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Items: 1 to 20 of 409

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6124282insertion1nstd186human GRCh37 chr4: 76,625,643-76,625,643 , GRCh38.p12 chr4: 75,700,459-75,700,459 G3BP2
    nsv6115267mobile element insertion1nstd186human GRCh37 chr4: 76,595,963-76,596,014 , GRCh38.p12 chr4: 75,670,779-75,670,830 G3BP2
    nsv5964108insertion1nstd209human GRCh38 chr4: 75,697,301-75,697,301 , GRCh37.p13 chr4: 76,622,485-76,622,485 G3BP2
    nsv5954424insertion1nstd209human GRCh38 chr4: 75,663,872-75,663,872 , GRCh37.p13 chr4: 76,589,056-76,589,056 G3BP2
    nsv5953056insertion1nstd209human GRCh38 chr4: 75,670,779-75,670,779 , GRCh37.p13 chr4: 76,595,963-76,595,963 G3BP2
    nsv5903268copy number variation1nstd209human GRCh38 chr4: 75,640,158-75,644,095 , GRCh37.p13 chr4: 76,565,342-76,569,279 G3BP2
    nsv5840387copy number variation1nstd209human GRCh38 chr4: 75,640,157-75,643,056 , GRCh37.p13 chr4: 76,565,341-76,568,240 G3BP2
    nsv5839797copy number variation2nstd209human GRCh38 chr4: 75,716,298-75,717,335 , GRCh37.p13 chr4: 76,641,482-76,642,519 G3BP2
    nsv5839796copy number variation1nstd209human GRCh38 chr4: 75,714,536-75,719,388 , GRCh37.p13 chr4: 76,639,720-76,644,572 G3BP2
    nsv5692533mobile element insertion2nstd211human GRCh38 chr4: 75,670,779-75,670,779 , GRCh37.p13 chr4: 76,595,963-76,595,963 G3BP2
    nsv5687778mobile element insertion1nstd211human GRCh38 chr4: 75,707,749-75,707,749 , GRCh37.p13 chr4: 76,632,933-76,632,933 G3BP2
    nsv5674237copy number variation1nstd102humanPathogenic GRCh38 chr4: 51,891,814-76,009,719 , GRCh37.p13 chr4: 52,757,980-76,930,872 FTLP10, RNU6-410P, 335 more genes
    nsv5613075insertion1nstd207human GRCh38 chr4: 75,670,761-75,670,761 , GRCh37.p13 chr4: 76,595,945-76,595,945 G3BP2
    nsv5612276insertion1nstd207human GRCh38 chr4: 75,676,582-75,676,582 , GRCh37.p13 chr4: 76,601,766-76,601,766 G3BP2
    nsv5611181insertion1nstd207human GRCh38 chr4: 75,663,872-75,663,872 , GRCh37.p13 chr4: 76,589,056-76,589,056 G3BP2
    nsv5611164insertion1nstd207human GRCh38 chr4: 75,700,473-75,700,473 , GRCh37.p13 chr4: 76,625,657-76,625,657 G3BP2
    nsv5574121copy number variation1nstd207human GRCh38 chr4: 75,674,870-75,676,489 , GRCh37.p13 chr4: 76,600,054-76,601,673 G3BP2
    nsv5562145sequence alteration1nstd206human GRCh38 chr4: 74,717,205-184,730,527 , GRCh37.p13 chr4: 75,689,880-185,651,681 , ASS1P8, 1307 more genes
    nsv5550077insertion1nstd206human GRCh38 chr4: 75,663,877-75,663,923 , GRCh37.p13 chr4: 76,589,061-76,589,107 G3BP2
    nsv5547961insertion1nstd206human GRCh38 chr4: 75,700,459-75,700,459 , GRCh37.p13 chr4: 76,625,643-76,625,643 G3BP2
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