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Items: 1 to 20 of 120

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7093485insertion1nstd102humanPathogenic GRCh37 chr11: 94,225,954-94,225,954 , GRCh38 chr11: 94,492,788-94,492,788 MRE11, ANKRD49
    nsv7075541inversion1nstd229human GRCh38 chr11: 94,207,671-94,586,565 , GRCh37.p13 chr11: 93,940,837-94,319,731 MIR548L, ANKRD49, 8 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
    nsv7059549inversion1nstd229human GRCh38 chr11: 94,203,472-94,594,522 , GRCh37.p13 chr11: 93,936,638-94,327,688 FUT4, MRE11, 8 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
    nsv6909251copy number variation1nstd229human GRCh38 chr11: 94,489,103-94,493,643 , GRCh37.p13 chr11: 94,222,269-94,226,809 ANKRD49, MRE11
    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
    nsv6902508copy number variation1nstd229human GRCh38 chr11: 94,200,856-94,580,935 , GRCh37.p13 chr11: 93,934,022-94,314,101 ANKRD49, MIR548L, 8 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
    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
    nsv6582429inversion1nstd223human GRCh38 chr11: 93,899,951-96,855,215 , GRCh37.p13 chr11: 93,633,117-96,726,215 MIR1260B, KDM4E, 51 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
    nsv6314859copy number variation1nstd102humanPathogenic GRCh37 chr11: 94,153,291-94,225,967 , GRCh38.p12 chr11: 94,420,125-94,492,801 MIR548L, MRE11, 1 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
    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
    nsv5672640copy number variation1nstd102humanPathogenic GRCh37 chr11: 94,153,285-111,965,700 , GRCh38.p12 chr11: 94,420,119-112,094,976 HSPD1P13, CARD17P, 239 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
    nsv5037979inversion1nstd200human GRCh38 chr11: 93,899,952-96,855,215 , GRCh37.p13 chr11: 93,633,118-96,726,215 , GPR83, 52 more genes
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