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Items: 1 to 20 of 170

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094186copy number variation1nstd102humanUncertain significance GRCh37 chr11: 721,044-3,988,932 , GRCh38.p12 chr11: 721,044-3,967,702 OR7E117P, RPLP2, 124 more genes
    nsv7093926copy number variation1nstd102humanUncertain significance GRCh37 chr11: 1,774,733-2,019,125 , GRCh38.p12 chr11: 1,753,503-1,997,895 LINC01219, MIR7847, 16 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
    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
    nsv6637463copy number variation1nstd102humanPathogenic GRCh37 chr11: 1,980,946-2,054,887 , GRCh38.p12 chr11: 1,959,716-2,033,657 MIR675, MRPL23, 3 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
    nsv6634781copy number variation2nstd227human GRCh37 chr11: 1,972,205-2,057,647 , GRCh38.p12 chr11: 1,950,975-2,036,417 MRPL23, H19, 3 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
    nsv6144247copy number variation1nstd206human GRCh38 chr11: 1,983,000-2,041,000 , GRCh37.p13 chr11: 2,004,230-2,062,230 H19, MRPL23, 3 more genes
    nsv5918738copy number variation1nstd209human GRCh38 chr11: 736,859-3,895,958 , GRCh37.p13 chr11: 736,859-3,917,188 , TALDO1, 128 more genes
    nsv5380885copy number variation1nstd102humanUncertain significance GRCh37 chr11: 298,501-4,113,028 , GRCh38.p12 chr11: 298,501-4,091,798 LINC02688, MIR210, 156 more genes
    nsv5259948copy number variation1nstd204human GRCh38.p13 chr11: 1,804,001-2,194,300 , GRCh37.p13 chr11: 1,825,231-2,215,530 H19, INS, 20 more genes
    nsv5251619copy number variation1nstd204human GRCh38.p13 chr11: 1,993,101-1,995,100 , GRCh37.p13 chr11: 2,014,331-2,016,330 MRPL23, LINC01219, 2 more genes
    nsv4768373copy number variation1nstd102humanPathogenic GRCh37 chr11: 210,300-8,664,358 , GRCh38.p12 chr11: 210,300-8,642,811 LOC107984302, STK33, 375 more genes
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