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Items: 1 to 20 of 147

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5713762mobile element insertion2nstd211human GRCh38 chr14: 103,557,554-103,557,554 , GRCh37.p13 chr14: 104,023,891-104,023,891 BAG5
    nsv5498590copy number variation1nstd206human GRCh38 chr14: 80,522,636-106,763,637 , GRCh37.p13 chr14: 80,988,980-106,929,356 , RPS18P2, 713 more genes
    nsv5426506mobile element insertion1nstd206human GRCh38 chr14: 103,557,554-103,557,605 , GRCh37.p13 chr14: 104,023,891-104,023,942 BAG5
    nsv5151030mobile element insertion1nstd203human GRCh38 chr14: 103,559,495-103,559,509 , GRCh37.p13 chr14: 104,025,832-104,025,846 BAG5
    nsv4991520copy number variation1nstd200human GRCh38 chr14: 103,556,380-103,557,894 , GRCh37.p13 chr14: 104,022,717-104,024,231 BAG5
    nsv4855088copy number variation1nstd200human GRCh37 chr14: 104,022,717-104,024,232 , GRCh38.p12 chr14: 103,556,380-103,557,895 BAG5
    nsv4729218copy number variation1nstd102humanPathogenic GRCh37 chr14: 102,615,953-107,285,437 , GRCh38.p12 chr14: 102,149,616-106,877,229 IGHV4-61, IGHD3-9, 308 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
    nsv4624902copy number variation1nstd183human GRCh37 chr14: 103,676,460-105,831,463 , GRCh38.p12 chr14: 103,210,123-105,365,126 , ZFYVE21, 69 more genes
    nsv4623254copy number variation1nstd183human GRCh37 chr14: 104,028,975-104,029,290 , GRCh38.p12 chr14: 103,562,638-103,562,953 BAG5, COA8
    nsv4620557copy number variation1nstd183human GRCh37 chr14: 104,023,858-104,025,833 , GRCh38.p12 chr14: 103,557,521-103,559,496 BAG5
    nsv4456944copy number variation1nstd102humanPathogenic GRCh37 chr14: 101,627,916-107,147,698 , GRCh38.p12 chr14: 101,161,579-106,691,681 IGHV1-58, IGHVII-60-1, 308 more genes
    nsv4456320copy number variation1nstd102humanPathogenic GRCh37 chr14: 102,931,119-107,285,437 , GRCh38.p12 chr14: 102,464,782-106,877,229 LOC105378184, LINC02298, 302 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
    nsv4430140copy number variation1nstd174human GRCh37 chr14: 103,982,866-104,021,347 , GRCh38.p12 chr14: 103,516,529-103,555,010 CKB, BAG5, 2 more genes
    nsv4350091copy number variation1nstd102humanLikely pathogenic GRCh37 chr14: 103,804,791-105,677,579 , GRCh38.p12 chr14: 103,338,454-105,211,242 AKT1, CKB, 58 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
    nsv4225313copy number variation1nstd166human GRCh37.p13 chr14: 104,022,473-104,210,691 , GRCh38.p12 chr14: 103,556,136-103,744,354 , XRCC3, 8 more genes
    nsv3923888copy number variation1nstd102humanUncertain significance NCBI36 chr14: 102,868,287-103,972,976 , GRCh38 chr14: 103,332,197-104,435,594 , GRCh37 chr14: 103,798,534-104,901,931 EIF5, MIR203B, 31 more genes
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