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    Number of Variants: 1

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5059939copy number variation1nstd202human GRCh37.p13 chr3: 2,339,656-2,377,802 , GRCh38 chr3: 2,297,972-2,336,118 CNTN4

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