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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137788copy number variation1nstd102humanPathogenic GRCh37 chr2: 24,601,818-43,466,284 , GRCh38.p12 chr2: 24,378,949-43,239,145 GTF3C2-AS1, MAPRE3-AS1, 316 more genes
    nsv6112680copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 24,881,528-43,460,021 , GRCh38.p12 chr2: 24,658,659-43,232,882 ADCY3, ALK, 314 more genes
    nsv5958970insertion1nstd209human GRCh38 chr2: 39,088,184-39,088,184 , GRCh37.p13 chr2: 39,315,325-39,315,325 SOS1
    nsv5956888insertion1nstd209human GRCh38 chr2: 39,038,732-39,038,732 , GRCh37.p13 chr2: 39,265,873-39,265,873 SOS1
    nsv5951633insertion1nstd209human GRCh38 chr2: 39,079,154-39,079,154 , GRCh37.p13 chr2: 39,306,295-39,306,295 SOS1
    nsv5877712copy number variation1nstd209human GRCh38 chr2: 39,036,843-39,036,938 , GRCh37.p13 chr2: 39,263,984-39,264,079 SOS1
    nsv5832986copy number variation1nstd209human GRCh38 chr2: 39,072,644-39,086,699 , GRCh37.p13 chr2: 39,299,785-39,313,840 RNU6-198P, SOS1
    nsv5832901copy number variation1nstd209human GRCh38 chr2: 39,085,350-39,096,861 , GRCh37.p13 chr2: 39,312,491-39,324,002 SOS1, HSPE1P13
    nsv5832900copy number variation1nstd209human GRCh38 chr2: 39,035,623-39,037,722 , GRCh37.p13 chr2: 39,262,764-39,264,863 SOS1
    nsv5720949mobile element insertion1nstd211human GRCh38 chr2: 39,024,765-39,024,765 , GRCh37.p13 chr2: 39,251,906-39,251,906 SOS1
    nsv5691168mobile element insertion1nstd211human GRCh38 chr2: 39,112,183-39,112,183 , GRCh37.p13 chr2: 39,339,324-39,339,324 SOS1
    nsv5687833mobile element insertion2nstd211human GRCh38 chr2: 39,088,198-39,088,198 , GRCh37.p13 chr2: 39,315,339-39,315,339 SOS1
    nsv5683239mobile element insertion1nstd211human GRCh38 chr2: 38,997,236-38,997,236 , GRCh37.p13 chr2: 39,224,377-39,224,377 SOS1
    nsv5681696mobile element insertion1nstd211human GRCh38 chr2: 39,112,180-39,112,180 , GRCh37.p13 chr2: 39,339,321-39,339,321 SOS1
    nsv5616161insertion1nstd207human GRCh38 chr2: 39,088,183-39,088,183 , GRCh37.p13 chr2: 39,315,324-39,315,324 SOS1
    nsv5608670insertion1nstd207human GRCh38 chr2: 39,079,154-39,079,154 , GRCh37.p13 chr2: 39,306,295-39,306,295 SOS1
    nsv5544970insertion1nstd206human GRCh38 chr2: 39,088,183-39,088,183 , GRCh37.p13 chr2: 39,315,324-39,315,324 SOS1
    nsv5541790insertion1nstd206human GRCh38 chr2: 39,079,156-39,079,205 , GRCh37.p13 chr2: 39,306,297-39,306,346 SOS1
    nsv5441166copy number variation1nstd206human GRCh38 chr2: 39,001,719-39,001,824 , GRCh37.p13 chr2: 39,228,860-39,228,965 SOS1
    nsv5437107copy number variation1nstd206human GRCh38 chr2: 39,089,991-39,090,585 , GRCh37.p13 chr2: 39,317,132-39,317,726 SOS1
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