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Items: 1 to 20 of 114

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094093copy number variation2nstd102humanUncertain significance GRCh37 chr11: 64,973,914-70,052,579 , GRCh38.p12 chr11: 65,206,443-70,206,473 B4GAT1, CHKA-DT, 208 more genes
    nsv7062888inversion1nstd229human GRCh38 chr11: 65,331,143-66,048,384 , GRCh37.p13 chr11: 65,098,614-65,815,855 FAUP4, MAP3K11, 50 more genes
    nsv7061449inversion1nstd229human GRCh38 chr11: 65,331,281-66,115,058 , GRCh37.p13 chr11: 65,098,752-65,882,529 LOC100420020, LINC02736, 53 more genes
    nsv6914921copy number variation1nstd229human GRCh38 chr11: 65,667,113-66,107,104 , GRCh37.p13 chr11: 65,434,584-65,874,575 SNX32, OVOL1, 28 more genes
    nsv6912389copy number variation1nstd229human GRCh38 chr11: 65,604,598-65,954,847 , GRCh37.p13 chr11: 65,372,069-65,722,318 RNASEH2C, C11orf68, 24 more genes
    nsv6910376copy number variation1nstd229human GRCh38 chr11: 65,882,708-65,883,043 , GRCh37.p13 chr11: 65,650,179-65,650,514 CTSW, FIBP
    nsv6905877copy number variation1nstd229human GRCh38 chr11: 60,405,001-68,536,600 , GRCh37.p13 chr11: 60,172,474-68,304,068 INCENP, SNRPCP12, 409 more genes
    nsv6903095copy number variation1nstd229human GRCh38 chr11: 59,466,654-66,168,743 , GRCh37.p13 chr11: 59,234,127-65,936,214 LINC02724, TMEM132A, 342 more genes
    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
    nsv6314192copy number variation1nstd102humanUncertain significance GRCh37 chr11: 64,935,724-66,405,514 , GRCh38.p12 chr11: 65,168,253-66,638,043 CNIH2, GAL3ST3, 95 more genes
    nsv6309121copy number variation2nstd102humanPathogenic GRCh37 chr11: 64,522,783-66,283,694 , GRCh38.p12 chr11: 64,755,311-66,516,223 SF3B2, ZNRD2-DT, 124 more genes
    nsv6132269copy number variation1nstd213human GRCh37 chr11: 64,390,000-65,950,001 , GRCh38.p12 chr11: 64,622,528-66,182,530 MRPL49, CTSW, 103 more genes
    nsv6132112copy number variation1nstd213human GRCh37 chr11: 64,220,000-68,010,001 , GRCh38.p12 chr11: 64,452,528-68,242,533 ACTN3, ALDH3B1, 212 more genes
    nsv5723155mobile element insertion1nstd211human GRCh38 chr11: 65,884,213-65,884,213 , GRCh37.p13 chr11: 65,651,684-65,651,684 FIBP, CTSW
    nsv5702670mobile element insertion2nstd211human GRCh38 chr11: 65,878,297-65,878,297 , GRCh37.p13 chr11: 65,645,768-65,645,768 CTSW
    nsv5648682insertion1nstd207human GRCh38 chr11: 65,883,339-65,883,339 , GRCh37.p13 chr11: 65,650,810-65,650,810 FIBP, CTSW
    nsv5561603mobile element insertion1nstd206human GRCh38 chr11: 65,884,228-65,884,264 , GRCh37.p13 chr11: 65,651,699-65,651,735 FIBP, CTSW
    nsv5407706mobile element insertion1nstd206human GRCh38 chr11: 65,878,297-65,878,348 , GRCh37.p13 chr11: 65,645,768-65,645,819 CTSW
    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
    nsv5277798copy number variation1nstd204human GRCh38.p13 chr11: 65,676,501-66,823,500 , GRCh37.p13 chr11: 65,443,972-66,590,971 , BBS1, 68 more genes
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