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Items: 1 to 20 of 144

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7093833copy number variation6nstd102humanUncertain significance GRCh37 chr11: 116,691,583-121,500,272 , GRCh38.p12 chr11: 116,820,867-121,629,563 RN7SL688P, MIR4492, 131 more genes
    nsv7093753copy number variation1nstd102humanUncertain significance GRCh37 chr11: 117,209,303-120,133,495 , GRCh38.p12 chr11: 117,338,587-120,262,786 TMEM25, HYOU1, 93 more genes
    nsv7074550inversion1nstd229human GRCh38 chr11: 118,332,309-119,477,352 , GRCh37.p13 chr11: 118,203,024-119,348,063 VPS11, LOC100131626, 55 more genes
    nsv7062420inversion1nstd229human GRCh38 chr11: 117,681,463-119,526,734 , GRCh37.p13 chr11: 117,552,178-119,397,444 RN7SL688P, MIR4492, 72 more genes
    nsv6903640copy number variation1nstd229human GRCh38 chr11: 118,856,131-119,169,941 , GRCh37.p13 chr11: 118,726,840-119,040,650 CENATAC, DPAGT1, 19 more genes
    nsv6902025copy number variation1nstd229human GRCh38 chr11: 118,757,701-119,235,300 , GRCh37.p13 chr11: 118,635,052-119,106,010 UPK2, VPS11, 25 more genes
    nsv6469765copy number variation1nstd223human GRCh38 chr11: 119,007,265-119,033,887 , GRCh37.p13 chr11: 118,877,975-118,904,597 , GRCh37.p13 chr11|NW_003871076.1: 28,865-55,486 RPS25, SLC37A4, 2 more genes
    nsv6315537copy number variation1nstd102humanPathogenic GRCh37 chr11: 32,799,481-134,938,470 , GRCh38.p12 chr11: 32,777,935-135,068,576 PYGM, ATL3, 2125 more genes
    nsv6308962copy number variation1nstd102humanUncertain significance GRCh37 chr11: 116,660,844-121,500,272 , GRCh38.p12 chr11: 116,790,128-121,629,563 LOC107984399, PCSK7, 132 more genes
    nsv6291385copy number variation1nstd102humanUncertain significance GRCh37 chr11: 118,849,155-119,067,781 , GRCh38.p12 chr11: 118,978,445-119,197,071 RPS25, C2CD2L, 17 more genes
    nsv6291074copy number variation1nstd102humanPathogenic GRCh37 chr11: 112,375,478-128,785,742 , GRCh38.p12 chr11: 112,504,755-128,915,847 ZW10, MPZL2, 378 more genes
    nsv6289927copy number variation1nstd102humanPathogenic GRCh37 chr11: 104,288,964-134,937,416 , GRCh38.p12 chr11: 104,418,236-135,067,522 IGSF9B, MIR10526, 592 more genes
    nsv4989358copy number variation1nstd200human GRCh38 chr11: 119,020,913-119,023,169 , GRCh37.p13 chr11: 118,891,623-118,893,879 , GRCh37.p13 chr11|NW_003871076.1: 42,513-44,769 SLC37A4, TRAPPC4
    nsv4989357copy number variation1nstd200human GRCh38 chr11: 119,007,186-119,033,957 , GRCh37.p13 chr11|NW_003871076.1: 28,786-55,556 , GRCh37.p13 chr11: 118,877,896-118,904,667 TRAPPC4, RPS25, 2 more genes
    nsv4980955copy number variation1nstd200human GRCh38 chr11: 119,021,124-119,033,372 , GRCh37.p13 chr11|NW_003871076.1: 42,724-54,971 , GRCh37.p13 chr11: 118,891,834-118,904,082 TRAPPC4, SLC37A4
    nsv4732750copy number variation1nstd199human GRCh37 chr11: 114,433,314-131,230,467 , GRCh38.p12 chr11: 114,562,592-131,360,572 , LINC02702, 392 more genes
    nsv4683551copy number variation9nstd102humanUncertain significance, Pathogenic GRCh37 chr11: 117,856,768-118,972,385 , GRCh38.p12 chr11: 117,986,053-119,101,675 MIR6716, TREHP1, 48 more genes
    nsv4675236copy number variation1nstd102humanUncertain significance GRCh37 chr11: 118,280,670-119,650,105 , GRCh38.p12 chr11: 118,409,955-119,779,396 SETP16, UPK2, 59 more genes
    nsv4674572copy number variation1nstd102humanLikely pathogenic GRCh37 chr11: 114,433,313-131,230,466 , GRCh38.p12 chr11: 114,562,591-131,360,571 ACRV1, APLP2, 382 more genes
    nsv4613248copy number variation1nstd183human GRCh37 chr11: 118,888,952-118,889,341 , GRCh38.p12 chr11: 119,018,242-119,018,631 , GRCh38.p12 chr11|NW_009646203.1: 39,842-40,231 TRAPPC4, RPS25
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