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Items: 2

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    Number of Variants: 2

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv27463sequence alteration1estd20human NCBI36 chr13: 97,592,718-97,594,370 , GRCh37.p13 chr13: 98,794,717-98,796,369 , GRCh38.p12 chr13: 98,142,463-98,144,115 FARP1, LOC105370328
    esv18781copy number variation4estd20human NCBI36 chr13: 97,592,718-97,594,370 , GRCh37.p13 chr13: 98,794,717-98,796,369 , GRCh38.p12 chr13: 98,142,463-98,144,115 FARP1, LOC105370328

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