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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5963006insertion1nstd209human GRCh38 chr2: 214,751,136-214,751,136 , GRCh37.p13 chr2: 215,615,860-215,615,860 BARD1
    nsv5903686copy number variation1nstd209human GRCh38 chr2: 214,750,332-214,750,416 , GRCh37.p13 chr2: 215,615,056-215,615,140 BARD1
    nsv5902361copy number variation1nstd209human GRCh38 chr2: 214,809,800-214,809,862 , GRCh37.p13 chr2: 215,674,524-215,674,586 SNHG31, BARD1
    nsv5898450copy number variation1nstd209human GRCh38 chr2: 214,726,966-214,727,026 , GRCh37.p13 chr2: 215,591,690-215,591,750 BARD1
    nsv5897787copy number variation1nstd209human GRCh38 chr2: 214,810,043-214,810,111 , GRCh37.p13 chr2: 215,674,767-215,674,835 SNHG31, BARD1
    nsv5897709copy number variation1nstd209human GRCh38 chr2: 214,785,026-214,786,284 , GRCh37.p13 chr2: 215,649,750-215,651,008 BARD1
    nsv5893298copy number variation1nstd209human GRCh38 chr2: 214,758,045-214,763,838 , GRCh37.p13 chr2: 215,622,769-215,628,562 BARD1
    nsv5892485copy number variation1nstd209human GRCh38 chr2: 214,803,037-214,806,859 , GRCh37.p13 chr2: 215,667,761-215,671,583 BARD1
    nsv5832452copy number variation1nstd209human GRCh38 chr2: 214,784,983-214,786,182 , GRCh37.p13 chr2: 215,649,707-215,650,906 BARD1
    nsv5832451copy number variation1nstd209human GRCh38 chr2: 214,758,022-214,763,784 , GRCh37.p13 chr2: 215,622,746-215,628,508 BARD1
    nsv5832197copy number variation1nstd209human GRCh38 chr2: 214,802,604-214,807,408 , GRCh37.p13 chr2: 215,667,328-215,672,132 BARD1
    nsv5679944mobile element insertion2nstd211human GRCh38 chr2: 214,771,943-214,771,943 , GRCh37.p13 chr2: 215,636,667-215,636,667 BARD1
    nsv5674265insertion1nstd102humanPathogenic GRCh37 chr2: 215,610,479-215,610,479 , GRCh38 chr2: 214,745,755-214,745,755 BARD1
    nsv5673693copy number variation1nstd102humanPathogenic GRCh37 chr2: 215,617,161-215,674,293 , GRCh38.p12 chr2: 214,752,437-214,809,569 BARD1, SNHG31
    nsv5673692copy number variation1nstd102humanPathogenic GRCh37 chr2: 215,593,400-215,657,179 , GRCh38.p12 chr2: 214,728,676-214,792,455 BARD1
    nsv5673691copy number variation2nstd102humanUncertain significance, Pathogenic GRCh37 chr2: 215,593,400-215,610,588 , GRCh38.p12 chr2: 214,728,676-214,745,864 BARD1
    nsv5673690copy number variation1nstd102humanPathogenic GRCh37 chr2: 215,590,360-215,674,445 , GRCh38.p12 chr2: 214,725,636-214,809,721 SNHG31, BARD1
    nsv5673378copy number variation1nstd102humanPathogenic GRCh37 chr2: 215,593,400-215,646,243 , GRCh38.p12 chr2: 214,728,676-214,781,519 BARD1
    nsv5673377copy number variation1nstd102humanPathogenic GRCh37 chr2: 215,593,394-215,634,042 , GRCh38.p12 chr2: 214,728,670-214,769,318 BARD1
    nsv5673301copy number variation1nstd102humanPathogenic GRCh37 chr2: 215,645,274-215,646,243 , GRCh38.p12 chr2: 214,780,550-214,781,519 BARD1
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