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Items: 1 to 20 of 210

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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
    nsv7093873copy number variation1nstd102humanUncertain significance GRCh37 chr10: 27,294,519-27,443,139 , GRCh38.p12 chr10: 27,005,590-27,154,210 ANKRD26, MASTL, 2 more genes
    nsv7093630copy number variation1nstd102humanUncertain significance GRCh37 chr10: 26,993,586-28,391,597 , GRCh38.p12 chr10: 26,704,657-28,102,668 PDSS1, SNORD130, 30 more genes
    nsv7074885inversion1nstd229human GRCh38 chr10: 26,205,604-28,491,184 , GRCh37.p13 chr10: 26,494,533-28,780,113 MPP7-DT, RAB18, 47 more genes
    nsv7071344inversion1nstd229human GRCh38 chr10: 27,072,454-27,965,833 , GRCh37.p13 chr10: 27,361,383-28,254,762 MASTL, ANKRD26, 21 more genes
    nsv7067110inversion1nstd229human GRCh38 chr10: 26,915,887-27,493,650 , GRCh37.p13 chr10: 27,204,816-27,782,579 RNU6-666P, MASTL, 15 more genes
    nsv7065972inversion1nstd229human GRCh38 chr10: 27,072,311-27,655,365 , GRCh37.p13 chr10: 27,361,240-27,944,294 PTCHD3, LINC02673, 16 more genes
    nsv7065269inversion1nstd229human GRCh38 chr10: 27,005,916-28,438,423 , GRCh37.p13 chr10: 27,294,845-28,727,352 RNU6-490P, ODAD2, 30 more genes
    nsv7061373inversion1nstd229human GRCh38 chr10: 26,891,336-27,355,825 , GRCh37.p13 chr10: 27,180,265-27,644,754 YME1L1, RNU6-490P, 13 more genes
    nsv7058187inversion1nstd229human GRCh38 chr10: 27,002,297-30,809,591 , GRCh37.p13 chr10: 27,291,226-31,098,520 RNU6-490P, LOC105376474, 87 more genes
    nsv6889671copy number variation1nstd229human GRCh38 chr10: 27,122,506-27,159,195 , GRCh37.p13 chr10: 27,411,435-27,448,124 YME1L1, MASTL
    nsv6637568copy number variation1nstd102humanUncertain significance GRCh37 chr10: 27,065,576-27,549,923 , GRCh38.p12 chr10: 26,776,647-27,260,994 RNU7-12P, ANKRD26, 10 more genes
    nsv6591139inversion1nstd223human GRCh38 chr10: 27,173,584-27,174,148 , GRCh37.p13 chr10: 27,462,513-27,463,077 MASTL
    nsv6587777inversion1nstd223human GRCh38 chr10: 27,171,837-27,172,648 , GRCh37.p13 chr10: 27,460,766-27,461,577 MASTL
    nsv6587016inversion1nstd223human GRCh38 chr10: 27,182,069-27,183,386 , GRCh37.p13 chr10: 27,470,998-27,472,315 MASTL, ACBD5
    nsv6586792inversion1nstd223human GRCh38 chr10: 26,903,566-27,312,250 , GRCh37.p13 chr10: 27,192,495-27,601,179 ANKRD26, MASTL, 9 more genes
    nsv6586065inversion1nstd223human GRCh38 chr10: 27,162,400-27,163,012 , GRCh37.p13 chr10: 27,451,329-27,451,941 MASTL
    nsv6582027inversion1nstd223human GRCh38 chr10: 26,903,422-36,846,484 , GRCh37.p13 chr10: 27,192,351-37,135,412 KIF5B, EPC1-AS1, 167 more genes
    nsv6577878inversion1nstd223human GRCh38 chr10: 27,173,589-27,174,031 , GRCh37.p13 chr10: 27,462,518-27,462,960 MASTL
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