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Items: 1 to 20 of 206

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5500005copy number variation1nstd206human GRCh38 chr11: 34,619,373-34,767,759 , GRCh37.p13 chr11: 34,640,920-34,789,306 EHF, NDUFB8P3, 1 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
    nsv5317920copy number variation1nstd204human GRCh38.p13 chr11: 34,619,372-34,767,760 , GRCh37.p13 chr11: 34,640,919-34,789,307 LOC102723568, EHF, 1 more genes
    nsv5277837copy number variation1nstd204human GRCh38.p13 chr11: 34,617,083-34,660,694 , GRCh37.p13 chr11: 34,638,630-34,682,241 EHF
    nsv5274022copy number variation1nstd204human GRCh38.p13 chr11: 34,620,501-34,682,700 , GRCh37.p13 chr11: 34,642,048-34,704,247 EHF, NDUFB8P3
    nsv5267276copy number variation1nstd204human GRCh38.p13 chr11: 34,644,901-34,647,300 , GRCh37.p13 chr11: 34,666,448-34,668,847 EHF
    nsv5139592mobile element insertion1nstd203human GRCh38 chr11: 34,619,612-34,619,625 , GRCh37.p13 chr11: 34,641,159-34,641,172 EHF
    nsv4984387copy number variation1nstd200human GRCh38 chr11: 34,619,373-34,767,759 , GRCh37.p13 chr11: 34,640,920-34,789,306 EHF, LOC102723568, 1 more genes
    nsv4843226copy number variation1nstd200human GRCh37 chr11: 34,640,920-34,789,306 , GRCh38.p12 chr11: 34,619,373-34,767,759 LOC102723568, EHF, 1 more genes
    nsv4831352copy number variation1nstd200human GRCh37 chr11: 34,659,298-34,659,762 , GRCh38.p12 chr11: 34,637,751-34,638,215 EHF
    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
    nsv4679857copy number variation1nstd189human GRCh37.p13 chr11: 34,592,853-34,952,574 , GRCh38.p12 chr11: 34,571,306-34,931,027 PDHX, EHF, 6 more genes
    nsv4674824copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,053,978-34,732,891 , GRCh38.p12 chr11: 11,032,431-34,711,344 SNORA88, LINC02729, 305 more genes
    nsv4604029copy number variation1nstd183human GRCh37 chr11: 34,641,598-34,789,343 , GRCh38.p12 chr11: 34,620,051-34,767,796 NDUFB8P3, LOC102723568, 1 more genes
    nsv4489989mobile element insertion1nstd166human GRCh37.p13 chr11: 34,678,929-34,678,929 , GRCh38.p12 chr11: 34,657,382-34,657,382 EHF
    nsv4455873copy number variation1nstd102humanPathogenic GRCh37 chr11: 22,079,154-35,597,645 , GRCh38.p12 chr11: 22,057,608-35,576,097 DNAJC24, LOC102723568, 153 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
    nsv4379178copy number variation1nstd173human GRCh37 chr11: 34,652,539-34,801,101 , GRCh38.p12 chr11: 34,630,992-34,779,554 NDUFB8P3, LOC102723568, 1 more genes
    nsv4366789copy number variation1nstd173human GRCh37 chr11: 34,652,966-34,789,109 , GRCh38.p12 chr11: 34,631,419-34,767,562 LOC102723568, NDUFB8P3, 1 more genes
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