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    Number of Variants: 1

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv1131120copy number variation2nstd106human GRCh37 chr16: 87,425,900-87,426,400 , GRCh38.p12 chr16: 87,392,294-87,392,794 MAP1LC3B, FBXO31

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