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    Number of Variants: 1

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6315210copy number variation1nstd102humanPathogenic GRCh37 chr1: 186,265,850-186,266,785 , GRCh38.p12 chr1: 186,296,718-186,297,653 PRG4

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