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    Number of Variants: 2

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4429460copy number variation1nstd174human GRCh37 chr12: 526,518-671,005 , GRCh38.p12 chr12: 417,352-561,839 CCDC77, B4GALNT3
    esv3628236copy number variation3estd214human GRCh37 chr12: 526,518-671,005 , GRCh38.p12 chr12: 417,352-561,839 CCDC77, B4GALNT3

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