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Items: 1 to 20 of 129

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5726069mobile element insertion1nstd211human GRCh38 chr11: 45,882,619-45,882,619 , GRCh37.p13 chr11: 45,904,170-45,904,170 CRY2
    nsv5600491copy number variation1nstd207human GRCh38 chr11: 45,874,484-45,874,549 , GRCh37.p13 chr11: 45,896,035-45,896,100 CRY2
    nsv5509497copy number variation1nstd206human GRCh38 chr11: 45,874,487-45,874,550 , GRCh37.p13 chr11: 45,896,038-45,896,101 CRY2
    nsv5380796copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397 FAUP4, MMP7, 2031 more genes
    nsv5380725copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chr11: 45,827,353-47,804,770 , GRCh38.p12 chr11: 45,805,802-47,783,218 MIR4688, LOC112268075, 58 more genes
    nsv5340078translocation1nstd200human GRCh37 chr11: 45,896,038-45,896,038 , GRCh37 chr11: 45,896,101-45,896,101 , GRCh38.p12 chr11: 45,874,487-45,874,487 , GRCh38.p12 chr11: 45,874,550-45,874,550 CRY2
    nsv5138050mobile element insertion1nstd203human GRCh38 chr11: 45,874,279-45,874,294 , GRCh37.p13 chr11: 45,895,830-45,895,845 CRY2
    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
    nsv4729649copy number variation1nstd102humanUncertain significance GRCh37 chr11: 44,266,593-46,123,796 , GRCh38.p12 chr11: 44,245,043-46,102,245 LOC105376654, PHF21A, 31 more genes
    nsv4714830copy number variation1nstd195human GRCh37 chr11: 45,760,601-46,177,151 , GRCh38.p12 chr11: 45,739,050-46,155,600 SLC35C1, LINC02716, 9 more genes
    nsv4682898copy number variation1nstd102humanUncertain significance GRCh37 chr11: 45,827,333-45,932,533 , GRCh38.p12 chr11: 45,805,782-45,910,982 MAPK8IP1, CRY2, 3 more genes
    nsv4555842insertion1nstd166human GRCh37.p13 chr11: 45,876,588-45,876,588 , GRCh38.p12 chr11: 45,855,037-45,855,037 CRY2
    nsv3924778copy number variation1nstd102humanPathogenic GRCh38 chr11: 41,118,322-48,643,003 , GRCh37 chr11: 41,139,872-48,664,555 , NCBI36 chr11: 41,096,448-48,621,131 F2, PSMC3, 140 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 MIR3160-2, LOC105376631, 122 more genes
    nsv3921841copy number variation1nstd102humanPathogenic NCBI36 chr11: 42,531,785-46,092,919 , GRCh37 chr11: 42,575,209-46,136,343 , GRCh38 chr11: 42,553,659-46,114,792 PEX16, LOC105376655, 51 more genes
    nsv3919271copy number variation1nstd102humanPathogenic GRCh38 chr11: 44,136,593-46,121,139 , NCBI36 chr11: 44,114,719-46,099,266 , GRCh37 chr11: 44,158,143-46,142,690 LOC105376646, ALX4, 31 more genes
    nsv3914563copy number variation1nstd102humanLikely pathogenic NCBI36 chr11: 42,705,681-49,113,863 , GRCh37 chr11: 42,749,105-49,157,287 , GRCh38 chr11: 42,727,555-49,135,735 ACP2, ARHGAP1, 143 more genes
    nsv3913842copy number variation1nstd102humanPathogenic GRCh37 chr11: 39,200,802-49,157,287 , NCBI36 chr11: 39,157,378-49,113,863 , GRCh38 chr11: 39,179,252-49,135,735 MIR3160-1, RPS20P26, 162 more genes
    nsv3908873copy number variation2nstd102humanPathogenic GRCh37 chr11: 230,616-134,938,470 , GRCh38.p12 chr11: 230,616-135,068,576 IGHMBP2, SYTL2, 2829 more genes
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