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Items: 1 to 20 of 179

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095727copy number variation1nstd102humanPathogenic GRCh37 chr19: 7,617,787-7,622,096 , GRCh38.p12 chr19: 7,552,901-7,557,210 PNPLA6
    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
    nsv7095676copy number variation1nstd102humanUncertain significance GRCh37 chr19: 7,586,521-8,670,595 , GRCh38.p12 chr19: 7,521,635-8,605,710 LRRC8E, ZNF414, 53 more genes
    nsv7095299copy number variation1nstd102humanPathogenic GRCh37 chr19: 7,618,738-7,619,178 , GRCh38.p12 chr19: 7,553,852-7,554,292 PNPLA6
    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
    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
    nsv7007519copy number variation1nstd229human GRCh38 chr19: 7,521,984-7,532,483 , GRCh37.p13 chr19: 7,586,870-7,597,369 PNPLA6, LOC105372261, 1 more genes
    nsv6597296inversion1nstd223human GRCh38 chr19: 2,282,380-7,636,598 , GRCh37.p13 chr19: 2,282,379-7,701,484 , ALKBH7, 192 more genes
    nsv6531760copy number variation1nstd223human GRCh38 chr19: 7,546,607-7,549,009 , GRCh37.p13 chr19: 7,611,493-7,613,895 PNPLA6
    nsv6518841copy number variation1nstd223human GRCh38 chr19: 7,544,070-7,545,284 , GRCh37.p13 chr19: 7,608,956-7,610,170 PNPLA6
    nsv6242773mobile element insertion1nstd215human GRCh38 chr19: 7,547,832-7,547,832 , GRCh37.p13 chr19: 7,612,718-7,612,718 PNPLA6
    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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