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    Number of Variants: 6

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6622123copy number variation14nstd224human GRCh37 chr13: 21,729,252-21,747,051 , GRCh38.p12 chr13: 21,155,113-21,172,912 SKA3
    nsv6623699copy number variation1nstd224human GRCh37 chr16: 6,879,217-6,972,216 , GRCh38.p12 chr16: 6,829,216-6,922,215 RBFOX1, RNU6-457P
    nsv6621722copy number variation15nstd224human GRCh37 chr12: 57,342,188-57,376,840 , GRCh38.p12 chr12: 56,948,404-56,983,056 RDH16, LOC390332
    nsv6625799copy number variation2nstd224human GRCh37 chr1: 16,367,339-16,388,605 , GRCh38.p12 chr1: 16,040,844-16,062,110 FAM131C, CLCNKB
    nsv6632453copy number variation5nstd224human GRCh37 chr7: 76,474,914-76,639,871 , GRCh38.p12 chr7: 76,845,597-77,010,554 FDPSP7, DTX2P1-UPK3BP1-PMS2P11, 4 more genes
    nsv6632364copy number variation1nstd224human GRCh37 chr7: 70,316,365-70,586,067 , GRCh38.p12 chr7: 70,851,379-71,121,081 0
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