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Items: 1 to 20 of 283

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6877718copy number variation1nstd229human GRCh38 chr9: 111,523,501-111,527,200 , GRCh37.p13 chr9: 114,285,781-114,289,480 ZNF483
    nsv6877102copy number variation1nstd229human GRCh38 chr9: 111,571,023-111,571,604 , GRCh37.p13 chr9: 114,333,303-114,333,884 ZNF483, PTGR1
    nsv6874906copy number variation1nstd229human GRCh38 chr9: 111,555,501-111,653,300 , GRCh37.p13 chr9: 114,317,781-114,415,580 ZNF483, DNAJC25-GNG10, 4 more genes
    nsv6873670copy number variation1nstd229human GRCh38 chr9: 111,574,909-111,575,659 , GRCh37.p13 chr9: 114,337,189-114,337,939 PTGR1, ZNF483
    nsv6873360copy number variation1nstd229human GRCh38 chr9: 111,494,875-111,906,695 , GRCh37.p13 chr9: 114,257,155-114,668,975 ZNF483, GNG10, 8 more genes
    nsv6872815copy number variation1nstd229human GRCh38 chr9: 111,557,667-111,558,315 , GRCh37.p13 chr9: 114,319,947-114,320,595 PTGR1, ZNF483
    nsv6867147copy number variation1nstd229human GRCh38 chr9: 111,569,993-111,605,081 , GRCh37.p13 chr9: 114,332,273-114,367,361 ZNF483, PTGR1, 1 more genes
    nsv6863209copy number variation1nstd229human GRCh38 chr9: 111,549,345-111,549,780 , GRCh37.p13 chr9: 114,311,625-114,312,060 PTGR1, ZNF483
    nsv6861205copy number variation1nstd229human GRCh38 chr9: 111,475,501-111,541,400 , GRCh37.p13 chr9: 114,237,781-114,303,680 ZNF483, ECPAS
    nsv6634454copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-131,603,223 , GRCh38.p12 chr9: 203,861-128,840,944 HNRNPA1P41, GAS1RR, 1868 more genes
    nsv6573485inversion1nstd223human GRCh38 chr9: 111,535,946-111,536,339 , GRCh37.p13 chr9: 114,298,226-114,298,619 ZNF483
    nsv6567363inversion1nstd223human GRCh38 chr9: 111,560,525-111,561,391 , GRCh37.p13 chr9: 114,322,805-114,323,671 ZNF483, PTGR1
    nsv6565310inversion1nstd223human GRCh38 chr9: 111,555,591-111,556,740 , GRCh37.p13 chr9: 114,317,871-114,319,020 ZNF483, PTGR1
    nsv6558908inversion1nstd223human GRCh38 chr9: 111,537,891-111,538,408 , GRCh37.p13 chr9: 114,300,171-114,300,688 ZNF483
    nsv6455199copy number variation1nstd223human GRCh38 chr9: 111,562,111-111,562,501 , GRCh37.p13 chr9: 114,324,391-114,324,781 ZNF483, PTGR1
    nsv6453080copy number variation1nstd223human GRCh38 chr9: 111,572,504-111,579,143 , GRCh37.p13 chr9: 114,334,784-114,341,423 ZNF483, PTGR1
    nsv6450046copy number variation1nstd223human GRCh38 chr9: 111,571,011-111,571,603 , GRCh37.p13 chr9: 114,333,291-114,333,883 ZNF483, PTGR1
    nsv6443381copy number variation1nstd223human GRCh38 chr9: 111,558,470-111,567,612 , GRCh37.p13 chr9: 114,320,750-114,329,892 PTGR1, ZNF483
    nsv6315460copy number variation1nstd102humanUncertain significance GRCh37 chr9: 113,673,200-115,935,268 , GRCh38.p12 chr9: 110,910,920-113,172,988 MIR4668, LINC02977, 40 more genes
    nsv6315405copy number variation1nstd102humanUncertain significance GRCh37 chr9: 19,356,861-119,513,311 , GRCh38.p12 chr9: 19,356,863-116,751,032 RNU6-156P, GDA, 1425 more genes
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