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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
    nsv5939564copy number variation1nstd209human GRCh38 chr14: 73,487,523-73,496,084 , GRCh37.p13 chr14: 73,954,228-73,962,788 HEATR4, RIOX1, 1 more genes
    nsv5859567copy number variation1nstd209human GRCh38 chr14: 73,487,581-73,495,263 , GRCh37.p13 chr14: 73,954,286-73,961,967 RIOX1, ACOT1, 1 more genes
    nsv5032025inversion1nstd200human GRCh38 chr14: 53,190,097-88,878,877 , GRCh37.p13 chr14: 53,656,815-89,345,221 , IFT43, 578 more genes
    nsv3961381copy number variation1nstd168human GRCh38 chr14: 73,452,756-73,592,245 , GRCh37.p13 chr14: 73,919,463-74,058,949 ACOT2, NT5CP2, 8 more genes
    nsv3923727copy number variation1nstd102humanPathogenic GRCh37 chr14: 70,028,816-82,441,728 , GRCh38 chr14: 69,562,099-81,975,384 , NCBI36 chr14: 69,098,569-81,511,481 CEP128, COX6CP11, 240 more genes
    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
    nsv3919051copy number variation1nstd102humanLikely pathogenic NCBI36 chr14: 72,879,674-78,371,155 , GRCh37 chr14: 73,809,921-79,301,402 , GRCh38 chr14: 73,343,213-78,835,059 ACYP1, ENTPD5, 137 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
    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
    nsv3898512copy number variation1nstd102humanPathogenic GRCh37 chr14: 73,750,741-107,285,437 , GRCh38.p12 chr14: 73,284,033-106,877,229 MEG3, IGHV7-27, 860 more genes
    nsv3168616copy number variation1nstd158human GRCh38.p12 chr14: 63,156,948-86,570,963 , GRCh37 chr14: 63,623,666-87,037,307 , ACTN1, 394 more genes
    nsv3158054copy number variation6nstd151human GRCh37 chr14: 73,957,721-73,962,096 , GRCh38.p12 chr14: 73,491,016-73,495,392 RIOX1, ACOT1, 1 more genes
    nsv3140276copy number variation1nstd151human GRCh37 chr14: 73,945,308-73,985,872 , GRCh38.p12 chr14: 73,478,603-73,519,168 RIOX1, HEATR4, 1 more genes
    nsv2785730copy number variation1nstd132human NCBI36 chr14: 72,999,324-73,207,613 , GRCh37.p13 chr14: 73,929,571-74,137,860 , GRCh38.p12 chr14: 73,462,865-73,671,157 ACOT2, ACOT4, 11 more genes
    nsv2738344copy number variation1nstd130human NCBI36 chr14: 72,999,324-73,063,122 , GRCh37.p13 chr14: 73,929,571-73,993,369 , GRCh38.p12 chr14: 73,462,865-73,526,665 RIOX1, HEATR4, 2 more genes
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