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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5715218mobile element insertion1nstd211human GRCh38 chr14: 20,677,401-20,677,401 , GRCh37.p13 chr14: 21,145,560-21,145,560 TRL-TAG4-1
    nsv1764564short tandem repeat1nstd128human GRCh37 chr14: 21,145,729-21,145,752 , GRCh38.p12 chr14: 20,677,570-20,677,593 TRL-TAG4-1
    nsv1764929short tandem repeat1nstd128human GRCh37 chr14: 21,145,706-21,145,727 , GRCh38.p12 chr14: 20,677,547-20,677,568 TRL-TAG4-1
    nsv1764557short tandem repeat3nstd128human GRCh37 chr14: 21,143,233-21,143,245 , GRCh38.p12 chr14: 20,675,074-20,675,086 TRL-TAG4-1
    nsv1777387short tandem repeat2nstd128human GRCh37 chr14: 21,143,563-21,143,574 , GRCh38.p12 chr14: 20,675,404-20,675,415 TRL-TAG4-1
    esv3800550inversion1estd192human GRCh37 chr14: 21,080,343-21,080,363 , GRCh37 chr14: 21,145,277-21,145,297 , GRCh38.p12 chr14: 20,612,184-20,612,204 , GRCh38.p12 chr14: 20,677,118-20,677,138 TRP-AGG2-6, TRT-TGT3-1, 1 more genes
    nsv3916277copy number variation1nstd102humanPathogenic NCBI36 chr14: 19,734,944-44,823,755 , GRCh38 chr14: 20,196,945-45,284,802 , GRCh37 chr14: 20,665,104-45,754,005 MIR208B, MRPL52, 600 more genes
    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 RNASE8, TRAV6, 271 more genes
    nsv6637318copy number variation1nstd102humanPathogenic GRCh37 chr14: 20,690,196-23,114,522 , GRCh38.p12 chr14: 20,222,037-22,645,313 TRAJ21, TRAJ44, 239 more genes
    nsv4676085copy number variation1nstd102humanPathogenic GRCh37 chr14: 21,143,933-23,297,667 , GRCh38.p12 chr14: 20,675,774-22,828,458 ANG, SNORD8, 209 more genes
    nsv4729394copy number variation1nstd102humanPathogenic GRCh37 chr14: 20,511,672-21,915,516 , GRCh38.p12 chr14: 20,043,513-21,447,357 SETP1, OR11H5P, 99 more genes
    nsv3914336copy number variation1nstd102humanPathogenic GRCh38 chr14: 20,475,357-21,613,255 , GRCh37 chr14: 20,943,516-22,081,409 , NCBI36 chr14: 20,013,356-21,151,249 TRP-TGG3-2, TRL-TAG2-1, 80 more genes
    nsv7094244copy number variation1nstd102humanPathogenic GRCh37 chr14: 20,915,399-22,005,055 , GRCh38.p12 chr14: 20,447,240-21,536,921 ARHGEF40, LOC105370398, 78 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
    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
    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
    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
    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
    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
    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
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