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Items: 1 to 20 of 128

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7071535inversion1nstd229human GRCh38 chr9: 124,246,999-128,875,010 , GRCh37.p13 chr9: 127,009,278-131,637,289 PTGES2-AS1, STXBP1, 130 more genes
    nsv6878043copy number variation1nstd229human GRCh38 chr9: 127,083,504-127,087,513 , GRCh37.p13 chr9: 129,845,783-129,849,792 RALGPS1, ANGPTL2
    nsv6868942copy number variation1nstd229human GRCh38 chr9: 127,098,301-127,104,500 , GRCh37.p13 chr9: 129,860,580-129,866,779 RALGPS1, ANGPTL2
    nsv6868366copy number variation1nstd229human GRCh38 chr9: 127,108,691-127,108,857 , GRCh37.p13 chr9: 129,870,970-129,871,136 ANGPTL2, RALGPS1
    nsv6863100copy number variation1nstd229human GRCh38 chr9: 127,094,770-127,100,132 , GRCh37.p13 chr9: 129,857,049-129,862,411 RALGPS1, ANGPTL2
    nsv6637981copy number variation1nstd102humanPathogenic GRCh37 chr9: 124,018,736-129,995,568 , GRCh38.p12 chr9: 121,256,458-127,233,289 PBX3-DT, ADGRD2, 119 more genes
    nsv6634454copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-131,603,223 , GRCh38.p12 chr9: 203,861-128,840,944 HNRNPA1P41, GAS1RR, 1868 more genes
    nsv6438803copy number variation1nstd223human GRCh38 chr9: 126,485,301-128,649,400 , GRCh37.p13 chr9: 129,247,580-131,411,679 MIR199B, FPGS, 72 more genes
    nsv6314001copy number variation1nstd102humanPathogenic GRCh37 chr9: 116,422,275-131,713,233 , GRCh38.p12 chr9: 113,659,995-128,950,954 LOC105376244, RN7SL187P, 286 more genes
    nsv6313546copy number variation1nstd102humanPathogenic GRCh37 chr9: 353,349-141,020,389 , GRCh38.p12 chr9: 353,349-138,125,937 FAM27C, DPM2, 2166 more genes
    nsv6291261copy number variation1nstd102humanPathogenic GRCh37 chr9: 128,523,763-132,604,808 , GRCh38.p12 chr9: 125,761,484-129,842,529 PTPA, AK1, 123 more genes
    nsv6240242mobile element insertion1nstd215human GRCh38 chr9: 127,098,494-127,098,494 , GRCh37.p13 chr9: 129,860,773-129,860,773 RALGPS1, ANGPTL2
    nsv6136817copy number variation1nstd213human GRCh37 chr9: 129,400,000-130,190,001 , GRCh38.p12 chr9: 126,637,721-127,427,722 LMX1B, RALGPS1, 10 more genes
    nsv5706474mobile element insertion1nstd211human GRCh38 chr9: 127,087,287-127,087,287 , GRCh37.p13 chr9: 129,849,566-129,849,566 RALGPS1, ANGPTL2
    nsv5564479copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chr9: 129,376,729-131,016,993 , GRCh38.p12 chr9: 126,614,450-128,254,714 PIP5KL1, MIR3911, 50 more genes
    nsv5410720mobile element insertion1nstd206human GRCh38 chr9: 127,087,287-127,087,338 , GRCh37.p13 chr9: 129,849,566-129,849,617 RALGPS1, ANGPTL2
    nsv5180861mobile element insertion1nstd203human GRCh38 chr9: 127,099,996-127,100,011 , GRCh37.p13 chr9: 129,862,275-129,862,290 ANGPTL2, RALGPS1
    nsv5134046mobile element insertion1nstd203human GRCh38 chr9: 127,092,564-127,092,578 , GRCh37.p13 chr9: 129,854,843-129,854,857 ANGPTL2, RALGPS1
    nsv5040732inversion1nstd200human GRCh38 chr9: 100,673,006-127,581,711 , GRCh37.p13 chr9: 103,435,288-130,343,990 , LOC105379839, 440 more genes
    nsv4768372copy number variation1nstd102humanPathogenic GRCh37 chr9: 128,512,347-130,702,572 , GRCh38.p12 chr9: 125,750,068-127,940,293 LOC105379841, PTRH1, 47 more genes
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