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Items: 1 to 20 of 320

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7073735inversion1nstd229human GRCh38 chr18: 56,617,786-56,622,433 , GRCh37.p13 chr18: 54,285,017-54,289,664 TXNL1
    nsv7073526inversion1nstd229human GRCh38 chr18: 53,651,514-59,638,513 , GRCh37.p13 chr18: 51,177,884-57,305,745 MBD2, LOC105372145, 78 more genes
    nsv7068858inversion1nstd229human GRCh38 chr18: 56,634,943-56,635,076 , GRCh37.p13 chr18: 54,302,174-54,302,307 TXNL1
    nsv7066250inversion1nstd229human GRCh38 chr18: 54,862,924-58,506,448 , GRCh37.p13 chr18: 52,530,155-56,173,680 NARS1, FECH, 48 more genes
    nsv7017795copy number variation1nstd229human GRCh38 chr18: 56,605,065-56,608,811 , GRCh37.p13 chr18: 54,272,296-54,276,042 TXNL1
    nsv7015773copy number variation1nstd229human GRCh38 chr18: 56,622,409-56,628,452 , GRCh37.p13 chr18: 54,289,640-54,295,683 TXNL1
    nsv7012313copy number variation1nstd229human GRCh38 chr18: 56,604,276-56,608,985 , GRCh37.p13 chr18: 54,271,507-54,276,216 TXNL1
    nsv7009559copy number variation1nstd229human GRCh38 chr18: 56,505,735-56,635,744 , GRCh37.p13 chr18: 54,172,966-54,302,975 TXNL1, LOC105372135
    nsv7007663copy number variation1nstd229human GRCh38 chr18: 56,559,244-56,614,624 , GRCh37.p13 chr18: 54,226,475-54,281,855 LOC105372135, TXNL1
    nsv7002490copy number variation1nstd229human GRCh38 chr18: 56,600,028-56,614,150 , GRCh37.p13 chr18: 54,267,259-54,281,381 TXNL1
    nsv6999098copy number variation1nstd229human GRCh38 chr18: 56,604,057-56,609,202 , GRCh37.p13 chr18: 54,271,288-54,276,433 TXNL1
    nsv6637467copy number variation1nstd102humanPathogenic GRCh37 chr18: 53,624,405-78,014,123 , GRCh38.p12 chr18: 55,957,174-80,256,240 RPL9P31, LOC100422317, 277 more genes
    nsv6593198inversion1nstd223human GRCh38 chr18: 56,611,431-56,611,706 , GRCh37.p13 chr18: 54,278,662-54,278,937 TXNL1
    nsv6582737inversion1nstd223human GRCh38 chr18: 56,613,112-56,613,678 , GRCh37.p13 chr18: 54,280,343-54,280,909 TXNL1
    nsv6582614inversion1nstd223human GRCh38 chr18: 56,619,516-56,620,175 , GRCh37.p13 chr18: 54,286,747-54,287,406 TXNL1
    nsv6582174inversion1nstd223human GRCh38 chr18: 56,611,315-56,611,706 , GRCh37.p13 chr18: 54,278,546-54,278,937 TXNL1
    nsv6533679copy number variation1nstd223human GRCh38 chr18: 56,505,735-56,635,744 , GRCh37.p13 chr18: 54,172,966-54,302,975 LOC105372135, TXNL1
    nsv6528780copy number variation1nstd223human GRCh38 chr18: 56,619,558-56,623,425 , GRCh37.p13 chr18: 54,286,789-54,290,656 TXNL1
    nsv6315530copy number variation1nstd102humanPathogenic GRCh37 chr18: 1-78,077,248 , GRCh38.p12 chr18: 10,001-80,259,271 LOC105372145, LOC105372016, 947 more genes
    nsv6314216copy number variation1nstd102humanPathogenic GRCh37 chr18: 52,675,201-78,014,123 , GRCh38.p12 chr18: 55,007,970-80,256,240 RNA5SP461, CYB5A, 290 more genes
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