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    Number of Variants: 1

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137051copy number variation1nstd102humanPathogenic GRCh37 chr16: 56,419,456-56,423,384 , GRCh38 chr16: 56,385,544-56,389,472 AMFR

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