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Items: 1 to 20 of 223

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5920885copy number variation1nstd209human GRCh38 chr8: 23,012,965-23,013,656 , GRCh37.p13 chr8: 22,870,478-22,871,169 RHOBTB2
    nsv5575779copy number variation1nstd207human GRCh38 chr8: 23,012,965-23,013,656 , GRCh37.p13 chr8: 22,870,478-22,871,169 RHOBTB2
    nsv5489234copy number variation1nstd206human GRCh38 chr8: 23,012,978-23,013,653 , GRCh37.p13 chr8: 22,870,491-22,871,166 RHOBTB2
    nsv5408565mobile element insertion1nstd206human GRCh38 chr8: 23,018,998-23,018,998 , GRCh37.p13 chr8: 22,876,511-22,876,511 TNFRSF10B, RHOBTB2
    nsv5388862copy number variation1nstd186human GRCh37 chr8: 22,870,517-22,871,135 , GRCh38.p12 chr8: 23,013,004-23,013,622 RHOBTB2
    nsv5312433copy number variation1nstd204human GRCh38.p13 chr8: 23,012,959-23,013,660 , GRCh37.p13 chr8: 22,870,472-22,871,173 RHOBTB2
    nsv5200364copy number variation1nstd102humanPathogenic GRCh37 chr8: 176,814-43,396,776 , GRCh38.p12 chr8: 226,814-43,541,633 LOC100130612, XPO7, 770 more genes
    nsv4959673copy number variation1nstd200human GRCh38 chr8: 22,938,646-23,018,508 , GRCh37.p13 chr8: 22,796,159-22,876,021 LOC107984124, RHOBTB2, 3 more genes
    nsv4821482copy number variation1nstd200human GRCh37 chr8: 22,870,514-22,871,136 , GRCh38.p12 chr8: 23,013,001-23,013,623 RHOBTB2
    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
    nsv4671472copy number variation1nstd186human GRCh37 chr8: 22,870,503-22,871,201 , GRCh38.p12 chr8: 23,012,990-23,013,688 RHOBTB2
    nsv4607576copy number variation1nstd183human GRCh37 chr8: 22,870,503-22,871,201 , GRCh38.p12 chr8: 23,012,990-23,013,688 RHOBTB2
    nsv4602130copy number variation1nstd183human GRCh37 chr8: 22,716,134-22,995,484 , GRCh38.p12 chr8: 22,858,621-23,137,971 , RN7SL303P, 9 more genes
    nsv4495014mobile element insertion1nstd166human GRCh37.p13 chr8: 22,876,511-22,876,511 , GRCh38.p12 chr8: 23,018,998-23,018,998 TNFRSF10B, RHOBTB2
    nsv4487800mobile element insertion1nstd166human GRCh37.p13 chr8: 22,876,463-22,876,463 , GRCh38.p12 chr8: 23,018,950-23,018,950 RHOBTB2, TNFRSF10B
    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
    nsv4396876copy number variation1nstd174human GRCh37 chr8: 22,870,414-22,871,298 , GRCh38.p12 chr8: 23,012,901-23,013,785 RHOBTB2
    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
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