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Items: 1 to 20 of 266

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5914816copy number variation1nstd209human GRCh38 chr9: 21,981,197-25,406,892 , GRCh37.p13 chr9: 21,981,196-25,406,890 , CLIC4P1, 20 more genes
    nsv5381686copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chr9: 21,968,228-22,160,087 , GRCh38.p12 chr9: 21,968,229-22,160,088 CDKN2A-AS1, CDKN2B-AS1, 3 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
    nsv4745683copy number variation1nstd199human GRCh37 chr9: 6,727,606-30,688,993 , GRCh38.p12 chr9: 6,727,606-30,688,995 , RPS6P10, 230 more genes
    nsv4728830copy number variation1nstd102humanUncertain significance GRCh37 chr9: 21,391,297-23,423,892 , GRCh38.p12 chr9: 21,391,298-23,423,894 LINC01239, LOC105375990, 22 more genes
    nsv4676038copy number variation1nstd102humanUncertain significance GRCh37 chr9: 21,936,290-22,082,568 , GRCh38.p12 chr9: 21,936,291-22,082,569 CDKN2A-AS1, UBA52P6, 3 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
    nsv4674944copy number variation1nstd102humanUncertain significance GRCh37 chr9: 20,829,681-22,069,144 , GRCh38.p12 chr9: 20,829,682-22,069,145 CDKN2B-AS1, IFNA2, 43 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
    nsv4388503copy number variation1nstd173human GRCh37 chr9: 19,569,670-27,574,515 , GRCh38.p12 chr9: 19,569,672-27,574,517 , RMRPP5, 104 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
    nsv4350534copy number variation1nstd102humanPathogenic GRCh37 chr9: 20,715,401-22,136,489 , GRCh38.p12 chr9: 20,715,402-22,136,490 IFNW1, IFNA7, 45 more genes
    nsv4187118copy number variation1nstd166human GRCh37.p13 chr9: 21,997,896-22,001,267 , GRCh38.p12 chr9: 21,997,897-22,001,268 CDKN2B, CDKN2B-AS1
    nsv4184515copy number variation1nstd166human GRCh37.p13 chr9: 21,703,458-22,598,302 , GRCh38.p12 chr9: 21,703,459-22,598,303 CDKN2A, CDKN2B, 7 more genes
    nsv3924627copy number variation1nstd102humandrug response GRCh37 chr9: 21,939,408-22,706,613 , GRCh38 chr9: 21,939,409-22,706,614 CDKN2B, LOC107987054, 6 more genes
    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
    nsv3923314copy number variation1nstd102humanPathogenic GRCh38 chr9: 220,257-29,424,848 , GRCh37 chr9: 220,257-29,424,846 , NCBI36 chr9: 210,257-29,414,846 DOCK8-AS2, IFNA14, 319 more genes
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