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Items: 1 to 20 of 133

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5940014copy number variation1nstd209human GRCh38 chr19: 57,241,633-57,241,702 , GRCh37.p13 chr19: 57,753,001-57,753,070 ZNF805
    nsv5933737copy number variation1nstd209human GRCh38 chr19: 57,244,632-57,244,743 , GRCh37.p13 chr19: 57,756,000-57,756,111 ZNF805
    nsv5595996copy number variation1nstd207human GRCh38 chr19: 57,241,633-57,241,702 , GRCh37.p13 chr19: 57,753,001-57,753,070 ZNF805
    nsv5292903copy number variation1nstd204human GRCh38.p13 chr19: 57,172,601-57,751,900 , GRCh37.p13 chr19: 57,683,969-58,263,268 TPRG1LP1, ZNF805, 30 more genes
    nsv5190863mobile element insertion1nstd203human GRCh38 chr19: 57,255,324-57,255,324 , GRCh37.p13 chr19: 57,766,692-57,766,692 ZNF805
    nsv4766985insertion1nstd199human GRCh37 chr19: 57,756,934-57,756,934 , GRCh38.p12 chr19: 57,245,566-57,245,566 ZNF805
    nsv4748480copy number variation1nstd199human GRCh37 chr19: 57,752,978-57,753,047 , GRCh38.p12 chr19: 57,241,610-57,241,679 ZNF805
    nsv4625260copy number variation1nstd183human GRCh37 chr19: 57,755,520-57,756,502 , GRCh38.p12 chr19: 57,244,152-57,245,134 ZNF805
    nsv4457735copy number variation1nstd102humanUncertain significance GRCh37 chr19: 57,737,113-57,771,792 , GRCh38.p12 chr19: 57,225,745-57,260,424 AURKC, ZNF805
    nsv4457364copy number variation1nstd102humanUncertain significance GRCh37 chr19: 57,718,739-57,760,953 , GRCh38.p12 chr19: 57,207,371-57,249,585 AURKC, ZNF805, 1 more genes
    nsv4422843copy number variation1nstd174human GRCh37 chr19: 57,752,745-57,753,401 , GRCh38.p12 chr19: 57,241,377-57,242,033 ZNF805
    nsv4373618copy number variation1nstd173human GRCh37 chr19: 57,658,220-57,780,096 , GRCh38.p12 chr19: 57,146,852-57,268,728 ZNF264, ZNF805, 4 more genes
    nsv4272334copy number variation1nstd166human GRCh37.p13 chr19: 57,773,003-57,778,373 , GRCh38.p12 chr19: 57,261,635-57,267,005 ZNF805, ZNF460-AS1
    nsv4265162copy number variation1nstd166human GRCh37.p13 chr19: 57,718,500-57,761,000 , GRCh38.p12 chr19: 57,207,132-57,249,632 ZNF264, ZNF805, 1 more genes
    nsv4260972copy number variation1nstd166human GRCh37.p13 chr19: 57,750,534-57,750,974 , GRCh38.p12 chr19: 57,239,166-57,239,606 ZNF805
    nsv4257830copy number variation1nstd166human GRCh37.p13 chr19: 57,756,900-57,757,018 , GRCh38.p12 chr19: 57,245,532-57,245,650 ZNF805
    nsv4255465copy number variation1nstd166human GRCh37.p13 chr19: 57,761,757-57,761,983 , GRCh38.p12 chr19: 57,250,389-57,250,615 ZNF805
    nsv4253572copy number variation1nstd166human GRCh37.p13 chr19: 57,741,900-57,761,000 , GRCh38.p12 chr19: 57,230,532-57,249,632 ZNF805, AURKC
    nsv3959946copy number variation1nstd168human GRCh38 chr19: 57,252,023-57,281,171 , GRCh37.p13 chr19: 57,763,391-57,792,539 ZNF805, ZNF460-AS1, 1 more genes
    nsv3924732copy number variation1nstd102humanPathogenic GRCh38 chr19: 49,907,832-58,557,889 , GRCh37 chr19: 50,411,089-59,069,256 , NCBI36 chr19: 55,102,901-63,761,068 RPL39P37, CCDC106, 556 more genes
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