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Items: 1 to 20 of 164

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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
    nsv7043816inversion1nstd229human GRCh38 chr6: 10,727,395-10,727,462 , GRCh37.p13 chr6: 10,727,628-10,727,695 TMEM14C
    nsv7042773inversion1nstd229human GRCh38 chr6: 8,542,608-11,835,677 , GRCh37.p13 chr6: 8,542,841-11,835,910 LOC112267952, RNU1-64P, 51 more genes
    nsv6791922copy number variation1nstd229human GRCh38 chr6: 10,692,401-10,762,600 , GRCh37.p13 chr6: 10,692,634-10,762,833 MAK, TMEM14C, 4 more genes
    nsv6791119copy number variation1nstd229human GRCh38 chr6: 10,721,930-10,721,951 , GRCh37.p13 chr6: 10,722,163-10,722,184 TMEM14C
    nsv6788410copy number variation1nstd229human GRCh38 chr6: 10,724,301-10,729,000 , GRCh37.p13 chr6: 10,724,534-10,729,233 TMEM14C
    nsv6778453copy number variation1nstd229human GRCh38 chr6: 10,536,801-11,071,500 , GRCh37.p13 chr6: 10,537,034-11,071,733 TMEM14B, GCNT2, 13 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
    nsv6404362copy number variation1nstd223human GRCh38 chr6: 10,545,723-10,821,818 , GRCh37.p13 chr6: 10,545,956-10,822,051 MAK, TMEM14C, 7 more genes
    nsv6401241copy number variation1nstd223human GRCh38 chr6: 10,726,981-10,752,017 , GRCh37.p13 chr6: 10,727,214-10,752,250 TMEM14C, TMEM14B, 1 more genes
    nsv6313544copy number variation1nstd102humanUncertain significance GRCh37 chr6: 10,620,217-10,901,049 , GRCh38.p12 chr6: 10,619,984-10,900,816 GCNT2, GCNT2P1, 8 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
    nsv6305841copy number variation1nstd186human GRCh37 chr6: 10,728,233-10,752,233 , GRCh38.p12 chr6: 10,728,000-10,752,000 TMEM14C, TMEM14B, 1 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
    nsv5464673copy number variation1nstd206human GRCh38 chr6: 10,728,000-10,752,000 , GRCh37.p13 chr6: 10,728,233-10,752,233 TMEM14B, TMEM14C, 1 more genes
    nsv5381380copy number variation1nstd102humanUncertain significance GRCh37 chr6: 10,556,657-10,775,712 , GRCh38.p12 chr6: 10,556,424-10,775,479 , GRCh38.p12 chr6|NW_018654713.1: 67,308-242,796 GCNT2P1, MAK, 7 more genes
    nsv4947776copy number variation1nstd200human GRCh38 chr6: 10,727,222-10,752,334 , GRCh37.p13 chr6: 10,727,455-10,752,567 TMEM14B, RNA5SP203, 1 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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