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    Number of Variants: 1

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv26702sequence alteration1estd20human NCBI36 chr9: 134,934,317-134,947,466 , GRCh37.p13 chr9: 135,944,496-135,957,645 , GRCh38.p12 chr9: 133,069,109-133,082,258 CEL, CELP

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