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Items: 1 to 20 of 247

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5972608insertion1nstd209human GRCh38 chr11: 63,901,448-63,901,448 , GRCh37.p13 chr11: 63,668,920-63,668,920 MARK2
    nsv5971139insertion1nstd209human GRCh38 chr11: 63,893,357-63,893,357 , GRCh37.p13 chr11: 63,660,829-63,660,829 TRR-CCT9-1, MARK2
    nsv5907786copy number variation1nstd209human GRCh38 chr11: 63,854,693-63,855,198 , GRCh37.p13 chr11: 63,622,165-63,622,670 MARK2
    nsv5722468mobile element insertion1nstd211human GRCh38 chr11: 63,852,364-63,852,364 , GRCh37.p13 chr11: 63,619,836-63,619,836 MARK2
    nsv5696625mobile element insertion1nstd211human GRCh38 chr11: 63,856,792-63,856,792 , GRCh37.p13 chr11: 63,624,264-63,624,264 MARK2
    nsv5663238insertion1nstd207human GRCh38 chr11: 63,871,738-63,871,738 , GRCh37.p13 chr11: 63,639,210-63,639,210 MARK2
    nsv5651630insertion1nstd207human GRCh38 chr11: 63,893,357-63,893,357 , GRCh37.p13 chr11: 63,660,829-63,660,829 TRR-CCT9-1, MARK2
    nsv5646574insertion1nstd207human GRCh38 chr11: 63,871,543-63,871,543 , GRCh37.p13 chr11: 63,639,015-63,639,015 MARK2
    nsv5598991copy number variation1nstd207human GRCh38 chr11: 63,871,618-63,871,707 , GRCh37.p13 chr11: 63,639,090-63,639,179 MARK2
    nsv5563434mobile element insertion1nstd206human GRCh38 chr11: 63,852,364-63,852,375 , GRCh37.p13 chr11: 63,619,836-63,619,847 MARK2
    nsv5540709insertion1nstd206human GRCh38 chr11: 63,893,357-63,893,357 , GRCh37.p13 chr11: 63,660,829-63,660,829 MARK2, TRR-CCT9-1
    nsv5513039copy number variation1nstd206human GRCh38 chr11: 63,859,142-63,863,855 , GRCh37.p13 chr11: 63,626,614-63,631,327 MARK2
    nsv5507993copy number variation1nstd206human GRCh38 chr11: 63,854,600-63,855,199 , GRCh37.p13 chr11: 63,622,072-63,622,671 MARK2
    nsv5504964copy number variation1nstd206human GRCh38 chr11: 63,883,577-63,883,642 , GRCh37.p13 chr11: 63,651,049-63,651,114 MARK2
    nsv5495948copy number variation1nstd206human GRCh38 chr11: 63,842,317-63,875,214 , GRCh37.p13 chr11: 63,609,789-63,642,686 MARK2
    nsv5380796copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397 FAUP4, MMP7, 2031 more genes
    nsv5355276translocation1nstd200human GRCh38 chr11: 63,854,695-63,854,695 , GRCh38 chr11: 63,855,199-63,855,199 , GRCh37.p13 chr11: 63,622,167-63,622,167 , GRCh37.p13 chr11: 63,622,671-63,622,671 MARK2
    nsv5339030translocation1nstd200human GRCh37 chr11: 63,651,049-63,651,049 , GRCh37 chr11: 63,651,114-63,651,114 , GRCh38.p12 chr11: 63,883,577-63,883,577 , GRCh38.p12 chr11: 63,883,642-63,883,642 MARK2
    nsv5305808copy number variation1nstd204human GRCh38.p13 chr11: 63,845,932-63,848,851 , GRCh37.p13 chr11: 63,613,404-63,616,323 MARK2
    nsv5277562copy number variation1nstd204human GRCh38.p13 chr11: 63,845,894-63,848,793 , GRCh37.p13 chr11: 63,613,366-63,616,265 MARK2
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