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Items: 1 to 20 of 247

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112661copy number variation1nstd102humanPathogenic GRCh37 chr1: 231,407,943-237,289,859 , GRCh38.p12 chr1: 231,272,197-237,126,559 LOC105373207, LOC105373210, 113 more genes
    nsv5972650inversion1nstd209human GRCh38 chr1: 229,174,728-232,234,598 , GRCh37.p13 chr1: 229,310,475-232,370,344 , ACTA1, 68 more genes
    nsv5971633inversion1nstd209human GRCh38 chr1: 229,416,331-231,831,980 , GRCh37.p13 chr1: 229,552,078-231,967,726 , ACTA1, 56 more genes
    nsv5966299insertion1nstd209human GRCh38 chr1: 231,589,470-231,589,470 , GRCh37.p13 chr1: 231,725,216-231,725,216 TSNAX-DISC1, LINC00582
    nsv5955278insertion1nstd209human GRCh38 chr1: 231,603,518-231,603,518 , GRCh37.p13 chr1: 231,739,264-231,739,264 LINC00582, TSNAX-DISC1
    nsv5876684copy number variation1nstd209human GRCh38 chr1: 231,589,485-231,589,611 , GRCh37.p13 chr1: 231,725,231-231,725,357 LINC00582, TSNAX-DISC1
    nsv5690962mobile element insertion2nstd211human GRCh38 chr1: 231,589,485-231,589,485 , GRCh37.p13 chr1: 231,725,231-231,725,231 TSNAX-DISC1, LINC00582
    nsv5623416insertion1nstd207human GRCh38 chr1: 231,589,470-231,589,470 , GRCh37.p13 chr1: 231,725,216-231,725,216 LINC00582, TSNAX-DISC1
    nsv5438247copy number variation1nstd206human GRCh38 chr1: 231,574,349-231,678,810 , GRCh37.p13 chr1: 231,710,095-231,814,556 TSNAX-DISC1, RNU5A-5P, 2 more genes
    nsv5434935copy number variation1nstd206human GRCh38 chr1: 231,607,840-231,608,256 , GRCh37.p13 chr1: 231,743,586-231,744,002 LINC00582, TSNAX-DISC1
    nsv5381285copy number variation2nstd102humanUncertain significance GRCh37 chr1: 130,980,840-248,900,000 , GRCh38.p12 chr1: 120,324,463-248,736,699 , DCST1, 2428 more genes
    nsv5356069translocation1nstd200human GRCh38 chr1: 231,608,241-231,608,241 , GRCh38 chr1: 231,607,840-231,607,840 , GRCh37.p13 chr1: 231,743,987-231,743,987 , GRCh37.p13 chr1: 231,743,586-231,743,586 LINC00582, TSNAX-DISC1
    nsv5341269translocation1nstd200human GRCh37 chr1: 231,743,987-231,743,987 , GRCh37 chr1: 231,743,586-231,743,586 , GRCh38.p12 chr1: 231,607,840-231,607,840 , GRCh38.p12 chr1: 231,608,241-231,608,241 LINC00582, TSNAX-DISC1
    nsv5286799copy number variation1nstd204human GRCh38.p13 chr1: 231,574,319-231,678,839 , GRCh37.p13 chr1: 231,710,065-231,814,585 TSNAX-DISC1, RNU5A-5P, 2 more genes
    nsv5219457copy number variation1nstd204human GRCh38.p13 chr1: 231,574,101-231,677,900 , GRCh37.p13 chr1: 231,709,847-231,813,646 TSNAX-DISC1, RNU5A-5P, 2 more genes
    nsv5077101mobile element insertion1nstd203human GRCh38 chr1: 231,589,475-231,589,485 , GRCh37.p13 chr1: 231,725,221-231,725,231 LINC00582, TSNAX-DISC1
    nsv5069634mobile element insertion1nstd203human GRCh38 chr1: 231,589,482-231,589,482 , GRCh37.p13 chr1: 231,725,228-231,725,228 LINC00582, TSNAX-DISC1
    nsv5069039mobile element insertion1nstd203human GRCh38 chr1: 231,589,472-231,589,485 , GRCh37.p13 chr1: 231,725,218-231,725,231 TSNAX-DISC1, LINC00582
    nsv5067674mobile element insertion1nstd203human GRCh38 chr1: 231,589,476-231,589,485 , GRCh37.p13 chr1: 231,725,222-231,725,231 TSNAX-DISC1, LINC00582
    nsv5066290mobile element insertion1nstd203human GRCh38 chr1: 231,589,473-231,589,485 , GRCh37.p13 chr1: 231,725,219-231,725,231 TSNAX-DISC1, LINC00582
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