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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5954423insertion1nstd209human GRCh38 chr1: 102,976,289-102,976,289 , GRCh37.p13 chr1: 103,441,845-103,441,845 COL11A1
    nsv5883830copy number variation1nstd209human GRCh38 chr1: 102,949,179-102,949,502 , GRCh37.p13 chr1: 103,414,735-103,415,058 COL11A1
    nsv5879219copy number variation1nstd209human GRCh38 chr1: 103,041,847-103,042,218 , GRCh37.p13 chr1: 103,507,403-103,507,774 COL11A1
    nsv5873416copy number variation1nstd209human GRCh38 chr1: 102,875,109-102,875,200 , GRCh37.p13 chr1: 103,340,665-103,340,756 COL11A1
    nsv5872282copy number variation1nstd209human GRCh38 chr1: 102,990,410-102,990,577 , GRCh37.p13 chr1: 103,455,966-103,456,133 COL11A1
    nsv5870961copy number variation1nstd209human GRCh38 chr1: 103,108,453-103,109,310 , GRCh37.p13 chr1: 103,574,009-103,574,866 COL11A1
    nsv5868861copy number variation1nstd209human GRCh38 chr1: 103,106,166-103,106,663 , GRCh37.p13 chr1: 103,571,722-103,572,219 COL11A1
    nsv5827673copy number variation1nstd209human GRCh38 chr1: 102,925,924-102,927,023 , GRCh37.p13 chr1: 103,391,480-103,392,579 COL11A1
    nsv5720155mobile element insertion1nstd211human GRCh38 chr1: 102,972,491-102,972,491 , GRCh37.p13 chr1: 103,438,047-103,438,047 COL11A1
    nsv5716222mobile element insertion1nstd211human GRCh38 chr1: 102,885,421-102,885,421 , GRCh37.p13 chr1: 103,350,977-103,350,977 COL11A1
    nsv5685743mobile element insertion1nstd211human GRCh38 chr1: 103,083,614-103,083,614 , GRCh37.p13 chr1: 103,549,170-103,549,170 COL11A1
    nsv5681240mobile element insertion1nstd211human GRCh38 chr1: 103,032,631-103,032,631 , GRCh37.p13 chr1: 103,498,187-103,498,187 COL11A1
    nsv5679279mobile element insertion2nstd211human GRCh38 chr1: 102,970,624-102,970,624 , GRCh37.p13 chr1: 103,436,180-103,436,180 COL11A1
    nsv5677333mobile element insertion1nstd211human GRCh38 chr1: 103,067,516-103,067,516 , GRCh37.p13 chr1: 103,533,072-103,533,072 COL11A1
    nsv5676631mobile element insertion1nstd211human GRCh38 chr1: 102,958,296-102,958,296 , GRCh37.p13 chr1: 103,423,852-103,423,852 COL11A1
    nsv5676000mobile element insertion1nstd211human GRCh38 chr1: 102,890,022-102,890,022 , GRCh37.p13 chr1: 103,355,578-103,355,578 COL11A1
    nsv5673148copy number variation1nstd102humanLikely pathogenic GRCh37 chr1: 103,380,260-103,548,528 , GRCh38.p12 chr1: 102,914,704-103,082,972 COL11A1
    nsv5621384insertion1nstd207human GRCh38 chr1: 103,043,216-103,043,216 , GRCh37.p13 chr1: 103,508,772-103,508,772 COL11A1
    nsv5619531insertion1nstd207human GRCh38 chr1: 102,938,423-102,938,423 , GRCh37.p13 chr1: 103,403,979-103,403,979 COL11A1
    nsv5581023copy number variation1nstd207human GRCh38 chr1: 102,949,179-102,949,502 , GRCh37.p13 chr1: 103,414,735-103,415,058 COL11A1
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