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    Number of Variants: 1

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv1057981copy number variation1nstd100human NCBI36 chr21: 41,584,092-41,716,628 , GRCh37.p13 chr21: 42,662,222-42,794,758 , GRCh38.p12 chr21: 41,290,295-41,422,831 FAM3B, MX2, 1 more genes

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