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    Number of Variants: 2

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4420379copy number variation1nstd174human GRCh37 chr18: 11,826,040-11,826,585 , GRCh38.p12 chr18: 11,826,041-11,826,586 GNAL
    esv2716803copy number variation52estd201human GRCh37 chr18: 11,825,619-11,826,585 , GRCh38.p12 chr18: 11,825,620-11,826,586 GNAL

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