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Items: 1 to 20 of 257

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112787copy number variation1nstd102humanUncertain significance GRCh37 chr22: 17,443,623-17,663,651 , GRCh38.p12 chr22: 16,962,733-17,182,761 IL17RA, HDHD5, 9 more genes
    nsv5975830insertion1nstd209human GRCh38 chr22: 17,094,666-17,094,666 , GRCh37.p13 chr22: 17,575,556-17,575,556 IL17RA
    nsv5707788mobile element insertion1nstd211human GRCh38 chr22: 17,113,014-17,113,014 , GRCh37.p13 chr22: 17,593,904-17,593,904 IL17RA
    nsv5671119insertion1nstd207human GRCh38 chr22: 17,103,951-17,103,951 , GRCh37.p13 chr22: 17,584,841-17,584,841 IL17RA
    nsv5666934insertion1nstd207human GRCh38 chr22: 17,094,665-17,094,665 , GRCh37.p13 chr22: 17,575,555-17,575,555 IL17RA
    nsv5602561copy number variation1nstd207human GRCh38 chr22: 17,104,031-17,104,108 , GRCh37.p13 chr22: 17,584,921-17,584,998 IL17RA
    nsv5597311copy number variation1nstd207human GRCh38 chr22: 17,103,953-17,104,112 , GRCh37.p13 chr22: 17,584,843-17,585,002 IL17RA
    nsv5381150copy number variation1nstd102humanUncertain significance GRCh37 chr22: 17,565,962-17,672,720 , GRCh38.p12 chr22: 17,085,072-17,191,830 ADA2, LINC01664, 6 more genes
    nsv5328655copy number variation1nstd204human GRCh38.p13 chr22: 17,101,257-17,161,299 , GRCh37.p13 chr22: 17,582,147-17,642,189 LINC01664, IL17RA, 3 more genes
    nsv5324343copy number variation1nstd204human GRCh38.p13 chr22: 17,098,951-17,100,089 , GRCh37.p13 chr22: 17,579,841-17,580,979 IL17RA
    nsv5294496copy number variation1nstd204human GRCh38.p13 chr22: 17,098,861-17,100,280 , GRCh37.p13 chr22: 17,579,751-17,581,170 IL17RA
    nsv5288966copy number variation1nstd204human GRCh38.p13 chr22: 17,101,306-17,124,335 , GRCh37.p13 chr22: 17,582,196-17,605,225 TMEM121B, LINC01664, 1 more genes
    nsv5285011copy number variation1nstd204human GRCh38.p13 chr22: 17,099,001-17,100,100 , GRCh37.p13 chr22: 17,579,891-17,580,990 IL17RA
    nsv5038027copy number variation1nstd200human GRCh38 chr22: 17,098,958-17,100,086 , GRCh37.p13 chr22: 17,579,848-17,580,976 IL17RA
    nsv5036743copy number variation1nstd200human GRCh38 chr22: 16,139,338-17,135,853 , GRCh37.p13 chr22: 16,884,806-17,616,743 , ANKRD62P1, 35 more genes
    nsv5033852copy number variation1nstd200human GRCh38 chr22: 17,093,761-17,096,862 , GRCh37.p13 chr22: 17,574,651-17,577,752 RPL31P62, IL17RA
    nsv5031564copy number variation1nstd200human GRCh38 chr22: 17,075,993-17,083,046 , GRCh37.p13 chr22: 17,556,883-17,563,936 IL17RA
    nsv4869333copy number variation1nstd200human GRCh37 chr22: 17,556,883-17,563,936 , GRCh38.p12 chr22: 17,075,993-17,083,046 IL17RA
    nsv4868934copy number variation1nstd200human GRCh37 chr22: 17,579,848-17,580,976 , GRCh38.p12 chr22: 17,098,958-17,100,086 IL17RA
    nsv4868933copy number variation1nstd200human GRCh37 chr22: 17,560,042-17,563,876 , GRCh38.p12 chr22: 17,079,152-17,082,986 IL17RA
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