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Items: 1 to 20 of 139

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137914insertion1nstd232human GRCh37.p13 chr17: 36,916,861-36,916,861 , GRCh38.p12 chr17: 38,760,608-38,760,608 , GRCh38.p12 chr17|NT_187614.1: 2,795,927-2,795,927 PSMB3
    nsv7095149copy number variation1nstd102humanUncertain significance GRCh37 chr17: 36,891,476-37,009,963 , GRCh38.p12 chr17|NT_187614.1: 2,770,542-2,877,074 , GRCh38.p12 chr17: 38,735,223-38,853,710 PSMB3, SPMAP1, 12 more genes
    nsv7074553inversion1nstd229human GRCh38 chr17: 37,597,996-39,028,846 , GRCh37.p13 chr17: 35,958,043-36,757,019 MRPL45, PCGF2, 62 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
    nsv7072263inversion1nstd229human GRCh38 chr17: 38,748,470-38,789,669 , GRCh37.p13 chr17: 36,904,723-36,945,922 PCGF2, RNU6-866P, 4 more genes
    nsv7066523inversion1nstd229human GRCh38 chr17: 36,977,322-38,870,747 , GRCh37.p13 chr17: 35,372,677-37,027,000 LOC101929950, LASP1, 68 more genes
    nsv6985552copy number variation1nstd229human GRCh38 chr17: 38,734,511-38,764,179 , GRCh37.p13 chr17: 36,890,764-36,920,432 TRN-GTT2-5, PCGF2, 5 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
    nsv6133355copy number variation2nstd213human GRCh37 chr17: 36,830,000-37,070,001 , GRCh38.p12 chr17: 38,673,747-38,913,748 , GRCh38.p12 chr17|NT_187614.1: 2,709,066-2,877,074 LASP1, MLLT6, 24 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
    nsv6036469copy number variation1nstd212human GRCh38 chr17: 38,763,598-38,763,670 , GRCh37.p13 chr17: 36,919,851-36,919,923 PSMB3
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5520034copy number variation1nstd206human GRCh38 chr17: 38,751,735-38,751,794 , GRCh37.p13 chr17: 36,907,988-36,908,047 PSMB3, TRN-GTT2-5, 1 more genes
    nsv4675332copy number variation1nstd102humanUncertain significance GRCh37 chr17: 36,710,984-37,295,662 , GRCh38.p12 chr17: 38,600,767-39,139,409 PIP4K2B, PSMB3, 32 more genes
    nsv4550156insertion1nstd166human GRCh37.p13 chr17: 36,907,988-36,907,988 , GRCh38.p12 chr17: 38,751,735-38,751,735 , GRCh38.p12 chr17|NT_187614.1: 2,787,054-2,787,054 PSMB3, TRN-GTT2-5, 1 more genes
    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
    nsv4366314copy number variation1nstd173human GRCh37 chr17: 36,898,585-36,932,200 , GRCh38.p12 chr17: 38,742,332-38,775,947 , GRCh38.p12 chr17|NT_187614.1: 2,777,651-2,811,266 PCGF2, RNU6-866P, 4 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
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