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Items: 1 to 20 of 582

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137756copy number variation1nstd102humanBenign GRCh38 chr4: 5,748,550-5,748,617 , GRCh37 chr4: 5,750,277-5,750,344 EVC
    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
    nsv5964709insertion1nstd209human GRCh38 chr4: 5,732,021-5,732,021 , GRCh37.p13 chr4: 5,733,748-5,733,748 EVC
    nsv5959039insertion1nstd209human GRCh38 chr4: 5,808,133-5,808,133 , GRCh37.p13 chr4: 5,809,860-5,809,860 EVC
    nsv5951279insertion1nstd209human GRCh38 chr4: 5,748,793-5,748,793 , GRCh37.p13 chr4: 5,750,520-5,750,520 EVC
    nsv5902067copy number variation1nstd209human GRCh38 chr4: 5,757,821-5,757,888 , GRCh37.p13 chr4: 5,759,548-5,759,615 EVC
    nsv5898073copy number variation1nstd209human GRCh38 chr4: 5,811,777-5,811,834 , GRCh37.p13 chr4: 5,813,504-5,813,561 EVC
    nsv5839975copy number variation1nstd209human GRCh38 chr4: 5,767,093-5,775,548 , GRCh37.p13 chr4: 5,768,820-5,777,275 EVC
    nsv5839694copy number variation1nstd209human GRCh38 chr4: 5,759,914-5,761,913 , GRCh37.p13 chr4: 5,761,641-5,763,640 EVC
    nsv5720848mobile element insertion1nstd211human GRCh38 chr4: 5,718,311-5,718,311 , GRCh37.p13 chr4: 5,720,038-5,720,038 EVC
    nsv5719183mobile element insertion1nstd211human GRCh38 chr4: 5,759,918-5,759,918 , GRCh37.p13 chr4: 5,761,645-5,761,645 EVC
    nsv5679981mobile element insertion1nstd211human GRCh38 chr4: 5,797,562-5,797,562 , GRCh37.p13 chr4: 5,799,289-5,799,289 EVC
    nsv5673744copy number variation1nstd102humanPathogenic GRCh37 chr4: 5,754,553-5,755,670 , GRCh38.p12 chr4: 5,752,826-5,753,943 EVC
    nsv5673653copy number variation1nstd102humanPathogenic GRCh37 chr4: 5,809,918-5,811,348 , GRCh38.p12 chr4: 5,808,191-5,809,621 EVC
    nsv5673652copy number variation1nstd102humanLikely pathogenic GRCh37 chr4: 5,733,142-5,735,172 , GRCh38.p12 chr4: 5,731,415-5,733,445 EVC
    nsv5673570copy number variation1nstd102humanLikely pathogenic GRCh37 chr4: 5,785,269-5,803,831 , GRCh38.p12 chr4: 5,783,542-5,802,104 EVC
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