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    Number of Variants: 2

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4394527copy number variation1nstd174human GRCh37 chr6: 136,597,458-136,599,042 , GRCh38.p12 chr6: 136,276,320-136,277,904 BCLAF1
    esv2732753copy number variation92estd201human GRCh37 chr6: 136,597,568-136,599,006 , GRCh38.p12 chr6: 136,276,430-136,277,868 BCLAF1

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