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Items: 1 to 20 of 81

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5718997mobile element insertion2nstd211human GRCh38 chr11: 43,063,971-43,063,971 , GRCh37.p13 chr11: 43,085,521-43,085,521 LOC100533710
    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
    nsv5186813mobile element insertion1nstd203human GRCh38 chr11: 43,063,957-43,063,971 , GRCh37.p13 chr11: 43,085,507-43,085,521 LOC100533710
    nsv5132993mobile element insertion1nstd203human GRCh38 chr11: 43,062,818-43,062,835 , GRCh37.p13 chr11: 43,084,368-43,084,385 LOC100533710
    nsv4970856copy number variation1nstd200human GRCh38 chr11: 42,915,412-43,067,245 , GRCh37.p13 chr11: 42,936,962-43,088,795 LOC100533710
    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
    nsv4706070copy number variation1nstd195human GRCh37 chr11: 43,026,651-43,116,701 , GRCh38.p12 chr11: 43,005,101-43,095,151 LOC100533710
    nsv4562909mobile element insertion1nstd166human GRCh37.p13 chr11: 43,085,507-43,085,507 , GRCh38.p12 chr11: 43,063,957-43,063,957 LOC100533710
    nsv4205214copy number variation1nstd166human GRCh37.p13 chr11: 42,993,191-43,106,702 , GRCh38.p12 chr11: 42,971,641-43,085,152 LOC100533710
    nsv3968197insertion1nstd168human GRCh38 chr11: 43,062,683-43,065,796 , GRCh37.p13 chr11: 43,084,233-43,087,346 LOC100533710
    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
    nsv3924016copy number variation1nstd102humanLikely pathogenic NCBI36 chr11: 40,666,800-44,162,262 , GRCh37 chr11: 40,710,224-44,205,686 , GRCh38 chr11: 40,688,674-44,184,136 EXT2, API5, 29 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
    nsv3921625copy number variation1nstd102humanUncertain significance GRCh37 chr11: 40,710,224-44,934,960 , NCBI36 chr11: 40,666,800-44,891,536 , GRCh38 chr11: 40,688,674-44,913,409 CTBP2P6, SEC14L1P1, 36 more genes
    nsv3917236copy number variation1nstd102humanPathogenic GRCh37 chr11: 39,706,376-44,866,811 , GRCh38 chr11: 39,684,826-44,845,260 , NCBI36 chr11: 39,662,952-44,823,387 LOC107984328, LRRC4C, 42 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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