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Items: 1 to 20 of 406

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5974834insertion1nstd209human GRCh38 chr17: 62,015,955-62,015,955 , GRCh37.p13 chr17: 60,093,316-60,093,316 MED13
    nsv5932179copy number variation1nstd209human GRCh38 chr17: 62,058,985-62,059,097 , GRCh37.p13 chr17: 60,136,346-60,136,458 MED13
    nsv5931068copy number variation1nstd209human GRCh38 chr17: 61,980,776-61,981,055 , GRCh37.p13 chr17: 60,058,137-60,058,416 MED13
    nsv5930514copy number variation1nstd209human GRCh38 chr17: 61,957,989-61,958,291 , GRCh37.p13 chr17: 60,035,350-60,035,652 MED13
    nsv5713604mobile element insertion2nstd211human GRCh38 chr17: 62,036,498-62,036,498 , GRCh37.p13 chr17: 60,113,859-60,113,859 MED13
    nsv5710888mobile element insertion2nstd211human GRCh38 chr17: 61,965,964-61,965,964 , GRCh37.p13 chr17: 60,043,325-60,043,325 MED13
    nsv5708996mobile element insertion1nstd211human GRCh38 chr17: 61,953,723-61,953,723 , GRCh37.p13 chr17: 60,031,084-60,031,084 MED13
    nsv5704063mobile element insertion1nstd211human GRCh38 chr17: 62,019,430-62,019,430 , GRCh37.p13 chr17: 60,096,791-60,096,791 MED13
    nsv5555542sequence alteration1nstd206human GRCh38 chr17: 62,013,503-62,013,865 , GRCh37.p13 chr17: 60,090,864-60,091,226 MED13
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5545409insertion1nstd206human GRCh38 chr17: 62,013,504-62,013,504 , GRCh37.p13 chr17: 60,090,865-60,090,865 MED13
    nsv5533104copy number variation1nstd206human GRCh38 chr17: 62,012,573-62,016,101 , GRCh37.p13 chr17: 60,089,934-60,093,462 MED13
    nsv5531157copy number variation1nstd206human GRCh38 chr17: 62,015,880-62,016,530 , GRCh37.p13 chr17: 60,093,241-60,093,891 MED13
    nsv5531085copy number variation1nstd206human GRCh38 chr17: 62,048,670-62,048,741 , GRCh37.p13 chr17: 60,126,031-60,126,102 MED13
    nsv5518055copy number variation1nstd206human GRCh38 chr17: 62,002,724-62,009,487 , GRCh37.p13 chr17: 60,080,085-60,086,848 MED13, RN7SL800P
    nsv5433703mobile element insertion1nstd206human GRCh38 chr17: 61,965,964-61,966,015 , GRCh37.p13 chr17: 60,043,325-60,043,376 MED13
    nsv5418358mobile element insertion1nstd206human GRCh38 chr17: 61,953,723-61,953,774 , GRCh37.p13 chr17: 60,031,084-60,031,135 MED13
    nsv5417148mobile element insertion1nstd206human GRCh38 chr17: 62,036,498-62,036,549 , GRCh37.p13 chr17: 60,113,859-60,113,910 MED13
    nsv5414070mobile element insertion1nstd206human GRCh38 chr17: 62,019,430-62,019,481 , GRCh37.p13 chr17: 60,096,791-60,096,842 MED13
    nsv5384970mobile element deletion1nstd186human GRCh37 chr17: 60,085,397-60,085,678 , GRCh38.p12 chr17: 62,008,036-62,008,317 MED13
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