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    Number of Variants: 1

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv997221copy number variation1nstd45humanPathogenic GRCh37 chr3: 69,788,586-70,017,488 , GRCh38.p12 chr3: 69,739,435-69,968,337 MITF, RN7SL418P

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