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Items: 1 to 20 of 157

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5944321copy number variation1nstd209human GRCh38 chr14: 100,843,817-100,846,399 , GRCh37.p13 chr14: 101,310,154-101,312,736 MEG3
    nsv5854453copy number variation1nstd209human GRCh38 chr14: 100,843,893-100,846,334 , GRCh37.p13 chr14: 101,310,230-101,312,671 MEG3
    nsv5498590copy number variation1nstd206human GRCh38 chr14: 80,522,636-106,763,637 , GRCh37.p13 chr14: 80,988,980-106,929,356 , RPS18P2, 713 more genes
    nsv4991400copy number variation1nstd200human GRCh38 chr14: 100,859,825-100,859,908 , GRCh37.p13 chr14: 101,326,162-101,326,245 MEG3
    nsv4991399copy number variation1nstd200human GRCh38 chr14: 100,833,751-100,833,824 , GRCh37.p13 chr14: 101,300,088-101,300,161 MEG3
    nsv4991398copy number variation1nstd200human GRCh38 chr14: 100,829,287-100,833,413 , GRCh37.p13 chr14: 101,295,624-101,299,750 MEG3
    nsv4854984copy number variation1nstd200human GRCh37 chr14: 101,326,162-101,326,245 , GRCh38.p12 chr14: 100,859,825-100,859,908 MEG3
    nsv4854983copy number variation1nstd200human GRCh37 chr14: 101,300,088-101,300,161 , GRCh38.p12 chr14: 100,833,751-100,833,824 MEG3
    nsv4854982copy number variation1nstd200human GRCh37 chr14: 101,295,624-101,299,750 , GRCh38.p12 chr14: 100,829,287-100,833,413 MEG3
    nsv4728990copy number variation1nstd102humanPathogenic GRCh37 chr14: 101,201,380-101,290,903 , GRCh38.p12 chr14: 100,735,043-100,824,566 DLK1, MIR2392, 1 more genes
    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
    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
    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
    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
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