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Items: 1 to 20 of 135

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7048729inversion1nstd229human GRCh38 chr2: 10,950,861-12,841,358 , GRCh37.p13 chr2: 11,090,987-12,981,484 LOC101929752, LOC105373431, 34 more genes
    nsv6666576copy number variation1nstd229human GRCh38 chr2: 6,592,339-11,769,396 , GRCh37.p13 chr2: 6,732,471-11,909,522 RN7SKP112, LOC101929861, 103 more genes
    nsv6658181copy number variation1nstd229human GRCh38 chr2: 11,291,814-11,791,449 , GRCh37.p13 chr2: 11,431,940-11,931,575 PPIAP60, TRG-CCC7-1, 17 more genes
    nsv6636815copy number variation1nstd102humanPathogenic GRCh37 chr2: 706,460-35,523,639 , GRCh38.p12 chr2: 706,460-35,298,573 LOC105374455, RN7SL674P, 504 more genes
    nsv6636734copy number variation1nstd102humanUncertain significance GRCh37 chr2: 11,410,615-12,064,438 , GRCh38.p12 chr2: 11,270,489-11,924,312 LINC00570, LOC105373429, 19 more genes
    nsv6634330copy number variation1nstd102humanPathogenic GRCh37 chr2: 11,504,318-111,365,996 , GRCh38.p12 chr2: 11,364,192-110,608,419 CYP1B1-AS1, LOC107985771, 1649 more genes
    nsv6346427copy number variation1nstd223human GRCh38 chr2: 11,457,558-11,468,815 , GRCh37.p13 chr2: 11,597,684-11,608,941 E2F6
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 more genes
    nsv6290643copy number variation1nstd102humanUncertain significance GRCh37 chr2: 8,935,077-15,722,794 , GRCh38.p12 chr2: 8,794,947-15,582,670 PPIAP60, LOC105373431, 95 more genes
    nsv6290363copy number variation1nstd102humanUncertain significance GRCh37 chr2: 9,717,186-12,013,065 , GRCh38.p12 chr2: 9,577,057-11,872,939 RNU4-73P, CYS1, 56 more genes
    nsv5873193copy number variation1nstd209human GRCh38 chr2: 11,453,798-11,465,770 , GRCh37.p13 chr2: 11,593,924-11,605,896 E2F6
    nsv5684780mobile element insertion1nstd211human GRCh38 chr2: 11,445,217-11,445,217 , GRCh37.p13 chr2: 11,585,343-11,585,343 E2F6
    nsv5400519mobile element insertion1nstd206human GRCh38 chr2: 11,445,217-11,445,268 , GRCh37.p13 chr2: 11,585,343-11,585,394 E2F6
    nsv5068870mobile element insertion1nstd203human GRCh38 chr2: 11,458,518-11,458,529 , GRCh37.p13 chr2: 11,598,644-11,598,655 E2F6
    nsv5068686mobile element insertion1nstd203human GRCh38 chr2: 11,458,520-11,458,529 , GRCh37.p13 chr2: 11,598,646-11,598,655 E2F6
    nsv5060265mobile element insertion1nstd203human GRCh38 chr2: 11,458,522-11,458,529 , GRCh37.p13 chr2: 11,598,648-11,598,655 E2F6
    nsv4728305copy number variation1nstd102humanUncertain significance GRCh37 chr2: 11,144,226-12,569,011 , GRCh38.p12 chr2: 11,004,100-12,428,885 RNA5SP85, TRG-CCC7-1, 30 more genes
    nsv4661841copy number variation1nstd186human GRCh37 chr2: 11,586,006-11,586,323 , GRCh38.p12 chr2: 11,445,880-11,446,197 E2F6
    nsv4594875copy number variation1nstd183human GRCh37 chr2: 11,585,486-11,586,713 , GRCh38.p12 chr2: 11,445,360-11,446,587 E2F6
    nsv4594874copy number variation2nstd183human GRCh37 chr2: 11,585,295-11,586,323 , GRCh38.p12 chr2: 11,445,169-11,446,197 E2F6
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