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Items: 1 to 20 of 125

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5644729insertion1nstd207human GRCh38 chr11: 67,291,397-67,291,397 , GRCh37.p13 chr11: 67,058,868-67,058,868 ANKRD13D
    nsv5496203copy number variation1nstd206human GRCh38 chr11: 67,297,447-67,297,777 , GRCh37.p13 chr11: 67,064,918-67,065,248 ANKRD13D
    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
    nsv5275203copy number variation1nstd204human GRCh38.p13 chr11: 66,946,001-67,700,500 , GRCh37.p13 chr11: 66,713,472-67,467,971 , PC, 38 more genes
    nsv5127841mobile element insertion1nstd203human GRCh38 chr11: 67,298,056-67,298,066 , GRCh37.p13 chr11: 67,065,527-67,065,537 ANKRD13D
    nsv4985091copy number variation1nstd200human GRCh38 chr11: 67,299,038-67,310,702 , GRCh37.p13 chr11: 67,066,509-67,078,173 SSH3, ANKRD13D
    nsv4832351copy number variation1nstd200human GRCh37 chr11: 67,065,124-67,065,629 , GRCh38.p12 chr11: 67,297,653-67,298,158 ANKRD13D
    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
    nsv4712776copy number variation1nstd195human GRCh37 chr11: 66,866,001-67,241,201 , GRCh38.p12 chr11: 67,098,530-67,473,730 PPP1CA, RPS6KB2, 19 more genes
    nsv4675137copy number variation1nstd102humanUncertain significance GRCh37 chr11: 66,820,585-67,979,510 , GRCh38.p12 chr11: 67,053,114-68,212,043 PPP1CA, RPS3AP40, 58 more genes
    nsv4618455copy number variation1nstd183human GRCh37 chr11: 67,025,374-67,084,761 , GRCh38.p12 chr11: 67,257,903-67,317,290 GRK2, KDM2A, 3 more genes
    nsv4611980copy number variation1nstd183human GRCh37 chr11: 67,056,967-67,057,024 , GRCh38.p12 chr11: 67,289,496-67,289,553 ANKRD13D
    nsv4607413copy number variation1nstd183human GRCh37 chr11: 67,056,967-67,057,413 , GRCh38.p12 chr11: 67,289,496-67,289,942 ANKRD13D
    nsv4349000copy number variation1nstd102humanPathogenic GRCh37 chr11: 65,138,976-67,574,402 , GRCh38.p12 chr11: 65,371,505-67,806,931 SNORD13F, ZNRD2, 141 more genes
    nsv3921639copy number variation1nstd102humanPathogenic NCBI36 chr11: 65,265,478-67,229,716 , GRCh37 chr11: 65,508,902-67,473,140 , GRCh38 chr11: 65,741,431-67,705,669 MIR6860, DOC2GP, 106 more genes
    nsv3920906copy number variation1nstd102humanLikely pathogenic NCBI36 chr11: 66,741,311-68,972,547 , GRCh37 chr11: 66,984,735-69,263,366 , GRCh38 chr11: 67,217,264-69,448,598 GRK2, ALDH3B1, 82 more genes
    nsv3917536copy number variation1nstd102humanPathogenic NCBI36 chr11: 66,409,957-67,222,297 , GRCh38 chr11: 66,885,910-67,698,250 , GRCh37 chr11: 66,653,381-67,465,721 PPP1CA, TBC1D10C, 39 more genes
    nsv3911732copy number variation1nstd102humanPathogenic GRCh38 chr11: 66,193,502-67,890,770 , GRCh37 chr11: 65,960,973-67,658,241 , NCBI36 chr11: 65,717,549-67,414,817 B4GAT1, KDM2A, 90 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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