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Items: 1 to 20 of 658

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112726copy number variation1nstd102humanPathogenic GRCh37 chr6: 133,810,210-140,046,615 , GRCh38.p12 chr6: 133,489,072-139,725,478 SIMALR, MTFR2, 99 more genes
    nsv5968494inversion1nstd209human GRCh38 chr6: 125,606,968-134,343,905 , GRCh37.p13 chr6: 125,928,114-134,665,043 , ARG1, 137 more genes
    nsv5957596insertion1nstd209human GRCh38 chr6: 133,439,049-133,439,049 , GRCh37.p13 chr6: 133,760,187-133,760,187 EYA4
    nsv5955096insertion1nstd209human GRCh38 chr6: 133,342,587-133,342,587 , GRCh37.p13 chr6: 133,663,725-133,663,725 EYA4
    nsv5954798insertion1nstd209human GRCh38 chr6: 133,410,619-133,410,619 , GRCh37.p13 chr6: 133,731,757-133,731,757 EYA4
    nsv5954037insertion1nstd209human GRCh38 chr6: 133,481,020-133,481,020 , GRCh37.p13 chr6: 133,802,158-133,802,158 EYA4
    nsv5907344copy number variation1nstd209human GRCh38 chr6: 133,388,280-133,393,431 , GRCh37.p13 chr6: 133,709,418-133,714,569 EYA4
    nsv5905255copy number variation1nstd209human GRCh38 chr6: 133,502,724-133,502,803 , GRCh37.p13 chr6: 133,823,862-133,823,941 TARID, EYA4
    nsv5904279copy number variation1nstd209human GRCh38 chr6: 133,346,690-133,346,982 , GRCh37.p13 chr6: 133,667,828-133,668,120 EYA4
    nsv5902457copy number variation1nstd209human GRCh38 chr6: 133,507,816-133,507,881 , GRCh37.p13 chr6: 133,828,954-133,829,019 EYA4, TARID
    nsv5901981copy number variation1nstd209human GRCh38 chr6: 133,258,105-133,258,192 , GRCh37.p13 chr6: 133,579,243-133,579,330 EYA4
    nsv5898669copy number variation1nstd209human GRCh38 chr6: 133,285,059-133,285,153 , GRCh37.p13 chr6: 133,606,197-133,606,291 EYA4
    nsv5887767copy number variation1nstd209human GRCh38 chr6: 133,424,630-133,426,223 , GRCh37.p13 chr6: 133,745,768-133,747,361 EYA4
    nsv5844379copy number variation1nstd209human GRCh38 chr6: 133,349,558-133,351,157 , GRCh37.p13 chr6: 133,670,696-133,672,295 EYA4
    nsv5844286copy number variation1nstd209human GRCh38 chr6: 133,424,584-133,426,283 , GRCh37.p13 chr6: 133,745,722-133,747,421 EYA4
    nsv5844029copy number variation1nstd209human GRCh38 chr6: 133,357,137-133,365,113 , GRCh37.p13 chr6: 133,678,275-133,686,251 EYA4
    nsv5722048mobile element insertion2nstd211human GRCh38 chr6: 133,304,863-133,304,863 , GRCh37.p13 chr6: 133,626,001-133,626,001 EYA4
    nsv5717124mobile element insertion1nstd211human GRCh38 chr6: 133,356,970-133,356,970 , GRCh37.p13 chr6: 133,678,108-133,678,108 EYA4
    nsv5716521mobile element insertion2nstd211human GRCh38 chr6: 133,374,874-133,374,874 , GRCh37.p13 chr6: 133,696,012-133,696,012 EYA4
    nsv5694238mobile element insertion2nstd211human GRCh38 chr6: 133,486,345-133,486,345 , GRCh37.p13 chr6: 133,807,483-133,807,483 EYA4
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