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    Number of Variants: 2

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4425071copy number variation1nstd174human GRCh37 chr13: 47,038,145-47,038,557 , GRCh38.p12 chr13: 46,464,010-46,464,422 LINC01198
    esv2676825copy number variation100estd199human GRCh37 chr13: 47,038,228-47,038,463 , GRCh38.p12 chr13: 46,464,093-46,464,328 LINC01198

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