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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
    nsv7099024copy number variation1nstd102humanPathogenic GRCh37 chr17: 17,119,280-17,119,281 , GRCh38 chr17: 17,215,966-17,215,967 FLCN
    nsv7098881copy number variation1nstd102humanPathogenic GRCh37 chr17: 17,116,969-20,217,378 , GRCh38.p12 chr17: 17,213,655-20,314,065 LOC105371578, SNORD3B-2, 119 more genes
    nsv7094958copy number variation1nstd102humanUncertain significance GRCh37 chr17: 17,118,289-17,140,502 , GRCh38.p12 chr17: 17,214,975-17,237,188 FLCN
    nsv7094862copy number variation1nstd102humanUncertain significance GRCh37 chr17: 17,135,108-17,135,196 , GRCh38.p12 chr17: 17,231,794-17,231,882 FLCN
    nsv7093606insertion1nstd102humanLikely benign GRCh37 chr17: 17,118,410-17,118,410 , GRCh38 chr17: 17,215,096-17,215,096 FLCN
    nsv7093230copy number variation2nstd102humanUncertain significance GRCh37 chr17: 17,116,999-17,117,000 , GRCh38 chr17: 17,213,685-17,213,686 FLCN
    nsv7077735inversion1nstd229human GRCh38 chr17: 17,217,581-17,220,758 , GRCh37.p13 chr17: 17,120,895-17,124,072 FLCN
    nsv7077567inversion1nstd229human GRCh38 chr17: 17,232,429-17,236,640 , GRCh37.p13 chr17: 17,135,743-17,139,954 FLCN
    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
    nsv7068050inversion1nstd229human GRCh38 chr17: 16,799,901-18,286,035 , GRCh37.p13 chr17: 16,703,215-18,189,349 ATPAF2, TNFRSF13B, 51 more genes
    nsv7067152inversion1nstd229human GRCh38 chr17: 16,993,913-17,832,711 , GRCh37.p13 chr17: 16,897,227-17,736,025 PLD6, TSEN15P1, 21 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
    nsv7062424inversion1nstd229human GRCh38 chr17: 17,236,070-17,239,954 , GRCh37.p13 chr17: 17,139,384-17,143,268 FLCN
    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
    nsv6989605copy number variation1nstd229human GRCh38 chr17: 17,130,501-17,247,600 , GRCh37.p13 chr17: 17,033,815-17,150,914 PLD6, RNU6-767P, 5 more genes
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