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Items: 1 to 20 of 215

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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
    nsv7064476inversion1nstd229human GRCh38 chr11: 123,462,060-125,907,500 , GRCh37.p13 chr11: 123,332,768-125,777,395 STT3A, OR8G1, 101 more genes
    nsv7064340inversion1nstd229human GRCh38 chr11: 124,323,161-124,401,935 , GRCh37.p13 chr11: 124,193,057-124,271,831 OR8B3, OR8C1P, 6 more genes
    nsv6905222copy number variation1nstd229human GRCh38 chr11: 124,397,792-124,404,956 , GRCh37.p13 chr11: 124,267,688-124,274,852 OR8B3, OR8X1P, 2 more genes
    nsv6904986copy number variation1nstd229human GRCh38 chr11: 124,263,058-124,406,683 , GRCh37.p13 chr11: 124,132,954-124,276,579 OR8G5, OR8D1, 12 more genes
    nsv6899548copy number variation1nstd229human GRCh38 chr11: 124,401,732-124,402,258 , GRCh37.p13 chr11: 124,271,628-124,272,154 OR8B3, OR8X1P
    nsv6898470copy number variation1nstd229human GRCh38 chr11: 124,224,728-124,517,025 , GRCh37.p13 chr11: 124,095,433-124,386,921 OR8C1P, SLC5A4P1, 21 more genes
    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
    nsv6472552copy number variation1nstd223human GRCh38 chr11: 124,398,901-124,408,400 , GRCh37.p13 chr11: 124,268,797-124,278,296 OR8B3, OR8X1P, 1 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
    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
    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
    nsv6035847copy number variation1nstd212human GRCh38 chr11: 124,395,245-124,395,400 , GRCh37.p13 chr11: 124,265,141-124,265,296 OR8B2, OR8B3
    nsv5968788inversion1nstd209human GRCh37.p13 chr11: 124,263,435-124,270,019 , GRCh38 chr11: 124,393,539-124,400,123 OR8B2, OR8B3
    nsv5926430copy number variation1nstd209human GRCh38 chr11: 124,384,523-124,398,838 , GRCh37.p13 chr11: 124,254,419-124,268,734 OR8B2, OR8B3
    nsv5513210copy number variation1nstd206human GRCh38 chr11: 124,332,483-124,404,353 , GRCh37.p13 chr11: 124,202,379-124,274,249 OR8C1P, OR8B1P, 6 more genes
    nsv5510615copy number variation1nstd206human GRCh38 chr11: 124,382,364-124,396,364 , GRCh37.p13 chr11: 124,252,260-124,266,260 OR8B2, OR8B3
    nsv4981119copy number variation1nstd200human GRCh38 chr11: 124,401,340-124,480,526 , GRCh37.p13 chr11: 124,271,236-124,350,422 OR8B8, OR8B9P, 5 more genes
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