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Items: 6

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    Number of Variants: 6

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6620878copy number variation140nstd224human GRCh37 chr11: 107,653,081-107,670,228 , GRCh38.p12 chr11: 107,782,355-107,799,502 SLC35F2
    nsv6622737copy number variation22nstd224human GRCh37 chr14: 48,250,202-48,271,636 , GRCh38.p12 chr14: 47,780,999-47,802,433 LINC00648, LOC100420098
    nsv6633357copy number variation8nstd224human GRCh37 chr8: 87,201,127-87,330,713 , GRCh38.p12 chr8: 86,188,898-86,318,484 LOC105375623, SLC7A13
    nsv6620363copy number variation2nstd224human GRCh37 chr10: 35,058,930-35,159,791 , GRCh38.p12 chr10: 34,770,002-34,870,863 PARD3-DT, PARD3
    nsv6631445copy number variation586nstd224human GRCh37 chr6: 67,017,543-67,044,431 , GRCh38.p12 chr6: 66,307,650-66,334,538 0
    nsv6627386copy number variation1nstd224human GRCh37 chr22: 25,658,525-25,910,315 , GRCh38.p12 chr22: 25,262,558-25,514,348 CRYBB2P1, IGLL3P, 4 more genes
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