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Items: 1 to 20 of 233

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5709296mobile element insertion1nstd211human GRCh38 chr8: 23,109,099-23,109,099 , GRCh37.p13 chr8: 22,966,612-22,966,612 TNFRSF10C
    nsv5486057copy number variation1nstd206human GRCh38 chr8: 23,102,093-23,111,421 , GRCh37.p13 chr8: 22,959,606-22,968,934 TNFRSF10C, LOC254896
    nsv5200364copy number variation1nstd102humanPathogenic GRCh37 chr8: 176,814-43,396,776 , GRCh38.p12 chr8: 226,814-43,541,633 LOC100130612, XPO7, 770 more genes
    nsv5105132mobile element insertion1nstd203human GRCh38 chr8: 23,108,673-23,108,690 , GRCh37.p13 chr8: 22,966,186-22,966,203 TNFRSF10C
    nsv4728911copy number variation1nstd102humanLikely pathogenic GRCh37 chr8: 12,528,482-29,886,483 , GRCh38.p12 chr8: 12,670,973-30,028,967 NAT1, NAT2, 272 more genes
    nsv4616329copy number variation1nstd183human GRCh37 chr8: 22,913,798-22,962,553 , GRCh38.p12 chr8: 23,056,285-23,105,040 , LOC254896, 3 more genes
    nsv4613229copy number variation1nstd183human GRCh37 chr8: 22,937,222-23,039,869 , GRCh38.p12 chr8: 23,079,709-23,182,356 , TNFRSF10D, 3 more genes
    nsv4602130copy number variation1nstd183human GRCh37 chr8: 22,716,134-22,995,484 , GRCh38.p12 chr8: 22,858,621-23,137,971 , RN7SL303P, 9 more genes
    nsv4494174mobile element insertion1nstd166human GRCh37.p13 chr8: 22,966,569-22,966,569 , GRCh38.p12 chr8: 23,109,056-23,109,056 TNFRSF10C
    nsv4491525mobile element insertion1nstd166human GRCh37.p13 chr8: 22,966,612-22,966,612 , GRCh38.p12 chr8: 23,109,099-23,109,099 TNFRSF10C
    nsv4457159copy number variation1nstd102humanPathogenic GRCh37 chr8: 21,662,847-24,199,218 , GRCh38.p12 chr8: 21,805,335-24,341,705 SINHCAFP3, RPL23AP55, 66 more genes
    nsv4455606copy number variation1nstd102humanPathogenic GRCh37 chr8: 22,442,548-27,369,334 , GRCh38.p12 chr8: 22,585,035-27,511,817 PPP2R2A, LOC102723395, 91 more genes
    nsv4412520copy number variation1nstd174human GRCh37 chr8: 22,913,786-22,963,960 , GRCh38.p12 chr8: 23,056,273-23,106,447 , TNFRSF10B, 3 more genes
    nsv4403316copy number variation1nstd174human GRCh37 chr8: 22,886,376-23,058,680 , GRCh38.p12 chr8: 23,028,863-23,201,167 , TNFRSF10D, 5 more genes
    nsv4349554copy number variation2nstd102humanPathogenic GRCh37 chr8: 158,048-146,295,771 , GRCh38.p12 chr8: 208,048-145,070,385 LOC101929488, TEX15, 2105 more genes
    nsv4348018copy number variation1nstd102humanLikely pathogenic GRCh37 chr8: 12,546,855-35,816,855 , GRCh38.p12 chr8: 12,689,346-35,959,337 NAT1, NAT2, 343 more genes
    nsv4158598copy number variation1nstd166human GRCh37.p13 chr8: 22,966,905-22,967,425 , GRCh38.p12 chr8: 23,109,392-23,109,912 TNFRSF10C
    nsv3972390copy number variation1nstd102humanLikely pathogenic GRCh37 chr8: 12,556,004-34,374,150 , GRCh38.p12 chr8: 12,698,495-34,516,632 NAT1, NAT2, 335 more genes
    nsv3966934insertion1nstd168human GRCh38 chr8: 23,111,130-23,138,099 , GRCh37.p13 chr8: 22,968,643-22,995,612 TNFRSF10D, TNFRSF10C
    nsv3924532copy number variation1nstd102humanPathogenic NCBI36 chr8: 181,605-31,068,132 , GRCh38 chr8: 241,605-31,091,074 , GRCh37 chr8: 191,605-30,948,590 DEFB109B, GATA4, 585 more genes
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