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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5727131mobile element insertion2nstd211human GRCh38 chr8: 123,522,102-123,522,102 , GRCh37.p13 chr8: 124,534,342-124,534,342 FBXO32
    nsv5720740mobile element insertion1nstd211human GRCh38 chr8: 123,516,059-123,516,059 , GRCh37.p13 chr8: 124,528,299-124,528,299 FBXO32
    nsv5715643mobile element insertion1nstd211human GRCh38 chr8: 123,496,833-123,496,833 , GRCh37.p13 chr8: 124,509,073-124,509,073 FBXO32
    nsv5379391translocation1nstd200human GRCh38 chr8: 123,503,233-123,503,233 , GRCh38 chr8: 123,507,514-123,507,514 , GRCh37.p13 chr8: 124,515,473-124,515,473 , GRCh37.p13 chr8: 124,519,754-124,519,754 FBXO32
    nsv5195742mobile element insertion1nstd203human GRCh38 chr8: 123,516,395-123,516,400 , GRCh37.p13 chr8: 124,528,635-124,528,640 FBXO32
    nsv5060033copy number variation1nstd102humanUncertain significance GRCh37 chr8: 121,938,227-125,485,728 , GRCh38.p12 chr8: 120,925,987-124,473,487 RNF139, TBC1D31, 56 more genes
    nsv5035989inversion1nstd200human GRCh38 chr8: 74,949,087-131,777,713 , GRCh37.p13 chr8: 75,861,322-132,789,960 SPAG1, RNU7-181P, 715 more genes
    nsv4675273copy number variation1nstd102humanPathogenic GRCh37 chr8: 121,042,467-146,295,771 , GRCh38.p12 chr8: 120,030,228-145,070,385 LOC105375747, LOC105375750, 390 more genes
    nsv4565485mobile element insertion1nstd166human GRCh37.p13 chr8: 124,534,328-124,534,328 , GRCh38.p12 chr8: 123,522,088-123,522,088 FBXO32
    nsv4558800mobile element insertion1nstd166human GRCh37.p13 chr8: 124,509,058-124,509,058 , GRCh38.p12 chr8: 123,496,818-123,496,818 FBXO32
    nsv4486779mobile element insertion1nstd166human GRCh37.p13 chr8: 124,539,037-124,539,037 , GRCh38.p12 chr8: 123,526,797-123,526,797 FBXO32
    nsv4457220copy number variation1nstd102humanPathogenic GRCh37 chr8: 123,074,293-131,113,892 , GRCh38.p12 chr8: 122,062,054-130,101,646 LOC105375754, LOC105375751, 123 more genes
    nsv4456811copy number variation1nstd102humanPathogenic GRCh37 chr8: 31,936,551-146,295,771 , GRCh38.p12 chr8: 32,079,035-145,070,385 LOC107984005, LY6D, 1545 more genes
    nsv4456783copy number variation1nstd102humanPathogenic GRCh37 chr8: 122,193,546-146,295,771 , GRCh38.p12 chr8: 121,181,306-145,070,385 LOC105375742, SQLE, 379 more genes
    nsv4456775copy number variation1nstd102humanUncertain significance GRCh37 chr8: 124,443,708-125,305,582 , GRCh38.p12 chr8: 123,431,468-124,293,341 ANXA13, FBXO32, 14 more genes
    nsv4455511copy number variation1nstd102humanPathogenic GRCh37 chr8: 124,120,772-135,265,846 , GRCh38.p12 chr8: 123,108,532-134,253,603 EFR3A, LOC105375763, 155 more genes
    nsv4380375copy number variation1nstd173human GRCh37 chr8: 124,522,427-124,546,676 , GRCh38.p12 chr8: 123,510,187-123,534,436 FBXO32
    nsv4349554copy number variation1nstd102humanPathogenic GRCh37 chr8: 158,048-146,295,771 , GRCh38.p12 chr8: 208,048-145,070,385 ARHGEF10, LOC105375901, 2159 more genes
    nsv4318515inversion1nstd166human GRCh37.p13 chr8: 75,861,320-132,789,960 , GRCh38.p12 chr8: 74,949,085-131,777,713 , ANXA13, 716 more genes
    nsv3923310copy number variation1nstd102humanPathogenic NCBI36 chr8: 166,452-146,264,902 , GRCh38 chr8: 226,452-145,068,712 , GRCh37 chr8: 176,452-146,294,098 LOC105375733, RPS4XP10, 2159 more genes
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