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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112761copy number variation1nstd102humanPathogenic GRCh37 chr4: 69,671-29,702,595 , GRCh38.p12 chr4: 69,779-29,700,973 LOC101928306, PDE6B-AS1, 460 more genes
    nsv6112747copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,598-18,912,995 , GRCh38.p12 chr4: 68,706-18,911,372 GPR78, LOC105374510, 362 more genes
    nsv5979532inversion1nstd209human GRCh38 chr4: 4,147,913-9,493,295 , GRCh37.p13 chr4: 4,149,640-9,494,939 , CRMP1, 130 more genes
    nsv5974394inversion1nstd209human GRCh38 chr4: 4,005,086-9,639,734 , GRCh37.p13 chr4: 4,006,813-9,641,358 , CRMP1, 142 more genes
    nsv5973087inversion1nstd209human GRCh38 chr4: 3,883,398-8,956,544 , GRCh37.p13 chr4: 3,885,125-8,958,270 , CRMP1, 102 more genes
    nsv5896443copy number variation1nstd209human GRCh38 chr4: 4,396,655-4,396,722 , GRCh37.p13 chr4: 4,398,382-4,398,449 NSG1
    nsv5839030copy number variation1nstd209human GRCh38 chr4: 4,412,205-4,414,468 , GRCh37.p13 chr4: 4,413,932-4,416,195 , NSG1
    nsv5691423mobile element insertion1nstd211human GRCh38 chr4: 4,394,275-4,394,275 , GRCh37.p13 chr4: 4,396,002-4,396,002 NSG1
    nsv5673743copy number variation1nstd102humanPathogenic GRCh37 chr4: 2,200,251-5,710,240 , GRCh38.p12 chr4: 2,198,524-5,708,513 ZFYVE28, LINC01587, 81 more genes
    nsv5614021insertion1nstd207human GRCh38 chr4: 4,411,786-4,411,786 , GRCh37.p13 chr4: 4,413,513-4,413,513 , NSG1
    nsv5572901copy number variation1nstd207human GRCh38 chr4: 4,396,655-4,396,722 , GRCh37.p13 chr4: 4,398,382-4,398,449 NSG1
    nsv5537914insertion1nstd206human GRCh38 chr4: 4,388,081-4,388,099 , GRCh37.p13 chr4: 4,389,808-4,389,826 NSG1
    nsv5400209mobile element insertion1nstd206human GRCh38 chr4: 4,394,275-4,394,326 , GRCh37.p13 chr4: 4,396,002-4,396,053 NSG1
    nsv5367338translocation1nstd200human GRCh38 chr4: 4,402,624-4,402,624 , GRCh38 chr4: 4,404,347-4,404,347 , GRCh37.p13 chr4: 4,404,351-4,404,351 , GRCh37.p13 chr4: 4,406,074-4,406,074 NSG1
    nsv5088483mobile element insertion1nstd203human GRCh38 chr4: 4,394,260-4,394,275 , GRCh37.p13 chr4: 4,395,987-4,396,002 NSG1
    nsv5085905mobile element insertion1nstd203human GRCh38 chr4: 4,415,027-4,415,041 , GRCh37.p13 chr4: 4,416,754-4,416,768 , NSG1
    nsv4925198copy number variation1nstd200human GRCh38 chr4: 4,403,331-4,427,921 , GRCh37.p13 chr4: 4,405,058-4,429,648 , NSG1, 1 more genes
    nsv4761770inversion1nstd199human GRCh37 chr4: 34,988-191,015,248 , GRCh38.p12 chr4: 34,988-190,094,093 , ADD1, 2433 more genes
    nsv4758212inversion1nstd199human GRCh37 chr4: 30,775-191,019,445 , GRCh38.p12 chr4: 30,775-190,098,290 , ADD1, 2433 more genes
    nsv4754592inversion1nstd199human GRCh37 chr4: 27,111-191,020,337 , GRCh38.p12 chr4: 27,111-190,099,182 , ADD1, 2433 more genes
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