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    Number of Variants: 2

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4427555copy number variation1nstd174human GRCh37 chr21: 47,530,701-47,582,102 , GRCh38.p12 chr21: 46,110,787-46,162,188 SPATC1L, COL6A2, 2 more genes
    nsv953658copy number variation1nstd73human GRCh37 chr21: 47,530,701-47,581,100 , GRCh38.p12 chr21: 46,110,787-46,161,186 COL6A2, FTCD, 2 more genes

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