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    Number of Variants: 2

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4425997copy number variation1nstd174human GRCh37 chr22: 18,126,406-18,129,662 , GRCh38.p12 chr22: 17,643,640-17,646,896 BCL2L13
    esv2669345copy number variation13estd199human GRCh37 chr22: 18,126,653-18,129,499 , GRCh38.p12 chr22: 17,643,887-17,646,733 BCL2L13

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