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    Number of Variants: 2

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4422232copy number variation1nstd174human GRCh37 chr22: 18,140,095-18,144,842 , GRCh38.p12 chr22: 17,657,329-17,662,076 BCL2L13
    esv2673622copy number variation10estd199human GRCh37 chr22: 18,140,095-18,144,842 , GRCh38.p12 chr22: 17,657,329-17,662,076 BCL2L13

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