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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5890300copy number variation1nstd209human GRCh38 chr3: 184,287,042-184,304,653 , GRCh37.p13 chr3: 184,004,830-184,022,441 EEF1AKMT4-ECE2, PSMD2, 1 more genes
    nsv5835425copy number variation1nstd209human GRCh38 chr3: 184,286,941-184,300,509 , GRCh37.p13 chr3: 184,004,729-184,018,297 EEF1AKMT4-ECE2, PSMD2, 1 more genes
    nsv5453639copy number variation1nstd206human GRCh38 chr3: 163,047,000-198,226,000 , GRCh37.p13 chr3: 162,764,788-197,952,871 , MIR922, 587 more genes
    nsv5442753copy number variation1nstd206human GRCh38 chr3: 184,290,396-184,321,664 , GRCh37.p13 chr3: 184,008,184-184,039,452 EIF4G1, PSMD2, 2 more genes
    nsv5441425copy number variation1nstd206human GRCh38 chr3: 184,287,002-184,304,711 , GRCh37.p13 chr3: 184,004,790-184,022,499 PSMD2, ECE2, 1 more genes
    nsv4924945copy number variation1nstd200human GRCh38 chr3: 184,293,355-184,295,368 , GRCh37.p13 chr3: 184,011,143-184,013,156 EEF1AKMT4-ECE2, ECE2
    nsv4924944copy number variation1nstd200human GRCh38 chr3: 184,290,396-184,321,664 , GRCh37.p13 chr3: 184,008,184-184,039,452 ECE2, PSMD2, 2 more genes
    nsv4924942copy number variation1nstd200human GRCh38 chr3: 184,108,733-184,353,203 , GRCh37.p13 chr3: 183,826,521-184,070,991 SNORD66, CAMK2N2, 17 more genes
    nsv4921196copy number variation1nstd200human GRCh38 chr3: 184,266,643-184,287,434 , GRCh37.p13 chr3: 183,984,431-184,005,222 EEF1AKMT4-ECE2, ECE2
    nsv4805052copy number variation1nstd200human GRCh37 chr3: 184,004,787-184,022,630 , GRCh38.p12 chr3: 184,286,999-184,304,842 ECE2, EEF1AKMT4-ECE2, 1 more genes
    nsv4798905copy number variation1nstd200human GRCh37 chr3: 183,984,396-184,005,268 , GRCh38.p12 chr3: 184,266,608-184,287,480 EEF1AKMT4-ECE2, ECE2
    nsv4769252copy number variation1nstd102humanPathogenic GRCh37 chr3: 181,171,210-184,706,091 , GRCh38.p12 chr3: 181,453,422-184,988,303 LOC107986054, LOC107986160, 83 more genes
    nsv4728604copy number variation1nstd102humanPathogenic GRCh37 chr3: 182,877,291-186,830,759 , GRCh38.p12 chr3: 183,159,503-187,112,971 LOC105374253, GPS2P2, 111 more genes
    nsv4674680copy number variation1nstd102humanPathogenic GRCh37 chr3: 169,617,690-190,593,854 , GRCh38.p12 chr3: 169,899,902-190,876,065 RNU6-1120P, LOC105374262, 323 more genes
    nsv4674171copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 183,789,584-186,034,649 , GRCh38.p12 chr3: 184,071,796-186,316,860 AP2M1, CLCN2, 54 more genes
    nsv4571153mobile element insertion1nstd166human GRCh37.p13 chr3: 184,004,765-184,004,765 , GRCh38.p12 chr3: 184,286,977-184,286,977 EEF1AKMT4-ECE2, ECE2
    nsv4327395inversion1nstd166human GRCh37.p13 chr3: 126,265,569-194,265,571 , GRCh38.p12 chr3: 126,546,726-194,544,842 , ACTG1P1, 1039 more genes
    nsv4110407copy number variation1nstd166human GRCh37.p13 chr3: 183,984,397-184,005,238 , GRCh38.p12 chr3: 184,266,609-184,287,450 EEF1AKMT4-ECE2, ECE2
    nsv4108955copy number variation1nstd166human GRCh37.p13 chr3: 184,004,798-184,022,459 , GRCh38.p12 chr3: 184,287,010-184,304,671 EEF1AKMT4-ECE2, ECE2, 1 more genes
    nsv4100232copy number variation1nstd166human GRCh37.p13 chr3: 184,008,184-184,039,452 , GRCh38.p12 chr3: 184,290,396-184,321,664 ECE2, EIF4G1, 2 more genes
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