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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112802copy number variation1nstd102humanPathogenic GRCh37 chr18: 23,626,739-78,014,976 , GRCh38.p12 chr18: 26,046,775-80,257,093 RPL9P31, LINC02582, 595 more genes
    nsv5713911mobile element insertion1nstd211human GRCh38 chr18: 54,934,019-54,934,019 , GRCh37.p13 chr18: 52,601,250-52,601,250 CCDC68
    nsv5696031mobile element insertion1nstd211human GRCh38 chr18: 54,923,272-54,923,272 , GRCh37.p13 chr18: 52,590,503-52,590,503 CCDC68
    nsv5652868insertion1nstd207human GRCh38 chr18: 54,930,653-54,930,653 , GRCh37.p13 chr18: 52,597,884-52,597,884 CCDC68
    nsv5548977insertion1nstd206human GRCh38 chr18: 54,911,240-54,911,283 , GRCh37.p13 chr18: 52,578,471-52,578,514 CCDC68
    nsv5521089copy number variation1nstd206human GRCh38 chr18: 54,936,216-54,937,574 , GRCh37.p13 chr18: 52,603,447-52,604,805 CCDC68
    nsv5514098copy number variation1nstd206human GRCh38 chr18: 54,909,566-54,909,739 , GRCh37.p13 chr18: 52,576,797-52,576,970 CCDC68
    nsv5421683mobile element insertion1nstd206human GRCh38 chr18: 54,923,272-54,923,323 , GRCh37.p13 chr18: 52,590,503-52,590,554 CCDC68
    nsv5381802copy number variation1nstd102humanPathogenic GRCh37 chr18: 51,925,586-78,010,032 , GRCh38.p12 chr18: 54,399,216-80,252,149 LOC105372200, LOC105372174, 298 more genes
    nsv5180493mobile element insertion1nstd203human GRCh38 chr18: 54,958,235-54,958,252 , GRCh37.p13 chr18: 52,625,466-52,625,483 CCDC68
    nsv5141655mobile element insertion1nstd203human GRCh38 chr18: 54,943,512-54,943,526 , GRCh37.p13 chr18: 52,610,743-52,610,757 CCDC68
    nsv5018184copy number variation1nstd200human GRCh38 chr18: 54,936,236-54,937,554 , GRCh37.p13 chr18: 52,603,467-52,604,785 CCDC68
    nsv4907437mobile element deletion1nstd200human GRCh38 chr18: 54,950,902-54,951,207 , GRCh37.p13 chr18: 52,618,133-52,618,438 CCDC68
    nsv4859697copy number variation1nstd200human GRCh37 chr18: 52,603,467-52,604,785 , GRCh38.p12 chr18: 54,936,236-54,937,554 CCDC68
    nsv4769649mobile element deletion1nstd200human GRCh37 chr18: 52,618,133-52,618,438 , GRCh38.p12 chr18: 54,950,902-54,951,207 CCDC68
    nsv4676239copy number variation1nstd102humanUncertain significance GRCh37 chr18: 51,802,787-53,000,275 , GRCh38.p12 chr18: 54,276,417-55,333,044 RAB27B, CUPIN1P, 13 more genes
    nsv4676105copy number variation1nstd102humanPathogenic GRCh37 chr18: 49,460,596-78,014,123 , GRCh38.p12 chr18: 51,934,226-80,256,240 MIR548AV, GTSCR1, 310 more genes
    nsv4633463copy number variation1nstd183human GRCh37 chr18: 52,569,737-52,574,824 , GRCh38.p12 chr18: 54,902,506-54,907,593 CCDC68
    nsv4551557insertion1nstd166human GRCh37.p13 chr18: 52,612,729-52,612,729 , GRCh38.p12 chr18: 54,945,498-54,945,498 CCDC68
    nsv4547433insertion1nstd166human GRCh37.p13 chr18: 52,612,545-52,612,545 , GRCh38.p12 chr18: 54,945,314-54,945,314 CCDC68
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