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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5672631copy number variation1nstd102humanPathogenic GRCh37 chr11: 36,614,125-36,615,728 , GRCh38.p12 chr11: 36,592,575-36,594,178 IFTAP, RAG2
    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
    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
    nsv4682728copy number variation1nstd102humanPathogenic GRCh37 chr11: 36,594,835-36,619,652 , GRCh38.p12 chr11: 36,573,285-36,598,102 RAG2, IFTAP, 1 more genes
    nsv4606802copy number variation1nstd183human GRCh37 chr11: 36,595,600-37,755,416 , GRCh38.p12 chr11: 36,574,050-37,733,866 RAG1, RAG2, 7 more genes
    nsv4455656copy number variation1nstd102humanUncertain significance GRCh37 chr11: 34,183,318-36,860,753 , GRCh38.p12 chr11: 34,161,771-36,839,203 LOC102723568, CAT, 39 more genes
    nsv3958906copy number variation1nstd168human GRCh38 chr11: 36,593,094-36,648,966 , GRCh37.p13 chr11: 36,614,644-36,670,516 IFTAP, RAG2
    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 PDHX, EHF, 39 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 CSTF3, LOC101928338, 170 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
    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 LOC100422241, TRAF6, 23 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 DNAAF11P1, TRIM44, 30 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 RAG1, RAG2, 30 more genes
    nsv3914209copy number variation1nstd102humanUncertain significance NCBI36 chr11: 36,465,362-40,886,061 , GRCh37 chr11: 36,508,786-40,929,485 , GRCh38 chr11: 36,487,236-40,907,935 LOC107984362, LOC105376631, 26 more genes
    nsv3913769copy number variation1nstd102humanUncertain significance NCBI36 chr11: 34,147,054-36,798,924 , GRCh37 chr11: 34,190,478-36,842,348 , GRCh38 chr11: 34,168,931-36,820,798 MMADHCP2, PAMR1, 39 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
    nsv3907644copy number variation1nstd102humanUncertain significance GRCh37 chr11: 35,126,357-38,814,431 , GRCh38.p12 chr11: 35,104,810-38,792,881 LOC105376632, PAMR1, 30 more genes
    nsv3907223copy number variation1nstd102humanPathogenic GRCh37 chr11: 24,469,451-37,524,085 , GRCh38.p12 chr11: 24,447,905-37,502,535 PIGCP1, HNRNPRP2, 151 more genes
    nsv3906552copy number variation1nstd102humanPathogenic GRCh37 chr11: 30,615,127-40,606,139 , GRCh38.p12 chr11: 30,593,580-40,584,589 MIR3973, HNRNPA3P9, 113 more genes
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