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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
    nsv6313948copy number variation1nstd102humanUncertain significance GRCh37 chr10: 37,697,888-38,677,334 , GRCh38.p12 chr10: 37,408,960-38,388,406 MTND1P18, RNU6-795P, 21 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
    nsv6011338copy number variation1nstd212human GRCh38 chr10: 38,226,818-38,445,958 , GRCh37.p13 chr10: 38,515,746-38,734,886 HSD17B7P2, SEPTIN7P9, 4 more genes
    nsv5190021mobile element insertion1nstd203human GRCh38 chr10: 38,376,563-38,376,577 , GRCh37.p13 chr10: 38,665,491-38,665,505 HSD17B7P2
    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
    nsv4988775copy number variation1nstd200human GRCh38 chr10: 38,305,317-38,826,633 , GRCh37.p13 chr10: 38,594,245-39,119,764 , HSD17B7P2, 12 more genes
    nsv4870857inversion1nstd200human GRCh37 chr10: 37,108,081-60,078,188 , GRCh38.p12 chr10: 36,819,153-58,318,428 , NCOA4, 306 more genes
    nsv4680714copy number variation1nstd189human GRCh37.p13 chr10: 38,144,259-38,655,478 , GRCh38.p12 chr10: 37,855,331-38,366,550 , ZNF33A, 12 more genes
    nsv4676011copy number variation1nstd102humanLikely benign GRCh37 chr10: 38,064,033-38,900,673 , GRCh38.p12 chr10: 37,775,105-38,607,542 EIF3LP3, CCNYL4, 20 more genes
    nsv4675921copy number variation1nstd102humanLikely benign GRCh37 chr10: 37,189,335-38,900,673 , GRCh38.p12 chr10: 36,900,407-38,607,542 ZNF248, RNU6-1118P, 38 more genes
    nsv4575461mobile element insertion1nstd166human GRCh37.p13 chr10: 38,665,491-38,665,491 , GRCh38.p12 chr10: 38,376,563-38,376,563 HSD17B7P2
    nsv4527167copy number variation1nstd166human GRCh37.p13 chr10: 38,454,999-38,735,000 , GRCh38.p12 chr10: 38,166,071-38,446,072 HSD17B7P2, SEPTIN7P9, 6 more genes
    nsv4430356copy number variation1nstd174human GRCh37 chr10: 38,641,508-39,154,633 , GRCh38.p12 chr10: 38,352,580-38,861,502 , CICP9, 11 more genes
    nsv4378369copy number variation1nstd173human GRCh37 chr10: 38,416,389-38,712,903 , GRCh38.p12 chr10: 38,127,461-38,423,975 CCNYL4, LOC101929540, 6 more genes
    nsv4368894copy number variation1nstd173human GRCh37 chr10: 38,414,822-38,914,648 , GRCh38.p12 chr10: 38,125,894-38,621,517 , ZNF37A, 11 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
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