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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5673238copy number variation1nstd102humanPathogenic GRCh37 chr1: 100,340,233-100,343,394 , GRCh38.p12 chr1: 99,874,677-99,877,838 AGL
    nsv4454953copy number variation1nstd102humanPathogenic GRCh38 chr1: 99,910,692-99,913,758 , GRCh37 chr1: 100,376,248-100,379,314 AGL
    nsv7095683copy number variation1nstd102humanPathogenic GRCh37 chr1: 100,366,182-100,368,360 , GRCh38.p12 chr1: 99,900,626-99,902,804 AGL
    nsv4674782copy number variation1nstd102humanPathogenic GRCh37 chr1: 100,366,308-100,367,832 , GRCh38 chr1: 99,900,752-99,902,276 AGL
    nsv3879039copy number variation1nstd102humanPathogenic GRCh37 chr1: 100,366,308-100,367,832 , GRCh38.p12 chr1: 99,900,752-99,902,276 AGL
    nsv4578358copy number variation1nstd102humanPathogenic GRCh37 chr1: 100,366,310-100,367,832 , GRCh38 chr1: 99,900,754-99,902,276 AGL
    nsv7095684copy number variation1nstd102humanPathogenic GRCh37 chr1: 100,380,935-100,382,063 , GRCh38.p12 chr1: 99,915,379-99,916,507 AGL
    nsv4683310copy number variation1nstd102humanPathogenic GRCh37 chr1: 100,357,978-100,358,173 , GRCh38.p12 chr1: 99,892,422-99,892,617 AGL
    nsv4683323copy number variation1nstd102humanPathogenic GRCh37 chr1: 100,376,248-100,376,423 , GRCh38.p12 chr1: 99,910,692-99,910,867 AGL
    nsv4451537copy number variation1nstd102humanPathogenic GRCh38 chr1: 99,902,663-99,902,814 , GRCh37 chr1: 100,368,219-100,368,370 AGL
    nsv7095734copy number variation1nstd102humanPathogenic GRCh37 chr1: 100,368,229-100,368,360 , GRCh38.p12 chr1: 99,902,673-99,902,804 AGL
    nsv6310714copy number variation1nstd102humanPathogenic GRCh37 chr1: 100,316,599-100,316,700 , GRCh38.p12 chr1: 99,851,043-99,851,144 AGL
    nsv5674300insertion1nstd102humanPathogenic GRCh37 chr1: 100,381,024-100,381,024 , GRCh38 chr1: 99,915,468-99,915,468 AGL
    nsv6310715copy number variation1nstd102humanLikely pathogenic GRCh37 chr1: 100,335,936-100,336,445 , GRCh38.p12 chr1: 99,870,380-99,870,889 AGL
    nsv4681591copy number variation1nstd102humanLikely pathogenic GRCh37 chr1: 100,387,070-100,387,227 , GRCh38.p12 chr1: 99,921,514-99,921,671 AGL
    nsv4681784copy number variation1nstd102humanLikely pathogenic GRCh37 chr1: 100,387,080-100,387,217 , GRCh38.p12 chr1: 99,921,524-99,921,661 AGL
    nsv6314981copy number variation1nstd102humanLikely pathogenic GRCh37 chr1: 100,340,170-100,340,171 , GRCh38 chr1: 99,874,614-99,874,615 AGL
    nsv6313606copy number variation1nstd102humanUncertain significance GRCh37 chr1: 100,345,603-100,352,899 , GRCh38.p12 chr1: 99,880,047-99,887,343 AGL
    nsv7095733copy number variation1nstd102humanUncertain significance GRCh37 chr1: 100,327,039-100,330,165 , GRCh38.p12 chr1: 99,861,483-99,864,609 AGL
    nsv5381284copy number variation1nstd102humanUncertain significance GRCh37 chr1: 100,314,640-100,390,579 , GRCh38.p12 chr1: 99,849,084-99,925,023 AGL
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