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Items: 2

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    Number of Variants: 2

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv22273sequence alteration4estd20human NCBI36 chr22: 43,513,946-43,517,622 , GRCh37.p13 chr22: 45,135,282-45,138,958 , GRCh38.p12 chr22: 44,739,402-44,743,078 PRR5-ARHGAP8
    esv19395copy number variation5estd20human NCBI36 chr22: 43,514,441-43,516,030 , GRCh37.p13 chr22: 45,135,777-45,137,366 , GRCh38.p12 chr22: 44,739,897-44,741,486 PRR5-ARHGAP8

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