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Items: 1 to 20 of 146

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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
    nsv7042773inversion1nstd229human GRCh38 chr6: 8,542,608-11,835,677 , GRCh37.p13 chr6: 8,542,841-11,835,910 LOC112267952, RNU1-64P, 51 more genes
    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
    nsv6636782copy number variation1nstd102humanUncertain significance GRCh37 chr6: 10,487,302-10,708,232 , GRCh38.p12 chr6: 10,487,069-10,707,999 , GRCh38.p12 chr6|NW_018654713.1: 1-218,883 C6orf52, RPL21P63, 5 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
    nsv6403222copy number variation1nstd223human GRCh38 chr6: 10,465,448-10,718,419 , GRCh37.p13 chr6: 10,465,681-10,718,652 GCNT2, PAK1IP1, 6 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
    nsv6291124copy number variation1nstd102humanLikely benign GRCh37 chr6: 10,543,098-10,640,180 , GRCh38.p12 chr6: 10,542,865-10,639,947 , GRCh38.p12 chr6|NW_018654713.1: 53,749-150,831 GCNT2, RPL21P63, 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
    nsv6019832copy number variation1nstd212human GRCh38 chr6: 10,630,764-10,636,371 , GRCh37.p13 chr6: 10,630,997-10,636,604 GCNT2P1
    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
    nsv4947748copy number variation1nstd200human GRCh38 chr6: 10,465,448-10,718,419 , GRCh37.p13 chr6: 10,465,681-10,718,652 , LOC101928146, 8 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
    nsv4729108copy number variation1nstd102humanUncertain significance GRCh37 chr6: 10,514,491-10,677,096 , GRCh38.p12 chr6: 10,514,258-10,676,863 , GRCh38.p12 chr6|NW_018654713.1: 25,142-187,747 GCNT2P1, RPL21P63, 4 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
    nsv4457033copy number variation1nstd102humanPathogenic GRCh37 chr6: 10,541,521-10,645,806 , GRCh38.p12 chr6: 10,541,288-10,645,573 , GRCh38.p12 chr6|NW_018654713.1: 52,172-156,457 GCNT2, GCNT2P1, 1 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
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