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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3911811copy number variation1nstd102humanPathogenic NCBI36 chr17: 31,824,931-78,654,742 , GRCh37.p13 chr17: 34,750,818-81,048,189 , GRCh38.p12 chr17: 36,382,248-83,103,577 CEP131, PRPSAP1, 1350 more genes
    nsv3903684copy number variation1nstd102humanPathogenic GRCh37 chr17: 8,547-81,060,040 , GRCh38.p12 chr17: 158,756-83,102,004 CEP131, MIR3185, 2366 more genes
    nsv3899740copy number variation1nstd102humanPathogenic GRCh37 chr17: 7,214-81,058,310 , GRCh38.p12 chr17: 157,423-83,100,564 CEP131, P4HB, 2366 more genes
    nsv3906245copy number variation1nstd102humanPathogenic GRCh37 chr17: 12,344-81,057,996 , GRCh38.p12 chr17: 162,553-83,100,251 CEP131, MIR21, 2366 more genes
    nsv3907261copy number variation2nstd102humanPathogenic GRCh37 chr17: 526-81,041,938 , GRCh38.p12 chr17: 150,733-83,084,062 CEP131, SMURF2, 2366 more genes
    nsv3914783copy number variation1nstd102humanPathogenic NCBI36 chr17: 16,698,288-78,654,742 , GRCh37.p13 chr17: 16,757,563-81,048,189 , GRCh38.p12 chr17: 16,854,249-83,103,577 CEP131, LOC105371922, 1855 more genes
    nsv3909511copy number variation1nstd102humanPathogenic GRCh37 chr17: 42,580,684-81,085,615 , GRCh38.p12 chr17: 44,503,316-83,137,846 CEP131, FOXK2, 958 more genes
    nsv4457646copy number variation1nstd102humanPathogenic GRCh37 chr17: 62,778,720-81,041,938 , GRCh38.p12 chr17: 64,782,602-83,084,062 CEP131, LOC107985089, 448 more genes
    nsv3909523copy number variation1nstd102humanPathogenic GRCh37 chr17: 63,689,671-81,041,938 , GRCh38.p12 chr17: 65,693,553-83,084,062 CEP131, RPL38, 428 more genes
    nsv3906075copy number variation1nstd102humanPathogenic GRCh37 chr17: 67,002,415-81,041,938 , GRCh38.p12 chr17: 69,006,274-83,084,062 CEP131, RPTOR, 374 more genes
    nsv3917654copy number variation1nstd102humanPathogenic NCBI36 chr17: 64,716,815-78,637,842 , GRCh37 chr17: 67,205,220-81,044,553 , GRCh38 chr17: 69,209,079-83,086,677 CEP131, LOC101928447, 368 more genes
    nsv3919156copy number variation1nstd102humanPathogenic GRCh38 chr17: 69,916,435-83,102,552 , GRCh37 chr17: 67,912,576-81,048,189 , NCBI36 chr17: 65,424,171-78,653,717 CEP131, CD300A, 359 more genes
    nsv6315182copy number variation1nstd102humanPathogenic GRCh37 chr17: 73,481,509-81,043,199 , GRCh38.p12 chr17: 75,485,428-83,085,323 CEP131, DUS1L, 252 more genes
    nsv3897835copy number variation1nstd102humanPathogenic GRCh37 chr17: 73,951,701-81,041,938 , GRCh38.p12 chr17: 75,955,620-83,084,062 CEP131, ARHGDIA, 230 more genes
    nsv3919635copy number variation1nstd102humanPathogenic GRCh37 chr17: 76,088,317-81,044,553 , NCBI36 chr17: 73,599,912-78,637,842 , GRCh38 chr17: 78,092,236-83,086,677 CEP131, LINC03048, 154 more genes
    nsv3914738copy number variation1nstd102humanPathogenic NCBI36 chr17: 74,409,636-78,637,842 , GRCh37 chr17: 76,898,041-81,044,553 , GRCh38 chr17: 78,901,959-83,086,677 CEP131, MIR338, 127 more genes
    nsv3911388copy number variation1nstd102humanPathogenic GRCh37 chr17: 76,914,732-80,978,971 , NCBI36 chr17: 74,426,327-78,572,260 , GRCh38 chr17: 78,918,650-83,021,095 CEP131, ANAPC11, 125 more genes
    nsv4457483copy number variation1nstd102humanPathogenic GRCh37 chr17: 78,608,912-81,041,938 , GRCh38.p12 chr17: 80,635,112-83,084,062 CEP131, HEXD, 94 more genes
    nsv3913720copy number variation1nstd102humanPathogenic GRCh38 chr17: 81,008,196-83,102,584 , GRCh37 chr17: 78,981,996-81,048,189 , NCBI36 chr17: 76,596,591-78,653,749 CEP131, LOC105376789, 89 more genes
    nsv3891353copy number variation1nstd102humanLikely pathogenic GRCh37 chr17: 76,552,611-81,041,938 , GRCh38.p12 chr17: 78,556,529-83,084,062 CEP131, ACTG1, 133 more genes
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