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Items: 1 to 20 of 485

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5916435copy number variation1nstd209human GRCh38 chr8: 143,618,314-143,632,521 , GRCh37.p13 chr8: 144,700,484-144,714,691 LOC105375798, GFUS
    nsv5861182copy number variation1nstd209human GRCh38 chr8: 143,618,326-143,624,981 , GRCh37.p13 chr8: 144,700,496-144,707,151 LOC105375798, GFUS
    nsv5573755copy number variation1nstd207human GRCh38 chr8: 143,618,314-143,632,521 , GRCh37.p13 chr8: 144,700,484-144,714,691 LOC105375798, GFUS
    nsv5476692copy number variation1nstd206human GRCh38 chr8: 143,618,296-143,632,542 , GRCh37.p13 chr8: 144,700,466-144,714,712 LOC105375798, GFUS
    nsv5386537copy number variation1nstd186human GRCh37 chr8: 144,700,487-144,714,690 , GRCh38.p12 chr8: 143,618,317-143,632,520 LOC105375798, GFUS
    nsv5308064copy number variation1nstd204human GRCh37.p13 chr8: 144,700,486-144,714,692 , GRCh38.p13 chr8: 143,618,316-143,632,522 LOC105375798, GFUS
    nsv5301183copy number variation1nstd204human GRCh38.p13 chr8: 143,160,494-143,803,360 , GRCh37.p13 chr8: 144,241,911-144,743,529 TIGD5, MAPK15, 36 more genes
    nsv5259424copy number variation1nstd204human GRCh38.p13 chr8: 143,617,201-143,632,500 , GRCh37.p13 chr8: 144,699,371-144,714,670 GFUS, LOC105375798
    nsv5254948copy number variation1nstd204human GRCh38.p13 chr8: 143,167,001-143,860,200 , GRCh37.p13 chr8: 144,248,418-144,743,525 LOC105375798, LINC02990, 41 more genes
    nsv5253861copy number variation1nstd204human GRCh38.p13 chr8: 143,618,301-143,619,200 , GRCh37.p13 chr8: 144,700,471-144,701,370 LOC105375798, GFUS
    nsv5253288copy number variation1nstd204human GRCh38.p13 chr8: 143,618,301-143,630,500 , GRCh37.p13 chr8: 144,700,471-144,712,670 LOC105375798, GFUS
    nsv5250708copy number variation1nstd204human GRCh37.p13 chr8: 144,636,271-144,700,470 , GRCh38.p13 chr8: 143,554,101-143,618,300 EEF1D, GFUS, 6 more genes
    nsv5249928copy number variation1nstd204human GRCh38.p13 chr8: 143,616,301-143,632,500 , GRCh37.p13 chr8: 144,698,471-144,714,670 LOC105375798, GFUS
    nsv5248414copy number variation1nstd204human GRCh38.p13 chr8: 143,618,526-143,632,467 , GRCh37.p13 chr8: 144,700,696-144,714,637 LOC105375798, GFUS
    nsv5245363copy number variation1nstd204human GRCh38.p13 chr8: 143,618,301-143,622,600 , GRCh37.p13 chr8: 144,700,471-144,704,770 GFUS, LOC105375798
    nsv4962647copy number variation1nstd200human GRCh38 chr8: 143,618,317-143,632,520 , GRCh37.p13 chr8: 144,700,487-144,714,690 LOC105375798, GFUS
    nsv4813889copy number variation1nstd200human GRCh37 chr8: 144,700,487-144,714,692 , GRCh38.p12 chr8: 143,618,317-143,632,522 LOC105375798, GFUS
    nsv4738611copy number variation1nstd199human GRCh37 chr8: 144,700,485-144,714,695 , GRCh38.p12 chr8: 143,618,315-143,632,525 GFUS, LOC105375798
    nsv4729603copy number variation1nstd102humanLikely pathogenic GRCh37 chr8: 144,262,042-146,295,771 , GRCh38.p12 chr8: 143,180,625-145,070,385 CYC1, EEF1D, 112 more genes
    nsv4676049copy number variation1nstd102humanPathogenic GRCh37 chr8: 143,616,831-144,930,611 , GRCh38.p12 chr8: 142,535,470-143,848,439 PYCR3, MROH4P, 69 more genes
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