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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112726copy number variation1nstd102humanPathogenic GRCh37 chr6: 133,810,210-140,046,615 , GRCh38.p12 chr6: 133,489,072-139,725,478 SIMALR, MTFR2, 99 more genes
    nsv5964143insertion1nstd209human GRCh38 chr6: 138,827,562-138,827,562 , GRCh37.p13 chr6: 139,148,699-139,148,699 ECT2L
    nsv5901861copy number variation1nstd209human GRCh38 chr6: 138,885,234-138,886,623 , GRCh37.p13 chr6: 139,206,371-139,207,760 ECT2L
    nsv5897026copy number variation1nstd209human GRCh38 chr6: 138,878,576-138,878,710 , GRCh37.p13 chr6: 139,199,713-139,199,847 ECT2L
    nsv5893389copy number variation1nstd209human GRCh38 chr6: 137,986,656-139,086,959 , GRCh37.p13 chr6: 138,307,793-139,408,096 ECT2L, NHSL1-AS1, 17 more genes
    nsv5844046copy number variation1nstd209human GRCh38 chr6: 138,885,204-138,886,803 , GRCh37.p13 chr6: 139,206,341-139,207,940 ECT2L
    nsv5692495mobile element insertion1nstd211human GRCh38 chr6: 138,874,235-138,874,235 , GRCh37.p13 chr6: 139,195,372-139,195,372 ECT2L
    nsv5544572insertion1nstd206human GRCh38 chr6: 138,827,574-138,827,611 , GRCh37.p13 chr6: 139,148,711-139,148,748 ECT2L
    nsv5473373copy number variation1nstd206human GRCh38 chr6: 138,885,234-138,886,608 , GRCh37.p13 chr6: 139,206,371-139,207,745 ECT2L
    nsv5471515copy number variation1nstd206human GRCh38 chr6: 138,875,886-138,884,365 , GRCh37.p13 chr6: 139,197,023-139,205,502 ECT2L
    nsv5468068copy number variation1nstd206human GRCh38 chr6: 138,876,749-138,876,983 , GRCh37.p13 chr6: 139,197,886-139,198,120 ECT2L
    nsv5468046copy number variation1nstd206human GRCh38 chr6: 138,878,594-138,878,711 , GRCh37.p13 chr6: 139,199,731-139,199,848 ECT2L
    nsv5463772copy number variation1nstd206human GRCh38 chr6: 138,842,417-138,842,757 , GRCh37.p13 chr6: 139,163,554-139,163,894 ECT2L
    nsv5459292copy number variation1nstd206human GRCh38 chr6: 138,869,688-138,870,440 , GRCh37.p13 chr6: 139,190,825-139,191,577 ECT2L
    nsv5458274copy number variation1nstd206human GRCh38 chr6: 138,829,869-138,838,862 , GRCh37.p13 chr6: 139,151,006-139,159,999 ECT2L
    nsv5457110copy number variation1nstd206human GRCh38 chr6: 138,798,471-138,802,664 , GRCh37.p13 chr6: 139,119,608-139,123,801 ECT2L
    nsv5413617mobile element insertion1nstd206human GRCh38 chr6: 138,874,235-138,874,286 , GRCh37.p13 chr6: 139,195,372-139,195,423 ECT2L
    nsv5366556translocation1nstd200human GRCh38 chr2: 155,671,570-155,671,570 , GRCh38 chr6: 138,873,424-138,873,424 , GRCh37.p13 chr2: 156,528,082-156,528,082 , GRCh37.p13 chr6: 139,194,561-139,194,561 ECT2L
    nsv5363414translocation1nstd200human GRCh38 chr6: 138,869,688-138,869,688 , GRCh38 chr6: 138,870,440-138,870,440 , GRCh37.p13 chr6: 139,191,577-139,191,577 , GRCh37.p13 chr6: 139,190,825-139,190,825 ECT2L
    nsv5362375translocation1nstd200human GRCh38 chr6: 138,847,535-138,847,535 , GRCh38 chr5: 85,087,146-85,087,146 , GRCh37.p13 chr6: 139,168,672-139,168,672 , GRCh37.p13 chr5: 84,382,964-84,382,964 ECT2L
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