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Items: 1 to 20 of 328

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7076323inversion1nstd229human GRCh38 chr19: 37,678,901-37,762,324 , GRCh37.p13 chr19: 38,169,802-38,252,964 ZNF607, SELENOKP1, 2 more genes
    nsv7059935inversion1nstd229human GRCh38 chr19: 37,679,174-37,873,698 , GRCh37.p13 chr19: 38,170,075-38,364,338 ZNF573, ZNF607, 9 more genes
    nsv7017756copy number variation1nstd229human GRCh38 chr19: 37,548,077-37,822,264 , GRCh37.p13 chr19: 38,038,979-38,312,904 MTND5P45, LOC728533, 14 more genes
    nsv7016680copy number variation1nstd229human GRCh38 chr19: 37,705,242-37,749,764 , GRCh37.p13 chr19: 38,196,143-38,240,404 ZNF607, ZNF573
    nsv7016466copy number variation1nstd229human GRCh38 chr19: 37,765,116-37,766,927 , GRCh37.p13 chr19: 38,255,756-38,257,567 ZNF573
    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
    nsv7013336copy number variation1nstd229human GRCh38 chr19: 37,745,993-37,764,372 , GRCh37.p13 chr19: 38,236,894-38,255,012 ZNF573
    nsv7010596copy number variation1nstd229human GRCh38 chr19: 37,735,136-37,739,882 , GRCh37.p13 chr19: 38,226,037-38,230,783 ZNF573
    nsv7010211copy number variation1nstd229human GRCh38 chr19: 37,764,201-37,776,700 , GRCh37.p13 chr19: 38,254,841-38,267,340 ZNF573
    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
    nsv7007664copy number variation1nstd229human GRCh38 chr19: 37,777,694-37,785,848 , GRCh37.p13 chr19: 38,268,334-38,276,488 ZNF573
    nsv7006960copy number variation1nstd229human GRCh38 chr19: 37,699,701-37,756,800 , GRCh37.p13 chr19: 38,190,602-38,247,440 ZNF607, ZNF573
    nsv7005713copy number variation1nstd229human GRCh38 chr19: 33,458,650-39,721,746 , GRCh37.p13 chr19: 33,949,556-40,212,386 , TYROBP, 259 more genes
    nsv7005506copy number variation1nstd229human GRCh38 chr19: 37,769,420-37,779,051 , GRCh37.p13 chr19: 38,260,060-38,269,691 ZNF573
    nsv7005377copy number variation1nstd229human GRCh38 chr19: 37,751,054-37,751,084 , GRCh37.p13 chr19: 38,241,694-38,241,724 ZNF573
    nsv7001110copy number variation1nstd229human GRCh38 chr19: 37,760,297-37,760,341 , GRCh37.p13 chr19: 38,250,937-38,250,981 ZNF573
    nsv6999147copy number variation1nstd229human GRCh38 chr19: 37,737,172-37,737,217 , GRCh37.p13 chr19: 38,228,073-38,228,118 ZNF573
    nsv6998938copy number variation1nstd229human GRCh38 chr19: 37,776,837-37,781,987 , GRCh37.p13 chr19: 38,267,477-38,272,627 ZNF573
    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
    nsv6599547inversion1nstd223human GRCh38 chr19: 37,744,499-37,745,071 , GRCh37.p13 chr19: 38,235,400-38,235,972 ZNF573
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