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Items: 1 to 20 of 202

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5976718insertion1nstd209human GRCh38 chr14: 88,859,857-88,859,857 , GRCh37.p13 chr14: 89,326,201-89,326,201 TTC8
    nsv5725969mobile element insertion1nstd211human GRCh38 chr14: 88,847,219-88,847,219 , GRCh37.p13 chr14: 89,313,563-89,313,563 TTC8
    nsv5701439mobile element insertion1nstd211human GRCh38 chr14: 88,833,738-88,833,738 , GRCh37.p13 chr14: 89,300,082-89,300,082 TTC8
    nsv5499171copy number variation1nstd206human GRCh38 chr14: 88,879,014-88,892,594 , GRCh37.p13 chr14: 89,345,358-89,358,938 TTC8
    nsv5498590copy number variation1nstd206human GRCh38 chr14: 80,522,636-106,763,637 , GRCh37.p13 chr14: 80,988,980-106,929,356 , RPS18P2, 713 more genes
    nsv5427598mobile element insertion1nstd206human GRCh38 chr14: 88,833,738-88,833,789 , GRCh37.p13 chr14: 89,300,082-89,300,133 TTC8
    nsv5380915copy number variation1nstd102humanUncertain significance GRCh37 chr14: 89,319,295-89,323,641 , GRCh38.p12 chr14: 88,852,951-88,857,297 TTC8
    nsv5380834copy number variation1nstd102humanUncertain significance GRCh37 chr14: 89,291,052-89,305,916 , GRCh38.p12 chr14: 88,824,708-88,839,572 TTC8
    nsv5357519translocation1nstd200human GRCh38 chr14: 88,879,014-88,879,014 , GRCh38 chr14: 88,892,594-88,892,594 , GRCh37.p13 chr14: 89,345,358-89,345,358 , GRCh37.p13 chr14: 89,358,938-89,358,938 TTC8
    nsv5272686copy number variation1nstd204human GRCh38.p13 chr14: 88,851,495-88,852,794 , GRCh37.p13 chr14: 89,317,839-89,319,138 TTC8
    nsv5153519mobile element insertion1nstd203human GRCh38 chr14: 88,876,030-88,876,045 , GRCh37.p13 chr14: 89,342,374-89,342,389 TTC8
    nsv5152923mobile element insertion1nstd203human GRCh38 chr14: 88,836,595-88,836,609 , GRCh37.p13 chr14: 89,302,939-89,302,953 TTC8
    nsv5144653mobile element insertion1nstd203human GRCh38 chr14: 88,845,196-88,845,209 , GRCh37.p13 chr14: 89,311,540-89,311,553 TTC8
    nsv5032025inversion1nstd200human GRCh38 chr14: 53,190,097-88,878,877 , GRCh37.p13 chr14: 53,656,815-89,345,221 , IFT43, 578 more genes
    nsv5004914copy number variation1nstd200human GRCh38 chr14: 88,702,145-89,001,512 , GRCh37.p13 chr14: 89,168,489-89,467,856 TTC8, EML5, 1 more genes
    nsv5000576copy number variation1nstd200human GRCh38 chr14: 88,859,391-88,859,883 , GRCh37.p13 chr14: 89,325,735-89,326,227 TTC8
    nsv4849407copy number variation1nstd200human GRCh37 chr14: 89,345,358-89,358,938 , GRCh38.p12 chr14: 88,879,014-88,892,594 TTC8
    nsv4726271insertion1nstd186human GRCh37 chr14: 89,326,201-89,326,201 , GRCh38.p12 chr14: 88,859,857-88,859,857 TTC8
    nsv4675107copy number variation1nstd102humanPathogenic GRCh37 chr14: 84,783,523-96,907,490 , GRCh38.p12 chr14: 84,317,179-96,441,153 SHLD2P2, RPL15P2, 175 more genes
    nsv4633001copy number variation1nstd183human GRCh37 chr14: 89,309,910-89,310,392 , GRCh38.p12 chr14: 88,843,566-88,844,048 TTC8
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