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Items: 1 to 20 of 182

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095478copy number variation1nstd102humanUncertain significance GRCh37 chr19: 33,167,170-36,643,309 , GRCh38.p12 chr19: 32,676,264-36,152,407 NFKBID, LRP3, 141 more genes
    nsv7074671inversion1nstd229human GRCh38 chr19: 33,126,299-36,006,645 , GRCh37.p13 chr19: 33,617,205-36,497,547 , ZNF30, 120 more genes
    nsv7074279inversion1nstd229human GRCh38 chr19: 33,135,428-36,017,833 , GRCh37.p13 chr19: 33,626,334-36,508,735 , PSENEN, 122 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
    nsv6310629copy number variation1nstd102humanUncertain significance GRCh37 chr19: 35,521,725-36,643,309 , GRCh38.p12 chr19: 35,030,821-36,152,407 KRTDAP, WDR62, 78 more genes
    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
    nsv6289587insertion2nstd214human GRCh38 chr19: 35,116,779-35,116,779 , GRCh37.p13 chr19: 35,607,683-35,607,683 FXYD3
    nsv6285217insertion1nstd214human GRCh38 chr19: 35,116,756-35,116,756 , GRCh37.p13 chr19: 35,607,660-35,607,660 FXYD3
    nsv6133523copy number variation1nstd213human GRCh37 chr19: 34,000,000-42,200,001 , GRCh38.p12 chr19: 33,509,094-41,696,083 , ACTN4, 345 more genes
    nsv6130693insertion1nstd186human GRCh37 chr19: 35,607,633-35,607,642 , GRCh38.p12 chr19: 35,116,729-35,116,738 FXYD3
    nsv6109456insertion1nstd212human GRCh38 chr19: 35,116,789-35,116,789 , GRCh37.p13 chr19: 35,607,693-35,607,693 FXYD3
    nsv5942955copy number variation1nstd209human GRCh38 chr19: 35,116,779-35,116,831 , GRCh37.p13 chr19: 35,607,683-35,607,735 FXYD3
    nsv5664306insertion1nstd207human GRCh38 chr19: 35,116,779-35,116,779 , GRCh37.p13 chr19: 35,607,683-35,607,683 FXYD3
    nsv5548322insertion1nstd206human GRCh38 chr19: 35,116,729-35,116,738 , GRCh37.p13 chr19: 35,607,633-35,607,642 FXYD3
    nsv5020443copy number variation1nstd200human GRCh38 chr19: 35,119,450-35,123,819 , GRCh37.p13 chr19: 35,610,354-35,614,723 LGI4, FXYD3, 1 more genes
    nsv4868168copy number variation1nstd200human GRCh37 chr19: 35,610,354-35,614,723 , GRCh38.p12 chr19: 35,119,450-35,123,819 MIR6887, LGI4, 1 more genes
    nsv4755608insertion1nstd199human GRCh37 chr19: 35,607,710-35,607,710 , GRCh38.p12 chr19: 35,116,806-35,116,806 FXYD3
    nsv4674329copy number variation1nstd102humanPathogenic GRCh37 chr19: 35,553,425-36,264,299 , GRCh38.p12 chr19: 35,062,521-35,773,397 LOC105372379, LSR, 50 more genes
    nsv4457800copy number variation1nstd102humanUncertain significance GRCh37 chr19: 35,613,953-36,183,886 , GRCh38.p12 chr19: 35,123,049-35,692,984 SBSN, UPK1A, 38 more genes
    nsv4457758copy number variation1nstd102humanUncertain significance GRCh37 chr19: 35,548,527-35,772,471 , GRCh38.p12 chr19: 35,057,623-35,281,568 LOC105372379, LSR, 15 more genes
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