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    Number of Variants: 2

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4429469copy number variation1nstd174human GRCh37 chr21: 46,370,797-46,372,049 , GRCh38.p12 chr21: 44,950,882-44,952,134 , SLX9
    esv2670703copy number variation5estd199human GRCh37 chr21: 46,370,797-46,371,790 , GRCh38.p12 chr21: 44,950,882-44,951,875 SLX9,

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