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Items: 1 to 20 of 134

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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
    nsv6910266copy number variation1nstd229human GRCh38 chr11: 119,001,692-119,001,744 , GRCh37.p13 chr11|NW_003871076.1: 23,292-23,344 , GRCh37.p13 chr11: 118,872,402-118,872,454 RPL23AP64, CENATAC
    nsv6908416copy number variation1nstd229human GRCh38 chr11: 118,971,614-119,014,416 , GRCh37.p13 chr11: 118,849,111-118,885,126 , GRCh37.p13 chr11|NW_003871076.1: 1-36,016 FOXR1, RPL23AP64, 3 more genes
    nsv6907231copy number variation1nstd229human GRCh38 chr11: 118,992,921-119,010,032 , GRCh37.p13 chr11|NW_003871076.1: 14,521-31,632 , GRCh37.p13 chr11: 118,863,631-118,880,742 CENATAC, CENATAC-DT, 1 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
    nsv6900299copy number variation1nstd229human GRCh38 chr11: 118,998,572-119,005,160 , GRCh37.p13 chr11|NW_003871076.1: 20,172-26,760 , GRCh37.p13 chr11: 118,869,282-118,875,870 CENATAC, RPL23AP64
    nsv6592315inversion1nstd223human GRCh38 chr11: 119,002,225-119,002,393 , GRCh37.p13 chr11|NW_003871076.1: 23,825-23,993 , GRCh37.p13 chr11: 118,872,935-118,873,103 RPL23AP64, CENATAC
    nsv6474632copy number variation1nstd223human GRCh38 chr11: 118,992,590-119,006,093 , GRCh37.p13 chr11: 118,863,300-118,876,803 , GRCh37.p13 chr11|NW_003871076.1: 14,190-27,693 RPL23AP64, CENATAC, 1 more genes
    nsv6461240copy number variation1nstd223human GRCh38 chr11: 119,001,423-119,004,800 , GRCh37.p13 chr11|NW_003871076.1: 23,023-26,400 , GRCh37.p13 chr11: 118,872,133-118,875,510 CENATAC, RPL23AP64
    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
    nsv6304672copy number variation1nstd186human GRCh37 chr11: 118,871,372-118,871,931 , GRCh38.p12 chr11: 119,000,662-119,001,221 , GRCh38.p12 chr11|NW_009646203.1: 22,262-22,821 RPL23AP64, CENATAC
    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
    nsv5502388copy number variation1nstd206human GRCh38 chr11: 119,000,662-119,001,221 , GRCh37.p13 chr11: 118,871,372-118,871,931 , GRCh37.p13 chr11|NW_003871076.1: 22,262-22,821 CENATAC, RPL23AP64
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