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Items: 1 to 20 of 232

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5730183mobile element insertion1nstd211human GRCh38 chr8: 124,463,273-124,463,273 , GRCh37.p13 chr8: 125,475,514-125,475,514 RNF139-DT
    nsv5562870mobile element insertion1nstd206human GRCh38 chr8: 124,463,286-124,463,324 , GRCh37.p13 chr8: 125,475,527-125,475,565 RNF139-DT
    nsv5478829copy number variation1nstd206human GRCh38 chr8: 124,420,455-124,471,155 , GRCh37.p13 chr8: 125,432,696-125,483,396 TRMT12, RNF139-DT
    nsv5476356copy number variation1nstd206human GRCh38 chr8: 124,453,346-124,461,923 , GRCh37.p13 chr8: 125,465,587-125,474,164 RNF139-DT, TRMT12
    nsv5315691copy number variation1nstd204human GRCh37.p13 chr8: 125,480,118-125,501,674 , GRCh38.p13 chr8: 124,467,877-124,489,433 RNF139, TATDN1, 1 more genes
    nsv5303615copy number variation1nstd204human GRCh38.p13 chr8: 124,420,425-124,471,177 , GRCh37.p13 chr8: 125,432,666-125,483,418 RNF139-DT, TRMT12
    nsv5259703copy number variation1nstd204human GRCh38.p13 chr8: 124,454,322-124,463,156 , GRCh37.p13 chr8: 125,466,563-125,475,397 RNF139-DT
    nsv5254794copy number variation1nstd204human GRCh38.p13 chr8: 124,467,802-124,480,217 , GRCh37.p13 chr8: 125,480,043-125,492,458 RNF139-DT, RNF139
    nsv5251523copy number variation1nstd204human GRCh38.p13 chr8: 124,420,401-124,471,200 , GRCh37.p13 chr8: 125,432,642-125,483,441 TRMT12, RNF139-DT
    nsv5250079copy number variation1nstd204human GRCh38.p13 chr8: 124,465,694-124,468,126 , GRCh37.p13 chr8: 125,477,935-125,480,367 RNF139-DT
    nsv5060033copy number variation1nstd102humanUncertain significance GRCh37 chr8: 121,938,227-125,485,728 , GRCh38.p12 chr8: 120,925,987-124,473,487 RNU6-756P, FAM83A, 53 more genes
    nsv5035989inversion1nstd200human GRCh38 chr8: 74,949,087-131,777,713 , GRCh37.p13 chr8: 75,861,322-132,789,960 , MIR7705, 715 more genes
    nsv4967950copy number variation1nstd200human GRCh38 chr8: 124,473,753-124,483,181 , GRCh37.p13 chr8: 125,485,994-125,495,422 RNF139-DT, RNF139
    nsv4967949copy number variation1nstd200human GRCh38 chr8: 124,455,184-124,462,095 , GRCh37.p13 chr8: 125,467,425-125,474,336 RNF139-DT
    nsv4965790copy number variation1nstd200human GRCh38 chr8: 124,420,455-124,471,155 , GRCh37.p13 chr8: 125,432,696-125,483,396 TRMT12, RNF139-DT
    nsv4829284copy number variation1nstd200human GRCh37 chr8: 125,432,696-125,483,396 , GRCh38.p12 chr8: 124,420,455-124,471,155 TRMT12, RNF139-DT
    nsv4827997copy number variation1nstd200human GRCh37 chr8: 125,467,425-125,474,336 , GRCh38.p12 chr8: 124,455,184-124,462,095 RNF139-DT
    nsv4813378copy number variation1nstd200human GRCh37 chr8: 125,485,994-125,495,422 , GRCh38.p12 chr8: 124,473,753-124,483,181 RNF139-DT, RNF139
    nsv4675718copy number variation1nstd102humanUncertain significance GRCh37 chr8: 124,878,368-126,737,708 , GRCh38.p12 chr8: 123,866,128-125,725,464 FER1L6-AS1, SQLE-DT, 30 more genes
    nsv4675273copy number variation1nstd102humanPathogenic GRCh37 chr8: 121,042,467-146,295,771 , GRCh38.p12 chr8: 120,030,228-145,070,385 TOP1MT, SLA, 379 more genes
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