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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5975846insertion1nstd209human GRCh38 chr11: 14,276,623-14,276,623 , GRCh37.p13 chr11|NW_003871075.1: 334,707-334,707 , GRCh37.p13 chr11: 14,298,169-14,298,169 RRAS2
    nsv5969539insertion1nstd209human GRCh38 chr11: 14,332,702-14,332,702 , GRCh37.p13 chr11|NW_003871075.1: 390,786-390,786 , GRCh37.p13 chr11: 14,354,248-14,354,248 RRAS2
    nsv5925270copy number variation1nstd209human GRCh38 chr11: 14,326,764-14,327,079 , GRCh37.p13 chr11|NW_003871075.1: 384,848-385,163 , GRCh37.p13 chr11: 14,348,310-14,348,625 RRAS2
    nsv5912009copy number variation1nstd209human GRCh38 chr11: 14,351,613-14,351,777 , GRCh37.p13 chr11|NW_003871075.1: 409,697-409,861 , GRCh37.p13 chr11: 14,373,159-14,373,323 RRAS2
    nsv5909565copy number variation1nstd209human GRCh38 chr11: 14,363,521-14,363,822 , GRCh37.p13 chr11: 14,385,067-14,385,368 , GRCh37.p13 chr11|NW_003871075.1: 421,605-421,906 RRAS2
    nsv5717024mobile element insertion1nstd211human GRCh38 chr11: 14,327,227-14,327,227 , GRCh37.p13 chr11|NW_003871075.1: 385,311-385,311 , GRCh37.p13 chr11: 14,348,773-14,348,773 RRAS2
    nsv5707389mobile element insertion1nstd211human GRCh38 chr11: 14,341,476-14,341,476 , GRCh37.p13 chr11|NW_003871075.1: 399,560-399,560 , GRCh37.p13 chr11: 14,363,022-14,363,022 RRAS2
    nsv5699604mobile element insertion2nstd211human GRCh38 chr11: 14,280,260-14,280,260 , GRCh37.p13 chr11|NW_003871075.1: 338,344-338,344 , GRCh37.p13 chr11: 14,301,806-14,301,806 RRAS2
    nsv5655807insertion1nstd207human GRCh38 chr11: 14,276,623-14,276,623 , GRCh37.p13 chr11|NW_003871075.1: 334,707-334,707 , GRCh37.p13 chr11: 14,298,169-14,298,169 RRAS2
    nsv5600390copy number variation1nstd207human GRCh38 chr11: 14,326,764-14,327,079 , GRCh37.p13 chr11|NW_003871075.1: 384,848-385,163 , GRCh37.p13 chr11: 14,348,310-14,348,625 RRAS2
    nsv5507832copy number variation1nstd206human GRCh38 chr11: 14,326,779-14,327,080 , GRCh37.p13 chr11: 14,348,325-14,348,626 , GRCh37.p13 chr11|NW_003871075.1: 384,863-385,164 RRAS2
    nsv5407419mobile element insertion1nstd206human GRCh38 chr11: 14,341,476-14,341,527 , GRCh37.p13 chr11|NW_003871075.1: 399,560-399,611 , GRCh37.p13 chr11: 14,363,022-14,363,073 RRAS2
    nsv5397942mobile element insertion1nstd206human GRCh38 chr11: 14,280,260-14,280,311 , GRCh37.p13 chr11: 14,301,806-14,301,857 , GRCh37.p13 chr11|NW_003871075.1: 338,344-338,395 RRAS2
    nsv5382137mobile element deletion2nstd186human GRCh37 chr11: 14,348,325-14,348,626 , GRCh38.p12 chr11: 14,326,779-14,327,080 RRAS2
    nsv5380796copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397 FAUP4, MMP7, 2031 more genes
    nsv5354761translocation1nstd200human GRCh38 chr11: 14,340,040-14,340,040 , GRCh38 chr11: 14,340,182-14,340,182 , GRCh37.p13 chr11|NW_003871075.1: 398,266-398,266 , GRCh37.p13 chr11: 14,361,728-14,361,728 , GRCh37.p13 chr11|NW_003871075.1: 398,124-398,124 , GRCh37.p13 chr11: 14,361,586-14,361,586 RRAS2
    nsv5241221copy number variation1nstd204human GRCh38.p13 chr11: 14,326,801-14,327,100 , GRCh37.p13 chr11|NW_003871075.1: 384,885-385,184 , GRCh37.p13 chr11: 14,348,347-14,348,646 RRAS2
    nsv5209907mobile element deletion1nstd204human GRCh38.p13 chr11: 14,326,779-14,327,080 , GRCh37.p13 chr11|NW_003871075.1: 384,863-385,164 , GRCh37.p13 chr11: 14,348,325-14,348,626 RRAS2
    nsv5134413mobile element insertion1nstd203human GRCh38 chr11: 14,350,736-14,350,743 , GRCh37.p13 chr11: 14,372,282-14,372,289 , GRCh37.p13 chr11|NW_003871075.1: 408,820-408,827 RRAS2
    nsv5130550mobile element insertion1nstd203human GRCh38 chr11: 14,296,185-14,296,192 , GRCh37.p13 chr11|NW_003871075.1: 354,269-354,276 , GRCh37.p13 chr11: 14,317,731-14,317,738 RRAS2
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