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    Number of Variants: 2

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4423886copy number variation1nstd174human GRCh37 chr18: 11,864,890-11,866,911 , GRCh38.p12 chr18: 11,864,891-11,866,912 GNAL
    esv3641818copy number variation224estd214human GRCh37 chr18: 11,864,772-11,867,304 , GRCh38.p12 chr18: 11,864,773-11,867,305 GNAL

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