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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6115628mobile element insertion1nstd186human GRCh37 chr3: 195,761,769-195,761,820 , GRCh38.p12 chr3: 196,034,898-196,034,949 TFRC
    nsv5980449copy number variation1nstd102humanrisk factor GRCh37 chr3: 195,693,872-197,376,871 , GRCh38.p12 chr3: 195,967,001-197,650,000 RN7SL434P, RNU6-1279P, 54 more genes
    nsv5974193inversion1nstd209human GRCh38 chr3: 195,962,345-196,237,115 , GRCh37.p13 chr3: 195,689,216-195,963,986 , PCYT1A, 9 more genes
    nsv5973794inversion1nstd209human GRCh38 chr3: 195,957,423-196,223,790 , GRCh37.p13 chr3: 195,684,294-195,950,661 , TFRC, 8 more genes
    nsv5971938inversion1nstd209human GRCh38 chr3: 195,938,968-196,228,057 , GRCh37.p13 chr3: 195,665,839-195,954,928 , TFRC, 9 more genes
    nsv5955966insertion1nstd209human GRCh38 chr3: 196,072,710-196,072,710 , GRCh37.p13 chr3: 195,799,581-195,799,581 TFRC, RNU7-18P
    nsv5952407insertion1nstd209human GRCh38 chr3: 196,028,433-196,028,433 , GRCh37.p13 chr3: 195,755,304-195,755,304 TFRC
    nsv5952398insertion1nstd209human GRCh38 chr3: 196,054,398-196,054,398 , GRCh37.p13 chr3: 195,781,269-195,781,269 TFRC
    nsv5902818copy number variation1nstd209human GRCh38 chr3: 196,047,041-196,048,103 , GRCh37.p13 chr3: 195,773,912-195,774,974 TFRC
    nsv5692863mobile element insertion2nstd211human GRCh38 chr3: 196,072,726-196,072,726 , GRCh37.p13 chr3: 195,799,597-195,799,597 RNU7-18P, TFRC
    nsv5690090mobile element insertion2nstd211human GRCh38 chr3: 196,034,898-196,034,898 , GRCh37.p13 chr3: 195,761,769-195,761,769 TFRC
    nsv5613369insertion1nstd207human GRCh38 chr3: 196,027,700-196,027,700 , GRCh37.p13 chr3: 195,754,571-195,754,571 TFRC
    nsv5612982insertion1nstd207human GRCh38 chr3: 196,072,710-196,072,710 , GRCh37.p13 chr3: 195,799,581-195,799,581 TFRC, RNU7-18P
    nsv5605039insertion1nstd207human GRCh38 chr3: 196,034,885-196,034,885 , GRCh37.p13 chr3: 195,761,756-195,761,756 TFRC
    nsv5578867copy number variation1nstd207human GRCh38 chr3: 196,047,041-196,048,103 , GRCh37.p13 chr3: 195,773,912-195,774,974 TFRC
    nsv5566979copy number variation1nstd207human GRCh38 chr3: 196,027,787-196,027,957 , GRCh37.p13 chr3: 195,754,658-195,754,828 TFRC
    nsv5453639copy number variation1nstd206human GRCh38 chr3: 163,047,000-198,226,000 , GRCh37.p13 chr3: 162,764,788-197,952,871 , MIR922, 587 more genes
    nsv5448315copy number variation1nstd206human GRCh38 chr3: 196,033,000-196,043,574 , GRCh37.p13 chr3: 195,759,871-195,770,445 TFRC
    nsv5447874copy number variation1nstd206human GRCh38 chr3: 196,078,813-196,079,297 , GRCh37.p13 chr3: 195,805,684-195,806,168 TFRC
    nsv5438623copy number variation1nstd206human GRCh38 chr3: 196,029,714-196,034,687 , GRCh37.p13 chr3: 195,756,585-195,761,558 TFRC
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