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Items: 1 to 20 of 153

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6931341copy number variation1nstd229human GRCh38 chr13: 18,913,647-19,007,190 , GRCh37.p13 chr13: 19,487,787-19,581,330 LINC00408, LINC00442, 1 more genes
    nsv6922377copy number variation1nstd229human GRCh38 chr13: 18,909,101-18,913,300 , GRCh37.p13 chr13: 19,483,241-19,487,440 LINC00408
    nsv6637646copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,436,287-22,089,005 , GRCh38.p12 chr13: 18,862,147-21,514,866 LOC105370104, RNU6-52P, 78 more genes
    nsv6637390copy number variation1nstd102humanUncertain significance GRCh37 chr13: 19,436,287-22,405,375 , GRCh38.p12 chr13: 18,862,147-21,831,236 SLC35E1P1, LOC107984553, 83 more genes
    nsv6634431copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,253,848-115,108,937 , GRCh38.p12 chr13: 18,679,708-114,343,462 MTUS2-AS1, LOC105370213, 1330 more genes
    nsv6621657copy number variation1nstd224human GRCh37 chr13: 19,121,950-20,440,020 , GRCh38.p12 chr13: 18,547,810-19,865,880 TERF1P5, MRPS31P2, 46 more genes
    nsv6315495copy number variation1nstd102humanPathogenic GRCh37 chr13: 1-115,169,878 , GRCh38.p12 chr13: 18,445,862-114,344,403 RNU6-80P, EFNB2, 1334 more genes
    nsv6314030copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,436,286-114,981,726 , GRCh38.p12 chr13: 18,862,146-114,216,251 RPSAP53, LOC105370213, 1310 more genes
    nsv6289999copy number variation1nstd102humanPathogenic GRCh37 chr13: 1-115,169,878 , GRCh38.p12 chr13: 18,445,862-114,344,403 LINC00363, LOC105370118, 1334 more genes
    nsv6248755mobile element insertion1nstd215human GRCh38 chr13: 18,912,717-18,912,717 , GRCh37.p13 chr13: 19,486,857-19,486,857 LINC00408
    nsv6132544copy number variation1nstd213human GRCh37 chr13: 19,030,000-21,540,001 , GRCh38.p12 chr13: 18,455,860-20,965,862 ZMYM2, IFT88, 73 more genes
    nsv6132543copy number variation1nstd213human GRCh37 chr13: 19,020,000-67,280,001 , GRCh38.p12 chr13: 18,445,862-66,705,869 , PARP4, 770 more genes
    nsv6106790inversion1nstd212human GRCh38 chr13: 18,875,033-18,930,111 , GRCh37.p13 chr13: 19,449,173-19,504,251 SNX19P2, LINC00408, 1 more genes
    nsv6085571insertion1nstd212human GRCh38 chr13: 18,904,360-18,904,360 , GRCh37.p13 chr13: 19,478,500-19,478,500 LINC00408
    nsv6037529copy number variation1nstd212human GRCh38 chr13: 18,904,100-18,904,241 , GRCh37.p13 chr13: 19,478,240-19,478,381 LINC00408
    nsv6029655copy number variation1nstd212human GRCh38 chr13: 18,904,238-18,904,334 , GRCh37.p13 chr13: 19,478,378-19,478,474 LINC00408
    nsv5705278mobile element insertion1nstd211human GRCh38 chr13: 18,912,717-18,912,717 , GRCh37.p13 chr13: 19,486,857-19,486,857 LINC00408
    nsv5700772mobile element insertion1nstd211human GRCh38 chr13: 18,921,169-18,921,169 , GRCh37.p13 chr13: 19,495,309-19,495,309 LINC00408
    nsv5657524insertion1nstd207human GRCh38 chr13: 18,904,351-18,904,351 , GRCh37.p13 chr13: 19,478,491-19,478,491 LINC00408
    nsv5564510copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,053,605-115,108,528 , GRCh38.p12 chr13: 18,479,465-114,343,053 RN7SL272P, DIAPH3, 1333 more genes
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