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Items: 1 to 20 of 414

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6716093copy number variation1nstd229human GRCh38 chr3: 40,264,601-40,273,000 , GRCh37.p13 chr3: 40,306,092-40,314,491 EIF1B-AS1
    nsv6715955copy number variation1nstd229human GRCh38 chr3: 40,229,490-40,229,514 , GRCh37.p13 chr3: 40,270,981-40,271,005 MYRIP, EIF1B-AS1
    nsv6712916copy number variation1nstd229human GRCh38 chr3: 40,201,862-40,207,570 , GRCh37.p13 chr3: 40,243,353-40,249,061 MYRIP, EIF1B-AS1, 1 more genes
    nsv6712575copy number variation1nstd229human GRCh38 chr3: 40,267,485-40,275,593 , GRCh37.p13 chr3: 40,308,976-40,317,084 EIF1B-AS1
    nsv6711902copy number variation1nstd229human GRCh38 chr3: 38,527,947-43,061,183 , GRCh37.p13 chr3: 38,569,438-43,102,675 ZBTB47, VIPR1-AS1, 90 more genes
    nsv6709392copy number variation1nstd229human GRCh38 chr3: 40,262,333-40,262,506 , GRCh37.p13 chr3: 40,303,824-40,303,997 EIF1B-AS1
    nsv6708550copy number variation1nstd229human GRCh38 chr3: 40,256,064-40,259,541 , GRCh37.p13 chr3: 40,297,555-40,301,032 MYRIP, EIF1B-AS1
    nsv6708523copy number variation1nstd229human GRCh38 chr3: 40,171,411-40,171,534 , GRCh37.p13 chr3: 40,212,902-40,213,025 EIF1B-AS1, MYRIP
    nsv6706707copy number variation1nstd229human GRCh38 chr3: 40,171,320-40,177,633 , GRCh37.p13 chr3: 40,212,811-40,219,124 MYRIP, EIF1B-AS1
    nsv6705875copy number variation1nstd229human GRCh38 chr3: 40,283,691-40,286,025 , GRCh37.p13 chr3: 40,325,182-40,327,516 EIF1B-AS1
    nsv6704610copy number variation1nstd229human GRCh38 chr3: 40,229,244-40,250,408 , GRCh37.p13 chr3: 40,270,735-40,291,899 EIF1B-AS1, MYRIP
    nsv6703196copy number variation1nstd229human GRCh38 chr3: 40,262,718-40,266,433 , GRCh37.p13 chr3: 40,304,209-40,307,924 EIF1B-AS1
    nsv6700581copy number variation1nstd229human GRCh38 chr3: 40,298,701-40,302,300 , GRCh37.p13 chr3: 40,340,192-40,343,791 EIF1B-AS1
    nsv6699544copy number variation1nstd229human GRCh38 chr3: 40,209,674-40,213,337 , GRCh37.p13 chr3: 40,251,165-40,254,828 MYRIP, EIF1B-AS1, 1 more genes
    nsv6628595copy number variation1nstd224human GRCh37 chr3: 40,231,814-40,342,347 , GRCh38.p12 chr3: 40,190,323-40,300,856 EIF1B-AS1, MYRIP, 1 more genes
    nsv6548378inversion1nstd223human GRCh38 chr3: 40,203,620-40,203,780 , GRCh37.p13 chr3: 40,245,111-40,245,271 EIF1B-AS1, MYRIP
    nsv6369713copy number variation1nstd223human GRCh38 chr3: 40,293,612-40,297,173 , GRCh37.p13 chr3: 40,335,103-40,338,664 EIF1B-AS1
    nsv6357675copy number variation1nstd223human GRCh38 chr3: 40,214,665-40,215,190 , GRCh37.p13 chr3: 40,256,156-40,256,681 EIF1B-AS1, MYRIP
    nsv6311966copy number variation1nstd102humanPathogenic GRCh37 chr3: 16,710,965-41,275,270 , GRCh38.p12 chr3: 16,669,458-41,233,779 LOC102724104, CRIP1P2, 291 more genes
    nsv6253903mobile element insertion1nstd215human GRCh37.p13 chr3: 40,241,622-40,241,622 , GRCh38 chr3: 40,200,131-40,200,131 , MYRIP, 1 more genes
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