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    Number of Variants: 2

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4397822copy number variation1nstd174human GRCh37 chr3: 1,029,987-1,040,021 , GRCh38.p12 chr3: 988,303-998,337 CNTN6
    esv2659086copy number variation5estd199human GRCh37 chr3: 1,032,710-1,039,581 , GRCh38.p12 chr3: 991,026-997,897 CNTN6

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