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Items: 1 to 20 of 77

  • The following term was not found in dbVar: microRNA.
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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6291429copy number variation1nstd102humanUncertain significance GRCh37 chr3: 35,471,543-35,879,518 , GRCh38.p12 chr3: 35,430,051-35,838,026 ARPP21, MIR128-2
    esv3032430copy number variation1estd209human GRCh37 chr3: 35,785,056-35,785,072 , GRCh38.p12 chr3: 35,743,564-35,743,580 MIR128-2, ARPP21
    nsv526191copy number variation1nstd21human NCBI35 chr3: 35,690,238-35,847,380 , GRCh37.p13 chr3: 35,715,234-35,872,376 , GRCh38.p12 chr3: 35,673,742-35,830,884 ARPP21, MIR128-2
    nsv3134604copy number variation6nstd151human GRCh37 chr3: 35,770,792-35,835,455 , GRCh38.p12 chr3: 35,729,300-35,793,963 MIR128-2, ARPP21
    nsv3137737copy number variation1nstd151human GRCh37 chr3: 35,723,241-35,785,462 , GRCh38.p12 chr3: 35,681,749-35,743,970 ARPP21, MIR128-2
    nsv3122490copy number variation1nstd151human GRCh37 chr3: 35,785,328-35,835,455 , GRCh38.p12 chr3: 35,743,836-35,793,963 MIR128-2, ARPP21
    nsv3132030copy number variation3nstd151human GRCh37 chr3: 35,785,967-35,835,455 , GRCh38.p12 chr3: 35,744,475-35,793,963 ARPP21, MIR128-2
    nsv5393961mobile element insertion1nstd206human GRCh38 chr3: 35,744,059-35,744,110 , GRCh37.p13 chr3: 35,785,551-35,785,602 MIR128-2, ARPP21
    nsv5693361mobile element insertion2nstd211human GRCh38 chr3: 35,744,059-35,744,059 , GRCh37.p13 chr3: 35,785,551-35,785,551 MIR128-2, ARPP21
    nsv4470577mobile element insertion1nstd166human GRCh37.p13 chr3: 35,785,535-35,785,535 , GRCh38.p12 chr3: 35,744,043-35,744,043 ARPP21, MIR128-2
    nsv2161062short tandem repeat1nstd128human GRCh37 chr3: 35,785,765-35,785,779 , GRCh38.p12 chr3: 35,744,273-35,744,287 ARPP21, MIR128-2
    nsv1004683copy number variation1nstd100human NCBI36 chr3: 35,739,213-35,916,620 , GRCh37.p13 chr3: 35,764,209-35,941,616 , GRCh38.p12 chr3: 35,722,717-35,900,124 ARPP21, RPL36AP17, 1 more genes
    nsv536534copy number variation1nstd54human NCBI36 chr3: 35,739,213-35,916,620 , GRCh37.p13 chr3: 35,764,209-35,941,616 , GRCh38.p12 chr3: 35,722,717-35,900,124 ARPP21, MIR128-2, 1 more genes
    nsv590055copy number variation1nstd54human NCBI36 chr3: 35,756,391-35,913,799 , GRCh37.p13 chr3: 35,781,387-35,938,795 , GRCh38.p12 chr3: 35,739,895-35,897,303 ARPP21, RPL36AP17, 1 more genes
    nsv432408copy number variation1nstd12human NCBI35 chr3: 35,613,300-35,928,200 , GRCh37.p13 chr3: 35,638,296-35,953,196 , GRCh38.p12 chr3: 35,596,804-35,911,704 ARPP21, MIR128-2, 1 more genes
    nsv6311966copy number variation1nstd102humanPathogenic GRCh37 chr3: 16,710,965-41,275,270 , GRCh38.p12 chr3: 16,669,458-41,233,779 LOC102724104, CRIP1P2, 291 more genes
    nsv3918147copy number variation1nstd102humanPathogenic GRCh38 chr3: 32,322,382-36,775,606 , NCBI36 chr3: 32,338,878-36,792,101 , GRCh37 chr3: 32,363,874-36,817,097 TRIM71, CMTM8, 46 more genes
    nsv3920512copy number variation1nstd102humanPathogenic GRCh37 chr3: 33,103,691-36,870,931 , NCBI36 chr3: 33,078,695-36,845,935 , GRCh38 chr3: 33,062,199-36,829,440 RN7SKP227, RNA5SP128, 33 more genes
    nsv3885606copy number variation1nstd102humanPathogenic GRCh37 chr3: 60,174-197,948,027 , GRCh38.p12 chr3: 18,496-198,221,156 RNU4-62P, SEMA3B-AS1, 2880 more genes
    nsv3889228copy number variation2nstd102humanPathogenic GRCh37 chr3: 61,892-197,851,986 , GRCh38.p12 chr3: 20,214-198,125,115 NDUFB4, LOC105374108, 2876 more genes
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