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Items: 1 to 20 of 126

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5709011mobile element insertion1nstd211human GRCh38 chr10: 43,637,598-43,637,598 , GRCh37.p13 chr10: 44,133,046-44,133,046 ZNF32-AS3
    nsv5354393translocation1nstd200human GRCh38 chr10: 43,654,370-43,654,370 , GRCh38 chr10: 43,654,516-43,654,516 , GRCh37.p13 chr10: 44,149,964-44,149,964 , GRCh37.p13 chr10: 44,149,818-44,149,818 ZNF32-AS3
    nsv5136511mobile element insertion1nstd203human GRCh38 chr10: 43,637,586-43,637,598 , GRCh37.p13 chr10: 44,133,034-44,133,046 ZNF32-AS3
    nsv5035636inversion1nstd200human GRCh38 chr10: 32,580,256-50,959,654 , GRCh37.p13 chr10: 32,869,184-52,719,414 , ZNF32-AS2, 320 more genes
    nsv5033632inversion1nstd200human GRCh38 chr10: 36,819,152-58,318,428 , GRCh37.p13 chr10: 37,108,080-60,078,188 , LOC107001062, 306 more genes
    nsv4973583copy number variation1nstd200human GRCh38 chr10: 43,633,408-43,640,242 , GRCh37.p13 chr10: 44,128,856-44,135,690 ZNF32-AS3
    nsv4969774copy number variation1nstd200human GRCh38 chr10: 43,658,677-43,659,708 , GRCh37.p13 chr10: 44,154,125-44,155,156 ZNF32-AS3
    nsv4870857inversion1nstd200human GRCh37 chr10: 37,108,081-60,078,188 , GRCh38.p12 chr10: 36,819,153-58,318,428 , NCOA4, 306 more genes
    nsv4844797copy number variation1nstd200human GRCh37 chr10: 44,154,125-44,155,156 , GRCh38.p12 chr10: 43,658,677-43,659,708 ZNF32-AS3
    nsv4602243copy number variation1nstd183human GRCh37 chr10: 44,144,107-44,144,354 , GRCh38.p12 chr10: 43,648,659-43,648,906 , ZNF32, 1 more genes
    nsv4554147insertion1nstd166human GRCh37.p13 chr10: 44,133,034-44,133,034 , GRCh38.p12 chr10: 43,637,586-43,637,586 ZNF32-AS3
    nsv4343722sequence alteration1nstd166human GRCh37.p13 chr10: 43,905,894-92,001,956 , GRCh38.p12 chr10: 43,410,446-90,242,199 , ALOX5, 749 more genes
    nsv4339713sequence alteration1nstd166human GRCh37.p13 chr10: 8,718,069-114,609,729 , GRCh38.p12 chr10: 8,676,106-112,849,970 , ADRA2A, 1651 more genes
    nsv4313384inversion1nstd166human GRCh37.p13 chr10: 37,108,081-60,078,188 , GRCh38.p12 chr10: 36,819,153-58,318,428 , RET, 306 more genes
    nsv4191015copy number variation1nstd166human GRCh37.p13 chr10: 44,149,818-44,149,964 , GRCh38.p12 chr10: 43,654,370-43,654,516 ZNF32-AS3
    nsv4190810copy number variation1nstd166human GRCh37.p13 chr10: 44,128,913-44,135,646 , GRCh38.p12 chr10: 43,633,465-43,640,198 ZNF32-AS3
    nsv3972353copy number variation1nstd102humanLikely pathogenic GRCh37 chr10: 37,149,872-46,169,876 , GRCh38.p12 chr10: 36,860,944-45,674,428 ALOX5, HNRNPF, 132 more genes
    nsv3923539inversion1nstd102humanLikely pathogenic GRCh38.p12 chr10: 43,115,743-59,903,521 , GRCh37 chr10: 43,611,191-61,663,279 ALOX5, CHAT, 248 more genes
    nsv3921181copy number variation1nstd102humanPathogenic NCBI36 chr10: 41,927,641-68,830,439 , GRCh38 chr10: 42,112,187-67,400,675 , GRCh37 chr10: 42,607,635-69,160,433 AGAP6, A1CF, 338 more genes
    nsv3920598copy number variation1nstd102humanBenign NCBI36 chr10: 4,636,926-47,125,152 , GRCh38 chr10: 4,604,734-48,074,662 , GRCh37 chr10: 4,646,926-47,531,169 LOC100420467, LOC105376474, 709 more genes
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