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Items: 1 to 20 of 347

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5692192mobile element insertion2nstd211human GRCh38 chr6: 87,215,153-87,215,153 , GRCh37.p13 chr6: 87,924,871-87,924,871 ZNF292
    nsv5684029mobile element insertion2nstd211human GRCh38 chr6: 87,204,580-87,204,580 , GRCh37.p13 chr6: 87,914,298-87,914,298 ZNF292
    nsv5626723insertion1nstd207human GRCh38 chr6: 87,215,139-87,215,139 , GRCh37.p13 chr6: 87,924,857-87,924,857 ZNF292
    nsv5471593copy number variation1nstd206human GRCh38 chr6: 87,201,475-87,204,708 , GRCh37.p13 chr6: 87,911,193-87,914,426 ZNF292
    nsv5456473copy number variation1nstd206human GRCh38 chr6: 87,175,011-87,175,081 , GRCh37.p13 chr6: 87,884,729-87,884,799 ZNF292
    nsv5409667mobile element insertion1nstd206human GRCh38 chr6: 87,215,153-87,215,204 , GRCh37.p13 chr6: 87,924,871-87,924,922 ZNF292
    nsv5369409translocation1nstd200human GRCh38 chr6: 87,211,452-87,211,452 , GRCh38 chr6: 87,211,380-87,211,380 , GRCh37.p13 chr6: 87,921,098-87,921,098 , GRCh37.p13 chr6: 87,921,170-87,921,170 ZNF292
    nsv5115340mobile element insertion1nstd203human GRCh38 chr6: 87,215,139-87,215,153 , GRCh37.p13 chr6: 87,924,857-87,924,871 ZNF292
    nsv5114717mobile element insertion1nstd203human GRCh38 chr6: 87,195,220-87,195,226 , GRCh37.p13 chr6: 87,904,938-87,904,944 ZNF292
    nsv5102724mobile element insertion1nstd203human GRCh38 chr6: 87,159,218-87,159,218 , GRCh37.p13 chr6: 87,868,936-87,868,936 ZNF292
    nsv5038830inversion1nstd200human GRCh38 chr6: 84,210,829-134,196,676 , GRCh37.p13 chr6: 84,920,547-134,517,814 , LOC105377981, 623 more genes
    nsv4945385copy number variation1nstd200human GRCh38 chr6: 87,201,407-87,204,758 , GRCh37.p13 chr6: 87,911,125-87,914,476 ZNF292
    nsv4942002copy number variation1nstd200human GRCh38 chr6: 87,202,097-87,202,251 , GRCh37.p13 chr6: 87,911,815-87,911,969 ZNF292
    nsv4816891copy number variation1nstd200human GRCh37 chr6: 87,911,815-87,911,969 , GRCh38.p12 chr6: 87,202,097-87,202,251 ZNF292
    nsv4717872mobile element insertion1nstd186human GRCh37 chr6: 87,924,857-87,924,857 , GRCh38.p12 chr6: 87,215,139-87,215,139 ZNF292
    nsv4675663copy number variation1nstd102humanLikely benign GRCh37 chr6: 87,564,055-87,921,049 , GRCh38.p12 chr6: 86,854,337-87,211,331 ZNF292, LOC100418923, 6 more genes
    nsv4675039copy number variation1nstd102humanPathogenic GRCh37 chr6: 86,024,761-90,023,713 , GRCh38.p12 chr6: 85,315,043-89,313,994 C6orf163, LOC100652960, 65 more genes
    nsv4487811mobile element insertion1nstd166human GRCh37.p13 chr6: 87,924,857-87,924,857 , GRCh38.p12 chr6: 87,215,139-87,215,139 ZNF292
    nsv4478938mobile element insertion1nstd166human GRCh37.p13 chr6: 87,946,305-87,946,305 , GRCh38.p12 chr6: 87,236,587-87,236,587 ZNF292
    nsv4456405copy number variation1nstd102humanUncertain significance GRCh37 chr6: 87,627,836-93,698,486 , GRCh38.p12 chr6: 86,918,118-92,988,768 MIR4643, LOC107986625, 82 more genes
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