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Items: 2

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    Number of Variants: 2

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv28778sequence alteration1estd20human NCBI36 chr16: 56,127,517-56,128,606 , GRCh37.p13 chr16: 57,570,016-57,571,105 , GRCh38.p12 chr16: 57,536,104-57,537,193 ADGRG5, CCDC102A
    esv14482copy number variation1estd20human NCBI36 chr16: 56,127,517-56,128,606 , GRCh37.p13 chr16: 57,570,016-57,571,105 , GRCh38.p12 chr16: 57,536,104-57,537,193 CCDC102A, ADGRG5

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