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    Number of Variants: 2

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4403526copy number variation1nstd174human GRCh37 chr5: 179,227,865-179,242,581 , GRCh38.p12 chr5: 179,800,865-179,815,581 , GRCh38.p12 chr5|NW_016107298.1: 566,438-581,141 MGAT4B, SQSTM1
    esv3570596copy number variation5estd212human GRCh37 chr5: 179,231,973-179,240,403 , GRCh38.p12 chr5: 179,804,973-179,813,403 , GRCh38.p12 chr5|NW_016107298.1: 570,546-578,958 MGAT4B, SQSTM1

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