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Items: 2

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    Number of Variants: 2

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv23382sequence alteration1estd20human NCBI36 chr19: 38,804,323-38,805,160 , GRCh37.p13 chr19: 34,112,483-34,113,320 , GRCh38.p12 chr19: 33,621,577-33,622,414 CHST8
    esv11860copy number variation1estd20human NCBI36 chr19: 38,804,323-38,805,160 , GRCh37.p13 chr19: 34,112,483-34,113,320 , GRCh38.p12 chr19: 33,621,577-33,622,414 CHST8

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