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Items: 1 to 20 of 121

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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
    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
    nsv6916891copy number variation1nstd229human GRCh38 chr11: 2,269,001-2,272,400 , GRCh37.p13 chr11: 2,290,231-2,293,630 ASCL2
    nsv6911864copy number variation1nstd229human GRCh38 chr11: 2,172,083-2,270,940 , GRCh37.p13 chr11: 2,193,313-2,292,170 ASCL2, MIR4686, 1 more genes
    nsv6906116copy number variation1nstd229human GRCh38 chr11: 2,211,996-2,356,501 , GRCh37.p13 chr11: 2,233,226-2,377,731 C11orf21, RPL26P30, 4 more genes
    nsv6901605copy number variation1nstd229human GRCh38 chr11: 2,257,028-2,326,666 , GRCh37.p13 chr11: 2,278,258-2,347,896 C11orf21, ASCL2, 2 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
    nsv6634327copy number variation1nstd102humanPathogenic GRCh38 chr11: 499,700-5,279,697 , GRCh37.p13 chr11: 499,700-5,300,927 SNORA54, PIDD1, 219 more genes
    nsv6446440copy number variation1nstd223human GRCh38 chr11: 2,172,083-2,270,940 , GRCh37.p13 chr11: 2,193,313-2,292,170 MIR4686, ASCL2, 1 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
    nsv6437128copy number variation1nstd223human GRCh38 chr11: 2,212,082-2,356,488 , GRCh37.p13 chr11: 2,233,312-2,377,718 ASCL2, CD81-AS1, 4 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
    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
    nsv4984134copy number variation1nstd200human GRCh38 chr11: 2,172,083-2,270,940 , GRCh37.p13 chr11: 2,193,313-2,292,170 TH, MIR4686, 1 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
    nsv4751865inversion1nstd199human GRCh37 chr11: 1,620,303-71,272,233 , GRCh38.p12 chr11: 1,599,073-71,561,187 , ACP2, 1686 more genes
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