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    Number of Variants: 2

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv22984sequence alteration2estd20human NCBI36 chr7: 6,089,789-6,111,243 , GRCh37.p13 chr7: 6,123,263-6,144,717 , GRCh38.p12 chr7: 6,083,632-6,105,086 USP42
    esv13824copy number variation5estd20human NCBI36 chr7: 6,089,789-6,111,243 , GRCh37.p13 chr7: 6,123,263-6,144,717 , GRCh38.p12 chr7: 6,083,632-6,105,086 USP42

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