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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
    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
    nsv7077532inversion1nstd229human GRCh38 chr17: 17,907,928-18,966,216 , GRCh37.p13 chr17: 17,811,242-18,869,529 SMCR8, PAIP1P2, 51 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
    nsv7073152inversion1nstd229human GRCh38 chr17: 17,317,750-18,724,343 , GRCh37.p13 chr17: 17,221,064-18,627,656 TOP3A, SMCR8, 60 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
    nsv6991708copy number variation1nstd229human GRCh38 chr17: 18,425,001-18,564,200 , GRCh37.p13 chr17: 18,328,315-18,467,514 LOC105371570, TNPO1P2, 11 more genes
    nsv6990165copy number variation1nstd229human GRCh38 chr17: 18,425,601-18,563,900 , GRCh37.p13 chr17: 18,328,915-18,467,214 TNPO1P2, USP32P2, 11 more genes
    nsv6637220copy number variation1nstd102humanPathogenic GRCh37 chr17: 17,103,571-19,331,028 , GRCh38.p12 chr17: 17,200,257-19,427,715 PRPSAP2, SNORD3A, 96 more genes
    nsv6634447copy number variation1nstd102humanUncertain significance GRCh37 chr17: 16,736,709-20,339,460 , GRCh38.p12 chr17: 16,833,395-20,436,147 KCTD9P1, MTCO1P39, 139 more genes
    nsv6624017copy number variation1nstd224human GRCh37 chr17: 18,155,870-18,702,230 , GRCh38.p12 chr17: 18,252,556-18,798,917 SHMT1, SRP68P2, 33 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
    nsv6590468inversion1nstd223human GRCh38 chr17: 15,738,295-18,638,514 , GRCh37.p13 chr17: 15,641,609-18,541,827 LOC105371570, RAI1-AS1, 120 more genes
    nsv6587833inversion1nstd223human GRCh38 chr17: 15,680,260-18,702,090 , GRCh37.p13 chr17: 15,583,574-18,605,403 RPLP1P11, KRT16P6, 128 more genes
    nsv6586690inversion1nstd223human GRCh38 chr17: 16,699,513-18,616,061 , GRCh37.p13 chr17: 16,602,827-18,519,374 KRT17P2, LOC105371569, 80 more genes
    nsv6579420inversion1nstd223human GRCh38 chr17: 15,711,972-18,674,503 , GRCh37.p13 chr17: 15,615,286-18,577,816 NOS2P2, LOC105371566, 124 more genes
    nsv6578694inversion1nstd223human GRCh38 chr17: 15,604,091-18,759,630 , GRCh37.p13 chr17: 15,507,405-18,662,943 TRPV2, SNORD49B, 131 more genes
    nsv6315488copy number variation1nstd102humanPathogenic GRCh37 chr17: 17,579,860-18,469,185 , GRCh38.p12 chr17: 17,676,546-18,565,871 FAM106A, EVPLL, 43 more genes
    nsv6315482copy number variation1nstd102humanPathogenic GRCh37 chr17: 17,151,140-20,187,953 , GRCh38.p12 chr17: 17,247,826-20,284,640 COPS3, KYNUP2, 116 more genes
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