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Items: 1 to 20 of 173

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6917369copy number variation1nstd229human GRCh38 chr11: 77,597,396-77,606,923 , GRCh37.p13 chr11: 77,308,441-77,317,968 AQP11
    nsv6911458copy number variation1nstd229human GRCh38 chr11: 77,594,199-77,656,355 , GRCh37.p13 chr11: 77,305,244-77,367,400 LOC107984369, AQP11, 1 more genes
    nsv6909596copy number variation1nstd229human GRCh38 chr11: 77,596,923-77,597,629 , GRCh37.p13 chr11: 77,307,968-77,308,674 AQP11
    nsv6904714copy number variation1nstd229human GRCh38 chr11: 77,569,709-77,724,648 , GRCh37.p13 chr11: 77,280,754-77,435,693 CLNS1A, LINC03030, 3 more genes
    nsv6901162copy number variation1nstd229human GRCh38 chr11: 77,605,967-77,608,056 , GRCh37.p13 chr11: 77,317,012-77,319,101 AQP11
    nsv6900271copy number variation1nstd229human GRCh38 chr11: 77,584,380-77,588,076 , GRCh37.p13 chr11: 77,295,425-77,299,121 AQP11
    nsv6637911copy number variation1nstd102humanUncertain significance GRCh37 chr11: 77,211,136-78,014,355 , GRCh38.p12 chr11: 77,500,091-78,303,309 RPS20P27, RNU7-59P, 22 more genes
    nsv6471682copy number variation1nstd223human GRCh38 chr11: 77,584,380-77,588,061 , GRCh37.p13 chr11: 77,295,425-77,299,106 AQP11
    nsv6466212copy number variation1nstd223human GRCh38 chr11: 77,595,001-77,611,600 , GRCh37.p13 chr11: 77,306,046-77,322,645 AQP11
    nsv6464792copy number variation1nstd223human GRCh38 chr11: 77,593,301-77,600,800 , GRCh37.p13 chr11: 77,304,346-77,311,845 AQP11
    nsv6464386copy number variation1nstd223human GRCh38 chr11: 77,569,795-77,724,740 , GRCh37.p13 chr11: 77,280,840-77,435,785 LINC03030, CLNS1A, 3 more genes
    nsv6462929copy number variation1nstd223human GRCh38 chr11: 77,593,364-77,604,922 , GRCh37.p13 chr11: 77,304,409-77,315,967 AQP11
    nsv6460994copy number variation1nstd223human GRCh38 chr11: 77,358,265-77,600,740 , GRCh37.p13 chr11: 77,069,310-77,311,785 LINC03030, RNU7-59P, 2 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
    nsv6304360copy number variation1nstd186human GRCh37 chr11: 77,307,596-77,310,023 , GRCh38.p12 chr11: 77,596,551-77,598,978 AQP11
    nsv6132116copy number variation1nstd213human GRCh37 chr11: 77,290,000-77,430,001 , GRCh38.p12 chr11: 77,578,955-77,718,956 CLNS1A, RSF1, 2 more genes
    nsv6039806copy number variation1nstd212human GRCh38 chr11: 77,599,139-77,601,581 , GRCh37.p13 chr11: 77,310,184-77,312,626 AQP11
    nsv5714799mobile element insertion1nstd211human GRCh38 chr11: 77,597,179-77,597,179 , GRCh37.p13 chr11: 77,308,224-77,308,224 AQP11
    nsv5558683mobile element insertion1nstd206human GRCh38 chr11: 77,597,190-77,597,230 , GRCh37.p13 chr11: 77,308,235-77,308,275 AQP11
    nsv5558384sequence alteration1nstd206human GRCh38 chr11: 77,600,839-77,600,841 , GRCh37.p13 chr11: 77,311,884-77,311,886 AQP11
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