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Items: 1 to 20 of 559

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148123copy number variation2nstd102humanPathogenic GRCh37 chr16: 29,517,464-30,200,058 , GRCh38.p12 chr16: 29,506,143-30,188,737 SMG1P2, QPRT, 39 more genes
    nsv7148104copy number variation1nstd102humanPathogenic GRCh37 chr16: 29,517,464-30,199,839 , GRCh38.p12 chr16: 29,506,143-30,188,518 QPRT, SMG1P2, 39 more genes
    nsv7148094copy number variation1nstd102humanPathogenic GRCh37 chr16: 29,511,270-30,243,006 , GRCh38.p12 chr16: 29,499,949-30,231,685 SMG1P2, KCTD13, 46 more genes
    nsv7137206copy number variation1nstd102humanPathogenic GRCh37 chr16: 29,620,748-30,250,606 , GRCh38.p12 chr16: 29,609,427-30,239,285 SMG1P2, QPRT, 43 more genes
    nsv7137124copy number variation1nstd102humanPathogenic GRCh37 chr16: 29,675,050-30,218,384 , GRCh38.p12 chr16: 29,663,729-30,207,063 LOC112694756, YPEL3-DT, 38 more genes
    nsv7137119copy number variation1nstd102humanPathogenic GRCh37 chr16: 29,495,011-30,206,548 , GRCh38.p12 chr16: 29,483,690-30,195,227 CORO1A-AS1, YPEL3-DT, 42 more genes
    nsv7098923copy number variation1nstd102humanPathogenic GRCh38 chr16: 29,653,297-30,181,026 , GRCh37.p13 chr16: 29,664,618-30,192,347 ALDOA, QPRT, 31 more genes
    nsv7093394copy number variation1nstd102humannot provided GRCh37 chr16: 29,670,770-30,207,956 , GRCh38.p12 chr16: 29,659,449-30,196,635 LOC105371167, CDIPTOSP, 36 more genes
    nsv7093385copy number variation1nstd102humannot provided GRCh37 chr16: 29,651,706-30,193,525 , GRCh38.p12 chr16: 29,640,385-30,182,204 PRRT2, KIF22, 33 more genes
    nsv7068091inversion1nstd229human GRCh38 chr16: 29,736,414-31,610,190 , GRCh37.p13 chr16: 29,747,735-31,621,511 C16orf92, TMEM219, 118 more genes
    nsv7062908inversion1nstd229human GRCh38 chr16: 29,953,046-29,965,136 , GRCh37.p13 chr16: 29,964,367-29,976,457 TMEM219
    nsv6991885copy number variation1nstd229human GRCh38 chr16: 29,972,857-29,973,124 , GRCh37.p13 chr16: 29,984,178-29,984,445 TAOK2, TMEM219
    nsv6990242copy number variation1nstd229human GRCh38 chr16: 29,880,907-29,972,522 , GRCh37.p13 chr16: 29,892,228-29,983,843 KCTD13-DT, KCTD13, 4 more genes
    nsv6985050copy number variation1nstd229human GRCh38 chr16: 29,967,581-29,970,205 , GRCh37.p13 chr16: 29,978,902-29,981,526 TMEM219
    nsv6982613copy number variation1nstd229human GRCh38 chr16: 29,968,255-29,971,406 , GRCh37.p13 chr16: 29,979,576-29,982,727 TMEM219
    nsv6982046copy number variation1nstd229human GRCh38 chr16: 29,966,033-29,969,447 , GRCh37.p13 chr16: 29,977,354-29,980,768 TMEM219
    nsv6637889copy number variation2nstd102humanPathogenic GRCh37 chr16: 29,567,296-30,240,227 , GRCh38.p12 chr16: 29,555,975-30,228,906 MIR3680-2, TLCD3B, 45 more genes
    nsv6637734copy number variation1nstd102humanPathogenic GRCh37 chr16: 29,432,213-30,240,227 , GRCh38.p12 chr16: 29,420,892-30,228,906 SLX1B, LOC606724, 54 more genes
    nsv6637633copy number variation1nstd102humanPathogenic GRCh37 chr16: 21,576,803-30,177,240 , GRCh38.p12 chr16: 21,565,482-30,165,919 USP31, CA5AP1, 200 more genes
    nsv6637578copy number variation1nstd102humanPathogenic GRCh37 chr16: 29,622,758-30,240,227 , GRCh38.p12 chr16: 29,611,437-30,228,906 PAGR1, SULT1A3, 43 more genes
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