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Items: 1 to 20 of 507

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098178copy number variation1nstd102humanUncertain significance GRCh37 chr8: 56,854,419-56,882,372 , GRCh38.p12 chr8: 55,941,860-55,969,813 LYN
    nsv7076454inversion1nstd229human GRCh38 chr8: 55,838,194-55,882,800 , GRCh37.p13 chr8: 56,750,753-56,795,359 LYN
    nsv7068582inversion1nstd229human GRCh38 chr8: 55,930,521-55,939,379 , GRCh37.p13 chr8: 56,843,080-56,851,938 LYN
    nsv7067508inversion1nstd229human GRCh38 chr8: 51,755,366-56,976,322 , GRCh37.p13 chr8: 52,667,926-57,888,881 CHCHD2P10, LOC105375850, 81 more genes
    nsv7064051inversion1nstd229human GRCh38 chr8: 53,370,406-56,357,942 , GRCh37.p13 chr8: 54,282,966-57,270,501 CHCHD2P10, RN7SL798P, 51 more genes
    nsv6857820copy number variation1nstd229human GRCh38 chr8: 55,749,799-55,963,538 , GRCh37.p13 chr8: 56,662,358-56,876,097 LYN, TMEM68, 2 more genes
    nsv6857790copy number variation1nstd229human GRCh38 chr8: 55,884,516-55,888,880 , GRCh37.p13 chr8: 56,797,075-56,801,439 LYN
    nsv6857642copy number variation1nstd229human GRCh38 chr8: 55,703,411-55,989,897 , GRCh37.p13 chr8: 56,615,970-56,902,456 TMEM68, SNORA1B, 5 more genes
    nsv6855499copy number variation1nstd229human GRCh38 chr8: 55,687,037-56,004,073 , GRCh37.p13 chr8: 56,599,596-56,916,632 TGS1, RN7SL798P, 5 more genes
    nsv6855099copy number variation1nstd229human GRCh38 chr8: 55,899,017-55,899,887 , GRCh37.p13 chr8: 56,811,576-56,812,446 LYN
    nsv6854491copy number variation1nstd229human GRCh38 chr8: 56,012,001-56,140,200 , GRCh37.p13 chr8: 56,924,560-57,052,759 MOS, PSMC6P1, 6 more genes
    nsv6853547copy number variation1nstd229human GRCh38 chr8: 55,887,707-55,902,064 , GRCh37.p13 chr8: 56,800,266-56,814,623 SNORA1B, LYN
    nsv6852688copy number variation1nstd229human GRCh38 chr8: 55,902,533-55,904,664 , GRCh37.p13 chr8: 56,815,092-56,817,223 SNORA1B, LYN
    nsv6852076copy number variation1nstd229human GRCh38 chr8: 55,891,155-55,897,913 , GRCh37.p13 chr8: 56,803,714-56,810,472 LYN
    nsv6849747copy number variation1nstd229human GRCh38 chr8: 55,942,501-55,948,300 , GRCh37.p13 chr8: 56,855,060-56,860,859 LYN
    nsv6847873copy number variation1nstd229human GRCh38 chr8: 55,983,695-55,994,058 , GRCh37.p13 chr8: 56,896,254-56,906,617 LYN
    nsv6845294copy number variation1nstd229human GRCh38 chr8: 55,936,876-55,936,933 , GRCh37.p13 chr8: 56,849,435-56,849,492 LYN
    nsv6842070copy number variation1nstd229human GRCh38 chr8: 55,999,547-56,009,905 , GRCh37.p13 chr8: 56,912,106-56,922,464 LYN
    nsv6841973copy number variation1nstd229human GRCh38 chr8: 55,977,832-56,025,126 , GRCh37.p13 chr8: 56,890,391-56,937,685 RN7SL323P, RN7SL798P, 1 more genes
    nsv6840339copy number variation1nstd229human GRCh38 chr8: 55,879,834-55,879,860 , GRCh37.p13 chr8: 56,792,393-56,792,419 LYN
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