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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5965822insertion1nstd209human GRCh38 chr9: 137,273,724-137,273,724 , GRCh37.p13 chr9: 140,168,176-140,168,176 NELFB
    nsv5922920copy number variation1nstd209human GRCh38 chr9: 137,260,793-137,261,074 , GRCh37.p13 chr9: 140,155,245-140,155,526 NELFB
    nsv5915241copy number variation1nstd209human GRCh38 chr9: 137,257,814-137,258,138 , GRCh37.p13 chr9: 140,152,266-140,152,590 NELFB
    nsv5910422copy number variation1nstd209human GRCh38 chr9: 137,257,363-137,257,536 , GRCh37.p13 chr9: 140,151,815-140,151,988 NELFB
    nsv5637437insertion1nstd207human GRCh38 chr9: 137,273,768-137,273,768 , GRCh37.p13 chr9: 140,168,220-140,168,220 NELFB
    nsv5601343copy number variation1nstd207human GRCh38 chr9: 137,263,295-137,263,378 , GRCh37.p13 chr9: 140,157,747-140,157,830 NELFB
    nsv5493165copy number variation1nstd206human GRCh38 chr9: 137,273,280-137,294,410 , GRCh37.p13 chr9: 140,167,732-140,188,862 NELFB, TOR4A
    nsv5474126copy number variation1nstd206human GRCh38 chr9: 137,268,101-137,268,169 , GRCh37.p13 chr9: 140,162,553-140,162,621 NELFB
    nsv5381762copy number variation1nstd102humanPathogenic GRCh37 chr9: 139,284,464-141,018,984 , GRCh38.p12 chr9: 136,390,012-138,124,532 ARRDC1, SETP5, 101 more genes
    nsv5381736copy number variation1nstd102humanPathogenic GRCh37 chr9: 139,764,148-141,066,491 , GRCh38.p12 chr9: 136,869,696-138,172,039 PTGDS, LCN12, 63 more genes
    nsv5243007copy number variation1nstd204human GRCh38.p13 chr9: 136,845,001-137,273,000 , GRCh37.p13 chr9: 139,739,453-140,167,452 ENTPD2, LINC02908, 43 more genes
    nsv5126040mobile element insertion1nstd203human GRCh38 chr9: 137,269,349-137,269,366 , GRCh37.p13 chr9: 140,163,801-140,163,818 NELFB
    nsv4973391copy number variation1nstd200human GRCh38 chr9: 137,257,614-137,259,808 , GRCh37.p13 chr9: 140,152,066-140,154,260 NELFB
    nsv4838680copy number variation1nstd200human GRCh37 chr9: 140,152,066-140,154,260 , GRCh38.p12 chr9: 137,257,614-137,259,808 NELFB
    nsv4768352copy number variation1nstd102humanPathogenic GRCh37 chr9: 139,018,777-141,018,984 , GRCh38.p12 chr9: 136,126,931-138,124,532 MIR6722, EXD3, 108 more genes
    nsv4752549insertion1nstd199human GRCh37 chr9: 140,168,140-140,168,140 , GRCh38.p12 chr9: 137,273,688-137,273,688 NELFB
    nsv4728942copy number variation1nstd102humanUncertain significance GRCh37 chr9: 139,776,707-140,234,193 , GRCh38.p12 chr9: 136,882,255-137,339,741 GRIN1, CYSRT1, 42 more genes
    nsv4685995copy number variation1nstd102humanPathogenic GRCh37 chr9: 138,225,001-141,015,001 , GRCh38.p12 chr9: 135,333,155-138,120,549 TPRN, CCDC183, 137 more genes
    nsv4683512copy number variation1nstd102humanPathogenic GRCh37 chr9: 140,033,919-140,729,425 , GRCh38.p12 chr9: 137,139,467-137,834,973 CIMIP2A, ENTPD8, 34 more genes
    nsv4681206copy number variation2nstd102humanUncertain significance, Pathogenic GRCh37 chr9: 138,645,763-140,729,425 , GRCh38.p12 chr9: 135,753,917-137,834,973 DPP7, MIR4673, 112 more genes
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