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Items: 1 to 20 of 96

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097046copy number variation1nstd102humanPathogenic GRCh37 chr6: 142,623,467-144,508,628 , GRCh38.p12 chr6: 142,302,330-144,187,491 ZC2HC1B, PHACTR2-AS1, 26 more genes
    nsv7054823inversion1nstd229human GRCh38 chr6: 143,170,072-148,803,855 , GRCh37.p13 chr6: 143,491,209-149,124,991 FBXO30, C4orf46P4, 56 more genes
    nsv7053989inversion1nstd229human GRCh38 chr6: 141,012,668-144,160,886 , GRCh37.p13 chr6: 141,333,805-144,482,023 LINC01277, SF3B5, 36 more genes
    nsv7053654inversion1nstd229human GRCh38 chr6: 143,517,092-147,615,699 , GRCh37.p13 chr6: 143,838,229-147,936,835 PHACTR2, LOC105378040, 37 more genes
    nsv7048770inversion1nstd229human GRCh38 chr6: 140,841,636-145,364,827 , GRCh37.p13 chr6: 141,162,773-145,685,963 SNORA98, HIVEP2, 44 more genes
    nsv6816300copy number variation1nstd229human GRCh38 chr6: 143,809,379-144,795,873 , GRCh37.p13 chr6: 144,130,516-145,117,009 LOC105378036, LOC100131041, 13 more genes
    nsv6810206copy number variation1nstd229human GRCh38 chr6: 144,092,944-144,095,638 , GRCh37.p13 chr6: 144,414,081-144,416,775 SF3B5
    nsv6313714copy number variation1nstd102humanPathogenic GRCh37 chr6: 143,331,663-145,817,051 , GRCh38.p12 chr6: 143,010,526-145,495,915 LOC100131041, RPL31P27, 31 more genes
    nsv6313657copy number variation1nstd102humanPathogenic GRCh37 chr6: 143,874,282-145,071,930 , GRCh38.p12 chr6: 143,553,145-144,750,794 LOC105378036, HYMAI, 14 more genes
    nsv6135235copy number variation1nstd213human GRCh37 chr6: 143,160,000-144,690,001 , GRCh38.p12 chr6: 142,838,863-144,368,865 FUCA2, HIVEP2, 27 more genes
    nsv5673595copy number variation1nstd102humanPathogenic GRCh37 chr6: 143,772,160-144,508,648 , GRCh38.p12 chr6: 143,451,023-144,187,511 LOC105378036, ZC2HC1B, 14 more genes
    nsv5100868mobile element insertion1nstd203human GRCh38 chr6: 144,093,078-144,093,095 , GRCh37.p13 chr6: 144,414,215-144,414,232 SF3B5
    nsv4943169copy number variation1nstd200human GRCh38 chr6: 144,092,944-144,095,636 , GRCh37.p13 chr6: 144,414,081-144,416,773 SF3B5
    nsv4810747copy number variation1nstd200human GRCh37 chr6: 144,414,081-144,416,773 , GRCh38.p12 chr6: 144,092,944-144,095,636 SF3B5
    nsv4675434copy number variation1nstd102humanUncertain significance GRCh37 chr6: 144,285,958-144,758,765 , GRCh38.p12 chr6: 143,964,821-144,437,629 LOC105378036, LOC100131041, 10 more genes
    nsv4350212copy number variation1nstd102humanPathogenic GRCh37 chr6: 135,239,633-146,997,510 , GRCh38.p12 chr6: 134,918,495-146,676,374 LOC100131041, ADGB-DT, 146 more genes
    nsv4330897inversion1nstd166human GRCh37.p13 chr6: 90,629,263-160,387,383 , GRCh38.p12 chr6: 89,919,544-159,966,351 , ACAT2, 894 more genes
    nsv4132595copy number variation1nstd166human GRCh37.p13 chr6: 144,413,533-144,433,476 , GRCh38.p12 chr6: 144,092,396-144,112,339 LOC105378036, SF3B5
    nsv3921844copy number variation1nstd102humanPathogenic GRCh37 chr6: 143,940,111-144,734,319 , GRCh38 chr6: 143,618,974-144,413,183 , NCBI36 chr6: 143,981,804-144,776,012 ZC2HC1B, LOC100420214, 13 more genes
    nsv3920975copy number variation1nstd102humanPathogenic GRCh37 chr6: 141,454,127-169,739,666 , GRCh38 chr6: 141,132,990-169,339,571 , NCBI36 chr6: 141,495,820-169,481,591 UST-AS2, LOC729681, 394 more genes
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