36.2UniSTS
Cytogenetic Map11q22.3UniSTS
Cytogenetic Map16p12UniSTS
Cytogenetic Map1q22-q23UniSTS
Cytogenetic Map13q22.1UniSTS
Cytogenetic Map2q12.2UniSTS
Cytogenetic Map8p12UniSTS
Cytogenetic Map4q21UniSTS
Cytogenetic Map13q12.2UniSTS
Cytogenetic Map9q31-q33UniSTS
Cytogenetic Map6p24.1UniSTS
Cytogenetic Map1q23UniSTS
Cytogenetic Map11q12-q13UniSTS
Cytogenetic Map11q13.3UniSTS
Cytogenetic Map11q24.2UniSTS
Cytogenetic Map11q12.1UniSTS
Cytogenetic Map3p26UniSTS
Cytogenetic Map5q13UniSTS
Cytogenetic Map8p21UniSTS
Cytogenetic Map19q13.1-q13.2UniSTS
Cytogenetic Map1p33-p32UniSTS
Cytogenetic Map7q36.2UniSTS
Cytogenetic Map4q32.3UniSTS
Cytogenetic Map16p13.2UniSTS
Cytogenetic Map14q32UniSTS
Cytogenetic Map10q11.23UniSTS
Cytogenetic Map10q26.1UniSTS
Cytogenetic Map9q32-q33.3UniSTS
Cytogenetic Map9q22.1-q22.2UniSTS
Cytogenetic Map3q26.1-q26.2UniSTS
Cytogenetic Map5q31-q34UniSTS
Cytogenetic Map9q33-q34UniSTS
Cytogenetic Map5q11.2-q13.2UniSTS
Cytogenetic Map13q32UniSTS
Cytogenetic Map9q22.32UniSTS
Cytogenetic Map1p36.3UniSTS
Cytogenetic Map1p36.3-p36.2UniSTS
Cytogenetic Map4q28.1UniSTS
Cytogenetic Map5q22UniSTS
Cytogenetic Map12p11.21UniSTS
Cytogenetic MapXq13.3UniSTS
Cytogenetic Map9q31.3UniSTS
Cytogenetic Map3p26.3UniSTS
Cytogenetic Map2q11.1UniSTS
Cytogenetic Map21q11.2UniSTS
Cytogenetic Map18q21.32UniSTS
Cytogenetic Map15q26.2UniSTS
Cytogenetic Map12q24.23UniSTS
Cytogenetic Map10q25.3UniSTS
Cytogenetic Map20q11.23UniSTS
Cytogenetic Map20p12.1UniSTS
Cytogenetic Map2q31.1-q31.2UniSTS
Cytogenetic MapXp22.31UniSTS
Cytogenetic MapXp21.3UniSTS
Cytogenetic Map5q33.3UniSTS
Cytogenetic Map4q28.2UniSTS
Cytogenetic Map3p14.2UniSTS
Cytogenetic Map3q24UniSTS
Cytogenetic Map2q13UniSTS
Cytogenetic Map20q13.2UniSTS
Cytogenetic Map14q11.2-q12UniSTS
Cytogenetic Map3p24UniSTS
Cytogenetic Map12q23.3UniSTS
Cytogenetic Map11q24.3UniSTS
Cytogenetic Map11q14.3UniSTS
Cytogenetic Map10q25.2UniSTS
Cytogenetic Map3q25.1UniSTS
Cytogenetic Map8q13UniSTS
Cytogenetic Map1p22.2UniSTS
Cytogenetic Map3p22.3UniSTS
Cytogenetic Map18q11.1UniSTS
Cytogenetic Map8q23.3UniSTS
Cytogenetic Map15q24UniSTS
Cytogenetic Map11cen-q12UniSTS
Cytogenetic Map11q25UniSTS
Cytogenetic Map3p22.2UniSTS
Cytogenetic MapXp21.1UniSTS
Cytogenetic Map7q36UniSTS
Cytogenetic Map7p14.3UniSTS
Cytogenetic Map12q21UniSTS
Cytogenetic Map7p15UniSTS
Cytogenetic Map7q22-q31UniSTS
Cytogenetic Map11q22UniSTS
Cytogenetic Map5p15.3UniSTS
Cytogenetic Map20q13.3-qterUniSTS
Cytogenetic Map1p35-p34UniSTS
Cytogenetic Map4p13-p12UniSTS
Cytogenetic Map10q21-q22UniSTS
Cytogenetic Map4q22UniSTS
Cytogenetic Map7p13-p11.1UniSTS
Cytogenetic Map9q31-q34UniSTS
Cytogenetic Map7q21.1-q22UniSTS
Cytogenetic Map15q26.1UniSTS
Cytogenetic Map3q13.13-q13.2UniSTS
Cytogenetic MapXp22.13UniSTS
Cytogenetic Map13q12.12UniSTS
Cytogenetic Map13q14.2UniSTS
Cytogenetic Map12qUniSTS
Cytogenetic Map1pUniSTS
Cytogenetic Map16pUniSTS
Cytogenetic Map15qUniSTS
Cytogenetic Map7qUniSTS
Cytogenetic Map2qUniSTS
Cytogenetic Map5q13.1UniSTS
Cytogenetic Map11p14.1UniSTS
Cytogenetic Map4q32UniSTS
Cytogenetic Map2p22UniSTS
Cytogenetic Map5q14.3UniSTS
Cytogenetic Map10p12.1UniSTS
Cytogenetic Map5q23.2UniSTS
Cytogenetic Map2p24.1UniSTS
Cytogenetic Map8q24.13UniSTS
Cytogenetic Map12p13.32UniSTS
Cytogenetic Map9p21.1UniSTS
Cytogenetic Map9q34.2-q34.3UniSTS
D1S1425  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map1p33UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map1p31.3UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map6q25.3UniSTS
Cytogenetic Map19p13.12UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map2p13.1UniSTS
Cytogenetic Map5q35.3UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map4q21.23UniSTS
Cytogenetic Map22q12.1UniSTS
Cytogenetic Map8q24.13UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map1q23.1UniSTS
Cytogenetic Map10q22UniSTS
Cytogenetic Map4q12UniSTS
Cytogenetic Map10p14UniSTS
Cytogenetic Map6p21.33UniSTS
Cytogenetic Map10q26.3UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map7p22.2UniSTS
Cytogenetic Map12q13.12UniSTS
Cytogenetic Map18p11.21UniSTS
Cytogenetic Map14q32.12UniSTS
Cytogenetic Map2q31.1UniSTS
Cytogenetic Map18p11.31UniSTS
Cytogenetic Map13q34UniSTS
Cytogenetic Map4p14UniSTS
Cytogenetic Map8p23.1UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map3q21.3UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map8q12.1UniSTS
Cytogenetic Map11q12.3UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map10p12UniSTS
Cytogenetic Map12q13UniSTS
Cytogenetic Map11p15.4UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map8q24UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic Map5q13.2UniSTS
Cytogenetic Map5q32UniSTS
Cytogenetic Map1q21.2UniSTS
Cytogenetic Map3q26.2UniSTS
Cytogenetic Map6q25.2-q25.3UniSTS
Cytogenetic Map20q11.2-q13.2UniSTS
Cytogenetic Map12q13.3UniSTS
Cytogenetic Map1q21-q23UniSTS
Cytogenetic Map17q21.32UniSTS
Cytogenetic Map1p35.3UniSTS
Cytogenetic Map1p12UniSTS
Cytogenetic Map2p23-p22UniSTS
Cytogenetic Map2q36.1UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic Map2p16.1UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map16q12.1UniSTS
Cytogenetic Map17q22-q23UniSTS
Cytogenetic Map2p11.1UniSTS
Cytogenetic Map16q12.2UniSTS
Cytogenetic Map2p12-p11.2UniSTS
Cytogenetic Map3q11.1UniSTS
Cytogenetic Map2p21UniSTS
Cytogenetic Map17q11.2-q12UniSTS
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map1p32-p31UniSTS
Cytogenetic Map1p21.3UniSTS
Cytogenetic Map1q32.2UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic Map7q21-q22UniSTS
Cytogenetic Map1q25.3UniSTS
Cytogenetic Map18p11.3-p11.2UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map21p11.1UniSTS
Cytogenetic Map12q24.31-q24.32UniSTS
Cytogenetic Map9q33.2UniSTS
Cytogenetic Map11q13.5UniSTS
Cytogenetic Map12p12.2-p11.2UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map2q14.3UniSTS
Cytogenetic Map19p13.3-p13.2UniSTS
Cytogenetic Map7q32.1UniSTS
Cytogenetic Map8p21.3UniSTS
Cytogenetic Map17q22-q23.2UniSTS
Cytogenetic Map3q27.1UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map4q21.21UniSTS
Cytogenetic Map1q32UniSTS
Cytogenetic Map14q32UniSTS
Cytogenetic Map14q24.2UniSTS
Cytogenetic Map20q13.33UniSTS
Cytogenetic Map3p21UniSTS
Cytogenetic Map10p11.23UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map1q25.2UniSTS
Cytogenetic Map18q12.1UniSTS
Cytogenetic Map1p34.3UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic Map15q23UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map13q12.11UniSTS
Cytogenetic Map1p36.31UniSTS
Cytogenetic Map3q21.1UniSTS
Cytogenetic Map12p12UniSTS
Cytogenetic Map21q22.11UniSTS
Cytogenetic Map15q15.3UniSTS
Cytogenetic MapXq12-q13UniSTS
Cytogenetic Map22q11.2UniSTS
Cytogenetic Map7q31.1-q31.3UniSTS
Cytogenetic MapXp22.11UniSTS
Cytogenetic Map3p21.1-p14.2UniSTS
Cytogenetic Map2p24UniSTS
Cytogenetic Map20p12.1UniSTS
Cytogenetic Map3q26.33UniSTS
Cytogenetic Map12q13.11-q14.3UniSTS
Cytogenetic Map2q37.3UniSTS
Cytogenetic Map9q21.33UniSTS
Cytogenetic Map12q12UniSTS
Cytogenetic MapXq13-q21UniSTS
Cytogenetic Map8q24.22UniSTS
Cytogenetic Map11p13UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map6q25.2-q27UniSTS
Cytogenetic Map12q24.32UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic MapXq13.1UniSTS
Cytogenetic Map22q12.2UniSTS
Cytogenetic Map14q12UniSTS
Cytogenetic Map12q23-q24.1UniSTS
Cytogenetic Map4q35.1UniSTS
Cytogenetic Map17q24.1UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map14q21UniSTS
Cytogenetic Map9p24.3UniSTS
Cytogenetic Map7p13UniSTS
Cytogenetic Map2p14UniSTS
Cytogenetic Map21q22.2UniSTS
Cytogenetic Map2q12.3UniSTS
Cytogenetic Map8p21.1UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map3q25.33UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic Map1p34UniSTS
Cytogenetic Map19p13.1UniSTS
Cytogenetic Map5q14.1UniSTS
Cytogenetic MapXq22.3UniSTS
Cytogenetic Map7p21.1UniSTS
Cytogenetic Map6p25.2UniSTS
Cytogenetic Map10q23.33UniSTS
Cytogenetic Map15q11-q12UniSTS
Cytogenetic Map3p22.2UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map15q21.1-q21.2UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic Map4q13.3UniSTS
Cytogenetic Map19p13.13UniSTS
Cytogenetic Map19q13.41UniSTS
Cytogenetic Map17q24.3UniSTS
Cytogenetic Map12p13.33UniSTS
Cytogenetic Map11q14.1UniSTS
Cytogenetic Map3p22-p21.3UniSTS
Cytogenetic Map16q22.3UniSTS
Cytogenetic Map1p22.1UniSTS
Cytogenetic Map6p12.1UniSTS
Cytogenetic Map19q13.33-q13.41UniSTS
Cytogenetic Map2p25.3UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map5p12UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map7q35UniSTS
Cytogenetic Map17p12UniSTS
Cytogenetic Map7q11.1UniSTS
Cytogenetic Map2p25.1-p24.1UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map4q31.21UniSTS
Cytogenetic Map5p13.1UniSTS
Cytogenetic MapXq22.1UniSTS
Cytogenetic Map9q21.11UniSTS
Cytogenetic Map5q13UniSTS
Cytogenetic Map1p22.2UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map12q24UniSTS
Cytogenetic MapXq24UniSTS
Cytogenetic Map1q24.2UniSTS
Cytogenetic Map22q13.31UniSTS
Cytogenetic Map8p11.23UniSTS
Cytogenetic Map1q23.3UniSTS
Cytogenetic Map16p12UniSTS
Cytogenetic Map10p15-p14UniSTS
Cytogenetic Map19q13UniSTS
Cytogenetic Map1q22-q23UniSTS
Cytogenetic Map20q11.23UniSTS
Cytogenetic Map7q31UniSTS
Cytogenetic Map10q26UniSTS
Cytogenetic Map7p22.1UniSTS
Cytogenetic Map6p22.3UniSTS
Cytogenetic Map6p21.2UniSTS
Cytogenetic Map11q13.4UniSTS
Cytogenetic Map11q24.2UniSTS
Cytogenetic MapXq28UniSTS
Cytogenetic Map1p33-p32UniSTS
Cytogenetic Map5q35.2UniSTS
Cytogenetic Map3p14.3UniSTS
Cytogenetic Map12q24.33UniSTS
Cytogenetic Map3q26.1-q26.2UniSTS
Cytogenetic Map12p13UniSTS
Cytogenetic Map7q36.1UniSTS
Cytogenetic Map8p11.21UniSTS
Cytogenetic Map12q13.1-q13.2UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map19q13.33UniSTS
Cytogenetic Map16p12.3UniSTS
Cytogenetic Map13q14.11UniSTS
Cytogenetic Map9p13.2UniSTS
Cytogenetic Map4q22.1UniSTS
Cytogenetic Map3q13.2UniSTS
Cytogenetic Map8p22UniSTS
Cytogenetic Map22q11.23UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map1q42.3UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map5q12.3UniSTS
Cytogenetic Map20q11.21UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map12q14.3UniSTS
Cytogenetic Map6q15UniSTS
Cytogenetic Map6q22.32UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map19q13.31UniSTS
Cytogenetic Map16p13.11UniSTS
Cytogenetic Map10q24.32UniSTS
Cytogenetic Map4p16.1UniSTS
Cytogenetic Map18q11.1UniSTS
Cytogenetic Map16q23.2UniSTS
Cytogenetic Map3q12.1UniSTS
Cytogenetic Map15q24-q25UniSTS
Cytogenetic Map7q31.1UniSTS
Cytogenetic Map15q26.1UniSTS
Cytogenetic Map8q13.1UniSTS
Cytogenetic Map6pter-p12.1UniSTS
Cytogenetic Map6q16UniSTS
Cytogenetic Map12q14.1UniSTS
Cytogenetic Map17q21.2UniSTS
Cytogenetic Map9q22.2UniSTS
Cytogenetic Map17q23.2UniSTS
Cytogenetic Map11q23.1-q23.2UniSTS
Cytogenetic Map13q14UniSTS
Cytogenetic Map4q23UniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map11q24.3UniSTS
Cytogenetic Map7p14UniSTS
Cytogenetic Map15q24.1UniSTS
Cytogenetic Map16q24.2UniSTS
Cytogenetic Map12q13.11UniSTS
Cytogenetic Map9p13.3UniSTS
Cytogenetic Map8q22.1UniSTS
Cytogenetic Map6q16.2UniSTS
Cytogenetic Map5p15.2UniSTS
Cytogenetic Map20q13.12UniSTS
Cytogenetic Map14q22.3UniSTS
Cytogenetic Map2q13UniSTS
Cytogenetic Map3p21.3UniSTS
Cytogenetic Map12q13.2UniSTS
Cytogenetic Map20p13UniSTS
Cytogenetic Map3q29UniSTS
Cytogenetic Map5q23.3-q31.1UniSTS
Cytogenetic Map1p36UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map2q35UniSTS
Cytogenetic Map17p11.2UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map12p13.31UniSTS
Cytogenetic Map3q12.3UniSTS
Cytogenetic Map11q23UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map20q11UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map5q23.3UniSTS
Cytogenetic Map15q15.1UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map1q42UniSTS
Cytogenetic MapXp11.23UniSTS
Cytogenetic Map12q24.13UniSTS
Cytogenetic Map3q27.3UniSTS
Cytogenetic Map14q21.3UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map2p15UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map20q13.32UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic MapXq21.1UniSTS
GDB:315881  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map3q27.3UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map19p13UniSTS
Cytogenetic Map18p11.31UniSTS
Cytogenetic Map20p13UniSTS
Cytogenetic Map3q13.33UniSTS
Cytogenetic Map21q22.11UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map2p14UniSTS
Cytogenetic Map8p23UniSTS
Cytogenetic Map2q35UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map17q12UniSTS


Expression

RNA-SEQ Expression

adipose tissue
alimentary part of gastrointestinal system
appendage
circulatory system
ectoderm
endocrine system
endoderm
entire extraembryonic component
exocrine system
hemolymphoid system
hepatobiliary system
integumental system
mesenchyme
mesoderm
musculoskeletal system
nervous system
pharyngeal arch
renal system
reproductive system
respiratory system
sensory system
visual system
1204 2439 2788 2253 4974 1726 2351 6 624 1951 465 2270 7306 6472 53 3734 1 852 1744 1617 175 1

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_000629 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001384498 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001384499 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001384500 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001384501 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001384502 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001384503 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001384504 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AF039907 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK123813 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK222770 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK222812 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK298051 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK312631 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AP000296 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AP000297 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AP000298 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AP001716 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AY654286 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC002590 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC014338 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC021825 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC035603 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC065751 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BG116121 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BG548299 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BX537636 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CA309858 (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
  J03171 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  JN543953 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  JN543954 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  JN543955 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  JN543956 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF510545 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  R15745 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  X60459 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Ensembl Acc Id: ENST00000270139   ⟹   ENSP00000270139
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2133,324,970 - 33,359,864 (+)Ensembl
Ensembl Acc Id: ENST00000442071   ⟹   ENSP00000400161
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2133,324,942 - 33,359,730 (+)Ensembl
Ensembl Acc Id: ENST00000651609   ⟹   ENSP00000498594
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2133,324,980 - 33,359,730 (+)Ensembl
Ensembl Acc Id: ENST00000652450   ⟹   ENSP00000498654
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2133,324,389 - 33,359,730 (+)Ensembl
Ensembl Acc Id: ENST00000652513   ⟹   ENSP00000498491
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2133,324,935 - 33,349,077 (+)Ensembl
Ensembl Acc Id: ENST00000652601   ⟹   ENSP00000498231
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2133,324,975 - 33,349,077 (+)Ensembl
Ensembl Acc Id: ENST00000652654   ⟹   ENSP00000498666
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2133,324,904 - 33,359,794 (+)Ensembl
Ensembl Acc Id: ENST00000700045
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2133,324,929 - 33,353,006 (+)Ensembl
Ensembl Acc Id: ENST00000700046   ⟹   ENSP00000514762
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2133,324,962 - 33,359,730 (+)Ensembl
Ensembl Acc Id: ENST00000700080   ⟹   ENSP00000514785
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2133,324,387 - 33,359,730 (+)Ensembl
Ensembl Acc Id: ENST00000700084   ⟹   ENSP00000514786
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2133,324,389 - 33,359,843 (+)Ensembl
Ensembl Acc Id: ENST00000700085
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2133,351,680 - 33,355,870 (+)Ensembl
Ensembl Acc Id: ENST00000700086
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2133,343,003 - 33,359,730 (+)Ensembl
Ensembl Acc Id: ENST00000700087
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2133,324,935 - 33,348,789 (+)Ensembl
Ensembl Acc Id: ENST00000700099
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2133,324,975 - 33,342,665 (+)Ensembl
Ensembl Acc Id: ENST00000700301
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2133,324,935 - 33,349,779 (+)Ensembl
Ensembl Acc Id: ENST00000703514   ⟹   ENSP00000515347
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2133,324,935 - 33,359,730 (+)Ensembl
Ensembl Acc Id: ENST00000703515   ⟹   ENSP00000515348
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2133,324,922 - 33,359,264 (+)Ensembl
Ensembl Acc Id: ENST00000703516   ⟹   ENSP00000515349
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2133,324,975 - 33,359,730 (+)Ensembl
Ensembl Acc Id: ENST00000703556   ⟹   ENSP00000515372
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2133,324,922 - 33,359,295 (+)Ensembl
Ensembl Acc Id: ENST00000703557   ⟹   ENSP00000515373
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2133,324,929 - 33,359,137 (+)Ensembl
Ensembl Acc Id: ENST00000703561   ⟹   ENSP00000515377
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2133,324,935 - 33,359,805 (+)Ensembl
Ensembl Acc Id: ENST00000703562   ⟹   ENSP00000515378
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2133,324,935 - 33,359,730 (+)Ensembl
Ensembl Acc Id: ENST00000703563   ⟹   ENSP00000515379
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2133,324,965 - 33,359,730 (+)Ensembl
Ensembl Acc Id: ENST00000703564   ⟹   ENSP00000515380
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2133,324,980 - 33,359,730 (+)Ensembl
Ensembl Acc Id: ENST00000703565   ⟹   ENSP00000515381
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2133,324,935 - 33,355,865 (+)Ensembl
Ensembl Acc Id: ENST00000703776
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2133,336,097 - 33,341,134 (+)Ensembl
Ensembl Acc Id: ENST00000703778
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2133,324,517 - 33,348,652 (+)Ensembl
Ensembl Acc Id: ENST00000703779   ⟹   ENSP00000515477
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2133,324,980 - 33,349,780 (+)Ensembl
RefSeq Acc Id: NM_000629   ⟹   NP_000620
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382133,324,970 - 33,359,864 (+)NCBI
GRCh372134,696,748 - 34,732,129 (+)NCBI
Build 362133,619,084 - 33,653,999 (+)NCBI Archive
HuRef2120,166,044 - 20,200,958 (+)ENTREZGENE
CHM1_12134,259,582 - 34,294,500 (+)NCBI
T2T-CHM13v2.02131,697,214 - 31,732,109 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001384498   ⟹   NP_001371427
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382133,324,970 - 33,359,864 (+)NCBI
T2T-CHM13v2.02131,697,214 - 31,732,109 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001384499   ⟹   NP_001371428
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382133,324,970 - 33,359,864 (+)NCBI
T2T-CHM13v2.02131,697,214 - 31,732,109 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001384500   ⟹   NP_001371429
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382133,324,970 - 33,359,864 (+)NCBI
T2T-CHM13v2.02131,697,214 - 31,732,109 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001384501   ⟹   NP_001371430
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382133,324,970 - 33,359,864 (+)NCBI
T2T-CHM13v2.02131,697,214 - 31,732,109 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001384502   ⟹   NP_001371431
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382133,324,970 - 33,359,864 (+)NCBI
T2T-CHM13v2.02131,697,214 - 31,732,109 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001384503   ⟹   NP_001371432
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382133,324,970 - 33,359,864 (+)NCBI
T2T-CHM13v2.02131,697,214 - 31,732,109 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001384504   ⟹   NP_001371433
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382133,324,395 - 33,359,864 (+)NCBI
T2T-CHM13v2.02131,696,639 - 31,732,109 (+)NCBI
Sequence: