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Items: 1 to 20 of 165

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv5381707copy number variation2nstd102humanUncertain significance GRCh37 chr9: 34,458,994-35,072,710 , GRCh38.p12 chr9: 34,458,996-35,072,713 YWHAZP6, IL11RA, 30 more genes
    nsv5372466translocation1nstd200human GRCh38 chr16: 50,799,296-50,799,296 , GRCh38 chr9: 34,829,696-34,829,696 , GRCh37.p13 chr16: 50,833,207-50,833,207 , GRCh37.p13 chr9: 34,829,693-34,829,693 CYLD, PHF24, 2 more genes
    nsv5347445translocation1nstd200human GRCh38 chr16: 50,798,125-50,798,125 , GRCh38 chr9: 34,829,681-34,829,681 , GRCh37.p13 chr16: 50,832,036-50,832,036 , GRCh37.p13 chr9: 34,829,678-34,829,678 CYLD, PHF24, 2 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
    nsv4675565copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-70,984,588 , GRCh38.p12 chr9: 203,861-68,369,672 LOC100132004, LOC105375993, 853 more genes
    nsv4675154copy number variation1nstd102humanUncertain significance GRCh37 chr9: 34,699,039-35,060,746 , GRCh38.p12 chr9: 34,699,042-35,060,749 SYF2P2, YWHAZP6, 13 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
    nsv4421969copy number variation1nstd174human GRCh37 chr9: 34,717,086-34,835,299 , GRCh38.p12 chr9: 34,717,089-34,835,302 SPATA31F1, SPATA31F2P, 1 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
    nsv4181598copy number variation1nstd166human GRCh37.p13 chr9: 34,830,520-34,830,768 , GRCh38.p12 chr9: 34,830,523-34,830,771 PHF24, SPATA31F2P
    nsv3923714copy number variation1nstd102humanPathogenic GRCh38 chr9: 193,412-70,630,731 , GRCh37 chr9: 220,253-73,245,647 , NCBI36 chr9: 210,253-72,435,467 LOC105379257, LOC105376002, 888 more genes
    nsv3922684copy number variation2nstd102humanPathogenic NCBI36 chr9: 194,193-140,193,718 , GRCh38 chr9: 193,412-138,179,445 , GRCh37 chr9: 204,193-141,073,897 TDRD7, CDK9, 2170 more genes
    nsv3921759copy number variation1nstd102humanPathogenic NCBI36 chr9: 2,934-65,222,364 , GRCh37.p13 chr9: 12,934-65,482,544 , GRCh38.p12 chr9: 12,934-66,233,120 SPATA31A6, CDRT15P14, 824 more genes
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