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Items: 1 to 20 of 276

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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
    nsv7076630inversion1nstd229human GRCh38 chr10: 29,313,096-30,347,685 , GRCh37.p13 chr10: 29,602,025-30,636,614 LOC105376475, RNU6-598P, 22 more genes
    nsv7070202inversion1nstd229human GRCh38 chr10: 27,330,033-30,802,827 , GRCh37.p13 chr10: 27,618,962-31,091,756 LINC00837, RPL21P93, 77 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
    nsv6897614copy number variation1nstd229human GRCh38 chr10: 30,084,654-30,084,753 , GRCh37.p13 chr10: 30,373,583-30,373,682 LOC101929256, JCAD
    nsv6895854copy number variation1nstd229human GRCh38 chr10: 30,016,555-30,234,058 , GRCh37.p13 chr10: 30,305,484-30,522,987 LOC105376477, LOC101929256, 2 more genes
    nsv6894893copy number variation1nstd229human GRCh38 chr10: 30,063,896-30,066,598 , GRCh37.p13 chr10: 30,352,825-30,355,527 LOC101929256, JCAD
    nsv6894377copy number variation1nstd229human GRCh38 chr10: 28,466,728-36,061,502 , GRCh37.p13 chr10: 28,755,657-36,350,430 LOC105376482, LOC101929431, 130 more genes
    nsv6885693copy number variation1nstd229human GRCh38 chr10: 29,996,035-30,020,326 , GRCh37.p13 chr10: 30,284,964-30,309,255 JCAD, LOC107984218
    nsv6885403copy number variation1nstd229human GRCh38 chr10: 30,034,493-30,043,479 , GRCh37.p13 chr10: 30,323,422-30,332,408 JCAD
    nsv6884083copy number variation1nstd229human GRCh38 chr10: 30,091,749-30,098,667 , GRCh37.p13 chr10: 30,380,678-30,387,596 JCAD, LOC101929256
    nsv6883198copy number variation1nstd229human GRCh38 chr10: 30,092,455-30,100,601 , GRCh37.p13 chr10: 30,381,384-30,389,530 JCAD, LOC101929256
    nsv6881373copy number variation1nstd229human GRCh38 chr10: 30,043,001-30,046,000 , GRCh37.p13 chr10: 30,331,930-30,334,929 JCAD
    nsv6593310inversion1nstd223human GRCh38 chr10: 29,384,765-30,593,038 , GRCh37.p13 chr10: 29,673,694-30,881,967 LOC105376479, RN7SL63P, 30 more genes
    nsv6585948inversion1nstd223human GRCh38 chr10: 29,962,200-31,017,471 , GRCh37.p13 chr10: 30,251,129-31,306,400 LYZL2, MIR7162, 22 more genes
    nsv6584945inversion1nstd223human GRCh38 chr10: 29,510,330-30,674,089 , GRCh37.p13 chr10: 29,799,259-30,963,018 LOC107984218, LOC102724333, 28 more genes
    nsv6582027inversion1nstd223human GRCh38 chr10: 26,903,422-36,846,484 , GRCh37.p13 chr10: 27,192,351-37,135,412 KIF5B, EPC1-AS1, 167 more genes
    nsv6581833inversion1nstd223human GRCh38 chr10: 30,081,673-30,082,699 , GRCh37.p13 chr10: 30,370,602-30,371,628 JCAD, LOC101929256
    nsv6575946inversion1nstd223human GRCh38 chr10: 30,081,571-30,082,592 , GRCh37.p13 chr10: 30,370,500-30,371,521 LOC101929256, JCAD
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