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    Number of Variants: 1

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6290358copy number variation1nstd219human GRCh37.p13 chr11: 5,247,419-5,252,321 , GRCh38 chr11: 5,226,189-5,231,091 HBB, HBD

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