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Items: 1 to 20 of 63

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137211copy number variation1nstd102humanPathogenic GRCh37 chr10: 11,138,692-135,427,143 , GRCh38.p12 chr10: 11,096,729-133,613,639 EXOC6, VCL, 1906 more genes
    nsv7137209copy number variation1nstd102humanPathogenic GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639 RNU7-12P, RNU1-65P, 1876 more genes
    nsv7071643inversion1nstd229human GRCh38 chr10: 42,146,783-43,722,055 , GRCh37.p13 chr10: 42,642,231-44,217,503 RNU6ATAC11P, EIF3LP2, 48 more genes
    nsv6888265copy number variation1nstd229human GRCh38 chr10: 43,648,409-43,648,909 , GRCh37.p13 chr10: 44,143,857-44,144,357 ZNF32-AS2, ZNF32-AS3, 1 more genes
    nsv6883580copy number variation1nstd229human GRCh38 chr10: 42,792,424-46,796,570 , GRCh37.p13 chr10: 43,287,872-46,224,333 RASSF4, AGAP14P, 107 more genes
    nsv6878657copy number variation1nstd229human GRCh38 chr10: 43,549,254-43,826,219 , GRCh37.p13 chr10: 44,044,702-44,321,667 LOC105378275, ELOCP30, 13 more genes
    nsv6878460copy number variation1nstd229human GRCh38 chr10: 43,644,760-43,666,402 , GRCh37.p13 chr10: 44,140,208-44,161,850 ZNF32-AS2, ZNF32, 2 more genes
    nsv6435871copy number variation1nstd223human GRCh38 chr10: 43,644,901-43,648,700 , GRCh37.p13 chr10: 44,140,349-44,144,148 ZNF32-AS3, ZNF32, 2 more genes
    nsv6314146copy number variation1nstd102humanUncertain significance GRCh37 chr10: 43,683,704-44,151,599 , GRCh38.p12 chr10: 43,188,256-43,656,151 ZNF32-AS2, LOC107984226, 19 more genes
    nsv6290893copy number variation1nstd102humannot provided GRCh37 chr10: 135,655-47,688,677 , GRCh38.p12 chr10: 89,715-47,923,579 C1QL3, LOC105376441, 774 more genes
    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
    nsv4870857inversion1nstd200human GRCh37 chr10: 37,108,081-60,078,188 , GRCh38.p12 chr10: 36,819,153-58,318,428 , NCOA4, 306 more genes
    nsv4602243copy number variation1nstd183human GRCh37 chr10: 44,144,107-44,144,354 , GRCh38.p12 chr10: 43,648,659-43,648,906 , ZNF32, 1 more genes
    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
    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
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