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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137103copy number variation1nstd102humanPathogenic GRCh37 chr17: 16,664,739-20,370,783 , GRCh38.p12 chr17: 16,761,425-20,467,470 NMTRQ-TTG12-1, NOS2P4, 148 more genes
    nsv7075073inversion1nstd229human GRCh38 chr17: 16,560,168-17,214,404 , GRCh37.p13 chr17: 16,463,482-17,117,718 ZNF624, TBC1D27P, 28 more genes
    nsv7073486inversion1nstd229human GRCh38 chr17: 15,622,817-18,740,940 , GRCh37.p13 chr17: 15,526,131-18,644,253 NCOR1, KRT16P6, 129 more genes
    nsv7073439inversion1nstd229human GRCh38 chr17: 15,962,151-19,146,977 , GRCh37.p13 chr17: 15,865,465-19,050,290 RNU6-767P, KRT17P5, 129 more genes
    nsv7066862inversion1nstd229human GRCh38 chr17: 15,664,455-18,717,083 , GRCh37.p13 chr17: 15,567,769-18,620,396 KRT16P6, RPLP1P11, 129 more genes
    nsv7059660inversion1nstd229human GRCh38 chr17: 16,041,448-17,186,703 , GRCh37.p13 chr17: 15,944,762-17,090,017 SNHG29, ZNF624, 46 more genes
    nsv7059394inversion1nstd229human GRCh38 chr17: 16,560,428-17,214,568 , GRCh37.p13 chr17: 16,463,742-17,117,882 TNFRSF13B, ZNF624, 28 more genes
    nsv7059177inversion1nstd229human GRCh38 chr17: 15,493,473-18,338,296 , GRCh37.p13 chr17: 15,396,787-18,241,610 TOM1L2, PPIAP53, 107 more genes
    nsv6995851copy number variation1nstd229human GRCh38 chr17: 16,261,589-17,283,740 , GRCh37.p13 chr17: 16,164,903-17,187,054 SRP68P1, SNORD49B, 42 more genes
    nsv6991129copy number variation1nstd229human GRCh38 chr17: 16,677,418-16,689,530 , GRCh37.p13 chr17: 16,580,732-16,592,844 CCDC144A, RNASEH1P2
    nsv6988358copy number variation1nstd229human GRCh38 chr17: 16,669,201-16,683,900 , GRCh37.p13 chr17: 16,572,515-16,587,214 CCDC144A, RNASEH1P2
    nsv6988041copy number variation1nstd229human GRCh38 chr17: 16,744,778-16,748,997 , GRCh37.p13 chr17: 16,648,092-16,652,311 UPF3AP1, CCDC144A
    nsv6987652copy number variation1nstd229human GRCh38 chr17: 16,700,145-16,700,651 , GRCh37.p13 chr17: 16,603,459-16,603,965 CCDC144A
    nsv6985542copy number variation1nstd229human GRCh38 chr17: 16,671,008-16,683,949 , GRCh37.p13 chr17: 16,574,322-16,587,263 CCDC144A, RNASEH1P2
    nsv6637693copy number variation1nstd102humanUncertain significance GRCh37 chr17: 15,754,174-16,657,319 , GRCh38.p12 chr17: 15,850,860-16,754,005 SNORD65, RN7SL442P, 29 more genes
    nsv6637557copy number variation1nstd102humanUncertain significance GRCh37 chr17: 15,722,840-16,653,256 , GRCh38.p12 chr17: 15,819,526-16,749,942 RPLP1P11, SNORD49A, 31 more genes
    nsv6624202copy number variation1nstd224human GRCh37 chr17: 16,608,260-16,725,877 , GRCh38.p12 chr17: 16,704,946-16,822,563 CCDC144A, UPF3AP1, 7 more genes
    nsv6624049copy number variation1nstd224human GRCh37 chr17: 16,351,932-16,576,609 , GRCh38.p12 chr17: 16,448,618-16,673,295 CCDC144A, ZNF287, 6 more genes
    nsv6593366inversion1nstd223human GRCh38 chr17: 15,604,136-18,759,631 , GRCh37.p13 chr17: 15,507,450-18,662,944 EEF1A1P43, ZNF624, 131 more genes
    nsv6590911inversion1nstd223human GRCh38 chr17: 16,675,953-16,676,183 , GRCh37.p13 chr17: 16,579,267-16,579,497 CCDC144A
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