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Items: 1 to 20 of 137

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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
    nsv6730601copy number variation1nstd229human GRCh38 chr3: 184,103,723-184,105,233 , GRCh37.p13 chr3: 183,821,511-183,823,021 HTR3E-AS1, HTR3E, 1 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
    nsv6561344inversion1nstd223human GRCh38 chr3: 184,100,996-184,102,016 , GRCh37.p13 chr3: 183,818,784-183,819,804 HTR3E, EIF2B5-DT, 1 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
    nsv6297687copy number variation1nstd186human GRCh37 chr3: 183,817,256-183,819,255 , GRCh38.p12 chr3: 184,099,468-184,101,467 HTR3E, EIF2B5-DT, 1 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
    nsv5992405copy number variation1nstd212human GRCh38 chr3: 184,099,714-184,103,605 , GRCh37.p13 chr3: 183,817,502-183,821,393 HTR3E, EIF2B5-DT, 1 more genes
    nsv5992269copy number variation1nstd212human GRCh38 chr3: 184,099,474-184,101,467 , GRCh37.p13 chr3: 183,817,262-183,819,255 HTR3E, EIF2B5-DT, 1 more genes
    nsv5900726copy number variation1nstd209human GRCh38 chr3: 184,099,468-184,101,466 , GRCh37.p13 chr3: 183,817,256-183,819,254 HTR3E, EIF2B5-DT, 1 more genes
    nsv5835693copy number variation1nstd209human GRCh38 chr3: 184,099,436-184,101,418 , GRCh37.p13 chr3: 183,817,224-183,819,206 EIF2B5-DT, HTR3E-AS1, 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
    nsv5436591copy number variation1nstd206human GRCh38 chr3: 184,099,468-184,101,467 , GRCh37.p13 chr3: 183,817,256-183,819,255 HTR3E-AS1, EIF2B5-DT, 1 more genes
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