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Items: 1 to 20 of 154

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5205810mobile element deletion1nstd204human GRCh37.p13 chr3: 120,066,220-120,066,546 , GRCh38.p13 chr3: 120,347,373-120,347,699 LRRC58, BTNL12P
    nsv5097220mobile element insertion1nstd203human GRCh38 chr3: 120,323,263-120,323,278 , GRCh37.p13 chr3: 120,042,110-120,042,125 LRRC58
    nsv5088512mobile element insertion1nstd203human GRCh38 chr3: 120,324,992-120,325,008 , GRCh37.p13 chr3: 120,043,839-120,043,855 LRRC58
    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
    nsv4777871mobile element deletion1nstd200human GRCh37 chr3: 120,066,230-120,066,537 , GRCh38.p12 chr3: 120,347,383-120,347,690 LRRC58, BTNL12P
    nsv4728369copy number variation1nstd102humanLikely benign GRCh37 chr3: 120,043,207-120,255,384 , GRCh38.p12 chr3: 120,324,360-120,536,537 FSTL1, LOC107986121, 5 more genes
    nsv4468321mobile element insertion1nstd166human GRCh37.p13 chr3: 120,054,509-120,054,509 , GRCh38.p12 chr3: 120,335,662-120,335,662 LRRC58
    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
    nsv3914171copy number variation1nstd102humanUncertain significance GRCh38 chr3: 120,286,468-121,375,425 , GRCh37 chr3: 120,005,315-121,094,272 , NCBI36 chr3: 121,488,005-122,576,962 MIR5682, HGD, 19 more genes
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