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Items: 1 to 20 of 158

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137702copy number variation1nstd102humanPathogenic GRCh37 chr9: 35,059,633-37,660,586 , GRCh38.p12 chr9: 35,059,636-37,660,589 ARHGEF39, LOC105376026, 84 more genes
    nsv5980379copy number variation1nstd102humanBenign GRCh37 chr9: 35,657,729-35,657,730 , GRCh38 chr9: 35,657,732-35,657,733 ARHGEF39, RMRP, 1 more genes
    nsv5912308copy number variation1nstd209human GRCh38 chr9: 35,657,732-35,657,801 , GRCh37.p13 chr9: 35,657,729-35,657,798 ARHGEF39, CCDC107, 1 more genes
    nsv5674274insertion1nstd102humanLikely pathogenic GRCh37 chr9: 35,658,017-35,658,017 , GRCh38 chr9: 35,658,020-35,658,020 RMRP, ARHGEF39, 1 more genes
    nsv5674074copy number variation1nstd102humanPathogenic GRCh37 chr9: 34,459,004-36,276,941 , GRCh38.p12 chr9: 34,459,006-36,276,944 SPAG8, DNAI1, 84 more genes
    nsv5624929insertion1nstd207human GRCh38 chr9: 35,657,732-35,657,732 , GRCh37.p13 chr9: 35,657,729-35,657,729 RMRP, ARHGEF39, 1 more genes
    nsv5486698copy number variation1nstd206human GRCh38 chr9: 35,657,732-35,657,802 , GRCh37.p13 chr9: 35,657,729-35,657,799 ARHGEF39, CCDC107, 1 more genes
    nsv4766654inversion1nstd199human GRCh37 chr9: 201,453-68,434,063 , GRCh38.p12 chr9: 201,453-67,920,552 , ACO1, 876 more genes
    nsv4755256inversion1nstd199human GRCh37 chr9: 200,777-70,835,468 , GRCh38.p12 chr9: 200,777-67,920,552 , ACO1, 876 more genes
    nsv4729230copy number variation1nstd102humanLikely pathogenic GRCh37 chr9: 32,192,406-38,311,776 , GRCh38.p12 chr9: 32,192,408-38,311,779 ACO1, ANXA2P2, 210 more genes
    nsv4681829copy number variation1nstd102humanPathogenic GRCh37 chr9: 35,657,738-35,658,025 , GRCh38.p12 chr9: 35,657,741-35,658,028 ARHGEF39, RMRP, 1 more genes
    nsv4675565copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-70,984,588 , GRCh38.p12 chr9: 203,861-68,369,672 LOC100132004, LOC105375993, 853 more genes
    nsv4649572copy number variation1nstd186human GRCh37 chr9: 35,657,729-35,657,799 , GRCh38.p12 chr9: 35,657,732-35,657,802 RMRP, ARHGEF39, 1 more genes
    nsv4526848copy number variation1nstd166human GRCh37.p13 chr9: 35,657,729-35,657,799 , GRCh38.p12 chr9: 35,657,732-35,657,802 ARHGEF39, RMRP, 1 more genes
    nsv4457273copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-141,020,388 , GRCh38.p12 chr9: 203,861-138,125,936 CDRT15P14, MIR548AW, 2167 more genes
    nsv4457200copy number variation2nstd102humanPathogenic GRCh37 chr9: 203,861-67,986,965 , GRCh38.p12 chr9: 203,861-67,919,519 ACO1, RNU6-1073P, 846 more genes
    nsv4456028copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-38,472,979 , GRCh38.p12 chr9: 203,861-38,472,982 SNORA30B, LOC100419692, 559 more genes
    nsv4455152copy number variation1nstd102humanPathogenic GRCh37 chr9: 34,542,635-68,210,033 , GRCh38.p12 chr9: 34,542,637-67,920,552 FAM74A6, RGP1, 415 more genes
    nsv4436161complex substitution1nstd102humanLikely pathogenic GRCh38.p12 chr9: 23,524,428-84,744,973 , GRCh37 chr9: 23,524,426-87,359,888 ACO1, ALDH1A1, 779 more genes
    nsv4350536copy number variation1nstd102humanPathogenic GRCh37 chr9: 214,309-39,156,958 , GRCh38.p12 chr9: 214,309-39,156,961 CSNK1G2P1, PAICSP1, 576 more genes
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