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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096705copy number variation1nstd102humanUncertain significance GRCh37 chr3: 183,368,145-184,094,097 , GRCh38.p12 chr3: 183,650,357-184,376,309 VWA5B2, MIR1224, 35 more genes
    nsv7096553copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chr3: 182,733,226-184,094,097 , GRCh38.p12 chr3: 183,015,438-184,376,309 DVL3, LOC105374247, 51 more genes
    nsv7054984inversion1nstd229human GRCh38 chr3: 183,912,767-184,153,412 , GRCh37.p13 chr3: 183,630,555-183,871,200 EEF1A1P8, HTR3C2P, 11 more genes
    nsv7053971inversion1nstd229human GRCh38 chr3: 183,609,736-184,280,209 , GRCh37.p13 chr3: 183,327,524-183,997,997 HTR3C2P, YEATS2-AS1, 31 more genes
    nsv6726682copy number variation1nstd229human GRCh38 chr3: 184,104,489-184,114,545 , GRCh37.p13 chr3: 183,822,277-183,832,333 HTR3E-AS1, HTR3E, 2 more genes
    nsv6634384copy number variation1nstd102humanPathogenic GRCh37 chr3: 181,062,175-185,474,509 , GRCh38.p12 chr3: 181,344,387-185,756,721 PRICKLE1P1, KLHL24, 99 more genes
    nsv6634371copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 171,549,421-198,022,430 , GRCh38.p12 chr3: 171,831,631-198,235,559 ACTL6A, AHSG, 466 more genes
    nsv6315437copy number variation1nstd102humanPathogenic GRCh37 chr3: 183,498,520-197,851,986 , GRCh38.p12 chr3: 183,780,732-198,125,115 LOC105374291, GP5, 315 more genes
    nsv6315366copy number variation1nstd102humanPathogenic GRCh37 chr3: 183,556,940-188,083,060 , GRCh38.p12 chr3: 183,839,152-188,365,272 MASP1, PSMD10P2, 115 more genes
    nsv6313539copy number variation1nstd102humanPathogenic GRCh37 chr3: 182,189,525-187,212,935 , GRCh38.p12 chr3: 182,471,737-187,495,147 ALG3, MIR4448, 133 more genes
    nsv6290246copy number variation1nstd102humanPathogenic GRCh37 chr3: 175,119,199-187,592,480 , GRCh38.p12 chr3: 175,401,410-187,874,692 RPL39L, MCF2L2, 220 more genes
    nsv5677636mobile element insertion1nstd211human GRCh38 chr3: 184,115,242-184,115,242 , GRCh37.p13 chr3: 183,833,030-183,833,030 EIF2B5-DT, HSP90AA5P
    nsv5453639copy number variation1nstd206human GRCh38 chr3: 163,047,000-198,226,000 , GRCh37.p13 chr3: 162,764,788-197,952,871 , MIR922, 587 more genes
    nsv5442644copy number variation1nstd206human GRCh38 chr3: 184,115,578-184,125,432 , GRCh37.p13 chr3: 183,833,366-183,843,220 HSP90AA5P, EIF2B5-DT
    nsv4924943copy number variation1nstd200human GRCh38 chr3: 184,115,578-184,125,432 , GRCh37.p13 chr3: 183,833,366-183,843,220 HSP90AA5P, EIF2B5-DT
    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
    nsv4805050copy number variation1nstd200human GRCh37 chr3: 183,833,366-183,843,220 , GRCh38.p12 chr3: 184,115,578-184,125,432 EIF2B5-DT, HSP90AA5P
    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
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