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Items: 1 to 20 of 108

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7070229inversion1nstd229human GRCh38 chr11: 92,451,554-94,033,544 , GRCh37.p13 chr11: 92,184,720-93,766,710 SNORA32, SNORA18, 30 more genes
    nsv7067820inversion1nstd229human GRCh38 chr11: 93,730,825-93,742,908 , GRCh37.p13 chr11: 93,463,991-93,476,074 CEP295, SNORA1, 10 more genes
    nsv7060154inversion1nstd229human GRCh38 chr11: 89,626,991-96,425,689 , GRCh37.p13 chr11: 89,360,159-96,158,853 LINC02756, OSBPL9P2, 119 more genes
    nsv6914121copy number variation1nstd229human GRCh38 chr11: 89,708,489-94,988,932 , GRCh37.p13 chr11: 89,441,657-94,611,845 SNORA40, PIWIL4-AS1, 89 more genes
    nsv6909837copy number variation1nstd229human GRCh38 chr11: 93,612,993-93,771,009 , GRCh37.p13 chr11: 93,346,159-93,504,175 SNORA1, CEP295, 11 more genes
    nsv6907347copy number variation1nstd229human GRCh38 chr11: 89,715,432-96,566,090 , GRCh37.p13 chr11: 89,448,600-96,287,584 DISC1FP1, RPL32P25, 120 more genes
    nsv6900323copy number variation1nstd229human GRCh38 chr11: 93,200,748-96,340,159 , GRCh37.p13 chr11: 92,933,914-96,073,323 FGFR3P2, LOC112268080, 67 more genes
    nsv6637499copy number variation1nstd102humanUncertain significance GRCh37 chr11: 92,875,858-93,489,964 , GRCh38.p12 chr11: 93,142,692-93,756,798 CEP295, SRP14P2, 18 more genes
    nsv6637396copy number variation1nstd102humanPathogenic GRCh37 chr11: 81,478,509-104,667,040 , GRCh38.p12 chr11: 81,767,467-104,796,313 LOC107984375, RN7SL222P, 295 more genes
    nsv6583138inversion1nstd223human GRCh38 chr11: 93,730,825-93,742,911 , GRCh37.p13 chr11: 93,463,991-93,476,077 MIR1304, SNORD5, 10 more genes
    nsv6471203copy number variation1nstd223human GRCh38 chr11: 93,730,001-93,733,100 , GRCh37.p13 chr11: 93,463,167-93,466,266 SNORD5, SNORD6, 8 more genes
    nsv6459070copy number variation1nstd223human GRCh38 chr11: 92,156,862-95,481,795 , GRCh37.p13 chr11: 91,890,028-95,214,959 FUT4, KDM4D, 66 more genes
    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
    nsv6314019copy number variation1nstd102humanUncertain significance GRCh37 chr11: 90,906,452-94,437,087 , GRCh38.p12 chr11: 91,173,284-94,703,921 PGAM1P9, C11orf97, 52 more genes
    nsv6313961copy number variation1nstd102humanPathogenic GRCh37 chr11: 77,855,209-98,002,445 , GRCh38.p12 chr11: 78,144,163-98,131,717 MTND5P38, XIAPP2, 252 more genes
    nsv6313939copy number variation1nstd102humanUncertain significance GRCh37 chr11: 93,434,593-93,506,496 , GRCh38.p12 chr11: 93,701,427-93,773,330 SNORA32, SNORA40, 11 more genes
    nsv6290834copy number variation1nstd102humanUncertain significance GRCh37 chr11: 85,422,071-118,022,671 , GRCh38.p12 chr11: 85,711,028-118,151,956 CARD17P, RNA5SP350, 480 more genes
    nsv5497804copy number variation1nstd206human GRCh38 chr11: 93,482,000-94,038,896 , GRCh37.p13 chr11: 93,215,166-93,772,062 SNORA1, HPRT1P3, 20 more genes
    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
    nsv4989175copy number variation1nstd200human GRCh38 chr11: 93,501,300-93,857,533 , GRCh37.p13 chr11: 93,234,466-93,590,699 VSTM5, SNORA18, 17 more genes
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