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Items: 1 to 20 of 941

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7070585inversion1nstd229human GRCh38 chr9: 20,885,919-20,909,265 , GRCh37.p13 chr9: 20,885,918-20,909,264 FOCAD
    nsv7068293inversion1nstd229human GRCh38 chr9: 12,453,912-21,375,878 , GRCh37.p13 chr9: 12,453,912-21,375,877 RNU6-264P, PSMC3P1, 115 more genes
    nsv7062632inversion1nstd229human GRCh38 chr9: 20,752,012-20,754,304 , GRCh37.p13 chr9: 20,752,011-20,754,303 FOCAD
    nsv7062404inversion1nstd229human GRCh38 chr9: 12,646,715-21,082,028 , GRCh37.p13 chr9: 12,646,715-21,082,027 RPS6, RPL7AP47, 95 more genes
    nsv7058551inversion1nstd229human GRCh38 chr9: 20,861,083-20,861,166 , GRCh37.p13 chr9: 20,861,082-20,861,165 FOCAD
    nsv6877210copy number variation1nstd229human GRCh38 chr9: 20,774,722-20,774,800 , GRCh37.p13 chr9: 20,774,721-20,774,799 FOCAD
    nsv6877154copy number variation1nstd229human GRCh38 chr9: 20,957,781-20,991,850 , GRCh37.p13 chr9: 20,957,780-20,991,849 FOCAD
    nsv6876881copy number variation1nstd229human GRCh38 chr9: 20,824,830-20,841,347 , GRCh37.p13 chr9: 20,824,829-20,841,346 FOCAD
    nsv6876498copy number variation1nstd229human GRCh38 chr9: 20,699,615-20,722,662 , GRCh37.p13 chr9: 20,699,614-20,722,661 MIR491, FOCAD
    nsv6876289copy number variation1nstd229human GRCh38 chr9: 20,913,103-20,984,281 , GRCh37.p13 chr9: 20,913,102-20,984,280 FOCAD
    nsv6875788copy number variation1nstd229human GRCh38 chr9: 20,978,454-20,981,425 , GRCh37.p13 chr9: 20,978,453-20,981,424 FOCAD
    nsv6875358copy number variation1nstd229human GRCh38 chr9: 20,671,501-20,673,900 , GRCh37.p13 chr9: 20,671,500-20,673,899 FOCAD
    nsv6875003copy number variation1nstd229human GRCh38 chr9: 20,727,868-20,730,925 , GRCh37.p13 chr9: 20,727,867-20,730,924 FOCAD
    nsv6874876copy number variation1nstd229human GRCh38 chr9: 20,862,098-20,865,405 , GRCh37.p13 chr9: 20,862,097-20,865,404 FOCAD
    nsv6874760copy number variation1nstd229human GRCh38 chr9: 20,698,546-20,743,200 , GRCh37.p13 chr9: 20,698,545-20,743,199 MIR491, FOCAD
    nsv6874355copy number variation1nstd229human GRCh38 chr9: 20,810,943-20,840,106 , GRCh37.p13 chr9: 20,810,942-20,840,105 FOCAD
    nsv6874247copy number variation1nstd229human GRCh38 chr9: 20,688,801-20,770,300 , GRCh37.p13 chr9: 20,688,800-20,770,299 MIR491, FOCAD
    nsv6874135copy number variation1nstd229human GRCh38 chr9: 20,763,858-20,812,410 , GRCh37.p13 chr9: 20,763,857-20,812,409 FOCAD, SNORA30B
    nsv6873832copy number variation1nstd229human GRCh38 chr9: 20,684,201-21,311,600 , GRCh37.p13 chr9: 20,684,200-21,311,599 IFNWP5, IFNWP18, 22 more genes
    nsv6873242copy number variation1nstd229human GRCh38 chr9: 20,898,897-20,901,726 , GRCh37.p13 chr9: 20,898,896-20,901,725 FOCAD
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