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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
    nsv5905013copy number variation1nstd209human GRCh38 chr6: 138,735,502-138,735,859 , GRCh37.p13 chr6: 139,056,639-139,056,996 CCDC28A-AS1
    nsv5903344copy number variation1nstd209human GRCh38 chr6: 138,735,311-138,738,051 , GRCh37.p13 chr6: 139,056,448-139,059,188 CCDC28A-AS1
    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
    nsv5467976copy number variation1nstd206human GRCh38 chr6: 138,742,675-138,759,105 , GRCh37.p13 chr6: 139,063,812-139,080,242 CCDC28A-AS1
    nsv5467271copy number variation1nstd206human GRCh38 chr6: 138,748,599-138,754,277 , GRCh37.p13 chr6: 139,069,736-139,075,414 CCDC28A-AS1
    nsv5460685copy number variation1nstd206human GRCh38 chr6: 138,735,068-138,738,242 , GRCh37.p13 chr6: 139,056,205-139,059,379 CCDC28A-AS1
    nsv5456800copy number variation1nstd206human GRCh38 chr6: 138,741,010-138,753,444 , GRCh37.p13 chr6: 139,062,147-139,074,581 CCDC28A-AS1
    nsv5363412translocation1nstd200human GRCh38 chr6: 138,732,261-138,732,261 , GRCh38 chr6: 138,730,127-138,730,127 , GRCh37.p13 chr6: 139,053,398-139,053,398 , GRCh37.p13 chr6: 139,051,264-139,051,264 CCDC28A-AS1
    nsv5330409translocation1nstd200human GRCh37 chr6: 139,051,264-139,051,264 , GRCh37 chr6: 139,053,398-139,053,398 , GRCh38.p12 chr6: 138,730,127-138,730,127 , GRCh38.p12 chr6: 138,732,261-138,732,261 CCDC28A-AS1
    nsv5236178copy number variation1nstd204human GRCh38.p13 chr6: 138,771,614-138,774,064 , GRCh37.p13 chr6: 139,092,751-139,095,201 CCDC28A-AS1, CCDC28A
    nsv5198854mobile element insertion1nstd203human GRCh38 chr6: 138,759,095-138,759,109 , GRCh37.p13 chr6: 139,080,232-139,080,246 CCDC28A-AS1
    nsv5116486mobile element insertion1nstd203human GRCh38 chr6: 138,748,598-138,748,611 , GRCh37.p13 chr6: 139,069,735-139,069,748 CCDC28A-AS1
    nsv5110807mobile element insertion1nstd203human GRCh38 chr6: 138,767,001-138,767,015 , GRCh37.p13 chr6: 139,088,138-139,088,152 CCDC28A-AS1
    nsv5110556mobile element insertion1nstd203human GRCh38 chr6: 138,748,592-138,748,611 , GRCh37.p13 chr6: 139,069,729-139,069,748 CCDC28A-AS1
    nsv5106890mobile element insertion1nstd203human GRCh38 chr6: 138,755,671-138,755,682 , GRCh37.p13 chr6: 139,076,808-139,076,819 CCDC28A-AS1
    nsv5101881mobile element insertion1nstd203human GRCh38 chr6: 138,748,594-138,748,611 , GRCh37.p13 chr6: 139,069,731-139,069,748 CCDC28A-AS1
    nsv5039909inversion1nstd200human GRCh38 chr6: 137,955,606-139,947,661 , GRCh37.p13 chr6: 138,276,743-140,268,798 , CCDC28A-AS1, 30 more genes
    nsv4945730copy number variation1nstd200human GRCh38 chr6: 138,748,561-138,754,317 , GRCh37.p13 chr6: 139,069,698-139,075,454 CCDC28A-AS1
    nsv4945729copy number variation1nstd200human GRCh38 chr6: 138,605,250-138,811,414 , GRCh37.p13 chr6: 138,926,387-139,132,551 ECT2L, NHSL1-AS1, 4 more genes
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