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Items: 1 to 20 of 186

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5696094mobile element insertion1nstd211human GRCh38 chr9: 33,272,410-33,272,410 , GRCh37.p13 chr9: 33,272,408-33,272,408 CHMP5
    nsv5381740copy number variation1nstd102humanUncertain significance GRCh37 chr9: 32,399,559-33,541,225 , GRCh38.p12 chr9: 32,399,561-33,541,227 SMU1, RNU4ATAC15P, 38 more genes
    nsv5372453translocation1nstd200human GRCh38 chr9: 33,269,126-33,269,126 , GRCh38 chr9: 33,269,209-33,269,209 , GRCh37.p13 chr9: 33,269,124-33,269,124 , GRCh37.p13 chr9: 33,269,207-33,269,207 CHMP5
    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
    nsv4729332copy number variation1nstd102humanUncertain significance GRCh37 chr9: 33,127,802-33,377,822 , GRCh38.p12 chr9: 33,127,804-33,377,824 LOC105376018, NFX1, 7 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
    nsv4675367copy number variation1nstd102humanUncertain significance GRCh37 chr9: 33,126,394-33,398,500 , GRCh38.p12 chr9: 33,126,396-33,398,502 LOC100862682, BAG1, 8 more genes
    nsv4610797copy number variation1nstd183human GRCh37 chr9: 33,094,979-33,274,474 , GRCh38.p12 chr9: 33,094,981-33,274,476 BAG1, B4GALT1, 5 more genes
    nsv4599120copy number variation1nstd183human GRCh37 chr9: 33,091,696-33,276,680 , GRCh38.p12 chr9: 33,091,698-33,276,682 BAG1, B4GALT1, 5 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
    nsv4455588copy number variation1nstd102humanUncertain significance GRCh37 chr9: 33,177,135-33,407,576 , GRCh38.p12 chr9: 33,177,137-33,407,578 LOC100862682, SPINK4, 7 more genes
    nsv4455571copy number variation1nstd102humanUncertain significance GRCh37 chr9: 33,087,213-33,274,455 , GRCh38.p12 chr9: 33,087,215-33,274,457 SPINK4, RNU4ATAC15P, 5 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
    nsv4418031copy number variation1nstd174human GRCh37 chr9: 33,042,017-33,278,844 , GRCh38.p12 chr9: 33,042,019-33,278,846 BAG1, B4GALT1, 6 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
    nsv4181347copy number variation1nstd166human GRCh37.p13 chr9: 33,262,741-33,262,900 , GRCh38.p12 chr9: 33,262,743-33,262,902 BAG1, CHMP5
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