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Items: 1 to 20 of 116

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7057713inversion1nstd229human GRCh38 chr6: 56,332,234-57,502,028 , GRCh37.p13 chr6: 56,197,032-57,366,927 OSTCP6, MIR548U, 16 more genes
    nsv6790884copy number variation1nstd229human GRCh38 chr6: 57,169,563-57,174,364 , GRCh37.p13 chr6: 57,034,361-57,039,162 BAG2, ZNF451-AS1, 1 more genes
    nsv6787867copy number variation1nstd229human GRCh38 chr6: 57,180,301-57,187,400 , GRCh37.p13 chr6: 57,045,099-57,052,198 BAG2, RAB23
    nsv6787575copy number variation1nstd229human GRCh38 chr6: 57,175,695-57,186,250 , GRCh37.p13 chr6: 57,040,493-57,051,048 BAG2, RAB23
    nsv6785488copy number variation1nstd229human GRCh38 chr6: 57,092,887-57,247,997 , GRCh37.p13 chr6: 56,957,685-57,112,795 BAG2, ZNF451-AS1, 2 more genes
    nsv6782136copy number variation1nstd229human GRCh38 chr6: 57,127,871-57,257,204 , GRCh37.p13 chr6: 56,992,669-57,122,002 ZNF451, RAB23, 2 more genes
    nsv6780170copy number variation1nstd229human GRCh38 chr6: 57,031,858-57,172,819 , GRCh37.p13 chr6: 56,896,656-57,037,617 KIAA1586, ZNF451, 2 more genes
    nsv6638066copy number variation1nstd102humanUncertain significance GRCh38 chr6: 53,151,508-58,400,428 , GRCh37.p13 chr6: 53,016,306-58,726,706 NPM1P36, LINC00680-GUSBP4, 73 more genes
    nsv6631511copy number variation1nstd224human GRCh37 chr6: 56,995,750-57,121,719 , GRCh38.p12 chr6: 57,130,952-57,256,921 ZNF451-AS1, ZNF451, 2 more genes
    nsv6631072copy number variation1nstd224human GRCh37 chr6: 56,995,750-57,054,008 , GRCh38.p12 chr6: 57,130,952-57,189,210 ZNF451-AS1, ZNF451, 2 more genes
    nsv6631070copy number variation1nstd224human GRCh37 chr6: 54,531,949-57,262,543 , GRCh38.p12 chr6: 54,667,151-57,397,745 DST, BAG2, 28 more genes
    nsv6560587inversion1nstd223human GRCh38 chr6: 56,332,312-57,501,978 , GRCh37.p13 chr6: 56,197,110-57,366,877 RCC2P7, COL21A1, 16 more genes
    nsv6405374copy number variation1nstd223human GRCh38 chr6: 57,187,553-57,188,045 , GRCh37.p13 chr6: 57,052,351-57,052,843 RAB23, BAG2
    nsv6314749copy number variation1nstd102humanLikely pathogenic GRCh37 chr6: 43,636,308-64,947,206 , GRCh38.p12 chr6: 43,668,571-64,237,313 ACTG1P9, CRISP1, 245 more genes
    nsv6313617copy number variation1nstd102humanUncertain significance GRCh37 chr6: 56,993,776-57,052,516 , GRCh38.p12 chr6: 57,128,978-57,187,718 RAB23, ZNF451, 2 more genes
    nsv5558551sequence alteration1nstd206human GRCh38 chr6: 40,895,286-71,029,944 , GRCh37.p13 chr6: 40,863,025-71,739,647 , ACTG1P9, 405 more genes
    nsv5367218translocation1nstd200human GRCh38 chr3: 179,488,071-179,488,071 , GRCh38 chr6: 57,174,881-57,174,881 , GRCh37.p13 chr3: 179,205,859-179,205,859 , GRCh37.p13 chr6: 57,039,679-57,039,679 , BAG2
    nsv5361789translocation1nstd200human GRCh38 chr3: 93,812,772-93,812,772 , GRCh38 chr6: 57,188,369-57,188,369 , GRCh37.p13 chr6: 57,053,167-57,053,167 , GRCh37.p13 chr3: 93,531,616-93,531,616 RAB23, BAG2
    nsv5340989translocation1nstd200human GRCh37 chr6: 57,053,167-57,053,167 , GRCh37 chr3: 93,531,616-93,531,616 , GRCh38.p12 chr6: 57,188,369-57,188,369 , GRCh38.p12 chr3: 93,812,772-93,812,772 BAG2, RAB23
    nsv4757608inversion1nstd199human GRCh37 chr6: 26,743,921-58,149,359 , GRCh38.p12 chr6: 26,823,536-61,119,912 , ABCF1, 1075 more genes
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