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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
    nsv7016993copy number variation1nstd229human GRCh38 chr19: 3,153,351-3,153,642 , GRCh37.p13 chr19: 3,153,349-3,153,640 GNA15-DT, GNA15
    nsv7016568copy number variation1nstd229human GRCh38 chr19: 3,105,739-3,136,463 , GRCh37.p13 chr19: 3,105,737-3,136,461 GNA15, GNA11, 1 more genes
    nsv7015701copy number variation1nstd229human GRCh38 chr19: 3,136,895-3,137,029 , GRCh37.p13 chr19: 3,136,893-3,137,027 GNA15
    nsv7008713copy number variation1nstd229human GRCh38 chr19: 3,134,565-3,134,881 , GRCh37.p13 chr19: 3,134,563-3,134,879 GNA15
    nsv7001756copy number variation1nstd229human GRCh38 chr19: 3,138,690-3,144,071 , GRCh37.p13 chr19: 3,138,688-3,144,069 GNA15-DT, GNA15
    nsv6597296inversion1nstd223human GRCh38 chr19: 2,282,380-7,636,598 , GRCh37.p13 chr19: 2,282,379-7,701,484 , ALKBH7, 192 more genes
    nsv6596938inversion1nstd223human GRCh38 chr19: 3,139,111-3,139,693 , GRCh37.p13 chr19: 3,139,109-3,139,691 GNA15, GNA15-DT
    nsv6596668inversion1nstd223human GRCh38 chr19: 3,138,702-3,139,888 , GRCh37.p13 chr19: 3,138,700-3,139,886 GNA15, GNA15-DT
    nsv6525691copy number variation1nstd223human GRCh38 chr19: 3,144,575-3,144,875 , GRCh37.p13 chr19: 3,144,573-3,144,873 GNA15-DT, GNA15
    nsv6518529copy number variation1nstd223human GRCh38 chr19: 3,153,711-3,154,176 , GRCh37.p13 chr19: 3,153,709-3,154,174 GNA15-DT, GNA15
    nsv6197275copy number variation1nstd214human GRCh38 chr19: 3,149,256-3,149,313 , GRCh37.p13 chr19: 3,149,254-3,149,311 GNA15, GNA15-DT
    nsv6145038copy number variation1nstd206human GRCh38 chr19: 3,158,000-3,166,000 , GRCh37.p13 chr19: 3,157,998-3,165,998 GNA15
    nsv6133698copy number variation1nstd213human GRCh37 chr19: 2,900,000-11,490,001 , GRCh38.p12 chr19: 2,900,002-11,379,325 , TLE5, 341 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
    nsv6130841insertion1nstd186human GRCh37 chr19: 3,145,581-3,145,581 , GRCh38.p12 chr19: 3,145,583-3,145,583 GNA15-DT, GNA15
    nsv6111229insertion1nstd212human GRCh38 chr19: 3,145,577-3,145,577 , GRCh37.p13 chr19: 3,145,575-3,145,575 GNA15-DT, GNA15
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