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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5347252translocation1nstd200human GRCh38 chr9: 87,726,758-87,726,758 , GRCh38 chr1: 154,031,416-154,031,416 , GRCh37.p13 chr1: 154,003,892-154,003,892 , GRCh37.p13 chr9: 90,341,673-90,341,673 CTSL, NUP210L
    nsv5338602translocation1nstd200human GRCh37 chr9: 90,341,673-90,341,673 , GRCh37 chr1: 154,003,892-154,003,892 , GRCh38.p12 chr1: 154,031,416-154,031,416 , GRCh38.p12 chr9: 87,726,758-87,726,758 CTSL, NUP210L
    nsv5312620copy number variation1nstd204human GRCh38.p13 chr9: 87,727,927-87,773,335 , GRCh37.p13 chr9: 90,342,842-90,388,250 EIF3JP3, CTSL, 1 more genes
    nsv5249323copy number variation1nstd204human GRCh38.p13 chr9: 87,726,027-87,727,026 , GRCh37.p13 chr9: 90,340,942-90,341,941 CTSL
    nsv5249301copy number variation1nstd204human GRCh38.p13 chr9: 87,727,568-87,741,723 , GRCh37.p13 chr9: 90,342,483-90,356,638 EIF3JP3, CTSL
    nsv5248688copy number variation1nstd204human GRCh38.p13 chr9: 87,728,618-87,758,014 , GRCh37.p13 chr9: 90,343,533-90,372,929 CTSL, EIF3JP3
    nsv5240994copy number variation1nstd204human GRCh38.p13 chr9: 87,727,968-87,748,907 , GRCh37.p13 chr9: 90,342,883-90,363,822 CTSL, EIF3JP3
    nsv5240991copy number variation1nstd204human GRCh38.p13 chr9: 87,728,101-87,735,100 , GRCh37.p13 chr9: 90,343,016-90,350,015 CTSL
    nsv4814843copy number variation1nstd200human GRCh37 chr9: 90,343,042-90,388,000 , GRCh38.p12 chr9: 87,728,127-87,773,085 EIF3JP3, CTSL, 1 more genes
    nsv4729419copy number variation1nstd102humanLikely pathogenic GRCh37 chr9: 90,031,614-93,173,691 , GRCh38.p12 chr9: 87,416,699-90,411,409 CKS2, CTSL, 60 more genes
    nsv4680900copy number variation1nstd189human GRCh37.p13 chr9: 90,185,615-90,731,440 , GRCh38.p12 chr9: 87,570,700-88,116,525 CTSL, CTSLP8, 20 more genes
    nsv4680239copy number variation1nstd189human GRCh37.p13 chr9: 90,201,816-90,722,897 , GRCh38.p12 chr9: 87,586,901-88,107,982 CTSL, CTSLP8, 20 more genes
    nsv4674876copy number variation1nstd102humanLikely pathogenic GRCh37 chr9: 90,002,910-94,567,835 , GRCh38.p12 chr9: 87,387,995-91,805,553 AUH, CKS2, 78 more genes
    nsv4457273copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-141,020,388 , GRCh38.p12 chr9: 203,861-138,125,936 CDRT15P14, MIR548AW, 2167 more genes
    nsv4455186copy number variation1nstd102humanPathogenic GRCh37 chr9: 71,416,475-141,020,389 , GRCh38.p12 chr9: 68,801,559-138,125,937 LOC105376327, ENG, 1304 more genes
    nsv4349215copy number variation1nstd102humanPathogenic GRCh37 chr9: 79,520,825-97,201,274 , GRCh38.p12 chr9: 76,905,909-94,438,992 SPATA31C1, LINC02893, 280 more genes
    nsv4188484copy number variation1nstd166human GRCh37.p13 chr9: 90,346,577-90,379,119 , GRCh38.p12 chr9: 87,731,662-87,764,204 EIF3JP3, CTSL
    nsv4183262copy number variation1nstd166human GRCh37.p13 chr9: 90,317,000-90,340,000 , GRCh38.p12 chr9: 87,702,085-87,725,085 CTSL, DAPK1
    nsv3922684copy number variation2nstd102humanPathogenic NCBI36 chr9: 194,193-140,193,718 , GRCh38 chr9: 193,412-138,179,445 , GRCh37 chr9: 204,193-141,073,897 TDRD7, CDK9, 2170 more genes
    nsv3921738copy number variation1nstd102humanUncertain significance GRCh38 chr9: 87,209,403-87,977,877 , NCBI36 chr9: 89,014,138-89,782,612 , GRCh37 chr9: 89,824,318-90,592,792 CTSL3P, CTSLP8, 22 more genes
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