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Items: 1 to 20 of 321

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5950278insertion1nstd209human GRCh38 chr2: 201,766,722-201,766,722 , GRCh37.p13 chr2: 202,631,445-202,631,445 ALS2
    nsv5888641copy number variation1nstd209human GRCh38 chr2: 201,739,128-201,740,215 , GRCh37.p13 chr2: 202,603,851-202,604,938 ALS2
    nsv5722200mobile element insertion1nstd211human GRCh38 chr2: 201,726,204-201,726,204 , GRCh37.p13 chr2: 202,590,927-202,590,927 ALS2
    nsv5682186mobile element insertion1nstd211human GRCh38 chr2: 201,752,555-201,752,555 , GRCh37.p13 chr2: 202,617,278-202,617,278 ALS2
    nsv5680683mobile element insertion2nstd211human GRCh38 chr2: 201,766,737-201,766,737 , GRCh37.p13 chr2: 202,631,460-202,631,460 ALS2
    nsv5678474mobile element insertion2nstd211human GRCh38 chr2: 201,777,277-201,777,277 , GRCh37.p13 chr2: 202,642,000-202,642,000 ALS2
    nsv5617399insertion1nstd207human GRCh38 chr2: 201,777,261-201,777,261 , GRCh37.p13 chr2: 202,641,984-202,641,984 ALS2
    nsv5607150insertion1nstd207human GRCh38 chr2: 201,766,722-201,766,722 , GRCh37.p13 chr2: 202,631,445-202,631,445 ALS2
    nsv5562343mobile element insertion1nstd206human GRCh38 chr2: 201,726,204-201,726,255 , GRCh37.p13 chr2: 202,590,927-202,590,978 ALS2
    nsv5560580sequence alteration1nstd206human GRCh38 chr2: 151,447,581-231,256,535 , GRCh37.p13 chr2: 152,304,095-232,121,248 , ATIC, 1163 more genes
    nsv5553030insertion1nstd206human GRCh38 chr2: 201,777,277-201,777,312 , GRCh37.p13 chr2: 202,642,000-202,642,035 ALS2
    nsv5449467copy number variation1nstd206human GRCh38 chr2: 201,752,021-201,752,177 , GRCh37.p13 chr2: 202,616,744-202,616,900 ALS2
    nsv5441922copy number variation1nstd206human GRCh38 chr2: 201,739,121-201,740,216 , GRCh37.p13 chr2: 202,603,844-202,604,939 ALS2
    nsv5399865mobile element insertion1nstd206human GRCh38 chr2: 201,752,555-201,752,566 , GRCh37.p13 chr2: 202,617,278-202,617,289 ALS2
    nsv5190325mobile element insertion1nstd203human GRCh38 chr2: 201,737,482-201,737,497 , GRCh37.p13 chr2: 202,602,205-202,602,220 ALS2
    nsv5079726mobile element insertion1nstd203human GRCh38 chr2: 201,766,724-201,766,737 , GRCh37.p13 chr2: 202,631,447-202,631,460 ALS2
    nsv5077821mobile element insertion1nstd203human GRCh38 chr2: 201,763,570-201,763,583 , GRCh37.p13 chr2: 202,628,293-202,628,306 RPS2P16, ALS2
    nsv5077496mobile element insertion1nstd203human GRCh38 chr2: 201,777,261-201,777,277 , GRCh37.p13 chr2: 202,641,984-202,642,000 ALS2
    nsv5076704mobile element insertion1nstd203human GRCh38 chr2: 201,766,726-201,766,737 , GRCh37.p13 chr2: 202,631,449-202,631,460 ALS2
    nsv5074563mobile element insertion1nstd203human GRCh38 chr2: 201,766,729-201,766,737 , GRCh37.p13 chr2: 202,631,452-202,631,460 ALS2
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