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Items: 1 to 20 of 93

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5980451copy number variation1nstd102humanLikely pathogenic GRCh37 chr14: 54,654,001-75,828,024 , GRCh38.p12 chr14: 54,187,283-75,361,321 ACTN1, ACYP1, 400 more genes
    nsv5938835copy number variation1nstd209human GRCh38 chr14: 50,842,894-59,394,609 , GRCh37.p13 chr14: 51,309,612-59,861,327 , TMX1, 148 more genes
    nsv5932908copy number variation1nstd209human GRCh38 chr14: 54,986,990-55,337,950 , GRCh37.p13 chr14: 55,453,708-55,804,668 LOC107984708, SOCS4, 12 more genes
    nsv5555347sequence alteration1nstd206human GRCh38 chr14: 54,915,499-55,646,544 , GRCh37.p13 chr14: 55,382,217-56,113,262 , ATG14, 21 more genes
    nsv5512824copy number variation1nstd206human GRCh38 chr14: 55,293,622-55,297,134 , GRCh37.p13 chr14: 55,760,340-55,763,852 FBXO34, CHMP4BP1
    nsv5032025inversion1nstd200human GRCh38 chr14: 53,190,097-88,878,877 , GRCh37.p13 chr14: 53,656,815-89,345,221 , IFT43, 578 more genes
    nsv5004640copy number variation1nstd200human GRCh38 chr14: 55,293,662-55,297,094 , GRCh37.p13 chr14: 55,760,380-55,763,812 CHMP4BP1, FBXO34
    nsv4675883copy number variation1nstd102humanPathogenic GRCh37 chr14: 55,615,073-58,043,694 , GRCh38.p12 chr14: 55,148,355-57,576,976 FBXO34-AS1, FBXO34, 39 more genes
    nsv4222195copy number variation1nstd166human GRCh37.p13 chr14: 55,764,450-55,772,593 , GRCh38.p12 chr14: 55,297,732-55,305,875 FBXO34, CHMP4BP1
    nsv4215065copy number variation1nstd166human GRCh37.p13 chr14: 55,760,331-55,763,812 , GRCh38.p12 chr14: 55,293,613-55,297,094 FBXO34, CHMP4BP1
    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
    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
    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
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