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Items: 1 to 20 of 112

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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
    nsv6891534copy number variation1nstd229human GRCh38 chr10: 43,482,916-43,587,800 , GRCh37.p13 chr10: 43,978,364-44,083,248 LOC100130881, ZNF239, 1 more genes
    nsv6884734copy number variation1nstd229human GRCh38 chr10: 43,560,572-43,572,775 , GRCh37.p13 chr10: 44,056,020-44,068,223 ZNF239
    nsv6884166copy number variation1nstd229human GRCh38 chr10: 43,561,019-43,569,624 , GRCh37.p13 chr10: 44,056,467-44,065,072 ZNF239
    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
    nsv6589496inversion1nstd223human GRCh38 chr10: 43,552,048-43,552,895 , GRCh37.p13 chr10: 44,047,496-44,048,343 ZNF239
    nsv6455348copy number variation1nstd223human GRCh38 chr10: 43,561,019-43,569,622 , GRCh37.p13 chr10: 44,056,467-44,065,070 ZNF239
    nsv6443372copy number variation1nstd223human GRCh38 chr10: 43,558,701-43,562,900 , GRCh37.p13 chr10: 44,054,149-44,058,348 ZNF239
    nsv6440130copy number variation1nstd223human GRCh38 chr10: 43,571,801-43,578,100 , GRCh37.p13 chr10: 44,067,249-44,073,548 ZNF239
    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
    nsv6301342copy number variation1nstd186human GRCh37 chr10: 44,067,254-44,067,334 , GRCh38.p12 chr10: 43,571,806-43,571,886 ZNF239
    nsv6290893copy number variation1nstd102humannot provided GRCh37 chr10: 135,655-47,688,677 , GRCh38.p12 chr10: 89,715-47,923,579 C1QL3, LOC105376441, 774 more genes
    nsv5916980copy number variation1nstd209human GRCh38 chr10: 43,563,387-43,564,572 , GRCh37.p13 chr10: 44,058,835-44,060,020 ZNF239
    nsv5861807copy number variation1nstd209human GRCh38 chr10: 43,563,183-43,564,582 , GRCh37.p13 chr10: 44,058,631-44,060,030 ZNF239
    nsv5703129mobile element insertion2nstd211human GRCh38 chr10: 43,573,082-43,573,082 , GRCh37.p13 chr10: 44,068,530-44,068,530 ZNF239
    nsv5484200copy number variation1nstd206human GRCh38 chr10: 43,571,806-43,571,886 , GRCh37.p13 chr10: 44,067,254-44,067,334 ZNF239
    nsv5403169mobile element insertion1nstd206human GRCh38 chr10: 43,573,082-43,573,133 , GRCh37.p13 chr10: 44,068,530-44,068,581 ZNF239
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