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Items: 1 to 20 of 82

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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
    nsv7048770inversion1nstd229human GRCh38 chr6: 140,841,636-145,364,827 , GRCh37.p13 chr6: 141,162,773-145,685,963 SNORA98, HIVEP2, 44 more genes
    nsv6812480copy number variation1nstd229human GRCh38 chr6: 143,012,001-143,489,000 , GRCh37.p13 chr6: 143,333,138-143,810,137 ADAT2, RNA5SP221, 9 more genes
    nsv6808308copy number variation1nstd229human GRCh38 chr6: 143,361,401-143,887,200 , GRCh37.p13 chr6: 143,682,538-144,208,337 ZC2HC1B, C4orf46P4, 11 more genes
    nsv6804347copy number variation1nstd229human GRCh38 chr6: 143,439,954-143,484,580 , GRCh37.p13 chr6: 143,761,091-143,805,717 PEX3, RNA5SP221, 1 more genes
    nsv6636975copy number variation1nstd102humanUncertain significance GRCh37 chr6: 143,645,794-143,860,372 , GRCh38.p12 chr6: 143,324,657-143,539,235 VDAC1P8, RNA5SP221, 10 more genes
    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
    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
    nsv4683714copy number variation1nstd102humanUncertain significance GRCh37 chr6: 143,654,419-143,832,771 , GRCh38.p12 chr6: 143,333,282-143,511,634 ADAT2, PEX3, 9 more genes
    nsv4496629mobile element insertion1nstd166human GRCh37.p13 chr6: 143,769,846-143,769,846 , GRCh38.p12 chr6: 143,448,709-143,448,709 RNA5SP221, ADAT2
    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
    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
    nsv3916499copy number variation1nstd102humanPathogenic NCBI36 chr6: 136,359,437-146,708,473 , GRCh37.p13 chr6: 136,317,744-146,666,780 , GRCh38.p12 chr6: 135,996,606-146,345,644 SLC35D3, SHPRH, 127 more genes
    nsv3915150copy number variation1nstd102humanPathogenic NCBI36 chr6: 124,322,082-156,156,864 , GRCh37.p13 chr6: 124,280,383-156,115,172 , GRCh38.p12 chr6: 123,959,238-155,794,038 KATNA1, RNF217-AS1, 422 more genes
    nsv3913689copy number variation1nstd102humanPathogenic NCBI36 chr6: 121,373,749-146,289,101 , GRCh37.p13 chr6: 121,332,050-146,247,408 , GRCh38.p12 chr6: 121,010,904-145,926,272 TPD52L1, MESTP1, 316 more genes
    nsv3912178copy number variation1nstd102humanPathogenic NCBI36 chr6: 142,070,748-145,748,578 , GRCh37.p13 chr6: 142,029,055-145,706,885 , GRCh38.p12 chr6: 141,707,918-145,385,749 GJE1, LOC105378030, 40 more genes
    nsv3911993copy number variation1nstd102humanPathogenic NCBI36 chr6: 133,900,102-166,209,023 , GRCh38 chr6: 133,537,271-165,875,545 , GRCh37 chr6: 133,858,409-166,289,033 LOC105369171, SHPRH, 418 more genes
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