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Items: 1 to 20 of 324

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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
    nsv6915628copy number variation1nstd229human GRCh38 chr11: 125,472,801-125,498,100 , GRCh37.p13 chr11: 125,342,697-125,367,996 LOC403312, FEZ1
    nsv6907958copy number variation1nstd229human GRCh38 chr11: 125,465,197-125,465,373 , GRCh37.p13 chr11: 125,335,093-125,335,269 FEZ1
    nsv6903661copy number variation1nstd229human GRCh38 chr11: 125,488,034-125,489,890 , GRCh37.p13 chr11: 125,357,930-125,359,786 FEZ1
    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
    nsv6587524inversion1nstd223human GRCh38 chr11: 125,474,342-125,474,978 , GRCh37.p13 chr11: 125,344,238-125,344,874 FEZ1
    nsv6586421inversion1nstd223human GRCh38 chr11: 125,466,288-125,467,040 , GRCh37.p13 chr11: 125,336,184-125,336,936 FEZ1
    nsv6585122inversion1nstd223human GRCh38 chr11: 125,473,540-125,474,338 , GRCh37.p13 chr11: 125,343,436-125,344,234 FEZ1
    nsv6580253inversion1nstd223human GRCh38 chr11: 125,473,508-125,474,167 , GRCh37.p13 chr11: 125,343,404-125,344,063 FEZ1
    nsv6473314copy number variation1nstd223human GRCh38 chr11: 125,461,563-125,463,262 , GRCh37.p13 chr11: 125,331,459-125,333,158 FEZ1
    nsv6470581copy number variation1nstd223human GRCh38 chr11: 125,490,736-125,491,260 , GRCh37.p13 chr11: 125,360,632-125,361,156 FEZ1
    nsv6468400copy number variation1nstd223human GRCh38 chr11: 125,449,671-125,451,769 , GRCh37.p13 chr11: 125,319,567-125,321,665 FEZ1
    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
    nsv6206099copy number variation1nstd214human GRCh38 chr11: 125,457,438-125,457,499 , GRCh37.p13 chr11: 125,327,334-125,327,395 FEZ1
    nsv6204502copy number variation1nstd214human GRCh38 chr11: 125,493,462-125,493,511 , GRCh37.p13 chr11: 125,363,358-125,363,407 FEZ1, LOC403312
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