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    Number of Variants: 1

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv22768sequence alteration1estd20human NCBI36 chr22: 16,506,982-16,509,450 , GRCh37.p13 chr22: 18,126,982-18,129,450 , GRCh38.p12 chr22: 17,644,216-17,646,684 BCL2L13

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