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    Number of Variants: 1

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6634306copy number variation1nstd102humanPathogenic GRCh38 chr1: 21,816,592-21,823,699 , GRCh37 chr1: 22,143,085-22,150,192 HSPG2, LDLRAD2

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