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Items: 1 to 20 of 114

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5506413copy number variation1nstd206human GRCh38 chr14: 100,658,704-100,658,787 , GRCh37.p13 chr14: 101,125,041-101,125,124 LINC00523
    nsv5498590copy number variation1nstd206human GRCh38 chr14: 80,522,636-106,763,637 , GRCh37.p13 chr14: 80,988,980-106,929,356 , RPS18P2, 713 more genes
    nsv4991390copy number variation1nstd200human GRCh38 chr14: 100,657,832-100,659,018 , GRCh37.p13 chr14: 101,124,169-101,125,355 LINC00523
    nsv4684265copy number variation1nstd102humanPathogenic GRCh37 chr14: 96,829,290-107,287,663 , GRCh38.p12 chr14: 96,362,953-106,879,456 NDUFB3P4, LINC02320, 502 more genes
    nsv4501102mobile element insertion1nstd166human GRCh37.p13 chr14: 101,137,986-101,137,986 , GRCh38.p12 chr14: 100,671,649-100,671,649 LINC00523
    nsv4456178copy number variation1nstd102humanPathogenic GRCh37 chr14: 91,969,028-107,285,437 , GRCh38.p12 chr14: 91,502,684-106,877,229 LOC105370639, SERPINA9, 600 more genes
    nsv4455156copy number variation1nstd102humanPathogenic GRCh37 chr14: 99,794,230-107,285,437 , GRCh38.p12 chr14: 99,327,893-106,877,229 IGHG4, IGHV3-57, 464 more genes
    nsv4414011copy number variation1nstd174human GRCh37 chr14: 101,005,158-101,192,103 , GRCh38.p12 chr14: 100,538,821-100,725,766 , DLK1, 4 more genes
    nsv4349898copy number variation1nstd102humanLikely pathogenic GRCh37 chr14: 99,737,888-101,847,855 , GRCh38.p12 chr14: 99,271,551-101,381,518 EML1, WARS1, 136 more genes
    nsv4349480copy number variation1nstd102humanPathogenic GRCh37 chr14: 100,575,917-107,281,934 , GRCh38.p12 chr14: 100,109,580-106,873,725 IGHD2-21, MIR300, 452 more genes
    nsv4219579copy number variation1nstd166human GRCh37.p13 chr14: 101,125,041-101,125,124 , GRCh38.p12 chr14: 100,658,704-100,658,787 LINC00523
    nsv3964933insertion1nstd168human GRCh38 chr14: 100,654,870-100,718,480 , GRCh37.p13 chr14: 101,121,207-101,184,817 , LINC00523, 2 more genes
    nsv3924299copy number variation1nstd102humanPathogenic GRCh37 chr14: 100,260,674-101,410,904 , GRCh38 chr14: 99,794,337-100,944,567 , NCBI36 chr14: 99,330,427-100,480,657 MIR433, RN7SKP92, 48 more genes
    nsv3922827copy number variation1nstd102humanPathogenic GRCh38 chr14: 100,309,382-106,855,263 , GRCh37 chr14: 100,775,719-107,263,478 , NCBI36 chr14: 99,845,472-106,334,523 RNU6-1316P, MIR136, 440 more genes
    nsv3922094copy number variation1nstd102humanPathogenic GRCh38 chr14: 73,655,772-106,879,298 , GRCh37 chr14: 74,122,475-107,287,505 , NCBI36 chr14: 73,192,228-106,358,550 LOC105370614, LOC105370617, 849 more genes
    nsv3921506copy number variation1nstd102humanPathogenic GRCh38 chr14: 99,831,655-106,855,263 , GRCh37 chr14: 100,297,992-107,263,478 , NCBI36 chr14: 99,367,745-106,334,523 RPL21P13, EXOC3L4, 453 more genes
    nsv3921292copy number variation1nstd102humanPathogenic GRCh38 chr14: 91,455,861-106,832,642 , GRCh37 chr14: 91,922,205-107,240,869 , NCBI36 chr14: 90,991,958-106,311,914 IGHVII-15-1, LINC03117, 594 more genes
    nsv3920123copy number variation1nstd102humanPathogenic GRCh37 chr14: 100,729,173-102,967,034 , GRCh38 chr14: 100,262,836-102,500,697 , NCBI36 chr14: 99,798,926-102,036,787 MIR1193, SNORD114-19, 147 more genes
    nsv3920105copy number variation1nstd102humanPathogenic GRCh37 chr14: 100,397,006-101,488,936 , GRCh38 chr14: 99,930,669-101,022,599 , NCBI36 chr14: 99,466,759-100,558,689 SNORD113-1, SNORD114-24, 82 more genes
    nsv3919106copy number variation1nstd102humanPathogenic GRCh37 chr14: 20,511,673-107,285,437 , GRCh38 chr14: 20,043,514-106,877,229 , NCBI36 chr14: 19,581,513-106,356,482 SRMP2, IGHV3-71, 1929 more genes
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