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Items: 1 to 20 of 339

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5978518insertion1nstd209human GRCh38 chr11: 111,642,824-111,642,824 , GRCh37.p13 chr11: 111,513,548-111,513,548 SIK2
    nsv5922139copy number variation1nstd209human GRCh38 chr11: 111,603,641-111,603,705 , GRCh37.p13 chr11: 111,474,365-111,474,429 SIK2
    nsv5920856copy number variation1nstd209human GRCh38 chr11: 111,722,480-111,725,268 , GRCh37.p13 chr11: 111,593,204-111,595,992 SIK2, PPP2R1B
    nsv5915084copy number variation1nstd209human GRCh38 chr11: 111,692,162-111,693,142 , GRCh37.p13 chr11: 111,562,886-111,563,866 SIK2, PPP2R1B
    nsv5913023copy number variation1nstd209human GRCh38 chr11: 111,624,753-111,624,808 , GRCh37.p13 chr11: 111,495,477-111,495,532 SIK2
    nsv5912418copy number variation1nstd209human GRCh38 chr11: 111,667,147-111,667,690 , GRCh37.p13 chr11: 111,537,871-111,538,414 SIK2
    nsv5699377mobile element insertion1nstd211human GRCh38 chr11: 111,701,714-111,701,714 , GRCh37.p13 chr11: 111,572,438-111,572,438 PPP2R1B, SIK2
    nsv5696701mobile element insertion2nstd211human GRCh38 chr11: 111,659,637-111,659,637 , GRCh37.p13 chr11: 111,530,361-111,530,361 SIK2
    nsv5695187mobile element insertion2nstd211human GRCh38 chr11: 111,609,114-111,609,114 , GRCh37.p13 chr11: 111,479,838-111,479,838 SIK2
    nsv5672640copy number variation1nstd102humanPathogenic GRCh37 chr11: 94,153,285-111,965,700 , GRCh38.p12 chr11: 94,420,119-112,094,976 HSPD1P13, CARD17P, 239 more genes
    nsv5662674insertion1nstd207human GRCh38 chr11: 111,642,824-111,642,824 , GRCh37.p13 chr11: 111,513,548-111,513,548 SIK2
    nsv5656676insertion1nstd207human GRCh38 chr11: 111,628,416-111,628,416 , GRCh37.p13 chr11: 111,499,140-111,499,140 SIK2
    nsv5652992insertion1nstd207human GRCh38 chr11: 111,628,414-111,628,414 , GRCh37.p13 chr11: 111,499,138-111,499,138 SIK2
    nsv5651087insertion1nstd207human GRCh38 chr11: 111,609,102-111,609,102 , GRCh37.p13 chr11: 111,479,826-111,479,826 SIK2
    nsv5549533insertion1nstd206human GRCh38 chr11: 111,642,868-111,642,895 , GRCh37.p13 chr11: 111,513,592-111,513,619 SIK2
    nsv5546011insertion1nstd206human GRCh38 chr11: 111,628,448-111,628,478 , GRCh37.p13 chr11: 111,499,172-111,499,202 SIK2
    nsv5509179copy number variation1nstd206human GRCh38 chr11: 106,441,255-114,742,965 , GRCh37.p13 chr11: 106,311,982-114,613,687 , ATM, 153 more genes
    nsv5508118copy number variation1nstd206human GRCh38 chr11: 111,692,192-111,693,120 , GRCh37.p13 chr11: 111,562,916-111,563,844 PPP2R1B, SIK2
    nsv5506973copy number variation1nstd206human GRCh38 chr11: 111,604,465-111,604,688 , GRCh37.p13 chr11: 111,475,189-111,475,412 SIK2
    nsv5495381copy number variation1nstd206human GRCh38 chr11: 111,636,652-111,636,735 , GRCh37.p13 chr11: 111,507,376-111,507,459 SIK2
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