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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5980305insertion1nstd209human GRCh38 chr18: 24,045,920-24,045,920 , GRCh37.p13 chr18: 21,625,884-21,625,884 TTC39C
    nsv5977576insertion1nstd209human GRCh38 chr18: 24,092,123-24,092,123 , GRCh37.p13 chr18: 21,672,087-21,672,087 TTC39C
    nsv5971729insertion1nstd209human GRCh38 chr18: 24,045,417-24,045,417 , GRCh37.p13 chr18: 21,625,381-21,625,381 TTC39C
    nsv5943335copy number variation1nstd209human GRCh38 chr18: 24,030,837-24,031,148 , GRCh37.p13 chr18: 21,610,801-21,611,112 TTC39C
    nsv5935856copy number variation1nstd209human GRCh38 chr18: 24,046,200-24,047,354 , GRCh37.p13 chr18: 21,626,164-21,627,318 TTC39C
    nsv5932371copy number variation1nstd209human GRCh38 chr18: 24,107,932-24,108,021 , GRCh37.p13 chr18: 21,687,896-21,687,985 TTC39C
    nsv5885424copy number variation1nstd209human GRCh38 chr18: 24,046,141-24,047,340 , GRCh37.p13 chr18: 21,626,105-21,627,304 TTC39C
    nsv5703941mobile element insertion1nstd211human GRCh38 chr18: 24,039,694-24,039,694 , GRCh37.p13 chr18: 21,619,658-21,619,658 TTC39C
    nsv5699716mobile element insertion1nstd211human GRCh38 chr18: 24,092,125-24,092,125 , GRCh37.p13 chr18: 21,672,089-21,672,089 TTC39C
    nsv5660103insertion1nstd207human GRCh38 chr18: 24,023,974-24,023,974 , GRCh37.p13 chr18: 21,603,938-21,603,938 TTC39C
    nsv5587599copy number variation1nstd207human GRCh38 chr18: 24,023,933-24,023,982 , GRCh37.p13 chr18: 21,603,897-21,603,946 TTC39C
    nsv5547210insertion1nstd206human GRCh38 chr18: 24,023,990-24,024,010 , GRCh37.p13 chr18: 21,603,954-21,603,974 TTC39C
    nsv5532142copy number variation1nstd206human GRCh38 chr18: 24,107,936-24,108,022 , GRCh37.p13 chr18: 21,687,900-21,687,986 TTC39C
    nsv5530918copy number variation1nstd206human GRCh38 chr18: 24,051,001-24,051,119 , GRCh37.p13 chr18: 21,630,965-21,631,083 TTC39C
    nsv5525979copy number variation1nstd206human GRCh38 chr18: 24,042,819-24,053,265 , GRCh37.p13 chr18: 21,622,783-21,633,229 TTC39C
    nsv5521067copy number variation1nstd206human GRCh38 chr18: 24,078,412-24,078,486 , GRCh37.p13 chr18: 21,658,376-21,658,450 TTC39C
    nsv5515630copy number variation1nstd206human GRCh38 chr18: 24,027,094-24,027,185 , GRCh37.p13 chr18: 21,607,058-21,607,149 TTC39C
    nsv5515380copy number variation1nstd206human GRCh38 chr18: 24,045,883-24,045,961 , GRCh37.p13 chr18: 21,625,847-21,625,925 TTC39C
    nsv5414315mobile element insertion1nstd206human GRCh38 chr18: 24,039,694-24,039,745 , GRCh37.p13 chr18: 21,619,658-21,619,709 TTC39C
    nsv5392382copy number variation1nstd186human GRCh37 chr18: 21,626,195-21,627,282 , GRCh38.p12 chr18: 24,046,231-24,047,318 TTC39C
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