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Items: 1 to 20 of 353

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148229copy number variation1nstd102humanPathogenic GRCh38 chr4: 2,904,667-42,963,232 , GRCh37.p13 chr4: 2,906,394-42,965,249 LINC01587, RN7SKP82, 509 more genes
    nsv7148161copy number variation1nstd102humanPathogenic GRCh38 chr4: 1-49,062,177 , GRCh37.p13 chr4: 507,005-49,064,194 SLIRPP2, STIM2-AS1, 659 more genes
    nsv7148157copy number variation1nstd102humanPathogenic GRCh38 chr4: 85,624-57,073,230 , GRCh37.p13 chr4: 507,005-57,939,396 OR7E84P, FAM193A, 764 more genes
    nsv7142624insertion1nstd232human GRCh37.p13 chr4: 40,754,839-40,754,839 , GRCh38.p12 chr4: 40,752,822-40,752,822 NSUN7
    nsv7137048copy number variation1nstd102humanPathogenic GRCh37 chr4: 40,337,485-41,941,400 , GRCh38.p12 chr4: 40,335,468-41,939,383 RNU6-1195P, RNU6-836P, 23 more genes
    nsv7057597inversion1nstd229human GRCh38 chr4: 40,706,162-41,294,144 , GRCh37.p13 chr4: 40,708,179-41,296,161 UCHL1-DT, UCHL1, 6 more genes
    nsv7055239inversion1nstd229human GRCh38 chr4: 40,146,946-41,050,224 , GRCh37.p13 chr4: 40,148,566-41,052,241 RHOH, RBM47, 10 more genes
    nsv7054319inversion1nstd229human GRCh38 chr4: 40,437,339-43,087,585 , GRCh37.p13 chr4: 40,439,356-43,089,602 RN7SKP82, RPS7P7, 33 more genes
    nsv7049429inversion1nstd229human GRCh38 chr4: 40,815,620-40,817,747 , GRCh37.p13 chr4: 40,817,637-40,819,764 APBB2, NSUN7
    nsv7040048inversion1nstd229human GRCh38 chr4: 40,793,549-40,807,098 , GRCh37.p13 chr4: 40,795,566-40,809,115 NSUN7
    nsv6737955copy number variation1nstd229human GRCh38 chr4: 40,799,001-40,811,900 , GRCh37.p13 chr4: 40,801,018-40,813,917 APBB2, NSUN7
    nsv6736906copy number variation1nstd229human GRCh38 chr4: 40,807,101-40,848,400 , GRCh37.p13 chr4: 40,809,118-40,850,417 NSUN7, APBB2
    nsv6735586copy number variation1nstd229human GRCh38 chr4: 40,757,159-40,758,758 , GRCh37.p13 chr4: 40,759,176-40,760,775 NSUN7
    nsv6735343copy number variation1nstd229human GRCh38 chr4: 40,791,036-40,794,677 , GRCh37.p13 chr4: 40,793,053-40,796,694 NSUN7
    nsv6731440copy number variation1nstd229human GRCh38 chr4: 40,798,995-40,799,042 , GRCh37.p13 chr4: 40,801,012-40,801,059 NSUN7
    nsv6731395copy number variation1nstd229human GRCh38 chr4: 40,780,568-40,784,960 , GRCh37.p13 chr4: 40,782,585-40,786,977 ARL4AP2, NSUN7
    nsv6728895copy number variation1nstd229human GRCh38 chr4: 40,753,313-40,762,875 , GRCh37.p13 chr4: 40,755,330-40,764,892 NSUN7
    nsv6728817copy number variation1nstd229human GRCh38 chr4: 40,787,013-40,791,231 , GRCh37.p13 chr4: 40,789,030-40,793,248 NSUN7, ARL4AP2
    nsv6728588copy number variation1nstd229human GRCh38 chr4: 40,801,901-40,812,300 , GRCh37.p13 chr4: 40,803,918-40,814,317 APBB2, NSUN7
    nsv6728232copy number variation1nstd229human GRCh38 chr4: 40,800,449-40,802,695 , GRCh37.p13 chr4: 40,802,466-40,804,712 NSUN7
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