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Items: 1 to 20 of 282

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6125099copy number variation1nstd186human GRCh37 chr20: 62,591,645-62,591,986 , GRCh38.p12 chr20: 63,960,292-63,960,633 ZNF512B
    nsv6125011copy number variation1nstd186human GRCh37 chr20: 62,595,911-62,597,421 , GRCh38.p12 chr20: 63,964,558-63,966,068 ZNF512B
    nsv6112778copy number variation1nstd102humanPathogenic GRCh37 chr20: 51,799,648-62,916,626 , GRCh38.p12 chr20: 53,183,109-64,285,273 LINC01742, MTCO2P1, 253 more genes
    nsv5965920copy number variation1nstd209human GRCh38 chr20: 63,956,453-63,956,514 , GRCh37.p13 chr20: 62,587,806-62,587,867 UCKL1, ZNF512B, 1 more genes
    nsv5962679copy number variation1nstd209human GRCh38 chr20: 63,965,894-63,966,117 , GRCh37.p13 chr20: 62,597,247-62,597,470 ZNF512B
    nsv5665835insertion1nstd207human GRCh38 chr20: 63,956,453-63,956,453 , GRCh37.p13 chr20: 62,587,806-62,587,806 UCKL1, ZNF512B, 1 more genes
    nsv5665795insertion1nstd207human GRCh38 chr20: 63,965,932-63,965,932 , GRCh37.p13 chr20: 62,597,285-62,597,285 ZNF512B
    nsv5604345copy number variation1nstd207human GRCh38 chr20: 63,965,484-63,965,621 , GRCh37.p13 chr20: 62,596,837-62,596,974 ZNF512B
    nsv5601983copy number variation1nstd207human GRCh38 chr20: 63,960,306-63,960,686 , GRCh37.p13 chr20: 62,591,659-62,592,039 ZNF512B
    nsv5596336copy number variation1nstd207human GRCh38 chr20: 63,965,937-63,966,117 , GRCh37.p13 chr20: 62,597,290-62,597,470 ZNF512B
    nsv5590846copy number variation1nstd207human GRCh38 chr20: 63,964,836-63,966,112 , GRCh37.p13 chr20: 62,596,189-62,597,465 ZNF512B
    nsv5589869copy number variation1nstd207human GRCh38 chr20: 63,965,067-63,965,152 , GRCh37.p13 chr20: 62,596,420-62,596,505 ZNF512B
    nsv5528735copy number variation1nstd206human GRCh38 chr20: 63,960,292-63,960,633 , GRCh37.p13 chr20: 62,591,645-62,591,986 ZNF512B
    nsv5525712copy number variation1nstd206human GRCh38 chr20: 63,964,558-63,966,068 , GRCh37.p13 chr20: 62,595,911-62,597,421 ZNF512B
    nsv5393038copy number variation1nstd186human GRCh37 chr20: 62,596,272-62,597,052 , GRCh38.p12 chr20: 63,964,919-63,965,699 ZNF512B
    nsv5392204copy number variation1nstd186human GRCh37 chr20: 62,596,252-62,597,283 , GRCh38.p12 chr20: 63,964,899-63,965,930 ZNF512B
    nsv5381307copy number variation1nstd102humanUncertain significance GRCh37 chr20: 62,559,699-62,656,066 , GRCh38.p12 chr20: 63,928,346-64,024,713 MIR1914, PRPF6, 6 more genes
    nsv5381223copy number variation2nstd102humanUncertain significance GRCh37 chr20: 60,831,241-62,664,346 , GRCh38.p12 chr20: 62,256,185-64,032,993 KCNQ2-AS1, HAR1B, 100 more genes
    nsv5328851copy number variation1nstd204human GRCh38.p13 chr20: 63,964,810-63,965,963 , GRCh37.p13 chr20: 62,596,163-62,597,316 ZNF512B
    nsv5323619copy number variation1nstd204human GRCh38.p13 chr20: 63,960,287-63,960,745 , GRCh37.p13 chr20: 62,591,640-62,592,098 ZNF512B
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