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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5658107insertion1nstd207human GRCh38 chr11: 69,813,600-69,813,600 , GRCh37.p13 chr11|NW_003571046.1: 13,583-13,583 , GRCh37.p13 chr11: 69,628,368-69,628,368 FGF3
    nsv5584748copy number variation1nstd207human GRCh38 chr11: 69,813,576-69,813,647 , GRCh37.p13 chr11|NW_003571046.1: 13,559-13,630 , GRCh37.p13 chr11: 69,628,344-69,628,415 FGF3
    nsv5380796copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397 FAUP4, MMP7, 2031 more genes
    nsv4980038copy number variation1nstd200human GRCh38 chr11: 69,818,186-69,818,988 , GRCh37.p13 chr11|NW_003571046.1: 18,169-18,971 , GRCh37.p13 chr11: 69,632,954-69,633,756 LOC107984368, FGF3
    nsv4831726copy number variation1nstd200human GRCh37 chr11: 69,632,954-69,633,756 , GRCh38.p12 chr11: 69,818,186-69,818,988 FGF3, LOC107984368
    nsv4754747insertion1nstd199human GRCh37 chr11: 69,628,340-69,628,340 , GRCh38.p12 chr11: 69,813,572-69,813,572 FGF3
    nsv4751865inversion1nstd199human GRCh37 chr11: 1,620,303-71,272,233 , GRCh38.p12 chr11: 1,599,073-71,561,187 , ACP2, 1686 more genes
    nsv4710825copy number variation1nstd195human GRCh37 chr11: 69,409,751-69,724,701 , GRCh38.p12 chr11: 69,594,983-69,909,959 CCND1, FGF3, 5 more genes
    nsv4706518copy number variation1nstd195human GRCh37 chr11: 69,139,801-69,724,701 , GRCh38.p12 chr11: 69,325,035-69,909,959 FGF3, LOC107984368, 9 more genes
    nsv4456202copy number variation1nstd102humanUncertain significance GRCh37 chr11: 69,540,125-69,711,472 , GRCh38.p12 chr11: 69,725,357-69,896,705 FGF3, FGF4, 2 more genes
    nsv4446347insertion1nstd175human GRCh37 chr11: 69,628,592-69,628,592 , GRCh38.p12 chr11: 69,813,824-69,813,824 FGF3
    nsv3950060insertion1nstd167human GRCh37 chr11: 69,628,353-69,628,353 , GRCh38.p12 chr11: 69,813,585-69,813,585 FGF3
    nsv3917463copy number variation1nstd102humanLikely pathogenic NCBI36 chr11: 67,555,736-70,982,189 , GRCh37 chr11: 67,799,160-71,304,541 , GRCh38 chr11: 68,031,693-71,593,495 CCND1, CHKA, 71 more genes
    nsv3909768copy number variation1nstd102humanLikely pathogenic GRCh37 chr11: 67,799,160-70,701,268 , GRCh38.p12 chr11: 68,031,693-70,855,163 CCND1, CHKA, 56 more genes
    nsv3908873copy number variation2nstd102humanPathogenic GRCh37 chr11: 230,616-134,938,470 , GRCh38.p12 chr11: 230,616-135,068,576 IGHMBP2, SYTL2, 2829 more genes
    nsv3900144copy number variation1nstd102humanPathogenic GRCh37 chr11: 198,510-134,934,063 , GRCh38.p12 chr11: 198,510-135,064,169 RTN3, KRTAP5-13P, 2833 more genes
    nsv3893233copy number variation1nstd102humanPathogenic GRCh37 chr11: 70,864-134,938,470 , GRCh38.p12 chr11: 70,864-135,068,576 LOC105376598, OSBPL9P2, 2842 more genes
    nsv3556501insertion1nstd152human GRCh38 chr11: 69,813,824-69,813,824 , GRCh37.p13 chr11|NW_003571046.1: 13,807-13,807 , GRCh37.p13 chr11: 69,628,592-69,628,592 FGF3
    nsv3334076insertion1nstd162human GRCh38 chr11: 69,813,825-69,813,825 , GRCh37.p13 chr11|NW_003571046.1: 13,808-13,808 , GRCh37.p13 chr11: 69,628,593-69,628,593 FGF3
    nsv3154722copy number variation1nstd151human GRCh37 chr11: 69,458,597-70,507,877 , GRCh38.p12 chr11: 69,643,829-70,661,772 , LTO1, 22 more genes
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