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Items: 1 to 20 of 140

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6985340copy number variation1nstd229human GRCh38 chr17: 42,003,901-42,110,700 , GRCh37.p13 chr17: 40,155,919-40,262,718 , GRCh37.p13 chr17|NW_003571052.1: 290,543-397,342 ZNF385C, NKIRAS2, 3 more genes
    nsv6984984copy number variation1nstd229human GRCh38 chr17: 38,377,708-42,855,253 , GRCh37.p13 chr17: 36,701,616-41,007,270 ZNF385C, AOC2, 248 more genes
    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
    nsv6133357copy number variation1nstd213human GRCh37 chr17: 39,920,000-40,260,001 , GRCh38.p12 chr17: 41,763,748-42,107,983 ACLY, CNP, 12 more genes
    nsv6133061copy number variation1nstd213human GRCh37 chr17: 39,870,000-40,890,001 , GRCh38.p12 chr17: 41,713,748-42,737,983 ACLY, ATP6V0A1, 51 more genes
    nsv6133060copy number variation1nstd213human GRCh37 chr17: 39,870,000-40,880,001 , GRCh38.p12 chr17: 41,713,748-42,727,983 ACLY, ATP6V0A1, 51 more genes
    nsv5562780sequence alteration1nstd206human GRCh38 chr17: 41,964,018-42,255,340 , GRCh37.p13 chr17|NW_003571052.1: 250,660-412,535 , GRCh37.p13 chr17: 40,116,036-40,277,911 KAT2A, STAT5B, 13 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
    nsv4680071copy number variation1nstd189human GRCh37.p13 chr17: 39,432,725-40,293,644 , GRCh38.p12 chr17: 41,276,473-42,141,626 ACLY, CNP, 50 more genes
    nsv4623642copy number variation1nstd183human GRCh37 chr17: 40,177,853-40,515,234 , GRCh38.p12 chr17: 42,025,835-42,363,216 NKIRAS2, STAT3, 12 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
    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
    nsv3907261copy number variation2nstd102humanPathogenic GRCh37 chr17: 526-81,041,938 , GRCh38.p12 chr17: 150,733-83,084,062 SMURF2, LOC112268199, 2366 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
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