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Items: 1 to 20 of 244

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7142123insertion1nstd232human GRCh37.p13 chr10: 33,212,668-33,212,668 , GRCh38.p12 chr10: 32,923,740-32,923,740 ITGB1
    nsv7140475insertion1nstd232human GRCh37.p13 chr10: 33,209,014-33,209,014 , GRCh38.p12 chr10: 32,920,086-32,920,086 ITGB1
    nsv7137798insertion1nstd232human GRCh37.p13 chr10: 33,209,013-33,209,013 , GRCh38.p12 chr10: 32,920,085-32,920,085 ITGB1
    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
    nsv7065010inversion1nstd229human GRCh38 chr10: 32,699,822-35,479,064 , GRCh37.p13 chr10: 32,988,750-35,767,992 RNU6-1167P, MIR3611, 34 more genes
    nsv6896181copy number variation1nstd229human GRCh38 chr10: 32,905,868-32,906,727 , GRCh37.p13 chr10: 33,194,796-33,195,655 ITGB1
    nsv6894569copy number variation1nstd229human GRCh38 chr10: 32,747,382-32,906,356 , GRCh37.p13 chr10: 33,036,310-33,195,284 ITGB1, SNORA86, 1 more genes
    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
    nsv6880702copy number variation1nstd229human GRCh38 chr10: 32,957,401-32,959,300 , GRCh37.p13 chr10: 33,246,329-33,248,228 ITGB1, ITGB1-DT
    nsv6878493copy number variation1nstd229human GRCh38 chr10: 32,913,719-32,918,580 , GRCh37.p13 chr10: 33,202,647-33,207,508 ITGB1
    nsv6582027inversion1nstd223human GRCh38 chr10: 26,903,422-36,846,484 , GRCh37.p13 chr10: 27,192,351-37,135,412 KIF5B, EPC1-AS1, 167 more genes
    nsv6453323copy number variation1nstd223human GRCh38 chr10: 32,747,382-32,906,356 , GRCh37.p13 chr10: 33,036,310-33,195,284 SNORA86, ITGB1, 1 more genes
    nsv6452484copy number variation1nstd223human GRCh38 chr10: 32,898,323-32,898,894 , GRCh37.p13 chr10: 33,187,251-33,187,822 ITGB1
    nsv6449450copy number variation1nstd223human GRCh38 chr10: 32,899,101-32,900,100 , GRCh37.p13 chr10: 33,188,029-33,189,028 ITGB1, SNORA86
    nsv6441686copy number variation1nstd223human GRCh38 chr10: 32,935,714-32,937,373 , GRCh37.p13 chr10: 33,224,642-33,226,301 ITGB1
    nsv6441310copy number variation1nstd223human GRCh38 chr10: 32,938,601-33,053,700 , GRCh37.p13 chr10: 33,227,529-33,342,628 MTND4LP11, ITGB1, 3 more genes
    nsv6436410copy number variation1nstd223human GRCh38 chr10: 32,897,828-32,898,351 , GRCh37.p13 chr10: 33,186,756-33,187,279 ITGB1
    nsv6313952copy number variation1nstd102humanPathogenic GRCh37 chr10: 6,273,934-34,732,521 , GRCh38.p12 chr10: 6,231,971-34,443,593 RPL36AP55, HNRNPA1P32, 418 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
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