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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6982861copy number variation1nstd229human GRCh38 chr17: 38,291,672-47,498,259 , GRCh37.p13 chr17: 36,510,266-45,575,625 KRT20, PLEKHH3, 442 more genes
    nsv6290455copy number variation1nstd102humanPathogenic GRCh38 chr17: 44,846,894-44,962,103 , GRCh37.p13 chr17: 42,924,262-43,039,471 RN7SL405P, LOC105371793, 8 more genes
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv4330632inversion1nstd166human GRCh37.p13 chr17: 18,838,526-72,042,289 , GRCh38.p12 chr17: 18,935,213-74,046,150 , ACACA, 1499 more genes
    nsv4259677copy number variation1nstd166human GRCh37.p13 chr17: 42,979,000-42,985,200 , GRCh38.p12 chr17: 44,901,632-44,907,832 FAM187A, CCDC103, 1 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
    nsv3913552copy number variation1nstd102humanPathogenic GRCh38 chr17: 36,449,220-75,053,130 , NCBI36 chr17: 54,950,518-70,560,820 , GRCh37 chr17: 57,595,736-73,049,225 RNU6-131P, ZNF652, 1075 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
    nsv3911563copy number variation1nstd102humanPathogenic NCBI36 chr17: 45,918,236-63,677,950 , GRCh37 chr17: 48,563,237-65,936,105 , GRCh38 chr17: 36,449,220-68,170,214 PLEKHH3, CHCT1, 958 more genes
    nsv3911344copy number variation1nstd102humanPathogenic GRCh37 chr17: 37,356,126-43,706,945 , NCBI36 chr17: 34,609,652-41,062,728 , GRCh38 chr17: 39,199,873-45,629,579 IFI35, RND2, 345 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
    nsv3907100copy number variation1nstd102humanPathogenic GRCh37 chr17: 42,969,980-42,993,118 , GRCh38.p12 chr17: 44,892,612-44,915,750 EFTUD2, CCDC103, 2 more genes
    nsv3906245copy number variation1nstd102humanPathogenic GRCh37 chr17: 12,344-81,057,996 , GRCh38.p12 chr17: 162,553-83,100,251 MIR21, LOC105371899, 2366 more genes
    nsv3903684copy number variation1nstd102humanPathogenic GRCh37 chr17: 8,547-81,060,040 , GRCh38.p12 chr17: 158,756-83,102,004 MIR3185, YWHAEP6, 2366 more genes
    nsv3899740copy number variation1nstd102humanPathogenic GRCh37 chr17: 7,214-81,058,310 , GRCh38.p12 chr17: 157,423-83,100,564 P4HB, LOC105371808, 2366 more genes
    nsv3899474copy number variation1nstd102humanUncertain significance GRCh37 chr17: 42,649,083-43,659,985 , GRCh38.p12 chr17: 44,571,715-45,582,619 PLEKHM1, HIGD1B, 45 more genes
    nsv3158725copy number variation1nstd151human GRCh37 chr17: 42,979,684-42,984,761 , GRCh38.p12 chr17: 44,902,316-44,907,393 FAM187A, GFAP, 1 more genes
    esv4010335copy number variation1estd233human GRCh37 chr17: 41,468,000-43,513,000 , GRCh38.p12 chr17: 43,390,632-45,435,634 , ARL4D, 102 more genes
    nsv2786536copy number variation1nstd132human NCBI36 chr17: 40,337,025-40,345,866 , GRCh37.p13 chr17: 42,981,499-42,990,340 , GRCh38.p12 chr17: 44,904,131-44,912,972 CCDC103, GFAP, 1 more genes
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