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    Number of Variants: 1

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv1072991copy number variation1nstd99human GRCh37 chr2: 170,709,899-170,712,400 , GRCh38.p12 chr2: 169,853,389-169,855,890 UBR3

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