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Items: 1 to 20 of 607

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7145973copy number variation1nstd232human GRCh37.p13 chr16: 18,855,831-18,855,891 , GRCh38.p12 chr16: 18,844,509-18,844,569 SMG1
    nsv7140277insertion1nstd232human GRCh37.p13 chr16: 18,826,604-18,826,604 , GRCh38.p12 chr16: 18,815,282-18,815,282 SMG1
    nsv7139411copy number variation1nstd232human GRCh37.p13 chr16: 18,823,189-18,823,268 , GRCh38.p12 chr16: 18,811,867-18,811,946 SMG1
    nsv7094815copy number variation1nstd102humanUncertain significance GRCh37 chr16: 18,794,331-19,089,480 , GRCh38.p12 chr16: 18,783,009-19,078,158 SMG1-DT, TMC7, 7 more genes
    nsv7076939inversion1nstd229human GRCh38 chr16: 15,569,413-22,730,334 , GRCh37.p13 chr16: 15,663,270-22,741,655 ACSM5P1, RNU6-213P, 154 more genes
    nsv7066233inversion1nstd229human GRCh38 chr16: 18,917,989-18,920,892 , GRCh37.p13 chr16: 18,929,311-18,932,214 SMG1
    nsv7061097inversion1nstd229human GRCh38 chr16: 18,806,607-18,806,642 , GRCh37.p13 chr16: 18,817,929-18,817,964 SMG1
    nsv7058379inversion1nstd229human GRCh38 chr16: 16,196,635-18,896,827 , GRCh37.p13 chr16: 16,290,492-18,908,149 LOC105376751, NOMO3, 46 more genes
    nsv6997878copy number variation1nstd229human GRCh38 chr16: 18,904,467-18,907,629 , GRCh37.p13 chr16: 18,915,789-18,918,951 SMG1
    nsv6997651copy number variation1nstd229human GRCh38 chr16: 18,911,601-18,918,900 , GRCh37.p13 chr16: 18,922,923-18,930,222 SMG1
    nsv6996720copy number variation1nstd229human GRCh38 chr16: 18,910,001-18,917,800 , GRCh37.p13 chr16: 18,921,323-18,929,122 SMG1
    nsv6993081copy number variation1nstd229human GRCh38 chr16: 18,909,080-18,909,125 , GRCh37.p13 chr16: 18,920,402-18,920,447 SMG1
    nsv6990643copy number variation1nstd229human GRCh38 chr16: 18,924,344-19,049,704 , GRCh37.p13 chr16: 18,935,666-19,061,026 SMG1-DT, RNU6-1340P, 2 more genes
    nsv6989721copy number variation1nstd229human GRCh38 chr16: 18,851,906-18,851,983 , GRCh37.p13 chr16: 18,863,228-18,863,305 SMG1
    nsv6987796copy number variation1nstd229human GRCh38 chr16: 18,908,711-18,926,040 , GRCh37.p13 chr16: 18,920,033-18,937,362 SMG1-DT, SMG1
    nsv6982836copy number variation1nstd229human GRCh38 chr16: 18,853,884-18,854,067 , GRCh37.p13 chr16: 18,865,206-18,865,389 SMG1
    nsv6982349copy number variation1nstd229human GRCh38 chr16: 18,911,568-18,917,735 , GRCh37.p13 chr16: 18,922,890-18,929,057 SMG1
    nsv6981314copy number variation1nstd229human GRCh38 chr16: 18,916,284-18,919,096 , GRCh37.p13 chr16: 18,927,606-18,930,418 SMG1
    nsv6979096copy number variation1nstd229human GRCh38 chr16: 18,904,201-18,907,600 , GRCh37.p13 chr16: 18,915,523-18,918,922 SMG1
    nsv6978839copy number variation1nstd229human GRCh38 chr16: 18,904,702-18,908,646 , GRCh37.p13 chr16: 18,916,024-18,919,968 SMG1
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