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Items: 1 to 20 of 144

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095726copy number variation1nstd102humanPathogenic GRCh37 chr19: 6,361,586-8,212,364 , GRCh38.p12 chr19: 6,361,575-8,147,480 SLC25A23, LYPLA2P2, 77 more genes
    nsv7095230copy number variation2nstd102humanUncertain significance GRCh37 chr19: 7,527,018-7,624,057 , GRCh38.p12 chr19: 7,462,132-7,559,171 SAXO5, PEX11G, 5 more genes
    nsv7070187inversion1nstd229human GRCh38 chr19: 6,518,823-8,315,881 , GRCh37.p13 chr19: 6,518,834-8,380,765 , ZNF557, 69 more genes
    nsv7067646inversion1nstd229human GRCh38 chr19: 2,282,380-7,636,598 , GRCh37.p13 chr19: 2,282,379-7,701,484 , UHRF1, 192 more genes
    nsv7066716inversion1nstd229human GRCh38 chr19: 6,518,017-8,344,162 , GRCh37.p13 chr19: 6,518,028-8,409,046 , STXBP2, 71 more genes
    nsv7062847inversion1nstd229human GRCh38 chr19: 7,473,530-8,349,302 , GRCh37.p13 chr19: 7,538,416-8,414,186 CERS4, LYPLA2P2, 47 more genes
    nsv7017151copy number variation1nstd229human GRCh38 chr19: 7,307,424-7,664,280 , GRCh37.p13 chr19: 7,396,129-7,729,166 , PNPLA6, 13 more genes
    nsv7017000copy number variation1nstd229human GRCh38 chr19: 7,476,462-7,476,975 , GRCh37.p13 chr19: 7,541,348-7,541,861 PEX11G, ARHGEF18
    nsv7015987copy number variation1nstd229human GRCh38 chr19: 7,476,901-7,480,800 , GRCh37.p13 chr19: 7,541,787-7,545,686 PEX11G, ARHGEF18
    nsv7014545copy number variation1nstd229human GRCh38 chr19: 7,478,449-7,485,659 , GRCh37.p13 chr19: 7,543,335-7,550,545 PEX11G
    nsv7011964copy number variation1nstd229human GRCh38 chr19: 7,354,369-9,019,195 , GRCh37.p13 chr19: 7,419,271-9,129,871 , MCOLN1, 66 more genes
    nsv7011121copy number variation1nstd229human GRCh38 chr19: 7,159,006-9,938,147 , GRCh37.p13 chr19: 7,159,017-10,048,823 , OR7G1, 117 more genes
    nsv7011065copy number variation1nstd229human GRCh38 chr19: 7,457,591-7,578,023 , GRCh37.p13 chr19: 7,522,477-7,642,909 ARHGEF18, ZNF358, 5 more genes
    nsv7004669copy number variation1nstd229human GRCh38 chr19: 7,478,363-7,481,935 , GRCh37.p13 chr19: 7,543,249-7,546,821 PEX11G
    nsv6597296inversion1nstd223human GRCh38 chr19: 2,282,380-7,636,598 , GRCh37.p13 chr19: 2,282,379-7,701,484 , ALKBH7, 192 more genes
    nsv6520986copy number variation1nstd223human GRCh38 chr19: 7,485,459-7,486,703 , GRCh37.p13 chr19: 7,550,345-7,551,589 PEX11G
    nsv6200118copy number variation1nstd214human GRCh38 chr19: 7,495,006-7,495,077 , GRCh37.p13 chr19: 7,559,892-7,559,963 PEX11G
    nsv6188734copy number variation1nstd214human GRCh38 chr19: 7,495,017-7,495,088 , GRCh37.p13 chr19: 7,559,903-7,559,974 PEX11G
    nsv6133698copy number variation1nstd213human GRCh37 chr19: 2,900,000-11,490,001 , GRCh38.p12 chr19: 2,900,002-11,379,325 , TLE5, 341 more genes
    nsv6133479copy number variation1nstd213human GRCh37 chr19: 7,400,000-13,280,001 , GRCh38.p12 chr19: 7,335,095-13,169,187 , ACP5, 299 more genes
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