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Items: 1 to 20 of 241

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137129copy number variation1nstd102humanPathogenic GRCh37 chr11: 120,531,028-134,257,553 , GRCh38.p12 chr11: 120,660,319-134,387,659 VSIG10L2, OR8B6P, 268 more genes
    nsv7077728inversion1nstd229human GRCh38 chr11: 124,239,803-134,089,458 , GRCh37.p13 chr11: 124,110,545-133,959,353 LOC283172, PPP1R10P1, 175 more genes
    nsv7076515inversion1nstd229human GRCh38 chr11: 125,894,211-125,926,861 , GRCh37.p13 chr11: 125,764,106-125,796,756 HYLS1, DDX25, 1 more genes
    nsv7070443inversion1nstd229human GRCh38 chr11: 125,887,512-126,792,902 , GRCh37.p13 chr11: 125,757,407-126,662,797 CDON, TIRAP, 21 more genes
    nsv7064476inversion1nstd229human GRCh38 chr11: 123,462,060-125,907,500 , GRCh37.p13 chr11: 123,332,768-125,777,395 STT3A, OR8G1, 101 more genes
    nsv6917175copy number variation1nstd229human GRCh38 chr11: 125,884,374-125,887,931 , GRCh37.p13 chr11: 125,754,269-125,757,826 HYLS1
    nsv6909722copy number variation1nstd229human GRCh38 chr11: 125,879,701-125,888,800 , GRCh37.p13 chr11: 125,749,596-125,758,695 HYLS1
    nsv6637558copy number variation1nstd102humanPathogenic GRCh37 chr11: 122,975,824-134,938,470 , GRCh38.p12 chr11: 123,105,116-135,068,576 OR8B8, LOC107984373, 234 more genes
    nsv6591177inversion1nstd223human GRCh38 chr11: 125,889,651-125,890,059 , GRCh37.p13 chr11: 125,759,546-125,759,954 HYLS1
    nsv6456177copy number variation1nstd223human GRCh38 chr11: 125,888,696-125,889,637 , GRCh37.p13 chr11: 125,758,591-125,759,532 HYLS1
    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
    nsv6309036copy number variation3nstd102humanUncertain significance GRCh37 chr11: 123,504,851-126,163,012 , GRCh38.p12 chr11: 123,634,143-126,293,117 CDON, PKNOX2-DT, 113 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
    nsv6291035copy number variation1nstd102humanUncertain significance GRCh37 chr11: 125,569,544-125,939,872 , GRCh38.p12 chr11: 125,699,649-126,069,977 CDON, PATE1, 9 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
    nsv6132092copy number variation1nstd213human GRCh37 chr11: 125,340,000-125,810,001 , GRCh38.p12 chr11: 125,470,104-125,940,106 DDX25, PUS3, 15 more genes
    nsv5925278copy number variation1nstd209human GRCh38 chr11: 125,895,043-125,895,110 , GRCh37.p13 chr11: 125,764,938-125,765,005 PUS3, HYLS1
    nsv5914508copy number variation1nstd209human GRCh38 chr11: 125,887,822-125,887,990 , GRCh37.p13 chr11: 125,757,717-125,757,885 HYLS1
    nsv5911765copy number variation1nstd209human GRCh38 chr11: 125,815,104-125,910,636 , GRCh37.p13 chr11: 125,684,999-125,780,531 , DDX25, 3 more genes
    nsv5861078copy number variation1nstd209human GRCh38 chr11: 125,895,477-125,899,476 , GRCh37.p13 chr11: 125,765,372-125,769,371 HYLS1, PUS3
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