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Items: 1 to 20 of 177

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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
    nsv6915889copy number variation1nstd229human GRCh38 chr11: 119,079,853-119,080,401 , GRCh37.p13 chr11|NW_003871076.1: 101,452-102,000 , GRCh37.p13 chr11: 118,950,563-118,951,111 VPS11
    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
    nsv6583781inversion1nstd223human GRCh38 chr11: 119,074,256-119,075,456 , GRCh37.p13 chr11: 118,944,966-118,946,166 , GRCh37.p13 chr11|NW_003871076.1: 95,855-97,055 VPS11
    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
    nsv6303159copy number variation1nstd186human GRCh37 chr11: 118,941,074-118,947,074 , GRCh38.p12 chr11: 119,070,364-119,076,364 , GRCh38.p12 chr11|NW_009646203.1: 91,963-97,963 VPS11
    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
    nsv6143633copy number variation1nstd206human GRCh38 chr11: 119,070,364-119,076,364 , GRCh37.p13 chr11|NW_003871076.1: 91,963-97,963 , GRCh37.p13 chr11: 118,941,074-118,947,074 VPS11
    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
    nsv5925223copy number variation1nstd209human GRCh38 chr11: 119,075,979-119,076,277 , GRCh37.p13 chr11: 118,946,689-118,946,987 , GRCh37.p13 chr11|NW_003871076.1: 97,578-97,876 VPS11
    nsv5496830copy number variation1nstd206human GRCh38 chr11: 119,067,691-119,067,768 , GRCh37.p13 chr11|NW_003871076.1: 89,291-89,368 , GRCh37.p13 chr11: 118,938,402-118,938,479 VPS11
    nsv5269165copy number variation1nstd204human GRCh38.p13 chr11: 119,078,381-119,080,780 , GRCh37.p13 chr11|NW_003871076.1: 99,980-102,379 , GRCh37.p13 chr11: 118,949,091-118,951,490 VPS11
    nsv5127889mobile element insertion1nstd203human GRCh38 chr11: 119,074,408-119,074,418 , GRCh37.p13 chr11|NW_003871076.1: 96,007-96,017 , GRCh37.p13 chr11: 118,945,118-118,945,128 VPS11
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