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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6806195copy number variation1nstd229human GRCh38 chr6: 136,702,974-136,712,421 , GRCh37.p13 chr6: 137,024,112-137,033,559 MAP3K5
    nsv6808703copy number variation1nstd229human GRCh38 chr6: 136,608,050-136,613,443 , GRCh37.p13 chr6: 136,929,188-136,934,581 MAP3K5
    nsv6808762copy number variation1nstd229human GRCh38 chr6: 136,683,234-136,687,982 , GRCh37.p13 chr6: 137,004,372-137,009,120 MAP3K5
    nsv6802415copy number variation1nstd229human GRCh38 chr6: 136,763,994-136,767,961 , GRCh37.p13 chr6: 137,085,132-137,089,099 MAP3K5
    nsv6815638copy number variation1nstd229human GRCh38 chr6: 136,757,019-136,760,338 , GRCh37.p13 chr6: 137,078,157-137,081,476 MAP3K5
    nsv6809894copy number variation1nstd229human GRCh38 chr6: 136,762,091-136,765,057 , GRCh37.p13 chr6: 137,083,229-137,086,195 MAP3K5
    nsv6808358copy number variation1nstd229human GRCh38 chr6: 136,763,301-136,766,100 , GRCh37.p13 chr6: 137,084,439-137,087,238 MAP3K5
    nsv6800723copy number variation1nstd229human GRCh38 chr6: 136,593,691-136,596,488 , GRCh37.p13 chr6: 136,914,829-136,917,626 MAP3K5
    nsv6799879copy number variation1nstd229human GRCh38 chr6: 136,686,322-136,687,007 , GRCh37.p13 chr6: 137,007,460-137,008,145 MAP3K5
    nsv6804813copy number variation1nstd229human GRCh38 chr6: 136,559,362-136,559,413 , GRCh37.p13 chr6: 136,880,500-136,880,551 MAP3K5
    nsv6814454copy number variation1nstd229human GRCh38 chr6: 136,622,813-136,622,844 , GRCh37.p13 chr6: 136,943,951-136,943,982 MAP3K5
    nsv6601627copy number variation1nstd223human GRCh38 chr6: 136,651,001-136,653,400 , GRCh37.p13 chr6: 136,972,139-136,974,538 MAP3K5
    nsv6612376copy number variation1nstd223human GRCh38 chr6: 136,554,407-136,555,359 , GRCh37.p13 chr6: 136,875,545-136,876,497 MAP3K5
    nsv6617154copy number variation1nstd223human GRCh38 chr6: 136,651,301-136,652,200 , GRCh37.p13 chr6: 136,972,439-136,973,338 MAP3K5
    nsv6609943copy number variation1nstd223human GRCh38 chr6: 136,686,290-136,687,039 , GRCh37.p13 chr6: 137,007,428-137,008,177 MAP3K5
    nsv6602604copy number variation1nstd223human GRCh38 chr6: 136,668,249-136,668,821 , GRCh37.p13 chr6: 136,989,387-136,989,959 MAP3K5
    nsv6612949copy number variation1nstd223human GRCh38 chr6: 136,717,574-136,717,969 , GRCh37.p13 chr6: 137,038,712-137,039,107 MAP3K5
    nsv5458927copy number variation1nstd206human GRCh38 chr6: 136,763,994-136,767,961 , GRCh37.p13 chr6: 137,085,132-137,089,099 MAP3K5
    nsv5463299copy number variation1nstd206human GRCh38 chr6: 136,663,901-136,665,598 , GRCh37.p13 chr6: 136,985,039-136,986,736 MAP3K5
    nsv5471089copy number variation1nstd206human GRCh38 chr6: 136,671,383-136,672,434 , GRCh37.p13 chr6: 136,992,521-136,993,572 MAP3K5
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