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Items: 1 to 20 of 155

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097168copy number variation1nstd102humanUncertain significance GRCh37 chr6: 10,402,705-10,415,218 , GRCh38.p12 chr6: 10,402,472-10,414,985 TFAP2A-AS1, TFAP2A, 1 more genes
    nsv7093363copy number variation1nstd102humanPathogenic GRCh37 chr6: 820,000-21,700,000 , GRCh38.p12 chr6: 820,000-21,699,769 LOC101928354, CNN3P1, 321 more genes
    nsv7042773inversion1nstd229human GRCh38 chr6: 8,542,608-11,835,677 , GRCh37.p13 chr6: 8,542,841-11,835,910 LOC112267952, RNU1-64P, 51 more genes
    nsv6785555copy number variation1nstd229human GRCh38 chr6: 10,419,086-10,425,489 , GRCh37.p13 chr6: 10,419,319-10,425,722 TFAP2A, LOC107986564
    nsv6784671copy number variation1nstd229human GRCh38 chr6: 10,419,801-10,422,500 , GRCh37.p13 chr6: 10,420,034-10,422,733 TFAP2A
    nsv6784012copy number variation1nstd229human GRCh38 chr6: 9,546,200-10,465,508 , GRCh37.p13 chr6: 9,546,433-10,465,741 TFAP2A-AS2, MIR5689HG, 16 more genes
    nsv6780528copy number variation1nstd229human GRCh38 chr6: 10,417,929-10,418,049 , GRCh37.p13 chr6: 10,418,162-10,418,282 TFAP2A
    nsv6409723copy number variation1nstd223human GRCh38 chr6: 7,366,072-12,459,745 , GRCh37.p13 chr6: 7,366,305-12,459,977 EEF1E1, RPS26P29, 82 more genes
    nsv6406154copy number variation1nstd223human GRCh38 chr6: 10,404,001-10,404,600 , GRCh37.p13 chr6: 10,404,234-10,404,833 TFAP2A, TFAP2A-AS2
    nsv6405108copy number variation1nstd223human GRCh38 chr6: 10,387,336-10,583,936 , GRCh37.p13 chr6: 10,387,569-10,584,169 MIR5689HG, MIR5689, 11 more genes
    nsv6312129copy number variation2nstd102humanUncertain significance GRCh37 chr6: 10,398,650-10,882,026 , GRCh38.p12 chr6: 10,398,417-10,881,793 , GRCh38.p12 chr6|NW_018654713.1: 1-242,796 GCM2, TFAP2A, 19 more genes
    nsv6256642mobile element insertion1nstd215human GRCh38 chr6: 10,397,382-10,397,382 , GRCh37.p13 chr6: 10,397,615-10,397,615 TFAP2A
    nsv6136505copy number variation1nstd213human GRCh37 chr6: 380,000-11,010,001 , GRCh38.p12 chr6: 380,000-11,009,768 BMP6, BPHL, 178 more genes
    nsv6135513copy number variation1nstd213human GRCh37 chr6: 380,000-10,980,001 , GRCh38.p12 chr6: 380,000-10,979,768 BMP6, BPHL, 178 more genes
    nsv5896105copy number variation1nstd209human GRCh38 chr6: 7,548,083-10,446,730 , GRCh37.p13 chr6: 7,548,316-10,446,963 , TFAP2A-AS2, 37 more genes
    nsv5674006copy number variation1nstd102humanPathogenic GRCh37 chr6: 10,393,732-10,439,975 , GRCh38.p12 chr6: 10,393,499-10,439,742 TFAP2A, LINC00518, 5 more genes
    nsv5456918copy number variation1nstd206human GRCh38 chr6: 10,419,220-10,419,372 , GRCh37.p13 chr6: 10,419,453-10,419,605 TFAP2A
    nsv4934411copy number variation1nstd200human GRCh38 chr6: 10,387,336-10,583,936 , GRCh37.p13 chr6: 10,387,569-10,584,169 GCNT2, MRPL48P1, 11 more genes
    nsv4934387copy number variation1nstd200human GRCh38 chr6: 7,366,072-12,459,747 , GRCh37.p13 chr6: 7,366,305-12,459,979 , DSP, 90 more genes
    nsv4683407copy number variation1nstd102humanUncertain significance GRCh37 chr6: 10,393,732-11,011,042 , GRCh38.p12 chr6: 10,393,499-11,010,809 MAK, TMEM14C, 22 more genes
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