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Items: 1 to 20 of 101

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7071761inversion1nstd229human GRCh38 chr11: 35,441,715-35,686,964 , GRCh37.p13 chr11: 35,463,263-35,708,512 FJX1, PAMR1, 1 more genes
    nsv6913781copy number variation1nstd229human GRCh38 chr11: 34,168,221-36,836,658 , GRCh37.p13 chr11: 34,189,768-36,858,208 TRAF6, LOC100422241, 39 more genes
    nsv6902081copy number variation1nstd229human GRCh38 chr11: 35,609,055-35,617,005 , GRCh37.p13 chr11: 35,630,603-35,638,553 FJX1
    nsv6638023copy number variation1nstd102humanPathogenic GRCh37 chr11: 31,372,721-38,259,316 , GRCh38.p12 chr11: 31,351,174-38,237,766 THEM7P, LOC105376624, 92 more genes
    nsv6469538copy number variation1nstd223human GRCh38 chr11: 35,617,801-35,621,700 , GRCh37.p13 chr11: 35,639,349-35,643,248 FJX1
    nsv6315537copy number variation1nstd102humanPathogenic GRCh37 chr11: 32,799,481-134,938,470 , GRCh38.p12 chr11: 32,777,935-135,068,576 PYGM, ATL3, 2125 more genes
    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
    nsv4614623copy number variation1nstd183human GRCh37 chr11: 35,580,590-35,687,725 , GRCh38.p12 chr11: 35,559,042-35,666,177 FJX1, TRIM44
    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
    nsv4206004copy number variation1nstd166human GRCh37.p13 chr11: 35,625,801-35,648,975 , GRCh38.p12 chr11: 35,604,253-35,627,427 FJX1
    nsv4196613copy number variation1nstd166human GRCh37.p13 chr11: 35,634,000-35,665,000 , GRCh38.p12 chr11: 35,612,452-35,643,452 FJX1
    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
    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
    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
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