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Items: 1 to 20 of 164

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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
    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
    nsv5639691insertion1nstd207human GRCh38 chr9: 35,906,592-35,906,592 , GRCh37.p13 chr9: 35,906,589-35,906,589 HRCT1
    nsv5625949insertion1nstd207human GRCh38 chr9: 35,906,568-35,906,568 , GRCh37.p13 chr9: 35,906,565-35,906,565 HRCT1
    nsv5381659copy number variation1nstd102humanUncertain significance GRCh37 chr9: 35,683,146-36,277,049 , GRCh38.p12 chr9: 35,683,149-36,277,052 CREB3, GBA2, 30 more genes
    nsv4768268insertion1nstd199human GRCh37 chr9: 35,906,607-35,906,607 , GRCh38.p12 chr9: 35,906,610-35,906,610 HRCT1
    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
    nsv4675565copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-70,984,588 , GRCh38.p12 chr9: 203,861-68,369,672 LOC100132004, LOC105375993, 853 more genes
    nsv4604795copy number variation1nstd183human GRCh37 chr9: 35,905,326-35,964,362 , GRCh38.p12 chr9: 35,905,329-35,964,365 SPAAR, PGAM1P2, 2 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
    nsv4178998copy number variation1nstd166human GRCh37.p13 chr9: 35,906,547-35,906,634 , GRCh38.p12 chr9: 35,906,550-35,906,637 HRCT1
    nsv3965190insertion1nstd168human GRCh38 chr9: 35,895,775-35,929,441 , GRCh37.p13 chr9: 35,895,772-35,929,438 HRCT1, SPAAR
    nsv3931136insertion1nstd167human GRCh37 chr9: 35,906,601-35,906,601 , GRCh38.p12 chr9: 35,906,604-35,906,604 HRCT1
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