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Items: 1 to 20 of 91

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5938835copy number variation1nstd209human GRCh38 chr14: 50,842,894-59,394,609 , GRCh37.p13 chr14: 51,309,612-59,861,327 , TMX1, 148 more genes
    nsv5931163copy number variation1nstd209human GRCh38 chr14: 53,953,525-53,953,622 , GRCh37.p13 chr14: 54,420,243-54,420,340 BMP4
    nsv5557576inversion1nstd206human GRCh38 chr14: 53,954,816-53,955,691 , GRCh37.p13 chr14: 54,421,534-54,422,409 BMP4
    nsv5032025inversion1nstd200human GRCh38 chr14: 53,190,097-88,878,877 , GRCh37.p13 chr14: 53,656,815-89,345,221 , IFT43, 578 more genes
    nsv4503994mobile element insertion1nstd166human GRCh37.p13 chr14: 54,423,918-54,423,918 , GRCh38.p12 chr14: 53,957,200-53,957,200 BMP4
    nsv4229755copy number variation1nstd166human GRCh37.p13 chr14: 54,420,248-54,420,341 , GRCh38.p12 chr14: 53,953,530-53,953,623 BMP4
    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
    nsv3917422copy number variation1nstd102humanPathogenic GRCh38 chr14: 20,151,149-106,855,263 , NCBI36 chr14: 19,689,148-106,334,523 , GRCh37 chr14: 20,619,308-107,263,478 MIR656, TRAJ59, 1918 more genes
    nsv3916278copy number variation1nstd102humanPathogenic GRCh38 chr14: 50,591,011-56,286,919 , GRCh37 chr14: 51,057,729-56,753,637 , NCBI36 chr14: 50,127,479-55,823,390 LOC105370507, ATG14, 98 more genes
    nsv3913833copy number variation1nstd102humanPathogenic NCBI36 chr14: 51,081,314-54,857,069 , GRCh38 chr14: 51,544,846-55,320,598 , GRCh37 chr14: 52,011,564-55,787,316 SOCS4, FRMD6, 65 more genes
    nsv3911849copy number variation1nstd102humanLikely pathogenic NCBI36 chr14: 38,735,127-56,250,932 , GRCh37 chr14: 39,665,376-57,181,179 , GRCh38 chr14: 39,196,172-56,714,461 ARF6, BMP4, 219 more genes
    nsv3907460copy number variation1nstd102humanPathogenic GRCh37 chr14: 19,280,733-107,287,663 , GRCh38.p12 chr14: 18,504,256-106,879,456 BANF1P1, IGHV1-68, 1996 more genes
    nsv3906134copy number variation1nstd102humanBenign GRCh37 chr14: 54,417,117-54,424,669 , GRCh38.p12 chr14: 53,950,399-53,957,951 BMP4
    nsv3904265copy number variation1nstd102humanPathogenic GRCh37 chr14: 20,511,673-107,285,437 , GRCh38.p12 chr14: 20,043,514-106,877,229 CRIP1, GPATCH2L, 1929 more genes
    nsv3903256copy number variation1nstd102humanPathogenic GRCh37 chr14: 19,794,561-107,234,280 , GRCh38.p12 chr14: 19,652,445-106,826,050 DHRS7, MIR548Y, 1946 more genes
    nsv3902883copy number variation1nstd102humanPathogenic GRCh37 chr14: 19,000,422-107,289,053 , GRCh38.p12 chr14: 18,223,945-106,880,863 LOC440181, HEATR5A-DT, 1998 more genes
    nsv3901842copy number variation1nstd102humanPathogenic GRCh37 chr14: 53,820,659-55,003,253 , GRCh38.p12 chr14: 53,353,941-54,536,535 LOC105370504, LOC105370507, 11 more genes
    nsv3899639copy number variation1nstd102humanPathogenic GRCh37 chr14: 19,327,823-107,287,663 , GRCh38.p12 chr14: 18,551,346-106,879,456 LOC100289511, RNU6-552P, 1996 more genes
    nsv3893957copy number variation1nstd102humanPathogenic GRCh37 chr14: 54,250,363-55,362,006 , GRCh38.p12 chr14: 53,783,645-54,895,288 CGRRF1, ATP5F1CP1, 16 more genes
    esv3873060inversion1estd219human GRCh37 chr14: 54,421,433-54,422,488 , GRCh38.p12 chr14: 53,954,715-53,955,770 BMP4
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