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Items: 1 to 20 of 515

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112754copy number variation1nstd102humanPathogenic GRCh37 chr4: 131,303,317-168,722,402 , GRCh38.p12 chr4: 130,382,162-167,801,251 MIR3139, CLGN, 407 more genes
    nsv5968756inversion1nstd209human GRCh38 chr4: 156,904,373-156,912,807 , GRCh37.p13 chr4: 157,825,525-157,833,959 PDGFC
    nsv5966377insertion1nstd209human GRCh38 chr4: 156,847,734-156,847,734 , GRCh37.p13 chr4: 157,768,886-157,768,886 PDGFC
    nsv5959015insertion1nstd209human GRCh38 chr4: 156,825,575-156,825,575 , GRCh37.p13 chr4: 157,746,727-157,746,727 PDGFC
    nsv5902244copy number variation1nstd209human GRCh38 chr4: 156,014,074-164,864,480 , GRCh37.p13 chr4: 156,935,226-165,785,632 , MIR3688-1, 67 more genes
    nsv5898576copy number variation1nstd209human GRCh38 chr4: 156,914,007-156,915,469 , GRCh37.p13 chr4: 157,835,159-157,836,621 PDGFC
    nsv5889457copy number variation1nstd209human GRCh38 chr4: 156,940,421-156,947,480 , GRCh37.p13 chr4: 157,861,573-157,868,632 PDGFC
    nsv5838317copy number variation1nstd209human GRCh38 chr4: 156,940,080-156,947,518 , GRCh37.p13 chr4: 157,861,232-157,868,670 PDGFC
    nsv5838080copy number variation2nstd209human GRCh38 chr4: 156,970,472-156,971,732 , GRCh37.p13 chr4: 157,891,624-157,892,884 PDGFC
    nsv5838079copy number variation1nstd209human GRCh38 chr4: 156,914,023-156,915,422 , GRCh37.p13 chr4: 157,835,175-157,836,574 PDGFC
    nsv5838078copy number variation1nstd209human GRCh38 chr4: 156,904,410-156,906,009 , GRCh37.p13 chr4: 157,825,562-157,827,161 PDGFC
    nsv5725028mobile element insertion1nstd211human GRCh38 chr4: 156,919,198-156,919,198 , GRCh37.p13 chr4: 157,840,350-157,840,350 PDGFC
    nsv5685286mobile element insertion2nstd211human GRCh38 chr4: 156,848,577-156,848,577 , GRCh37.p13 chr4: 157,769,729-157,769,729 PDGFC
    nsv5682790mobile element insertion1nstd211human GRCh38 chr4: 156,951,118-156,951,118 , GRCh37.p13 chr4: 157,872,270-157,872,270 PDGFC
    nsv5680110mobile element insertion1nstd211human GRCh38 chr4: 156,804,268-156,804,268 , GRCh37.p13 chr4: 157,725,420-157,725,420 PDGFC
    nsv5667363inversion1nstd207human GRCh38 chr4: 156,904,334-156,912,852 , GRCh37.p13 chr4: 157,825,486-157,834,004 PDGFC
    nsv5621567insertion1nstd207human GRCh38 chr4: 156,825,590-156,825,590 , GRCh37.p13 chr4: 157,746,742-157,746,742 PDGFC
    nsv5620868insertion1nstd207human GRCh38 chr4: 156,847,740-156,847,740 , GRCh37.p13 chr4: 157,768,892-157,768,892 PDGFC
    nsv5615959insertion2nstd207human GRCh38 chr4: 156,825,575-156,825,575 , GRCh37.p13 chr4: 157,746,727-157,746,727 PDGFC
    nsv5608459insertion1nstd207human GRCh38 chr4: 156,848,564-156,848,564 , GRCh37.p13 chr4: 157,769,716-157,769,716 PDGFC
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