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Items: 1 to 20 of 207

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4963634copy number variation1nstd200human GRCh38 chr9: 21,365,598-21,390,670 , GRCh37.p13 chr9: 21,365,597-21,390,669 IFNA13, IFNA2
    nsv4954550copy number variation1nstd200human GRCh38 chr9: 21,133,080-21,557,413 , GRCh37.p13 chr9: 21,133,079-21,557,412 IFNWP15, IFNA12P, 27 more genes
    nsv4814668copy number variation1nstd200human GRCh37 chr9: 21,133,079-21,557,412 , GRCh38.p12 chr9: 21,133,080-21,557,413 IFNA4, IFNA11P, 27 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
    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
    nsv4188353copy number variation1nstd166human GRCh37.p13 chr9: 21,365,597-21,390,669 , GRCh38.p12 chr9: 21,365,598-21,390,670 IFNA13, IFNA2
    nsv4182818copy number variation1nstd166human GRCh37.p13 chr9: 21,375,728-21,430,925 , GRCh38.p12 chr9: 21,375,729-21,430,926 IFNA2, IFNA8, 3 more genes
    nsv4177112copy number variation1nstd166human GRCh37.p13 chr9: 21,318,305-21,428,187 , GRCh38.p12 chr9: 21,318,306-21,428,188 IFNA20P, IFNA13, 8 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
    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
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