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Items: 1 to 20 of 126

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5898228copy number variation1nstd209human GRCh38 chr3: 119,675,412-119,675,525 , GRCh37.p13 chr3: 119,394,259-119,394,372 COX17
    nsv5889494copy number variation1nstd209human GRCh38 chr3: 119,662,960-119,757,421 , GRCh37.p13 chr3: 119,381,807-119,476,268 LOC105374064, CFAP91, 2 more genes
    nsv5834859copy number variation1nstd209human GRCh38 chr3: 119,662,779-119,679,095 , GRCh37.p13 chr3: 119,381,626-119,397,942 LOC105374063, COX17
    nsv5092470mobile element insertion1nstd203human GRCh38 chr3: 119,676,371-119,676,383 , GRCh37.p13 chr3: 119,395,218-119,395,230 COX17
    nsv5036857inversion1nstd200human GRCh38 chr3: 97,392,267-146,717,859 , GRCh37.p13 chr3: 97,111,111-146,435,646 , FBRSL1P1, 801 more genes
    nsv5031637inversion1nstd200human GRCh38 chr3: 112,181,184-125,673,487 , GRCh37.p13 chr3: 111,900,031-125,392,331 , ARHGAP31, 218 more genes
    nsv4919779copy number variation1nstd200human GRCh38 chr3: 119,640,730-119,691,506 , GRCh37.p13 chr3: 119,359,577-119,410,353 COX17, POPDC2, 1 more genes
    nsv4794317copy number variation1nstd200human GRCh37 chr3: 119,381,807-119,476,273 , GRCh38.p12 chr3: 119,662,960-119,757,426 LOC105374064, CFAP91, 2 more genes
    nsv4400646copy number variation1nstd174human GRCh37 chr3: 119,360,506-119,413,339 , GRCh38.p12 chr3: 119,641,659-119,694,492 COX17, LOC105374063, 1 more genes
    nsv4317801inversion1nstd166human GRCh37.p13 chr3: 106,160,269-123,476,086 , GRCh38.p12 chr3: 106,441,422-123,757,239 , ADPRH, 270 more genes
    nsv3924082copy number variation1nstd102humanPathogenic NCBI36 chr3: 119,875,435-127,742,263 , GRCh38 chr3: 118,673,898-126,540,730 , GRCh37 chr3: 118,392,745-126,259,573 MYLK-AS2, RPL7AP11, 165 more genes
    nsv3923097copy number variation1nstd102humanPathogenic NCBI36 chr3: 120,318,703-127,122,267 , GRCh38 chr3: 119,117,166-125,920,734 , GRCh37 chr3: 118,836,013-125,639,577 POGLUT1, RN7SL397P, 141 more genes
    nsv3922717copy number variation1nstd102humanPathogenic NCBI36 chr3: 95,002,154-146,895,858 , GRCh38 chr3: 93,800,620-145,695,381 , GRCh37 chr3: 93,519,464-145,413,168 OR7E53P, HSPA8P9, 794 more genes
    nsv3919464copy number variation1nstd102humanPathogenic GRCh38 chr3: 114,122,562-124,532,374 , GRCh37 chr3: 113,841,409-124,251,221 , NCBI36 chr3: 115,324,099-125,733,911 B4GALT4-AS1, LSAMP, 144 more genes
    nsv3919094copy number variation1nstd102humanPathogenic GRCh37 chr3: 114,737,921-122,232,245 , GRCh38 chr3: 115,019,074-122,513,398 , NCBI36 chr3: 116,220,611-123,714,935 LOC105374054, CSTA, 106 more genes
    nsv3918981copy number variation1nstd102humanPathogenic GRCh37 chr3: 103,145,726-197,837,049 , GRCh38 chr3: 103,426,882-198,110,178 , NCBI36 chr3: 104,628,416-199,321,446 LINC02614, LINC02054, 1469 more genes
    nsv3918661copy number variation1nstd102humanPathogenic NCBI36 chr3: 95,088,205-124,418,220 , GRCh37 chr3: 93,605,515-122,935,530 , GRCh38 chr3: 93,886,671-123,216,683 MTCO2P29, GAP43, 401 more genes
    nsv3918094copy number variation1nstd102humanPathogenic NCBI36 chr3: 113,822,514-129,935,667 , GRCh38 chr3: 112,620,977-128,734,134 , GRCh37 chr3: 112,339,824-128,452,977 QTRT2, MIR544B, 284 more genes
    nsv3917839copy number variation1nstd102humanUncertain significance NCBI36 chr3: 119,046,495-122,028,158 , GRCh38 chr3: 117,844,958-120,826,621 , GRCh37 chr3: 117,563,805-120,545,468 ADPRH, HGD, 52 more genes
    nsv3916767copy number variation1nstd102humanUncertain significance GRCh37 chr3: 117,563,805-120,515,873 , GRCh38 chr3: 117,844,958-120,797,026 , NCBI36 chr3: 119,046,495-121,998,563 TEX55, ARHGAP31-AS1, 50 more genes
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