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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3908664copy number variation1nstd102humanBenign GRCh37 chr11: 36,294,301-36,310,900 , GRCh38.p12 chr11: 36,272,751-36,289,350 COMMD9
    nsv3899456copy number variation1nstd102humanBenign GRCh37 chr11: 36,093,840-36,407,102 , GRCh38.p12 chr11: 36,072,290-36,385,552 COMMD9, LDLRAD3, 2 more genes
    nsv5380796copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397 COMMD9, FAUP4, 2031 more genes
    nsv3922664copy number variation1nstd102humanPathogenic GRCh38 chr11: 22,550,115-38,199,159 , NCBI36 chr11: 22,528,237-38,177,285 , GRCh37 chr11: 22,571,661-38,220,709 COMMD9, CSTF3, 170 more genes
    nsv3898805copy number variation1nstd102humanPathogenic GRCh37 chr11: 27,588,560-41,770,792 , GRCh38.p12 chr11: 27,567,013-41,749,242 COMMD9, LINC02707, 150 more genes
    nsv3907223copy number variation1nstd102humanPathogenic GRCh37 chr11: 24,469,451-37,524,085 , GRCh38.p12 chr11: 24,447,905-37,502,535 COMMD9, PIGCP1, 151 more genes
    nsv3922177copy number variation1nstd102humanPathogenic GRCh38 chr11: 35,663,578-46,959,820 , GRCh37 chr11: 35,685,126-46,981,371 , NCBI36 chr11: 35,641,702-46,937,947 COMMD9, MIR3160-2, 122 more genes
    nsv3906552copy number variation1nstd102humanPathogenic GRCh37 chr11: 30,615,127-40,606,139 , GRCh38.p12 chr11: 30,593,580-40,584,589 COMMD9, MIR3973, 113 more genes
    nsv6638023copy number variation1nstd102humanPathogenic GRCh37 chr11: 31,372,721-38,259,316 , GRCh38.p12 chr11: 31,351,174-38,237,766 COMMD9, THEM7P, 92 more genes
    nsv3893233copy number variation1nstd102humanPathogenic GRCh37 chr11: 70,864-134,938,470 , GRCh38.p12 chr11: 70,864-135,068,576 COMMD9, LOC105376598, 2842 more genes
    nsv3900144copy number variation1nstd102humanPathogenic GRCh37 chr11: 198,510-134,934,063 , GRCh38.p12 chr11: 198,510-135,064,169 COMMD9, RTN3, 2833 more genes
    nsv3908873copy number variation2nstd102humanPathogenic GRCh37 chr11: 230,616-134,938,470 , GRCh38.p12 chr11: 230,616-135,068,576 COMMD9, IGHMBP2, 2829 more genes
    nsv6315537copy number variation1nstd102humanPathogenic GRCh37 chr11: 32,799,481-134,938,470 , GRCh38.p12 chr11: 32,777,935-135,068,576 COMMD9, PYGM, 2125 more genes
    nsv3898926copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,615-37,698,540 , GRCh38.p12 chr11: 230,615-37,676,990 COMMD9, OR51L1, 771 more genes
    nsv3923805copy number variation1nstd102humanPathogenic GRCh38 chr11: 34,161,694-36,799,127 , GRCh37 chr11: 34,183,241-36,820,677 , NCBI36 chr11: 34,139,817-36,777,253 COMMD9, PDHX, 39 more genes
    nsv3917992copy number variation1nstd102humanLikely pathogenic NCBI36 chr11: 35,985,503-40,296,250 , GRCh37 chr11: 36,028,927-40,339,674 , GRCh38 chr11: 36,007,377-40,318,124 COMMD9, RAG1, 30 more genes
    nsv3920531copy number variation1nstd102humanUncertain significance NCBI36 chr11: 35,081,341-38,769,618 , GRCh37 chr11: 35,124,765-38,813,042 , GRCh38 chr11: 35,103,218-38,791,492 COMMD9, DNAAF11P1, 30 more genes
    nsv3907644copy number variation1nstd102humanUncertain significance GRCh37 chr11: 35,126,357-38,814,431 , GRCh38.p12 chr11: 35,104,810-38,792,881 COMMD9, LOC105376632, 30 more genes
    nsv3921953copy number variation1nstd102humanUncertain significance GRCh38 chr11: 35,135,480-37,649,168 , NCBI36 chr11: 35,113,603-37,627,294 , GRCh37 chr11: 35,157,027-37,670,718 COMMD9, LOC100422241, 23 more genes
    nsv3896459copy number variation1nstd102humanUncertain significance GRCh37 chr11: 32,782,607-36,404,823 , GRCh38.p12 chr11: 32,761,061-36,383,273 COMMD9, HIPK3, 58 more genes
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