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Items: 5

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    Number of Variants: 5

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6633178copy number variation15nstd224human GRCh37 chr9: 17,585,896-17,633,023 , GRCh38.p12 chr9: 17,585,898-17,633,025 PABPC1P11, SH3GL2
    nsv6622960copy number variation7nstd224human GRCh37 chr15: 22,368,918-22,383,300 , GRCh38.p12 chr15: 22,080,967-22,095,349 OR4M2, OR4M2-OT1, 1 more genes
    nsv6625130copy number variation188nstd224human GRCh37 chr19: 43,344,686-43,528,980 , GRCh38.p12 chr19: 42,840,534-43,024,828 CEACAMP7, PSG1, 4 more genes
    nsv6624269copy number variation7nstd224human GRCh37 chr17: 33,680,941-33,768,284 , GRCh38.p12 chr17: 35,353,922-35,441,265 SLFN12, SLFN11, 4 more genes
    nsv6630107copy number variation584nstd224human GRCh37 chr5: 140,223,185-140,238,124 , GRCh38.p12 chr5: 140,843,600-140,858,539 PCDHA4, PCDHA1, 9 more genes
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