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Items: 6

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    Number of Variants: 6

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6626716copy number variation32nstd224human GRCh37 chr20: 58,440,438-58,502,456 , GRCh38.p12 chr20: 59,865,383-59,927,401 SYCP2
    nsv6622737copy number variation22nstd224human GRCh37 chr14: 48,250,202-48,271,636 , GRCh38.p12 chr14: 47,780,999-47,802,433 LINC00648, LOC100420098
    nsv6628116copy number variation277nstd224human GRCh37 chr2: 38,956,836-38,972,328 , GRCh38.p12 chr2: 38,729,694-38,745,186 SRSF7, GALM
    nsv6620484copy number variation1nstd224human GRCh37 chr10: 47,543,322-47,667,164 , GRCh38.p12 chr10: 46,172,086-46,295,928 AHCYP1, LOC105378577, 2 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
    nsv6622838copy number variation31nstd224human GRCh37 chr15: 22,770,994-23,236,972 , GRCh38.p12 chr15: 22,636,124-23,102,074 NIPA1, LOC100133165, 10 more genes
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