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Items: 1 to 20 of 131

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5913961copy number variation1nstd209human GRCh38 chr11: 71,421,936-71,423,460 , GRCh37.p13 chr11: 71,132,982-71,134,506 ACTE1P
    nsv5858072copy number variation1nstd209human GRCh38 chr11: 71,421,953-71,423,196 , GRCh37.p13 chr11: 71,132,999-71,134,242 ACTE1P
    nsv5705212mobile element insertion1nstd211human GRCh38 chr11: 71,412,814-71,412,814 , GRCh37.p13 chr11: 71,123,860-71,123,860 ACTE1P
    nsv5645712insertion1nstd207human GRCh38 chr11: 71,403,893-71,403,893 , GRCh37.p13 chr11: 71,114,939-71,114,939 ACTE1P
    nsv5584585copy number variation1nstd207human GRCh38 chr11: 71,422,062-71,422,111 , GRCh37.p13 chr11: 71,133,108-71,133,157 ACTE1P
    nsv5502676copy number variation1nstd206human GRCh38 chr11: 71,421,898-71,423,474 , GRCh37.p13 chr11: 71,132,944-71,134,520 ACTE1P
    nsv5394035mobile element insertion1nstd206human GRCh38 chr11: 71,412,814-71,412,865 , GRCh37.p13 chr11: 71,123,860-71,123,911 ACTE1P
    nsv5380796copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397 FAUP4, MMP7, 2031 more genes
    nsv4980089copy number variation1nstd200human GRCh38 chr11: 71,409,315-71,411,360 , GRCh37.p13 chr11: 71,120,361-71,122,406 ACTE1P
    nsv4980088copy number variation1nstd200human GRCh38 chr11: 71,398,611-71,405,783 , GRCh37.p13 chr11: 71,109,657-71,116,829 ACTE1P
    nsv4840823copy number variation1nstd200human GRCh37 chr11: 71,120,361-71,122,406 , GRCh38.p12 chr11: 71,409,315-71,411,360 ACTE1P
    nsv4835966copy number variation1nstd200human GRCh37 chr11: 71,109,679-71,116,804 , GRCh38.p12 chr11: 71,398,633-71,405,758 ACTE1P
    nsv4751865inversion1nstd199human GRCh37 chr11: 1,620,303-71,272,233 , GRCh38.p12 chr11: 1,599,073-71,561,187 , ACP2, 1686 more genes
    nsv4737658copy number variation1nstd199human GRCh37 chr11: 71,133,053-71,133,110 , GRCh38.p12 chr11: 71,422,007-71,422,064 ACTE1P
    nsv4715246copy number variation1nstd195human GRCh37 chr11: 70,879,801-71,222,251 , GRCh38.p12 chr11: 71,168,755-71,511,205 DHCR7, SHANK2, 4 more genes
    nsv4669093copy number variation1nstd186human GRCh37 chr11: 71,132,964-71,134,500 , GRCh38.p12 chr11: 71,421,918-71,423,454 ACTE1P
    nsv4605013copy number variation1nstd183human GRCh37 chr11: 71,132,964-71,134,500 , GRCh38.p12 chr11: 71,421,918-71,423,454 ACTE1P
    nsv4553255insertion1nstd166human GRCh37.p13 chr11: 71,117,843-71,117,843 , GRCh38.p12 chr11: 71,406,797-71,406,797 ACTE1P
    nsv4413825copy number variation1nstd174human GRCh37 chr11: 71,132,854-71,134,500 , GRCh38.p12 chr11: 71,421,808-71,423,454 ACTE1P
    nsv4211304copy number variation1nstd166human GRCh37.p13 chr11: 71,109,669-71,116,804 , GRCh38.p12 chr11: 71,398,623-71,405,758 ACTE1P
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