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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
    nsv7094186copy number variation1nstd102humanUncertain significance GRCh37 chr11: 721,044-3,988,932 , GRCh38.p12 chr11: 721,044-3,967,702 OR7E117P, RPLP2, 124 more genes
    nsv7076913inversion1nstd229human GRCh38 chr11: 3,013,798-3,118,704 , GRCh37.p13 chr11: 3,035,028-3,139,934 OSBPL5, RNU1-91P, 2 more genes
    nsv6917011copy number variation1nstd229human GRCh38 chr11: 2,693,282-9,207,515 , GRCh37.p13 chr11: 2,714,512-9,229,062 LOC105376526, OR51E2, 279 more genes
    nsv6906261copy number variation1nstd229human GRCh38 chr11: 2,908,710-3,043,741 , GRCh37.p13 chr11: 2,929,940-3,064,971 CARS1, PHLDA2, 4 more genes
    nsv6903353copy number variation1nstd229human GRCh38 chr11: 3,029,362-3,029,533 , GRCh37.p13 chr11: 3,050,592-3,050,763 CARS1-AS1, CARS1
    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
    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
    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
    nsv6143476copy number variation1nstd206human GRCh38 chr11: 2,994,000-3,064,000 , GRCh37.p13 chr11: 3,015,230-3,085,230 CARS1-AS1, RNU1-91P, 1 more genes
    nsv6086589insertion1nstd212human GRCh38 chr11: 3,031,998-3,031,998 , GRCh37.p13 chr11: 3,053,228-3,053,228 CARS1-AS1, CARS1
    nsv6035484copy number variation1nstd212human GRCh38 chr11: 3,031,982-3,032,050 , GRCh37.p13 chr11: 3,053,212-3,053,280 CARS1-AS1, CARS1
    nsv5918738copy number variation1nstd209human GRCh38 chr11: 736,859-3,895,958 , GRCh37.p13 chr11: 736,859-3,917,188 , TALDO1, 128 more genes
    nsv5660982insertion1nstd207human GRCh38 chr11: 3,031,996-3,031,996 , GRCh37.p13 chr11: 3,053,226-3,053,226 CARS1-AS1, CARS1
    nsv5380885copy number variation1nstd102humanUncertain significance GRCh37 chr11: 298,501-4,113,028 , GRCh38.p12 chr11: 298,501-4,091,798 LINC02688, MIR210, 156 more genes
    nsv4977904copy number variation1nstd200human GRCh38 chr11: 3,032,233-3,032,358 , GRCh37.p13 chr11: 3,053,463-3,053,588 CARS1-AS1, CARS1
    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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