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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148179copy number variation1nstd102humanLikely pathogenic GRCh38 chr9: 78,235,965-78,243,734 , GRCh37.p13 chr9: 80,850,881-80,858,650 CEP78
    nsv7145337insertion1nstd232human GRCh37.p13 chr9: 80,869,886-80,869,886 , GRCh38.p12 chr9: 78,254,970-78,254,970 CEP78
    nsv7138989insertion1nstd232human GRCh37.p13 chr9: 80,861,698-80,861,698 , GRCh38.p12 chr9: 78,246,782-78,246,782 CEP78
    nsv7138829insertion1nstd232human GRCh37.p13 chr9: 80,866,959-80,866,959 , GRCh38.p12 chr9: 78,252,043-78,252,043 CEP78
    nsv7098474copy number variation1nstd102humanUncertain significance GRCh37 chr9: 80,881,338-80,881,678 , GRCh38.p12 chr9: 78,266,422-78,266,762 CEP78
    nsv7098203copy number variation1nstd102humanPathogenic GRCh37 chr9: 80,854,919-80,856,735 , GRCh38.p12 chr9: 78,240,003-78,241,819 CEP78
    nsv7098101copy number variation1nstd102humanPathogenic GRCh37 chr9: 80,851,266-80,856,548 , GRCh38.p12 chr9: 78,236,350-78,241,632 CEP78
    nsv7073661inversion1nstd229human GRCh38 chr9: 78,228,782-78,234,842 , GRCh37.p13 chr9: 80,843,698-80,849,758 CEP78
    nsv7059631inversion1nstd229human GRCh38 chr9: 78,234,547-78,244,766 , GRCh37.p13 chr9: 80,849,463-80,859,682 CEP78
    nsv6876296copy number variation1nstd229human GRCh38 chr9: 78,255,615-78,255,893 , GRCh37.p13 chr9: 80,870,531-80,870,809 CEP78
    nsv6876290copy number variation1nstd229human GRCh38 chr9: 78,262,501-78,264,200 , GRCh37.p13 chr9: 80,877,417-80,879,116 CEP78
    nsv6872939copy number variation1nstd229human GRCh38 chr9: 78,273,124-78,280,909 , GRCh37.p13 chr9: 80,888,040-80,895,825 CEP78
    nsv6872056copy number variation1nstd229human GRCh38 chr9: 78,252,554-78,256,781 , GRCh37.p13 chr9: 80,867,470-80,871,697 CEP78
    nsv6870651copy number variation1nstd229human GRCh38 chr9: 78,252,276-78,252,404 , GRCh37.p13 chr9: 80,867,192-80,867,320 CEP78
    nsv6867703copy number variation1nstd229human GRCh38 chr9: 78,230,063-78,244,730 , GRCh37.p13 chr9: 80,844,979-80,859,646 CEP78
    nsv6865588copy number variation1nstd229human GRCh38 chr9: 78,266,123-78,272,883 , GRCh37.p13 chr9: 80,881,039-80,887,799 CEP78
    nsv6863671copy number variation1nstd229human GRCh38 chr9: 78,096,930-78,331,884 , GRCh37.p13 chr9: 80,711,846-80,946,800 RN7SKP59, SYNGR2P2, 6 more genes
    nsv6860949copy number variation1nstd229human GRCh38 chr9: 78,170,995-78,521,869 , GRCh37.p13 chr9: 80,785,911-81,136,785 RPL21P84, ASS1P3, 4 more genes
    nsv6858421copy number variation1nstd229human GRCh38 chr9: 77,965,302-78,341,298 , GRCh37.p13 chr9: 80,580,218-80,956,214 LOC107987031, PSAT1, 7 more genes
    nsv6637642copy number variation1nstd102humanUncertain significance GRCh37 chr9: 80,582,026-80,948,266 , GRCh38.p12 chr9: 77,967,110-78,333,350 GNAQ, LOC107987082, 7 more genes
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