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Items: 1 to 20 of 281

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv7066523inversion1nstd229human GRCh38 chr17: 36,977,322-38,870,747 , GRCh37.p13 chr17: 35,372,677-37,027,000 LOC101929950, LASP1, 68 more genes
    nsv6997574copy number variation1nstd229human GRCh38 chr17: 38,379,101-38,388,400 , GRCh37.p13 chr17|NW_003315948.2: 162,312-171,952 SOCS7
    nsv6995802copy number variation1nstd229human GRCh38 chr17: 38,376,449-38,376,657 , GRCh37.p13 chr17|NW_003315948.2: 159,660-159,868 SOCS7
    nsv6994124copy number variation1nstd229human GRCh38 chr17: 38,379,384-38,388,425 , GRCh37.p13 chr17|NW_003315948.2: 162,595-171,977 SOCS7
    nsv6986387copy number variation1nstd229human GRCh38 chr17: 38,339,301-38,451,300 , GRCh37.p13 chr17: 36,546,160-36,607,544 LOC101929494, GPR179, 2 more genes
    nsv6985648copy number variation1nstd229human GRCh38 chr17: 38,371,414-38,376,845 , GRCh37.p13 chr17|NW_003315948.2: 154,685-160,056 SOCS7
    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
    nsv6978369copy number variation1nstd229human GRCh38 chr17: 38,377,844-38,385,219 , GRCh37.p13 chr17|NW_003315948.2: 161,055-168,428 SOCS7
    nsv6589276inversion1nstd223human GRCh38 chr17: 38,384,891-38,385,977 , GRCh37.p13 chr17|NW_003315948.2: 168,101-169,183 SOCS7
    nsv6587018inversion1nstd223human GRCh38 chr17: 38,398,263-38,399,114 , GRCh37.p13 chr17: 36,554,516-36,555,367 SOCS7
    nsv6509654copy number variation1nstd223human GRCh38 chr17: 38,374,096-38,376,561 , GRCh37.p13 chr17|NW_003315948.2: 157,307-159,772 SOCS7
    nsv6509104copy number variation1nstd223human GRCh38 chr17: 38,378,491-38,380,570 , GRCh37.p13 chr17|NW_003315948.2: 161,702-163,781 SOCS7
    nsv6503559copy number variation1nstd223human GRCh38 chr17: 38,379,431-38,388,394 , GRCh37.p13 chr17|NW_003315948.2: 162,642-171,946 SOCS7
    nsv6499649copy number variation1nstd223human GRCh38 chr17: 38,351,401-38,352,400 , GRCh37.p13 chr17|NW_003315948.2: 134,668-135,667 SOCS7
    nsv6197691copy number variation1nstd214human GRCh38 chr17: 38,371,489-38,371,548 , GRCh37.p13 chr17|NW_003315948.2: 154,760-154,819 SOCS7
    nsv6192798copy number variation1nstd214human GRCh38 chr17: 38,371,503-38,371,564 , GRCh37.p13 chr17|NW_003315948.2: 154,774-154,820 SOCS7
    nsv6133354copy number variation1nstd213human GRCh37 chr17: 36,490,000-36,590,001 , GRCh38.p12 chr17: 38,334,117-38,433,758 , GRCh38.p12 chr17|NT_187614.1: 2,369,065-2,469,067 SOCS7, ARHGAP23, 1 more genes
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