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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
    nsv7098718copy number variation1nstd102humanUncertain significance GRCh37 chr19: 1,206,913-3,771,740 , GRCh38.p12 chr19: 1,206,914-3,771,742 GIPC3, GNG7, 117 more genes
    nsv7095297copy number variation1nstd102humanUncertain significance GRCh37 chr19: 589,946-5,696,788 , GRCh38.p12 chr19: 589,946-5,696,777 NCLN, RN7SL202P, 223 more genes
    nsv7095226copy number variation1nstd102humanUncertain significance GRCh37 chr19: 589,946-4,818,389 , GRCh38.p12 chr19: 589,946-4,818,377 ATP5F1D, LOC102723798, 204 more genes
    nsv7067646inversion1nstd229human GRCh38 chr19: 2,282,380-7,636,598 , GRCh37.p13 chr19: 2,282,379-7,701,484 , UHRF1, 192 more genes
    nsv7013864copy number variation1nstd229human GRCh38 chr19: 2,847,532-2,862,262 , GRCh37.p13 chr19: 2,847,530-2,862,260 ZNF555
    nsv7013581copy number variation1nstd229human GRCh38 chr19: 2,859,909-2,876,223 , GRCh37.p13 chr19: 2,859,907-2,876,221 ZNF556, LOC107985264, 1 more genes
    nsv7012667copy number variation1nstd229human GRCh38 chr19: 2,848,766-2,899,014 , GRCh37.p13 chr19: 2,848,764-2,899,012 LOC100419704, ZNF57, 3 more genes
    nsv7001877copy number variation1nstd229human GRCh38 chr19: 2,852,997-2,859,888 , GRCh37.p13 chr19: 2,852,995-2,859,886 ZNF555
    nsv6598886inversion1nstd223human GRCh38 chr19: 2,851,018-2,852,126 , GRCh37.p13 chr19: 2,851,016-2,852,124 ZNF555
    nsv6597296inversion1nstd223human GRCh38 chr19: 2,282,380-7,636,598 , GRCh37.p13 chr19: 2,282,379-7,701,484 , ALKBH7, 192 more genes
    nsv6535231copy number variation1nstd223human GRCh38 chr19: 2,848,404-2,851,248 , GRCh37.p13 chr19: 2,848,402-2,851,246 ZNF555
    nsv6530405copy number variation1nstd223human GRCh38 chr19: 2,839,015-2,842,872 , GRCh37.p13 chr19: 2,839,013-2,842,870 ZNF555
    nsv6526733copy number variation1nstd223human GRCh38 chr19: 2,827,127-2,840,725 , GRCh37.p13 chr19: 2,827,125-2,840,723 ZNF554, ZNF555
    nsv6516156copy number variation1nstd223human GRCh38 chr19: 2,832,137-2,848,716 , GRCh37.p13 chr19: 2,832,135-2,848,714 ZNF555, ZNF554
    nsv6144742copy number variation1nstd206human GRCh38 chr19: 2,825,000-3,005,000 , GRCh37.p13 chr19: 2,824,998-3,004,998 , ZNF57, 8 more genes
    nsv6144680copy number variation1nstd206human GRCh38 chr19: 2,850,000-2,862,000 , GRCh37.p13 chr19: 2,849,998-2,861,998 ZNF555
    nsv6144439copy number variation1nstd206human GRCh38 chr19: 2,846,000-2,854,000 , GRCh37.p13 chr19: 2,845,998-2,853,998 ZNF555
    nsv6133471copy number variation1nstd213human GRCh37 chr19: 2,830,000-2,900,001 , GRCh38.p12 chr19: 2,830,002-2,900,003 ZNF556, ZNF554, 4 more genes
    nsv6133468copy number variation1nstd213human GRCh37 chr19: 2,040,000-7,300,001 , GRCh38.p12 chr19: 2,040,001-7,299,990 TLE5, AMH, 192 more genes
    nsv5970408inversion1nstd209human GRCh38 chr19: 2,282,477-7,636,587 , GRCh37.p13 chr19: 2,282,476-7,701,473 , TLE5, 195 more genes
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