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Items: 1 to 20 of 209

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095479copy number variation1nstd102humanUncertain significance GRCh37 chr19: 38,375,572-39,738,787 , GRCh38.p12 chr19: 37,884,932-39,248,147 HNRNPL, RN7SL663P, 45 more genes
    nsv7016444copy number variation1nstd229human GRCh38 chr19: 37,878,601-37,884,900 , GRCh37.p13 chr19: 38,369,241-38,375,540 WDR87, LOC105372395
    nsv7015040copy number variation1nstd229human GRCh38 chr19: 37,887,752-37,932,673 , GRCh37.p13 chr19: 38,378,392-38,423,313 LOC107985301, LOC105372395, 2 more genes
    nsv7014727copy number variation1nstd229human GRCh38 chr19: 37,571,795-38,134,006 , GRCh37.p13 chr19: 38,062,697-38,624,646 LOC105372395, ZNF573, 19 more genes
    nsv7013528copy number variation1nstd229human GRCh38 chr19: 37,882,550-37,883,196 , GRCh37.p13 chr19: 38,373,190-38,373,836 LOC105372395, WDR87
    nsv7012650copy number variation1nstd229human GRCh38 chr19: 37,897,794-37,901,473 , GRCh37.p13 chr19: 38,388,434-38,392,113 WDR87, LOC107985301
    nsv7008156copy number variation1nstd229human GRCh38 chr19: 36,851,242-46,031,790 , GRCh37.p13 chr19: 37,342,144-46,535,048 LOC105372390, LOC107985291, 396 more genes
    nsv7005713copy number variation1nstd229human GRCh38 chr19: 33,458,650-39,721,746 , GRCh37.p13 chr19: 33,949,556-40,212,386 , TYROBP, 259 more genes
    nsv7004121copy number variation1nstd229human GRCh38 chr19: 37,877,746-37,883,783 , GRCh37.p13 chr19: 38,368,386-38,374,423 WDR87, LOC105372395
    nsv7001772copy number variation1nstd229human GRCh38 chr19: 37,876,757-37,883,701 , GRCh37.p13 chr19: 38,367,397-38,374,341 WDR87, LOC105372395
    nsv7000496copy number variation1nstd229human GRCh38 chr19: 37,896,701-37,897,821 , GRCh37.p13 chr19: 38,387,341-38,388,461 LOC105372395, WDR87, 1 more genes
    nsv6998746copy number variation1nstd229human GRCh38 chr19: 37,877,513-37,906,201 , GRCh37.p13 chr19: 38,368,153-38,396,841 LOC107985301, SIPA1L3, 2 more genes
    nsv6637740copy number variation1nstd102humanUncertain significance GRCh37 chr19: 37,389,799-38,562,489 , GRCh38.p12 chr19: 36,898,897-38,071,849 MTND5P45, ZNF568, 36 more genes
    nsv6529405copy number variation1nstd223human GRCh38 chr19: 37,878,807-37,896,858 , GRCh37.p13 chr19: 38,369,447-38,387,498 LOC105372395, WDR87, 1 more genes
    nsv6528802copy number variation1nstd223human GRCh38 chr19: 37,602,649-38,484,499 , GRCh37.p13 chr19: 38,093,550-38,975,139 SPRED3, PSMD8, 30 more genes
    nsv6519775copy number variation1nstd223human GRCh38 chr19: 37,876,504-37,885,905 , GRCh37.p13 chr19: 38,367,144-38,376,545 WDR87, LOC105372395
    nsv6517324copy number variation1nstd223human GRCh38 chr19: 37,879,293-37,882,944 , GRCh37.p13 chr19: 38,369,933-38,373,584 WDR87, LOC105372395
    nsv6290300copy number variation1nstd102humanPathogenic GRCh37 chr19: 19,546,923-41,313,229 , GRCh38.p12 chr19: 19,436,114-40,807,324 ZNF420, LOC105372330, 574 more genes
    nsv6133523copy number variation1nstd213human GRCh37 chr19: 34,000,000-42,200,001 , GRCh38.p12 chr19: 33,509,094-41,696,083 , ACTN4, 345 more genes
    nsv6048541copy number variation1nstd212human GRCh38 chr19: 37,880,951-37,883,191 , GRCh37.p13 chr19: 38,371,591-38,373,831 LOC105372395, WDR87
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