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Items: 1 to 20 of 107

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5918738copy number variation1nstd209human GRCh38 chr11: 736,859-3,895,958 , GRCh37.p13 chr11: 736,859-3,917,188 , TALDO1, 128 more genes
    nsv5513578copy number variation1nstd206human GRCh38 chr11: 3,598,372-3,731,278 , GRCh37.p13 chr11: 3,619,602-3,752,508 ART1, NUP98, 6 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
    nsv4977930copy number variation1nstd200human GRCh38 chr11: 3,669,783-3,671,768 , GRCh37.p13 chr11: 3,691,013-3,692,998 CHRNA10
    nsv4849316copy number variation1nstd200human GRCh37 chr11: 3,691,013-3,692,998 , GRCh38.p12 chr11: 3,669,783-3,671,768 CHRNA10
    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
    nsv4741272copy number variation1nstd199human GRCh37 chr11: 3,487,146-67,605,076 , GRCh38.p12 chr11: 3,465,916-67,837,605 , DRAP1, 1535 more genes
    nsv4729112copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,615-4,851,537 , GRCh38.p12 chr11: 230,615-4,830,307 OR51E1, TNNI2, 203 more genes
    nsv4679705copy number variation1nstd189human GRCh37.p13 chr11: 2,339,823-3,832,257 , GRCh38.p12 chr11: 2,318,593-3,811,027 , ART1, 50 more genes
    nsv4675604copy number variation1nstd102humanUncertain significance GRCh37 chr11: 3,667,691-4,039,971 , GRCh38.p12 chr11: 3,646,461-4,018,741 STIM1, ART1, 12 more genes
    nsv4674879copy number variation1nstd102humanPathogenic GRCh37 chr11: 235,934-33,826,995 , GRCh38.p12 chr11: 235,934-33,805,449 BGLT3, RPL21P97, 723 more genes
    nsv4605212copy number variation1nstd183human GRCh37 chr11: 3,647,274-3,904,364 , GRCh38.p12 chr11: 3,626,044-3,883,134 NUP98, RHOG, 10 more genes
    nsv4578642copy number variation1nstd102humanUncertain significance GRCh37 chr11: 3,659,968-3,746,449 , GRCh38.p12 chr11: 3,638,738-3,725,219 ART5, RNU6-1143P, 3 more genes
    nsv4421715copy number variation1nstd174human GRCh37 chr11: 3,628,837-3,774,215 , GRCh38.p12 chr11: 3,607,607-3,752,985 ART1, NUP98, 5 more genes
    nsv4350476copy number variation1nstd102humanPathogenic GRCh37 chr11: 193,146-12,643,136 , GRCh38.p12 chr11: 193,146-12,621,589 KRTAP5-3, OR56A7P, 457 more genes
    nsv4207154copy number variation1nstd166human GRCh37.p13 chr11: 3,691,013-3,692,998 , GRCh38.p12 chr11: 3,669,783-3,671,768 CHRNA10
    nsv4194821copy number variation1nstd166human GRCh37.p13 chr11: 3,544,404-3,910,736 , GRCh38.p12 chr11: 3,523,174-3,889,506 CHRNA10, PGAP2, 17 more genes
    nsv3966774insertion1nstd168human GRCh37.p13 chr11: 3,619,501-3,720,458 , GRCh38 chr11: 3,598,271-3,699,228 ART1, NUP98, 5 more genes
    nsv3919565copy number variation1nstd102humanPathogenic GRCh38 chr11: 61,793-10,727,969 , GRCh37 chr11: 61,793-10,749,516 , NCBI36 chr11: 51,793-10,706,092 OR51A7, OR51F5P, 437 more genes
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