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Items: 1 to 20 of 153

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7078062inversion1nstd229human GRCh38 chr9: 99,955,191-100,728,757 , GRCh37.p13 chr9: 102,717,473-103,491,039 CAVIN4, UPF3AP3, 13 more genes
    nsv7075365inversion1nstd229human GRCh38 chr9: 94,549,389-100,549,990 , GRCh37.p13 chr9: 97,311,671-103,312,272 PCAT7, ANKS6, 128 more genes
    nsv6634454copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-131,603,223 , GRCh38.p12 chr9: 203,861-128,840,944 HNRNPA1P41, GAS1RR, 1868 more genes
    nsv6569211inversion1nstd223human GRCh38 chr9: 100,440,932-100,441,309 , GRCh37.p13 chr9: 103,203,214-103,203,591 MSANTD3-TMEFF1, MSANTD3
    nsv6558336inversion1nstd223human GRCh38 chr9: 99,955,191-100,728,759 , GRCh37.p13 chr9: 102,717,473-103,491,041 RPS2P35, STX17, 13 more genes
    nsv6448725copy number variation1nstd223human GRCh38 chr9: 100,451,609-100,471,804 , GRCh37.p13 chr9: 103,213,891-103,234,086 MSANTD3-TMEFF1, TMEFF1, 1 more genes
    nsv6315405copy number variation1nstd102humanUncertain significance GRCh37 chr9: 19,356,861-119,513,311 , GRCh38.p12 chr9: 19,356,863-116,751,032 RNU6-156P, GDA, 1425 more genes
    nsv6315179copy number variation1nstd102humanPathogenic GRCh37 chr9: 93,864,974-106,661,581 , GRCh38.p12 chr9: 91,102,692-103,899,300 SUGT1P4-STRA6LP, NR4A3, 255 more genes
    nsv6313900copy number variation1nstd102humanLikely pathogenic GRCh37 chr9: 71,349,994-122,603,410 , GRCh38.p12 chr9: 68,735,078-119,841,132 ABCA1, ALAD, 793 more genes
    nsv6313546copy number variation1nstd102humanPathogenic GRCh37 chr9: 353,349-141,020,389 , GRCh38.p12 chr9: 353,349-138,125,937 FAM27C, DPM2, 2166 more genes
    nsv6290765copy number variation1nstd102humanUncertain significance GRCh37 chr9: 102,858,276-110,624,997 , GRCh38.p12 chr9: 100,095,994-107,862,716 RNF20, SMC2, 120 more genes
    nsv6136626copy number variation1nstd213human GRCh37 chr9: 102,930,000-103,760,001 , GRCh38.p12 chr9: 100,167,718-100,997,719 NANOGP5, LOC105376181, 12 more genes
    nsv6019850copy number variation1nstd212human GRCh38 chr9: 100,421,053-100,435,461 , GRCh37.p13 chr9: 103,183,335-103,197,743 MSANTD3
    nsv5712616mobile element insertion1nstd211human GRCh38 chr9: 100,437,765-100,437,765 , GRCh37.p13 chr9: 103,200,047-103,200,047 MSANTD3
    nsv5398146mobile element insertion1nstd206human GRCh38 chr9: 100,437,765-100,437,816 , GRCh37.p13 chr9: 103,200,047-103,200,098 MSANTD3
    nsv5381561copy number variation1nstd102humanPathogenic GRCh37 chr9: 97,834,573-107,199,088 , GRCh38.p12 chr9: 95,072,291-104,436,807 TBC1D2, ZNF782, 170 more genes
    nsv5372885translocation1nstd200human GRCh38 chr9: 100,431,290-100,431,290 , GRCh38 chr9: 100,431,559-100,431,559 , GRCh37.p13 chr9: 103,193,572-103,193,572 , GRCh37.p13 chr9: 103,193,841-103,193,841 MSANTD3
    nsv4684256copy number variation1nstd102humanPathogenic GRCh37 chr9: 96,126,075-108,535,272 , GRCh38.p12 chr9: 93,363,793-105,772,991 RPS26P37, MIR27B, 238 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
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