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Items: 1 to 20 of 189

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5898176copy number variation1nstd209human GRCh38 chr6: 49,461,564-49,480,584 , GRCh37.p13 chr6: 49,429,277-49,448,297 MMUT, CENPQ
    nsv5844927copy number variation1nstd209human GRCh38 chr6: 49,461,562-49,469,563 , GRCh37.p13 chr6: 49,429,275-49,437,276 MMUT, CENPQ
    nsv5558551sequence alteration1nstd206human GRCh38 chr6: 40,895,286-71,029,944 , GRCh37.p13 chr6: 40,863,025-71,739,647 , ACTG1P9, 405 more genes
    nsv5473307copy number variation1nstd206human GRCh38 chr6: 49,461,544-49,480,609 , GRCh37.p13 chr6: 49,429,257-49,448,322 MMUT, CENPQ
    nsv5302118copy number variation1nstd204human GRCh38.p13 chr6: 49,461,562-49,480,590 , GRCh37.p13 chr6: 49,429,275-49,448,303 CENPQ, MMUT
    nsv5237570copy number variation1nstd204human GRCh38.p13 chr6: 49,461,601-49,480,600 , GRCh37.p13 chr6: 49,429,314-49,448,313 CENPQ, MMUT
    nsv5229864copy number variation1nstd204human GRCh38.p13 chr6: 49,460,962-49,462,961 , GRCh37.p13 chr6: 49,428,675-49,430,674 MMUT, CENPQ
    nsv5226725copy number variation1nstd204human GRCh38.p13 chr6: 49,462,025-49,481,121 , GRCh37.p13 chr6: 49,429,738-49,448,834 CENPQ, MMUT
    nsv5225314copy number variation1nstd204human GRCh38.p13 chr6: 49,462,501-49,470,400 , GRCh37.p13 chr6: 49,430,214-49,438,113 MMUT, CENPQ
    nsv4934727copy number variation1nstd200human GRCh38 chr6: 49,461,564-49,480,589 , GRCh37.p13 chr6: 49,429,277-49,448,302 CENPQ, MMUT
    nsv4828703copy number variation1nstd200human GRCh37 chr6: 49,429,277-49,448,302 , GRCh38.p12 chr6: 49,461,564-49,480,589 MMUT, CENPQ
    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
    nsv4729270copy number variation1nstd102humanLikely pathogenic GRCh37 chr6: 48,626,041-55,575,545 , GRCh38.p12 chr6: 48,658,305-55,710,747 CRISP1, SLC25A20P1, 105 more genes
    nsv4729154copy number variation1nstd102humanUncertain significance GRCh37 chr6: 48,566,675-50,063,411 , GRCh38.p12 chr6: 48,598,939-50,095,698 MMUT, RHAG, 21 more genes
    nsv4683173copy number variation2nstd102humanPathogenic GRCh37 chr6: 49,415,373-49,427,219 , GRCh38.p12 chr6: 49,447,660-49,459,506 MMUT
    nsv4660083copy number variation1nstd186human GRCh37 chr6: 49,430,723-49,455,283 , GRCh38.p12 chr6: 49,463,010-49,487,570 CENPQ, MMUT
    nsv4593638copy number variation1nstd183human GRCh37 chr6: 49,416,522-49,419,045 , GRCh38.p12 chr6: 49,448,809-49,451,332 MMUT
    nsv4592711copy number variation1nstd183human GRCh37 chr6: 49,430,723-49,455,283 , GRCh38.p12 chr6: 49,463,010-49,487,570 MMUT, CENPQ
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