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Items: 1 to 20 of 291

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7055386inversion1nstd229human GRCh38 chr3: 14,829,475-14,829,561 , GRCh37.p13 chr3: 14,870,982-14,871,068 FGD5
    nsv7038316inversion1nstd229human GRCh38 chr3: 14,836,403-14,838,051 , GRCh37.p13 chr3: 14,877,910-14,879,558 FGD5
    nsv6717628copy number variation1nstd229human GRCh38 chr3: 14,853,837-14,853,872 , GRCh37.p13 chr3: 14,895,344-14,895,379 FGD5
    nsv6713320copy number variation1nstd229human GRCh38 chr3: 14,873,491-14,873,561 , GRCh37.p13 chr3: 14,914,998-14,915,068 FGD5
    nsv6712034copy number variation1nstd229human GRCh38 chr3: 14,670,901-15,564,100 , GRCh37.p13 chr3: 14,712,408-15,605,607 COLQ, RNU6-1024P, 22 more genes
    nsv6710540copy number variation1nstd229human GRCh38 chr3: 14,845,585-14,865,509 , GRCh37.p13 chr3: 14,887,092-14,907,016 FGD5
    nsv6703695copy number variation1nstd229human GRCh38 chr3: 14,866,585-14,870,613 , GRCh37.p13 chr3: 14,908,092-14,912,120 FGD5
    nsv6699314copy number variation1nstd229human GRCh38 chr3: 14,885,044-14,888,692 , GRCh37.p13 chr3: 14,926,551-14,930,199 FGD5
    nsv6698724copy number variation1nstd229human GRCh38 chr3: 14,824,965-14,829,791 , GRCh37.p13 chr3: 14,866,472-14,871,298 FGD5
    nsv6698394copy number variation1nstd229human GRCh38 chr3: 14,832,826-14,835,301 , GRCh37.p13 chr3: 14,874,333-14,876,808 FGD5
    nsv6698163copy number variation1nstd229human GRCh38 chr3: 14,844,213-14,847,335 , GRCh37.p13 chr3: 14,885,720-14,888,842 FGD5
    nsv6634367copy number variation1nstd102humanPathogenic GRCh37 chr3: 13,836,340-25,357,427 , GRCh38.p12 chr3: 13,794,843-25,315,936 TMEM43, SLC6A6, 132 more genes
    nsv6374076copy number variation1nstd223human GRCh38 chr3: 14,873,703-14,874,465 , GRCh37.p13 chr3: 14,915,210-14,915,972 FGD5
    nsv6371104copy number variation1nstd223human GRCh38 chr3: 14,898,483-14,898,861 , GRCh37.p13 chr3: 14,939,990-14,940,368 FGD5
    nsv6315249copy number variation1nstd102humanPathogenic GRCh38 chr3: 13,371,737-20,095,506 , GRCh37.p13 chr3: 13,413,237-20,136,998 RNU6-905P, PRR3P1, 99 more genes
    nsv6299157copy number variation1nstd186human GRCh37 chr3: 14,954,287-15,038,185 , GRCh38.p12 chr3: 14,912,780-14,996,678 NR2C2, FGD5, 2 more genes
    nsv6298975copy number variation1nstd186human GRCh37 chr3: 14,915,000-14,915,068 , GRCh38.p12 chr3: 14,873,493-14,873,561 FGD5
    nsv6253724mobile element insertion1nstd215human GRCh38 chr3: 14,818,634-14,818,634 , GRCh37.p13 chr3: 14,860,141-14,860,141 FGD5
    nsv6160242copy number variation1nstd214human GRCh38 chr3: 14,927,629-14,927,693 , GRCh37.p13 chr3: 14,969,136-14,969,200 FGD5
    nsv6134411copy number variation1nstd213human GRCh37 chr3: 14,620,000-15,140,001 , GRCh38.p12 chr3: 14,578,493-15,098,494 NR2C2, CCDC174, 9 more genes
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