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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5936903copy number variation1nstd209human GRCh38 chr12: 132,943,180-133,182,732 , GRCh37.p13 chr12: 133,519,766-133,759,318 ZNF84-DT, ZNF891, 10 more genes
    nsv5936503copy number variation1nstd209human GRCh38 chr12: 133,111,291-133,240,412 , GRCh37.p13 chr12: 133,687,877-133,816,998 ZNF10, ZNF268, 4 more genes
    nsv5932789copy number variation1nstd209human GRCh38 chr12: 133,101,121-133,186,346 , GRCh37.p13 chr12: 133,677,707-133,762,932 ZNF140, ZNF10, 3 more genes
    nsv5866302copy number variation2nstd209human GRCh38 chr12: 133,132,197-133,134,996 , GRCh37.p13 chr12: 133,708,783-133,711,582 ZNF10
    nsv5863444copy number variation2nstd209human GRCh38 chr12: 133,157,972-133,161,071 , GRCh37.p13 chr12: 133,734,558-133,737,657 ZNF10
    nsv5861688copy number variation2nstd209human GRCh38 chr12: 133,141,865-133,147,369 , GRCh37.p13 chr12: 133,718,451-133,723,955 ZNF10
    nsv5861537copy number variation2nstd209human GRCh38 chr12: 133,153,020-133,159,571 , GRCh37.p13 chr12: 133,729,606-133,736,157 ZNF10
    nsv5859463copy number variation2nstd209human GRCh38 chr12: 133,157,472-133,160,271 , GRCh37.p13 chr12: 133,734,058-133,736,857 ZNF10
    nsv5857366copy number variation2nstd209human GRCh38 chr12: 133,129,768-133,132,196 , GRCh37.p13 chr12: 133,706,354-133,708,782 ZNF891, ZNF10
    nsv5856742copy number variation2nstd209human GRCh38 chr12: 133,135,897-133,143,719 , GRCh37.p13 chr12: 133,712,483-133,720,305 ZNF10
    nsv5852529copy number variation2nstd209human GRCh38 chr12: 133,159,672-133,163,371 , GRCh37.p13 chr12: 133,736,258-133,739,957 ZNF10
    nsv5852108copy number variation2nstd209human GRCh38 chr12: 133,150,420-133,153,019 , GRCh37.p13 chr12: 133,727,006-133,729,605 ZNF10
    nsv5848742copy number variation2nstd209human GRCh38 chr12: 133,128,668-133,131,496 , GRCh37.p13 chr12: 133,705,254-133,708,082 ZNF891, ZNF10
    nsv5848099copy number variation2nstd209human GRCh38 chr12: 133,149,520-133,151,919 , GRCh37.p13 chr12: 133,726,106-133,728,505 ZNF10
    nsv5512936copy number variation1nstd206human GRCh38 chr12: 133,139,966-133,249,374 , GRCh37.p13 chr12: 133,716,552-133,825,960 ANHX, RNU6-717P, 2 more genes
    nsv5509019copy number variation1nstd206human GRCh38 chr12: 133,146,249-133,146,362 , GRCh37.p13 chr12: 133,722,835-133,722,948 ZNF10
    nsv5499188copy number variation1nstd206human GRCh38 chr12: 133,101,132-133,186,349 , GRCh37.p13 chr12: 133,677,718-133,762,935 ZNF10, ZNF268, 3 more genes
    nsv5495330copy number variation1nstd206human GRCh38 chr12: 133,158,288-133,181,241 , GRCh37.p13 chr12: 133,734,874-133,757,827 ZNF268, ZNF10
    nsv5356579translocation1nstd200human GRCh38 chr12: 133,146,362-133,146,362 , GRCh38 chr12: 133,146,249-133,146,249 , GRCh37.p13 chr12: 133,722,948-133,722,948 , GRCh37.p13 chr12: 133,722,835-133,722,835 ZNF10
    nsv5345922translocation1nstd200human GRCh37 chr12: 133,722,835-133,722,835 , GRCh37 chr12: 133,722,948-133,722,948 , GRCh38.p12 chr12: 133,146,249-133,146,249 , GRCh38.p12 chr12: 133,146,362-133,146,362 ZNF10
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