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Items: 1 to 20 of 152

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    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
    nsv6900951copy number variation1nstd229human GRCh38 chr11: 94,226,301-94,447,000 , GRCh37.p13 chr11: 93,959,467-94,180,166 MRE11, LOC105369435, 2 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
    nsv6621229copy number variation1nstd224human GRCh37 chr11: 93,651,071-94,149,349 , GRCh38.p12 chr11: 93,917,905-94,416,183 HEPHL1, ARPC3P3, 8 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
    nsv6468885copy number variation1nstd223human GRCh38 chr11: 94,389,463-94,391,610 , GRCh37.p13 chr11: 94,122,629-94,124,776 GPR83
    nsv6462187copy number variation1nstd223human GRCh38 chr11: 94,383,886-94,387,677 , GRCh37.p13 chr11: 94,117,052-94,120,843 GPR83
    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
    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
    nsv5511708copy number variation1nstd206human GRCh38 chr11: 94,376,171-94,376,288 , GRCh37.p13 chr11: 94,109,337-94,109,454 GPR83
    nsv5501054copy number variation1nstd206human GRCh38 chr11: 94,374,439-94,390,344 , GRCh37.p13 chr11: 94,107,605-94,123,510 GPR83
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