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Items: 1 to 20 of 194

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7093994copy number variation1nstd102humanPathogenic GRCh37 chr13: 24,293,859-26,594,123 , GRCh38.p12 chr13: 23,719,720-26,019,985 IRX1P1, MTCO3P2, 54 more genes
    nsv7063835inversion1nstd229human GRCh38 chr13: 22,751,036-26,757,157 , GRCh37.p13 chr13: 23,325,175-27,331,294 SPATA13, LOC105370122, 86 more genes
    nsv6936632copy number variation1nstd229human GRCh38 chr13: 25,281,051-25,282,237 , GRCh37.p13 chr13: 25,855,189-25,856,375 MTMR6
    nsv6928869copy number variation1nstd229human GRCh38 chr13: 25,277,018-25,287,222 , GRCh37.p13 chr13: 25,851,156-25,861,360 MTMR6
    nsv6926965copy number variation1nstd229human GRCh38 chr13: 25,245,551-25,245,631 , GRCh37.p13 chr13: 25,819,689-25,819,769 MTMR6
    nsv6924314copy number variation1nstd229human GRCh38 chr13: 25,265,926-25,266,312 , GRCh37.p13 chr13: 25,840,064-25,840,450 MTMR6
    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
    nsv6581943inversion1nstd223human GRCh38 chr13: 25,014,412-26,066,804 , GRCh37.p13 chr13: 25,588,550-26,640,942 ATP8A2, LINC00463, 18 more genes
    nsv6577502inversion1nstd223human GRCh38 chr13: 25,014,167-26,066,860 , GRCh37.p13 chr13: 25,588,305-26,640,998 LSP1P1, LOC100133284, 18 more genes
    nsv6494008copy number variation1nstd223human GRCh38 chr13: 25,276,676-25,277,176 , GRCh37.p13 chr13: 25,850,814-25,851,314 MTMR6
    nsv6487491copy number variation1nstd223human GRCh38 chr13: 25,246,672-25,247,405 , GRCh37.p13 chr13: 25,820,810-25,821,543 MTMR6
    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
    nsv6132543copy number variation1nstd213human GRCh37 chr13: 19,020,000-67,280,001 , GRCh38.p12 chr13: 18,445,862-66,705,869 , PARP4, 770 more genes
    nsv6132473copy number variation1nstd213human GRCh37 chr13: 25,320,000-25,940,001 , GRCh38.p12 chr13: 24,745,862-25,365,863 PABPC3, MTMR6, 19 more genes
    nsv6132472copy number variation1nstd213human GRCh37 chr13: 24,340,000-26,020,001 , GRCh38.p12 chr13: 23,765,861-25,445,863 PABPC3, MTMR6, 49 more genes
    nsv6129524insertion1nstd186human GRCh37 chr13: 25,838,909-25,838,946 , GRCh38.p12 chr13: 25,264,771-25,264,808 MTMR6
    nsv6097326insertion1nstd212human GRCh38 chr13: 25,264,753-25,264,753 , GRCh37.p13 chr13: 25,838,891-25,838,891 MTMR6
    nsv6091608insertion1nstd212human GRCh38 chr13: 25,278,668-25,278,668 , GRCh37.p13 chr13: 25,852,806-25,852,806 MTMR6
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