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Items: 1 to 20 of 169

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5924430copy number variation1nstd209human GRCh38 chr10: 17,163,285-17,163,334 , GRCh37.p13 chr10: 17,205,284-17,205,333 TRDMT1
    nsv5909086copy number variation1nstd209human GRCh38 chr10: 16,761,962-17,211,984 , GRCh37.p13 chr10: 16,803,961-17,253,983 TRDMT1, RSU1, 2 more genes
    nsv5867175copy number variation1nstd209human GRCh38 chr10: 17,164,223-17,165,342 , GRCh37.p13 chr10: 17,206,222-17,207,341 TRDMT1
    nsv5861931copy number variation2nstd209human GRCh38 chr10: 17,142,015-17,144,014 , GRCh37.p13 chr10: 17,184,014-17,186,013 TRDMT1
    nsv5859831copy number variation1nstd209human GRCh38 chr10: 17,169,455-17,178,565 , GRCh37.p13 chr10: 17,211,454-17,220,564 TRDMT1
    nsv5854912copy number variation1nstd209human GRCh38 chr10: 17,154,759-17,156,458 , GRCh37.p13 chr10: 17,196,758-17,198,457 TRDMT1
    nsv5851222copy number variation2nstd209human GRCh38 chr10: 17,197,882-17,198,881 , GRCh37.p13 chr10: 17,239,881-17,240,880 TRDMT1
    nsv5850996copy number variation1nstd209human GRCh38 chr10: 17,150,194-17,166,559 , GRCh37.p13 chr10: 17,192,193-17,208,558 TRDMT1
    nsv5848749copy number variation1nstd209human GRCh38 chr10: 17,196,115-17,211,046 , GRCh37.p13 chr10: 17,238,114-17,253,045 TRDMT1
    nsv5848735copy number variation2nstd209human GRCh38 chr10: 17,186,092-17,187,691 , GRCh37.p13 chr10: 17,228,091-17,229,690 TRDMT1
    nsv5633424insertion1nstd207human GRCh38 chr10: 17,148,730-17,148,730 , GRCh37.p13 chr10: 17,190,729-17,190,729 TRDMT1
    nsv5381768copy number variation1nstd102humanPathogenic GRCh37 chr10: 9,137,489-17,227,168 , GRCh38.p12 chr10: 9,095,526-17,185,169 PROSER2, C1QL3, 110 more genes
    nsv4975166copy number variation1nstd200human GRCh38 chr10: 17,178,737-17,185,209 , GRCh37.p13 chr10: 17,220,736-17,227,208 TRDMT1
    nsv4613026copy number variation1nstd183human GRCh37 chr10: 17,216,503-17,216,631 , GRCh38.p12 chr10: 17,174,504-17,174,632 TRDMT1
    nsv4525645copy number variation1nstd166human GRCh37.p13 chr10: 17,079,999-17,206,000 , GRCh38.p12 chr10: 17,038,000-17,164,001 CUBN, TRDMT1
    nsv4490745mobile element insertion1nstd166human GRCh37.p13 chr10: 17,223,735-17,223,735 , GRCh38.p12 chr10: 17,181,736-17,181,736 TRDMT1
    nsv4456784copy number variation1nstd102humanUncertain significance GRCh37 chr10: 17,191,691-17,663,784 , GRCh38.p12 chr10: 17,149,692-17,621,785 LOC105376436, LOC105376437, 7 more genes
    nsv4389275copy number variation1nstd171human GRCh37 chr10: 17,230,032-17,230,062 , GRCh38.p12 chr10: 17,188,033-17,188,063 TRDMT1
    nsv4339713sequence alteration1nstd166human GRCh37.p13 chr10: 8,718,069-114,609,729 , GRCh38.p12 chr10: 8,676,106-112,849,970 , ADRA2A, 1651 more genes
    nsv4188103copy number variation1nstd166human GRCh37.p13 chr10: 17,177,839-17,177,993 , GRCh38.p12 chr10: 17,135,840-17,135,994 TRDMT1
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