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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5014073copy number variation1nstd200human GRCh38 chr17: 78,919,633-79,477,545 , GRCh37.p13 chr17: 76,915,715-77,412,183 TIMP2, LGALS3BP, 5 more genes
    nsv4729773copy number variation1nstd102humanUncertain significance GRCh37 chr17: 76,852,029-77,297,898 , GRCh38.p12 chr17: 78,855,947-79,301,816 C1QTNF1, CANT1, 6 more genes
    nsv4676104copy number variation1nstd102humanPathogenic GRCh37 chr17: 73,261,871-78,608,763 , GRCh38.p12 chr17: 75,265,790-80,634,963 LLGL2, TSEN54, 165 more genes
    nsv4457695copy number variation2nstd102humanUncertain significance GRCh37 chr17: 76,857,398-77,308,782 , GRCh38.p12 chr17: 78,861,316-79,312,700 CEP295NL, C1QTNF1-AS1, 6 more genes
    nsv4457646copy number variation1nstd102humanPathogenic GRCh37 chr17: 62,778,720-81,041,938 , GRCh38.p12 chr17: 64,782,602-83,084,062 LOC107985089, ARSG, 448 more genes
    nsv4271462copy number variation1nstd166human GRCh37.p13 chr17: 77,022,301-77,026,768 , GRCh38.p12 chr17: 79,026,219-79,030,686 C1QTNF1-AS1, C1QTNF1
    nsv4262229copy number variation1nstd166human GRCh37.p13 chr17: 76,649,383-77,059,909 , GRCh38.p12 chr17: 78,653,301-79,063,827 , CEP295NL, 9 more genes
    nsv3959638copy number variation1nstd168human GRCh38 chr17: 79,008,351-79,090,101 , GRCh37.p13 chr17: 77,004,433-77,086,183 CANT1, RBFOX3, 3 more genes
    nsv3920061copy number variation1nstd102humanLikely pathogenic NCBI36 chr17: 73,733,032-75,688,373 , GRCh37 chr17: 76,221,437-78,073,778 , GRCh38 chr17: 78,225,356-80,099,979 BIRC5, GAA, 38 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 LINC03048, MIR3186, 154 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 CD300A, RNF213, 359 more genes
    nsv3917730copy number variation1nstd102humanUncertain significance GRCh38 chr17: 78,484,862-79,436,025 , NCBI36 chr17: 73,992,539-74,943,702 , GRCh37 chr17: 76,480,944-77,432,107 C1QTNF1, TIMP2, 15 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 LOC101928447, GRB2, 368 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 LOC105371922, GJD3, 1855 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 MIR338, DUS1L, 127 more genes
    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 PRPSAP1, CACNG1, 1350 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 ANAPC11, GPS1, 125 more genes
    nsv3909523copy number variation1nstd102humanPathogenic GRCh37 chr17: 63,689,671-81,041,938 , GRCh38.p12 chr17: 65,693,553-83,084,062 RPL38, RNF157-AS1, 428 more genes
    nsv3909511copy number variation1nstd102humanPathogenic GRCh37 chr17: 42,580,684-81,085,615 , GRCh38.p12 chr17: 44,503,316-83,137,846 FOXK2, SOCS3-DT, 958 more genes
    nsv3907261copy number variation2nstd102humanPathogenic GRCh37 chr17: 526-81,041,938 , GRCh38.p12 chr17: 150,733-83,084,062 SMURF2, LOC112268199, 2366 more genes
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