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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7140501insertion1nstd232human GRCh37.p13 chr13: 26,923,317-26,923,317 , GRCh38.p12 chr13: 26,349,180-26,349,180 CDK8
    nsv7066195inversion1nstd229human GRCh38 chr13: 26,262,981-26,263,024 , GRCh37.p13 chr13: 26,837,118-26,837,161 CDK8
    nsv7063835inversion1nstd229human GRCh38 chr13: 22,751,036-26,757,157 , GRCh37.p13 chr13: 23,325,175-27,331,294 SPATA13, LOC105370122, 86 more genes
    nsv6936982copy number variation1nstd229human GRCh38 chr13: 26,371,282-26,371,456 , GRCh37.p13 chr13: 26,945,419-26,945,593 CDK8
    nsv6936903copy number variation1nstd229human GRCh38 chr13: 26,300,496-26,304,936 , GRCh37.p13 chr13: 26,874,633-26,879,073 CDK8
    nsv6935449copy number variation1nstd229human GRCh38 chr13: 26,268,654-26,271,841 , GRCh37.p13 chr13: 26,842,791-26,845,978 CDK8
    nsv6934562copy number variation1nstd229human GRCh38 chr13: 26,384,701-26,663,300 , GRCh37.p13 chr13: 26,958,838-27,237,437 RPS3AP44, CDK8, 1 more genes
    nsv6933388copy number variation1nstd229human GRCh38 chr13: 26,309,060-26,317,959 , GRCh37.p13 chr13: 26,883,197-26,892,096 CDK8
    nsv6932077copy number variation1nstd229human GRCh38 chr13: 26,227,454-26,349,705 , GRCh37.p13 chr13: 26,801,591-26,923,842 THAP12P6, CDK8
    nsv6931069copy number variation1nstd229human GRCh38 chr13: 26,327,315-26,335,497 , GRCh37.p13 chr13: 26,901,452-26,909,634 CDK8
    nsv6928587copy number variation1nstd229human GRCh38 chr13: 26,308,900-26,325,520 , GRCh37.p13 chr13: 26,883,037-26,899,657 CDK8
    nsv6927708copy number variation1nstd229human GRCh38 chr13: 26,184,757-26,327,926 , GRCh37.p13 chr13: 26,758,894-26,902,063 CDK8, THAP12P6, 1 more genes
    nsv6927572copy number variation1nstd229human GRCh38 chr13: 26,343,903-26,345,941 , GRCh37.p13 chr13: 26,918,040-26,920,078 CDK8
    nsv6925489copy number variation1nstd229human GRCh38 chr13: 26,313,374-26,326,732 , GRCh37.p13 chr13: 26,887,511-26,900,869 CDK8
    nsv6925194copy number variation1nstd229human GRCh38 chr13: 26,314,901-26,320,900 , GRCh37.p13 chr13: 26,889,038-26,895,037 CDK8
    nsv6922209copy number variation1nstd229human GRCh38 chr13: 26,365,854-26,407,231 , GRCh37.p13 chr13: 26,939,991-26,981,368 CDK8
    nsv6920523copy number variation1nstd229human GRCh38 chr13: 26,350,792-26,351,095 , GRCh37.p13 chr13: 26,924,929-26,925,232 CDK8
    nsv6919805copy number variation1nstd229human GRCh38 chr13: 26,261,052-26,267,586 , GRCh37.p13 chr13: 26,835,189-26,841,723 CDK8
    nsv6634431copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,253,848-115,108,937 , GRCh38.p12 chr13: 18,679,708-114,343,462 MTUS2-AS1, LOC105370213, 1330 more genes
    nsv6592883inversion1nstd223human GRCh38 chr13: 26,303,402-26,304,221 , GRCh37.p13 chr13: 26,877,539-26,878,358 CDK8
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