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Items: 1 to 20 of 220

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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
    nsv6912639copy number variation1nstd229human GRCh38 chr11: 125,562,901-125,619,700 , GRCh37.p13 chr11: 125,432,797-125,489,595 RNU6-1156P, STT3A, 2 more genes
    nsv6901070copy number variation1nstd229human GRCh38 chr11: 125,584,077-125,588,380 , GRCh37.p13 chr11: 125,453,972-125,458,275 STT3A-AS1, EI24
    nsv6898357copy number variation1nstd229human GRCh38 chr11: 125,548,701-125,602,100 , GRCh37.p13 chr11: 125,418,597-125,471,995 STT3A-AS1, EI24, 2 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
    nsv6589250inversion1nstd223human GRCh38 chr11: 125,581,620-125,582,057 , GRCh37.p13 chr11: 125,451,516-125,451,953 STT3A-AS1, EI24
    nsv6580002inversion1nstd223human GRCh38 chr11: 125,568,296-125,568,538 , GRCh37.p13 chr11: 125,438,192-125,438,434 EI24, STT3A-AS1
    nsv6577721inversion1nstd223human GRCh38 chr11: 125,567,711-125,568,842 , GRCh37.p13 chr11: 125,437,607-125,438,738 STT3A-AS1, EI24
    nsv6463538copy number variation1nstd223human GRCh38 chr11: 125,569,201-125,569,700 , GRCh37.p13 chr11: 125,439,097-125,439,596 EI24, STT3A-AS1
    nsv6456261copy number variation1nstd223human GRCh38 chr11: 125,563,403-125,567,657 , GRCh37.p13 chr11: 125,433,299-125,437,553 EI24, STT3A-AS1
    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
    nsv6301027copy number variation1nstd186human GRCh37 chr11: 125,433,306-125,437,540 , GRCh38.p12 chr11: 125,563,410-125,567,644 EI24, STT3A-AS1
    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
    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
    nsv5512921copy number variation1nstd206human GRCh38 chr11: 125,563,410-125,567,644 , GRCh37.p13 chr11: 125,433,306-125,437,540 EI24, STT3A-AS1
    nsv5500041copy number variation1nstd206human GRCh38 chr11: 125,584,513-125,584,579 , GRCh37.p13 chr11: 125,454,408-125,454,474 EI24, STT3A-AS1
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