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Items: 1 to 20 of 141

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7139819insertion1nstd232human GRCh37.p13 chr6: 52,134,025-52,134,025 , GRCh38.p12 chr6: 52,269,227-52,269,227 MCM3
    nsv7139517insertion1nstd232human GRCh37.p13 chr6: 52,138,715-52,138,715 , GRCh38.p12 chr6: 52,273,917-52,273,917 MCM3
    nsv7056672inversion1nstd229human GRCh38 chr6: 51,226,717-52,446,371 , GRCh37.p13 chr6: 51,095,293-52,311,169 MIR206, LOC101927082, 16 more genes
    nsv6791146copy number variation1nstd229human GRCh38 chr6: 52,180,101-52,369,800 , GRCh37.p13 chr6: 52,044,899-52,234,598 MCM3, IL17A, 4 more genes
    nsv6565647inversion1nstd223human GRCh38 chr6: 52,267,528-52,270,025 , GRCh37.p13 chr6: 52,132,326-52,134,823 MCM3
    nsv6563073inversion1nstd223human GRCh38 chr6: 52,107,269-56,893,586 , GRCh37.p13 chr6: 51,972,067-56,758,384 GSTA1, LOC730101, 79 more genes
    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
    nsv6245153mobile element insertion1nstd215human GRCh38 chr6: 52,283,898-52,283,898 , GRCh37.p13 chr6: 52,148,696-52,148,696 MCM3
    nsv6135921copy number variation1nstd213human GRCh37 chr6: 34,700,000-52,650,001 , GRCh38.p12 chr6: 34,732,223-52,785,203 ACTG1P9, CRISP1, 361 more genes
    nsv6135848copy number variation1nstd213human GRCh37 chr6: 50,080,000-52,650,001 , GRCh38.p12 chr6: 50,112,287-52,785,203 SLC25A20P1, FTH1P5, 32 more genes
    nsv5682245mobile element insertion1nstd211human GRCh38 chr6: 52,270,581-52,270,581 , GRCh37.p13 chr6: 52,135,379-52,135,379 MCM3
    nsv5558551sequence alteration1nstd206human GRCh38 chr6: 40,895,286-71,029,944 , GRCh37.p13 chr6: 40,863,025-71,739,647 , ACTG1P9, 405 more genes
    nsv5407834mobile element insertion1nstd206human GRCh38 chr6: 52,270,581-52,270,632 , GRCh37.p13 chr6: 52,135,379-52,135,430 MCM3
    nsv5381452copy number variation1nstd102humanUncertain significance GRCh37 chr6: 51,930,764-52,906,034 , GRCh38.p12 chr6: 52,065,966-53,041,236 GSTA4, LOC730101, 30 more genes
    nsv5362979translocation1nstd200human GRCh38 chr6: 52,263,497-52,263,497 , GRCh38 chr6: 52,263,384-52,263,384 , GRCh37.p13 chr6: 52,128,295-52,128,295 , GRCh37.p13 chr6: 52,128,182-52,128,182 MCM3
    nsv5116556mobile element insertion1nstd203human GRCh38 chr6: 52,280,747-52,280,763 , GRCh37.p13 chr6: 52,145,545-52,145,561 MCM3
    nsv5106185mobile element insertion1nstd203human GRCh38 chr6: 52,280,456-52,280,467 , GRCh37.p13 chr6: 52,145,254-52,145,265 MCM3
    nsv4757608inversion1nstd199human GRCh37 chr6: 26,743,921-58,149,359 , GRCh38.p12 chr6: 26,823,536-61,119,912 , ABCF1, 1075 more genes
    nsv4756329inversion1nstd199human GRCh37 chr6: 26,745,246-58,149,317 , GRCh38.p12 chr6: 26,823,536-61,119,912 , ABCF1, 1075 more genes
    nsv4735754copy number variation1nstd199human GRCh37 chr6: 26,776,020-58,144,810 , GRCh38.p12 chr6: 26,823,536-61,119,912 , RNU6-250P, 1075 more genes
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