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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137270copy number variation1nstd232human GRCh37.p13 chr11: 61,578,350-61,578,443 , GRCh38.p12 chr11: 61,810,878-61,810,971 FADS1
    nsv7093694copy number variation2nstd102humanUncertain significance GRCh37 chr11: 58,916,346-64,972,349 , GRCh38.p12 chr11: 59,148,873-65,204,878 VPS37C, POLR2G, 298 more genes
    nsv7076174inversion1nstd229human GRCh38 chr11: 57,437,573-64,138,990 , GRCh37.p13 chr11: 57,205,046-63,906,462 RNU2-2P, SLC43A1, 299 more genes
    nsv7073883inversion1nstd229human GRCh38 chr11: 61,802,175-61,802,267 , GRCh37.p13 chr11: 61,569,647-61,569,739 FADS1
    nsv6917433copy number variation1nstd229human GRCh38 chr11: 61,472,401-62,010,600 , GRCh37.p13 chr11: 61,239,873-61,778,072 LOC105369329, FADS3, 24 more genes
    nsv6909200copy number variation1nstd229human GRCh38 chr11: 61,458,001-62,069,400 , GRCh37.p13 chr11: 61,225,473-61,836,872 RPS2P37, BEST1, 25 more genes
    nsv6905915copy number variation1nstd229human GRCh38 chr11: 61,787,251-61,820,694 , GRCh37.p13 chr11: 61,554,723-61,588,166 FADS2, MYRF, 5 more genes
    nsv6905877copy number variation1nstd229human GRCh38 chr11: 60,405,001-68,536,600 , GRCh37.p13 chr11: 60,172,474-68,304,068 INCENP, SNRPCP12, 409 more genes
    nsv6904042copy number variation1nstd229human GRCh38 chr11: 61,456,701-62,012,000 , GRCh37.p13 chr11: 61,224,173-61,779,472 LOC399900, LRRC10B, 24 more genes
    nsv6903095copy number variation1nstd229human GRCh38 chr11: 59,466,654-66,168,743 , GRCh37.p13 chr11: 59,234,127-65,936,214 LINC02724, TMEM132A, 342 more genes
    nsv6899072copy number variation1nstd229human GRCh38 chr11: 61,801,418-61,801,619 , GRCh37.p13 chr11: 61,568,890-61,569,091 FADS1
    nsv6591399inversion1nstd223human GRCh38 chr11: 61,798,160-61,798,916 , GRCh37.p13 chr11: 61,565,632-61,566,388 FADS1
    nsv6315537copy number variation1nstd102humanPathogenic GRCh37 chr11: 32,799,481-134,938,470 , GRCh38.p12 chr11: 32,777,935-135,068,576 PYGM, ATL3, 2125 more genes
    nsv5922208copy number variation1nstd209human GRCh38 chr11: 61,815,124-61,815,180 , GRCh37.p13 chr11: 61,582,596-61,582,652 FADS1, FADS2, 1 more genes
    nsv5851041copy number variation2nstd209human GRCh38 chr11: 61,816,293-61,817,335 , GRCh37.p13 chr11: 61,583,765-61,584,807 FADS1, FADS2
    nsv5503897copy number variation1nstd206human GRCh38 chr11: 61,815,230-61,815,282 , GRCh37.p13 chr11: 61,582,702-61,582,754 FADS2, FADS1, 1 more genes
    nsv5500867copy number variation1nstd206human GRCh38 chr11: 61,801,930-61,802,010 , GRCh37.p13 chr11: 61,569,402-61,569,482 FADS1
    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
    nsv4979659copy number variation1nstd200human GRCh38 chr11: 61,801,930-61,802,010 , GRCh37.p13 chr11: 61,569,402-61,569,482 FADS1
    nsv4831453copy number variation1nstd200human GRCh37 chr11: 61,569,402-61,569,482 , GRCh38.p12 chr11: 61,801,930-61,802,010 FADS1
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