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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5979093inversion1nstd209human GRCh38 chr7: 150,023,235-154,074,108 , GRCh37.p13 chr7: 149,720,324-153,771,193 , AOC1, 98 more genes
    nsv5921021copy number variation1nstd209human GRCh38 chr7: 151,999,215-152,001,677 , GRCh37.p13 chr7: 151,696,300-151,698,762 GALNTL5
    nsv5918922copy number variation1nstd209human GRCh38 chr7: 151,979,377-151,981,002 , GRCh37.p13 chr7: 151,676,462-151,678,087 GALNTL5
    nsv5917259copy number variation1nstd209human GRCh38 chr7: 152,008,209-152,008,311 , GRCh37.p13 chr7: 151,705,294-151,705,396 GALNTL5
    nsv5915134copy number variation1nstd209human GRCh38 chr7: 151,974,113-151,974,288 , GRCh37.p13 chr7: 151,671,198-151,671,373 GALNTL5
    nsv5863821copy number variation1nstd209human GRCh38 chr7: 151,971,671-151,982,341 , GRCh37.p13 chr7: 151,668,756-151,679,426 GALNTL5
    nsv5861958copy number variation2nstd209human GRCh38 chr7: 151,979,379-151,981,048 , GRCh37.p13 chr7: 151,676,464-151,678,133 GALNTL5
    nsv5860467copy number variation2nstd209human GRCh38 chr7: 151,999,173-152,001,672 , GRCh37.p13 chr7: 151,696,258-151,698,757 GALNTL5
    nsv5706029mobile element insertion1nstd211human GRCh38 chr7: 151,995,390-151,995,390 , GRCh37.p13 chr7: 151,692,475-151,692,475 GALNTL5
    nsv5696922mobile element insertion2nstd211human GRCh38 chr7: 151,962,451-151,962,451 , GRCh37.p13 chr7: 151,659,536-151,659,536 GALNTL5
    nsv5571296copy number variation1nstd207human GRCh38 chr7: 151,974,113-151,974,288 , GRCh37.p13 chr7: 151,671,198-151,671,373 GALNTL5
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5542239insertion1nstd206human GRCh38 chr7: 151,969,577-151,969,577 , GRCh37.p13 chr7: 151,666,662-151,666,662 GALNTL5
    nsv5491406copy number variation1nstd206human GRCh38 chr7: 151,974,117-151,974,289 , GRCh37.p13 chr7: 151,671,202-151,671,374 GALNTL5
    nsv5489433copy number variation1nstd206human GRCh38 chr7: 151,989,259-151,991,165 , GRCh37.p13 chr7: 151,686,344-151,688,250 GALNTL5
    nsv5486472copy number variation1nstd206human GRCh38 chr7: 151,979,403-151,980,926 , GRCh37.p13 chr7: 151,676,488-151,678,011 GALNTL5
    nsv5484984copy number variation1nstd206human GRCh38 chr7: 152,012,850-152,015,323 , GRCh37.p13 chr7: 151,709,935-151,712,408 GALNTL5
    nsv5480747copy number variation1nstd206human GRCh38 chr7: 151,971,417-151,974,769 , GRCh37.p13 chr7: 151,668,502-151,671,854 GALNTL5
    nsv5381638copy number variation1nstd102humanUncertain significance GRCh37 chr7: 151,262,800-152,373,170 , GRCh38.p12 chr7: 151,565,714-152,676,085 KMT2C, RPS20P19, 17 more genes
    nsv5381637copy number variation1nstd102humanUncertain significance GRCh37 chr7: 150,642,453-152,373,165 , GRCh38.p12 chr7: 150,945,365-152,676,080 WDR86-AS1, XRCC2, 44 more genes
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