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    Number of Variants: 2

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv28903sequence alteration1estd20human NCBI36 chr1: 153,926,378-153,931,106 , GRCh37.p13 chr1: 155,659,754-155,664,482 , GRCh38.p12 chr1: 155,689,963-155,694,691 DAP3
    esv15603copy number variation15estd20human NCBI36 chr1: 153,926,378-153,931,106 , GRCh37.p13 chr1: 155,659,754-155,664,482 , GRCh38.p12 chr1: 155,689,963-155,694,691 DAP3

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