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Items: 1 to 20 of 209

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099226copy number variation1nstd231human GRCh38.p12 chr1: 115,063,638-119,984,872 , GRCh37 chr1: 115,606,259-120,527,495 ATP1A1, CASQ2, 103 more genes
    nsv7041105inversion1nstd229human GRCh38 chr1: 117,078,493-117,078,506 , GRCh37.p13 chr1: 117,621,115-117,621,128 TTF2
    nsv6640665copy number variation1nstd229human GRCh38 chr1: 117,054,415-117,066,575 , GRCh37.p13 chr1: 117,597,037-117,609,197 CD101-AS1, TTF2
    nsv6640592copy number variation1nstd229human GRCh38 chr1: 117,066,098-117,066,964 , GRCh37.p13 chr1: 117,608,720-117,609,586 TTF2
    nsv6640489copy number variation1nstd229human GRCh38 chr1: 117,070,001-117,090,900 , GRCh37.p13 chr1: 117,612,623-117,633,522 TTF2
    nsv6640488copy number variation1nstd229human GRCh38 chr1: 117,065,468-117,071,876 , GRCh37.p13 chr1: 117,608,090-117,614,498 TTF2
    nsv6640485copy number variation1nstd229human GRCh38 chr1: 116,936,483-117,173,099 , GRCh37.p13 chr1: 117,479,105-117,715,721 CD101, CD101-AS1, 7 more genes
    nsv6636499copy number variation1nstd102humanUncertain significance GRCh37 chr1: 117,590,849-117,994,398 , GRCh38.p12 chr1: 117,048,227-117,451,776 RPS15AP9, CD101-AS1, 6 more genes
    nsv6625102copy number variation1nstd224human GRCh37 chr1: 117,524,022-117,675,943 , GRCh38.p12 chr1: 116,981,400-117,133,321 PTGFRN, TTF2, 4 more genes
    nsv6548874inversion1nstd223human GRCh38 chr1: 117,066,697-117,067,250 , GRCh37.p13 chr1: 117,609,319-117,609,872 TTF2
    nsv6539475inversion1nstd223human GRCh38 chr1: 117,078,998-117,080,021 , GRCh37.p13 chr1: 117,621,620-117,622,643 TTF2
    nsv6334222copy number variation1nstd223human GRCh38 chr1: 117,100,223-117,440,236 , GRCh37.p13 chr1: 117,642,845-117,982,858 MAN1A2, TRIM45, 4 more genes
    nsv6330157copy number variation1nstd223human GRCh38 chr1: 117,060,716-117,061,162 , GRCh37.p13 chr1: 117,603,338-117,603,784 TTF2
    nsv6326280copy number variation1nstd223human GRCh38 chr1: 117,048,625-117,440,243 , GRCh37.p13 chr1: 117,591,247-117,982,865 VTCN1, RPS15AP9, 6 more genes
    nsv6313671copy number variation1nstd102humanPathogenic GRCh37 chr1: 111,647,582-121,343,783 , GRCh38.p12 chr1: 111,104,960-121,601,985 GAPDHP23, RNA5SP56, 243 more genes
    nsv6133921copy number variation1nstd213human GRCh37 chr1: 117,510,000-117,770,001 , GRCh38.p12 chr1: 116,967,378-117,227,379 PTGFRN, TTF2, 6 more genes
    nsv6133550copy number variation1nstd213human GRCh37 chr1: 117,260,000-118,670,001 , GRCh38.p12 chr1: 116,717,378-118,127,378 PTGFRN, CD101, 23 more genes
    nsv5882498copy number variation1nstd209human GRCh38 chr1: 117,066,098-117,066,963 , GRCh37.p13 chr1: 117,608,720-117,609,585 TTF2
    nsv5689305mobile element insertion2nstd211human GRCh38 chr1: 117,095,600-117,095,600 , GRCh37.p13 chr1: 117,638,222-117,638,222 TTF2
    nsv5677985mobile element insertion1nstd211human GRCh38 chr1: 117,059,386-117,059,386 , GRCh37.p13 chr1: 117,602,008-117,602,008 CD101-AS1, TTF2
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