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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3917301copy number variation1nstd102humanPathogenic GRCh38 chr14: 19,755,249-22,741,281 , GRCh37 chr14: 20,223,408-23,210,490 , NCBI36 chr14: 19,293,248-22,280,330 OR4M1, RNASE8, 271 more genes
    nsv3902883copy number variation1nstd102humanPathogenic GRCh37 chr14: 19,000,422-107,289,053 , GRCh38.p12 chr14: 18,223,945-106,880,863 OR4M1, LOC440181, 1998 more genes
    nsv3907460copy number variation1nstd102humanPathogenic GRCh37 chr14: 19,280,733-107,287,663 , GRCh38.p12 chr14: 18,504,256-106,879,456 OR4M1, BANF1P1, 1996 more genes
    nsv3899639copy number variation1nstd102humanPathogenic GRCh37 chr14: 19,327,823-107,287,663 , GRCh38.p12 chr14: 18,551,346-106,879,456 OR4M1, LOC100289511, 1996 more genes
    nsv3903256copy number variation1nstd102humanPathogenic GRCh37 chr14: 19,794,561-107,234,280 , GRCh38.p12 chr14: 19,652,445-106,826,050 OR4M1, DHRS7, 1946 more genes
    nsv3898685copy number variation1nstd102humanPathogenic GRCh37 chr14: 19,794,561-34,049,214 , GRCh38.p12 chr14: 19,652,445-33,580,008 OR4M1, LOC105370419, 480 more genes
    nsv4349901copy number variation1nstd102humanPathogenic GRCh37 chr14: 19,100,682-28,730,087 , GRCh38.p12 chr14: 18,324,205-28,260,881 OR4M1, TRAV4, 458 more genes
    nsv3898291copy number variation1nstd102humanPathogenic GRCh37 chr14: 19,794,561-27,768,254 , GRCh38.p12 chr14: 19,652,445-27,299,048 OR4M1, HOMEZ, 411 more genes
    nsv3913448copy number variation1nstd102humanBenign NCBI36 chr14: 18,431,410-19,515,166 , GRCh37.p13 chr14: 19,361,410-20,445,326 , GRCh38.p12 chr14: 18,584,933-19,977,167 OR4M1, LOC100421751, 61 more genes
    nsv3920451copy number variation2nstd102humanBenign NCBI36 chr14: 18,431,410-19,496,965 , GRCh37.p13 chr14: 19,361,410-20,427,125 , GRCh38.p12 chr14: 18,584,933-19,958,966 OR4M1, NEK2P1, 60 more genes
    nsv3919105copy number variation1nstd102humanBenign GRCh37 chr14: 19,376,792-20,435,888 , NCBI36 chr14: 18,446,792-19,505,728 , GRCh38 chr14: 18,600,315-19,967,729 OR4M1, RNU6-1268P, 60 more genes
    nsv3916424copy number variation1nstd102humanBenign GRCh38 chr14: 18,658,128-19,967,729 , NCBI36 chr14: 18,504,605-19,505,728 , GRCh37 chr14: 19,434,605-20,435,888 OR4M1, NEK2P1, 53 more genes
    nsv3911532copy number variation1nstd102humanBenign GRCh37 chr14: 19,474,802-20,435,888 , NCBI36 chr14: 18,544,802-19,505,728 , GRCh38 chr14: 18,698,325-19,967,729 OR4M1, LOC107984133, 52 more genes
    nsv3911101copy number variation1nstd102humanBenign NCBI36 chr14: 19,155,022-19,505,728 , GRCh38 chr14: 19,617,023-19,967,729 , GRCh37 chr14: 20,085,860-20,435,888 OR4M1, OR4K4P, 20 more genes
    nsv3920345copy number variation1nstd102humanBenign NCBI36 chr14: 19,050,910-19,496,965 , GRCh37.p13 chr14: 19,980,910-20,427,125 , GRCh38.p12 chr14: 19,611,715-19,958,966 OR4M1, OR4N1P, 20 more genes
    nsv3918643copy number variation1nstd102humanBenign NCBI36 chr14: 19,216,406-19,496,965 , GRCh37.p13 chr14: 20,146,566-20,427,125 , GRCh38.p12 chr14: 19,678,407-19,958,966 OR4M1, OR4K16P, 16 more genes
    nsv3920889copy number variation1nstd102humanBenign NCBI36 chr14: 19,256,384-19,496,965 , GRCh37.p13 chr14: 20,186,544-20,427,125 , GRCh38.p12 chr14: 19,718,385-19,958,966 OR4M1, OR4Q3, 12 more genes
    nsv3915583copy number variation1nstd102humanLikely benign GRCh37 chr14: 20,202,176-20,406,327 , GRCh38 chr14: 19,734,017-19,938,168 , NCBI36 chr14: 19,272,016-19,476,167 OR4M1, OR4K5, 11 more genes
    nsv3917464copy number variation1nstd102humanBenign NCBI36 chr14: 18,127,055-19,496,965 , GRCh37.p13 chr14: 19,057,055-20,427,125 , GRCh38.p12 chr14: 18,280,578-19,958,966 OR4M1, LOC107984133, 62 more genes
    nsv3914777copy number variation1nstd102humanBenign NCBI36 chr14: 18,170,771-19,496,965 , GRCh37.p13 chr14: 19,100,771-20,427,125 , GRCh38.p12 chr14: 18,324,294-19,958,966 OR4M1, POTEG, 62 more genes
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