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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5479439copy number variation1nstd206human GRCh38 chr9: 4,704,675-4,704,812 , GRCh37.p13 chr9: 4,704,675-4,704,812 CDC37L1
    nsv5381785copy number variation1nstd102humanPathogenic GRCh37 chr9: 2,854,435-6,937,677 , GRCh38.p12 chr9: 2,854,435-6,937,677 GLIS3-AS1, RFX3-DT, 70 more genes
    nsv5381767copy number variation1nstd102humanPathogenic GRCh37 chr9: 204,193-18,654,812 , GRCh38.p12 chr9: 204,193-18,654,814 ACTG1P14, DMAC1, 191 more genes
    nsv5381702copy number variation1nstd102humanUncertain significance GRCh37 chr9: 2,029,023-5,300,444 , GRCh38.p12 chr9: 2,029,023-5,300,444 MTND5P36, MTND2P36, 53 more genes
    nsv5306927copy number variation1nstd204human GRCh37.p13 chr9: 4,665,427-4,707,952 , GRCh38.p13 chr9: 4,665,427-4,707,952 AK3, SPATA6L, 3 more genes
    nsv5242038copy number variation1nstd204human GRCh38.p13 chr9: 4,665,305-4,684,370 , GRCh37.p13 chr9: 4,665,305-4,684,370 CDC37L1, SPATA6L, 2 more genes
    nsv5116683mobile element insertion1nstd203human GRCh38 chr9: 4,682,329-4,682,344 , GRCh37.p13 chr9: 4,682,329-4,682,344 CDC37L1
    nsv4969281copy number variation1nstd200human GRCh38 chr9: 4,704,675-4,704,812 , GRCh37.p13 chr9: 4,704,675-4,704,812 CDC37L1
    nsv4969280copy number variation1nstd200human GRCh38 chr9: 4,684,807-4,740,066 , GRCh37.p13 chr9: 4,684,807-4,740,066 CDC37L1, AK3
    nsv4969272copy number variation1nstd200human GRCh38 chr9: 4,065,650-4,678,397 , GRCh37.p13 chr9: 4,065,650-4,678,397 CDC37L1, RPS6P11, 7 more genes
    nsv4963057copy number variation1nstd200human GRCh38 chr9: 4,682,002-4,682,088 , GRCh37.p13 chr9: 4,682,002-4,682,088 CDC37L1
    nsv4963056copy number variation1nstd200human GRCh38 chr9: 4,665,437-4,707,943 , GRCh37.p13 chr9: 4,665,437-4,707,943 SPATA6L, PLPP6, 3 more genes
    nsv4823113copy number variation1nstd200human GRCh37 chr9: 4,682,002-4,682,088 , GRCh38.p12 chr9: 4,682,002-4,682,088 CDC37L1
    nsv4823112copy number variation1nstd200human GRCh37 chr9: 4,665,437-4,707,943 , GRCh38.p12 chr9: 4,665,437-4,707,943 AK3, PLPP6, 3 more genes
    nsv4768366copy number variation1nstd102humanPathogenic GRCh37 chr9: 204,193-18,073,357 , GRCh38.p12 chr9: 204,193-18,073,359 DOCK8-AS1, RN7SL25P, 186 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
    nsv4729111copy number variation1nstd102humanUncertain significance GRCh37 chr9: 4,611,869-4,791,622 , GRCh38.p12 chr9: 4,611,869-4,791,622 RPS5P6, SPATA6L, 7 more genes
    nsv4680534copy number variation1nstd189human GRCh37.p13 chr9: 4,062,061-4,680,530 , GRCh38.p12 chr9: 4,062,061-4,680,530 SLC1A1, SPATA6L, 7 more genes
    nsv4680037copy number variation1nstd189human GRCh37.p13 chr9: 4,611,876-4,894,234 , GRCh38.p12 chr9: 4,611,876-4,894,234 RCL1, AK3, 9 more genes
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