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Items: 1 to 20 of 184

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095150copy number variation1nstd102humanUncertain significance GRCh37 chr17: 37,821,613-38,458,253 , GRCh38.p12 chr17: 39,665,360-40,302,001 ZPBP2, MED24, 28 more genes
    nsv7073998inversion1nstd229human GRCh38 chr17: 32,918,710-41,148,753 , GRCh37.p13 chr17: 31,245,728-39,305,005 LOC105371750, C17orf78, 298 more genes
    nsv6988913copy number variation1nstd229human GRCh38 chr17: 40,094,124-40,094,931 , GRCh37.p13 chr17: 38,250,377-38,251,184 THRA, NR1D1
    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
    nsv6983429copy number variation1nstd229human GRCh38 chr17: 40,091,247-40,091,272 , GRCh37.p13 chr17: 38,247,500-38,247,525 THRA, NR1D1
    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
    nsv6133056copy number variation1nstd213human GRCh37 chr17: 36,400,000-39,740,001 , GRCh38.p12 chr17: 38,545,381-41,583,749 CACNB1, CDC6, 176 more genes
    nsv6021715copy number variation1nstd212human GRCh38 chr17: 40,079,307-40,079,773 , GRCh37.p13 chr17: 38,235,560-38,236,026 THRA
    nsv6021310copy number variation1nstd212human GRCh38 chr17: 40,069,083-40,069,163 , GRCh37.p13 chr17: 38,225,336-38,225,416 THRA
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5283669copy number variation1nstd204human GRCh38.p13 chr17: 39,851,001-40,379,500 , GRCh37.p13 chr17: 38,007,254-38,535,752 , CASC3, 27 more genes
    nsv5013689copy number variation1nstd200human GRCh38 chr17: 40,056,050-40,061,350 , GRCh37.p13 chr17: 38,212,303-38,217,603 THRA
    nsv4628986copy number variation1nstd183human GRCh37 chr17: 38,215,916-38,530,107 , GRCh38.p12 chr17: 40,059,663-40,373,855 PPIAP54, MSL1, 14 more genes
    nsv4531196copy number variation1nstd166human GRCh37.p13 chr17: 38,243,387-38,243,463 , GRCh38.p12 chr17: 40,087,134-40,087,210 THRA
    nsv4457831copy number variation1nstd102humanPathogenic GRCh37 chr17: 21,690,653-38,772,647 , GRCh38.p12 chr17: 22,164,047-40,616,395 LOC105371753, TAOK1, 474 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
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