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Items: 1 to 20 of 129

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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
    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
    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
    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
    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
    nsv4457104copy number variation1nstd102humanUncertain significance GRCh37 chr6: 10,329,349-10,553,787 , GRCh38.p12 chr6: 10,329,116-10,553,554 MIR5689, MIR5689HG, 13 more genes
    nsv4456780copy number variation1nstd102humanPathogenic GRCh37 chr6: 156,974-23,221,621 , GRCh38.p12 chr6: 156,974-23,221,393 LOC105374960, LOC101928573, 342 more genes
    nsv3922052copy number variation1nstd102humanPathogenic GRCh37 chr6: 155,807-17,058,645 , NCBI36 chr6: 100,807-17,166,624 , GRCh38 chr6: 155,807-17,058,414 ECI2-DT, RNU1-11P, 268 more genes
    nsv3921817copy number variation1nstd102humanPathogenic GRCh37 chr6: 2,862,874-16,698,019 , GRCh38 chr6: 2,862,640-16,697,788 , NCBI36 chr6: 2,807,873-16,805,998 RN7SKP293, LOC105374906, 230 more genes
    nsv3921027copy number variation1nstd102humanPathogenic GRCh38 chr6: 389,423-13,474,956 , GRCh37 chr6: 389,423-13,475,188 , NCBI36 chr6: 334,423-13,583,167 LOC105374898, HIVEP1, 215 more genes
    nsv3920564copy number variation1nstd102humanPathogenic GRCh38 chr6: 3,224,310-30,657,190 , GRCh37 chr6: 3,224,544-30,624,967 , NCBI36 chr6: 3,169,543-30,732,946 PRELID1P2, RPL7AP7, 785 more genes
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