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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7093922copy number variation1nstd102humanUncertain significance GRCh37 chr11: 118,955,303-118,956,445 , GRCh38.p12 chr11|NW_009646203.1: 106,192-107,334 , GRCh38.p12 chr11: 119,084,593-119,085,735 HMBS
    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
    nsv6912561copy number variation1nstd229human GRCh38 chr11: 119,083,429-119,086,936 , GRCh37.p13 chr11: 118,954,139-118,957,646 , GRCh37.p13 chr11|NW_003871076.1: 105,028-108,535 HMBS
    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
    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
    nsv6309100copy number variation1nstd102humanPathogenic GRCh37 chr11: 118,955,589-118,955,796 , GRCh38.p12 chr11: 119,084,879-119,085,086 , GRCh38.p12 chr11|NW_009646203.1: 106,478-106,685 HMBS
    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
    nsv6258396mobile element insertion1nstd215human GRCh38 chr11: 119,089,653-119,089,653 , GRCh37.p13 chr11: 118,960,363-118,960,363 HMBS
    nsv6143009copy number variation1nstd206human GRCh38 chr11: 119,058,364-119,114,364 , GRCh37.p13 chr11|NW_003871076.1: 79,964-108,875 , GRCh37.p13 chr11: 118,929,075-118,957,986 , DPAGT1, 4 more genes
    nsv6092784insertion1nstd212human GRCh38 chr11: 119,086,692-119,086,692 , GRCh37.p13 chr11|NW_003871076.1: 108,291-108,291 , GRCh37.p13 chr11: 118,957,402-118,957,402 HMBS
    nsv5710907mobile element insertion1nstd211human GRCh38 chr11: 119,089,653-119,089,653 , GRCh37.p13 chr11: 118,960,363-118,960,363 HMBS
    nsv5431217mobile element insertion1nstd206human GRCh38 chr11: 119,089,653-119,089,704 , GRCh37.p13 chr11: 118,960,363-118,960,414 HMBS
    nsv5134445mobile element insertion1nstd203human GRCh38 chr11: 119,089,639-119,089,653 , GRCh37.p13 chr11: 118,960,349-118,960,363 HMBS
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