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    Number of Variants: 1

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv1160898copy number variation2nstd111human GRCh38.p12 chr2: 201,196,327-201,213,771 , GRCh37 chr2: 202,061,050-202,078,494 CASP10, MTND4P23, 2 more genes

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