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    Number of Variants: 2

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv1398330copy number variation3nstd102humannot provided, Pathogenic GRCh37 chr3: 37,064,799-37,068,325 , GRCh38 chr3: 37,023,308-37,026,834 MLH1
    nsv6634562copy number variation1nstd102humanPathogenic GRCh38 chr9: 139,481-407,477 , GRCh37.p13 chr9: 139,481-407,477 ZNG1A, DOCK8, 3 more genes

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