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Items: 1 to 20 of 275

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5957699insertion1nstd209human GRCh38 chr2: 201,297,309-201,297,309 , GRCh37.p13 chr2: 202,162,032-202,162,032 FLACC1
    nsv5952875insertion1nstd209human GRCh38 chr2: 201,309,925-201,309,925 , GRCh37.p13 chr2: 202,174,648-202,174,648 FLACC1
    nsv5905198copy number variation1nstd209human GRCh38 chr2: 201,332,775-201,341,868 , GRCh37.p13 chr2: 202,197,498-202,206,591 FLACC1
    nsv5897454copy number variation1nstd209human GRCh38 chr2: 201,221,824-201,490,725 , GRCh37.p13 chr2: 202,086,547-202,355,448 CASP8, CASP10, 5 more genes
    nsv5889121copy number variation1nstd209human GRCh38 chr2: 201,356,124-201,356,221 , GRCh37.p13 chr2: 202,220,847-202,220,944 FLACC1
    nsv5832365copy number variation1nstd209human GRCh38 chr2: 201,332,879-201,341,826 , GRCh37.p13 chr2: 202,197,602-202,206,549 FLACC1
    nsv5832147copy number variation1nstd209human GRCh38 chr2: 201,335,820-201,337,619 , GRCh37.p13 chr2: 202,200,543-202,202,342 FLACC1
    nsv5831847copy number variation1nstd209human GRCh38 chr2: 201,295,027-201,304,011 , GRCh37.p13 chr2: 202,159,750-202,168,734 FLACC1
    nsv5693930mobile element insertion1nstd211human GRCh38 chr2: 201,288,645-201,288,645 , GRCh37.p13 chr2: 202,153,368-202,153,368 FLACC1
    nsv5680584mobile element insertion2nstd211human GRCh38 chr2: 201,339,071-201,339,071 , GRCh37.p13 chr2: 202,203,794-202,203,794 FLACC1
    nsv5607661insertion1nstd207human GRCh38 chr2: 201,339,055-201,339,055 , GRCh37.p13 chr2: 202,203,778-202,203,778 FLACC1
    nsv5604713insertion1nstd207human GRCh38 chr2: 201,288,631-201,288,631 , GRCh37.p13 chr2: 202,153,354-202,153,354 FLACC1
    nsv5560580sequence alteration1nstd206human GRCh38 chr2: 151,447,581-231,256,535 , GRCh37.p13 chr2: 152,304,095-232,121,248 , ATIC, 1163 more genes
    nsv5549575insertion1nstd206human GRCh38 chr2: 201,297,308-201,297,310 , GRCh37.p13 chr2: 202,162,031-202,162,033 FLACC1
    nsv5447167copy number variation1nstd206human GRCh38 chr2: 201,332,775-201,341,869 , GRCh37.p13 chr2: 202,197,498-202,206,592 FLACC1
    nsv5444013copy number variation1nstd206human GRCh38 chr2: 201,285,753-201,286,753 , GRCh37.p13 chr2: 202,150,476-202,151,476 CASP8, FLACC1
    nsv5439636copy number variation1nstd206human GRCh38 chr2: 201,344,341-201,359,800 , GRCh37.p13 chr2: 202,209,064-202,224,523 FLACC1
    nsv5437794copy number variation1nstd206human GRCh38 chr2: 201,292,036-201,301,432 , GRCh37.p13 chr2: 202,156,759-202,166,155 FLACC1
    nsv5411480mobile element insertion1nstd206human GRCh38 chr2: 201,288,645-201,288,696 , GRCh37.p13 chr2: 202,153,368-202,153,419 FLACC1
    nsv5405926mobile element insertion1nstd206human GRCh38 chr2: 201,339,071-201,339,122 , GRCh37.p13 chr2: 202,203,794-202,203,845 FLACC1
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