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Items: 1 to 20 of 239

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7145792copy number variation1nstd232human GRCh37.p13 chr11: 2,148,416-2,148,475 , GRCh38.p12 chr11: 2,127,186-2,127,245 IGF2, INS-IGF2
    nsv7142403copy number variation1nstd232human GRCh37.p13 chr11: 2,148,386-2,148,445 , GRCh38.p12 chr11: 2,127,156-2,127,215 IGF2, INS-IGF2
    nsv7139274copy number variation1nstd232human GRCh37.p13 chr11: 2,148,476-2,148,527 , GRCh38.p12 chr11: 2,127,246-2,127,297 IGF2, INS-IGF2
    nsv7094186copy number variation1nstd102humanUncertain significance GRCh37 chr11: 721,044-3,988,932 , GRCh38.p12 chr11: 721,044-3,967,702 OR7E117P, RPLP2, 124 more genes
    nsv7093761copy number variation1nstd102humanUncertain significance GRCh37 chr11: 1,278,740-2,906,719 , GRCh38.p12 chr11: 1,257,510-2,885,489 TOLLIP-DT, KRTAP5-6, 58 more genes
    nsv7067623inversion1nstd229human GRCh38 chr11: 2,149,471-2,149,627 , GRCh37.p13 chr11: 2,170,701-2,170,857 IGF2, INS-IGF2
    nsv6903743copy number variation1nstd229human GRCh38 chr11: 2,100,601-2,164,400 , GRCh37.p13 chr11: 2,121,831-2,185,630 TH, INS-IGF2, 4 more genes
    nsv6885276copy number variation1nstd229human GRCh38 chr11: 1,136,035-3,145,463 , GRCh37.p13 chr11: 1,129,943-3,166,693 KRTAP5-1, MIR675, 69 more genes
    nsv6637864copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,616-8,250,724 , GRCh38.p12 chr11: 230,616-8,229,177 PNPLA2, OR52H1, 372 more genes
    nsv6637212copy number variation1nstd102humanPathogenic GRCh37 chr11: 461,373-2,157,956 , GRCh38.p12 chr11: 461,373-2,136,726 MIR6744, PTDSS2, 80 more genes
    nsv6634327copy number variation1nstd102humanPathogenic GRCh38 chr11: 499,700-5,279,697 , GRCh37.p13 chr11: 499,700-5,300,927 SNORA54, PIDD1, 219 more genes
    nsv6438165copy number variation1nstd223human GRCh38 chr11: 737,066-3,896,161 , GRCh37.p13 chr11: 737,066-3,917,391 RNU6-878P, CARS1-AS1, 123 more genes
    nsv6315550copy number variation1nstd102humanPathogenic GRCh37 chr11: 1,621,232-2,228,572 , GRCh38.p12 chr11: 1,600,002-2,207,342 IGF2-AS, SNORD131, 31 more genes
    nsv6315535copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,615-26,881,146 , GRCh38.p12 chr11: 230,615-26,859,599 OR52Q1P, RNU6-593P, 630 more genes
    nsv6291427copy number variation1nstd102humannot provided GRCh37 chr11: 230,615-5,525,355 , GRCh38.p12 chr11: 230,615-5,504,125 OR52J1P, IFITM1, 255 more genes
    nsv6291085copy number variation1nstd102humanLikely pathogenic GRCh37 chr11: 1,719,815-2,321,109 , GRCh38.p12 chr11: 1,698,585-2,299,879 ASCL2, CTSD, 27 more genes
    nsv6198422copy number variation1nstd214human GRCh38 chr11: 2,127,246-2,127,297 , GRCh37.p13 chr11: 2,148,476-2,148,527 IGF2, INS-IGF2
    nsv6132258copy number variation1nstd213human GRCh37 chr11: 2,060,000-2,280,001 , GRCh38.p12 chr11: 2,038,770-2,258,771 IGF2, INS, 5 more genes
    nsv6098363insertion1nstd212human GRCh38 chr11: 2,127,286-2,127,286 , GRCh37.p13 chr11: 2,148,516-2,148,516 INS-IGF2, IGF2
    nsv6082968insertion1nstd212human GRCh38 chr11: 2,127,170-2,127,170 , GRCh37.p13 chr11: 2,148,400-2,148,400 INS-IGF2, IGF2
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