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    Number of Variants: 1

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv1138956copy number variation2nstd106human GRCh37 chr20: 35,522,737-35,522,796 , GRCh38.p12 chr20: 36,894,334-36,894,393 SAMHD1, TLDC2

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