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Items: 1 to 20 of 215

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5675988mobile element insertion2nstd211human GRCh38 chr6: 87,476,163-87,476,163 , GRCh37.p13 chr6: 88,185,881-88,185,881 SLC35A1
    nsv5630780insertion1nstd207human GRCh38 chr6: 87,507,828-87,507,828 , GRCh37.p13 chr6: 88,217,546-88,217,546 SLC35A1
    nsv5556757sequence alteration1nstd206human GRCh38 chr6: 87,507,828-87,507,832 , GRCh37.p13 chr6: 88,217,546-88,217,550 SLC35A1
    nsv5540073insertion1nstd206human GRCh38 chr6: 87,507,828-87,507,828 , GRCh37.p13 chr6: 88,217,546-88,217,546 SLC35A1
    nsv5457546copy number variation1nstd206human GRCh38 chr6: 87,486,903-87,488,275 , GRCh37.p13 chr6: 88,196,621-88,197,993 RNU6-444P, SLC35A1
    nsv5412605mobile element insertion1nstd206human GRCh38 chr6: 87,476,163-87,476,214 , GRCh37.p13 chr6: 88,185,881-88,185,932 SLC35A1
    nsv5117474mobile element insertion1nstd203human GRCh38 chr6: 87,507,827-87,507,827 , GRCh37.p13 chr6: 88,217,545-88,217,545 SLC35A1
    nsv5115648mobile element insertion1nstd203human GRCh38 chr6: 87,507,826-87,507,865 , GRCh37.p13 chr6: 88,217,544-88,217,583 SLC35A1
    nsv5111867mobile element insertion1nstd203human GRCh38 chr6: 87,503,738-87,503,757 , GRCh37.p13 chr6: 88,213,456-88,213,475 SLC35A1
    nsv5108118mobile element insertion1nstd203human GRCh38 chr6: 87,507,828-87,507,828 , GRCh37.p13 chr6: 88,217,546-88,217,546 SLC35A1
    nsv5107456mobile element insertion1nstd203human GRCh38 chr6: 87,476,153-87,476,160 , GRCh37.p13 chr6: 88,185,871-88,185,878 SLC35A1
    nsv5038830inversion1nstd200human GRCh38 chr6: 84,210,829-134,196,676 , GRCh37.p13 chr6: 84,920,547-134,517,814 , LOC105377981, 623 more genes
    nsv4942011copy number variation1nstd200human GRCh38 chr6: 87,486,903-87,488,275 , GRCh37.p13 chr6: 88,196,621-88,197,993 RNU6-444P, SLC35A1
    nsv4816899copy number variation1nstd200human GRCh37 chr6: 88,196,621-88,197,993 , GRCh38.p12 chr6: 87,486,903-87,488,275 SLC35A1, RNU6-444P
    nsv4751469insertion1nstd199human GRCh37 chr6: 88,217,543-88,217,543 , GRCh38.p12 chr6: 87,507,825-87,507,825 SLC35A1
    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
    nsv4484849mobile element insertion1nstd166human GRCh37.p13 chr6: 88,185,871-88,185,871 , GRCh38.p12 chr6: 87,476,153-87,476,153 SLC35A1
    nsv4481385mobile element insertion1nstd166human GRCh37.p13 chr6: 88,202,878-88,202,878 , GRCh38.p12 chr6: 87,493,160-87,493,160 SLC35A1
    nsv4457169copy number variation1nstd102humanUncertain significance GRCh37 chr6: 88,095,499-88,341,035 , GRCh38.p12 chr6: 87,385,781-87,631,317 ST13P16, CFAP206, 7 more genes
    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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