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    Number of Variants: 2

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4414126copy number variation1nstd174human GRCh37 chr12: 117,005,116-117,007,770 , GRCh38.p12 chr12: 116,567,311-116,569,965 MAP1LC3B2
    esv3630852copy number variation3estd214human GRCh37 chr12: 117,005,221-117,007,704 , GRCh38.p12 chr12: 116,567,416-116,569,899 MAP1LC3B2

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