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Items: 1 to 20 of 199

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7093363copy number variation1nstd102humanPathogenic GRCh37 chr6: 820,000-21,700,000 , GRCh38.p12 chr6: 820,000-21,699,769 LOC101928354, CNN3P1, 321 more genes
    nsv7054910inversion1nstd229human GRCh38 chr6: 10,441,999-10,442,092 , GRCh37.p13 chr6: 10,442,232-10,442,325 MIR5689HG
    nsv7042773inversion1nstd229human GRCh38 chr6: 8,542,608-11,835,677 , GRCh37.p13 chr6: 8,542,841-11,835,910 LOC112267952, RNU1-64P, 51 more genes
    nsv6792110copy number variation1nstd229human GRCh38 chr6: 10,433,128-10,433,530 , GRCh37.p13 chr6: 10,433,361-10,433,763 LINC00518, MIR5689HG
    nsv6788288copy number variation1nstd229human GRCh38 chr6: 10,453,301-10,467,600 , GRCh37.p13 chr6: 10,453,534-10,467,833 MIR5689HG, LINC02522, 1 more genes
    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
    nsv6782843copy number variation1nstd229human GRCh38 chr6: 10,456,794-10,462,974 , GRCh37.p13 chr6: 10,457,027-10,463,207 MRPL48P1, MIR5689HG
    nsv6630702copy number variation1nstd224human GRCh37 chr6: 10,449,258-10,506,976 , GRCh38.p12 chr6: 10,449,025-10,506,743 MIR5689HG, LOC101928146, 2 more genes
    nsv6572367inversion1nstd223human GRCh38 chr6: 10,454,650-10,455,094 , GRCh37.p13 chr6: 10,454,883-10,455,327 MIR5689HG
    nsv6413144copy number variation1nstd223human GRCh38 chr6: 10,435,500-10,436,266 , GRCh37.p13 chr6: 10,435,733-10,436,499 MIR5689HG
    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
    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
    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
    nsv5843957copy number variation1nstd209human GRCh38 chr6: 10,446,762-10,451,891 , GRCh37.p13 chr6: 10,446,995-10,452,124 MIR5689HG
    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
    nsv5097598mobile element insertion1nstd203human GRCh38 chr6: 10,454,020-10,454,066 , GRCh37.p13 chr6: 10,454,253-10,454,299 MIR5689HG
    nsv4947747copy number variation1nstd200human GRCh38 chr6: 10,436,206-10,436,326 , GRCh37.p13 chr6: 10,436,439-10,436,559 MIR5689HG
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