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    Number of Variants: 2

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4427044copy number variation1nstd174human GRCh37 chr13: 47,038,244-47,040,113 , GRCh38.p12 chr13: 46,464,109-46,465,978 LINC01198
    esv2659526copy number variation10estd199human GRCh37 chr13: 47,038,244-47,039,808 , GRCh38.p12 chr13: 46,464,109-46,465,673 LINC01198

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