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    Number of Variants: 2

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4406075copy number variation1nstd174human GRCh37 chr3: 2,877,373-2,879,787 , GRCh38.p12 chr3: 2,835,689-2,838,103 CNTN4, LOC105376926
    esv2669901copy number variation1estd199human GRCh37 chr3: 2,877,373-2,879,745 , GRCh38.p12 chr3: 2,835,689-2,838,061 CNTN4, LOC105376926

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