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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
    esv3647139copy number variation15estd214human GRCh37 chr21: 46,370,789-46,372,146 , GRCh38.p12 chr21: 44,950,874-44,952,231 SLX9,

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