U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Search results

Items: 1 to 20 of 88

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4769363copy number variation1nstd102humanUncertain significance GRCh37 chr7: 6,406,506-6,466,407 , GRCh38.p12 chr7: 6,366,875-6,426,776 RAC1, DAGLB
    nsv3894630copy number variation1nstd102humanUncertain significance GRCh37 chr7: 6,426,906-6,457,236 , GRCh38.p12 chr7: 6,387,275-6,417,605 RAC1, DAGLB
    nsv3911665copy number variation1nstd102humanPathogenic NCBI36 chr7: 6,143,255-6,404,722 , GRCh37 chr7: 6,176,729-6,438,197 , GRCh38 chr7: 6,137,098-6,398,566 RAC1, CYTH3, 3 more genes
    nsv4349855copy number variation1nstd102humanPathogenic GRCh37 chr7: 6,385,256-6,431,775 , GRCh38.p12 chr7: 6,345,625-6,392,144 RAC1, FAM220A, 1 more genes
    nsv4456774copy number variation1nstd102humanUncertain significance GRCh37 chr7: 6,262,721-6,488,220 , GRCh38.p12 chr7: 6,223,090-6,448,589 RAC1, RPSAP73, 3 more genes
    nsv4674954copy number variation1nstd102humanUncertain significance GRCh37 chr7: 6,278,609-6,415,520 , GRCh38.p12 chr7: 6,238,978-6,375,889 RAC1, RPSAP73, 2 more genes
    nsv3893654copy number variation1nstd102humanUncertain significance GRCh37 chr14: 21,249,293-21,270,474 , GRCh38.p12 chr14: 20,781,134-20,802,315 LOC107984671, RNASE1, 2 more genes
    nsv4728862copy number variation1nstd102humanUncertain significance GRCh37 chr7: 6,237,905-6,443,802 , GRCh38.p12 chr7: 6,198,274-6,404,171 RAC1, RPSAP73, 2 more genes
    nsv4455436copy number variation1nstd102humanUncertain significance GRCh37 chr7: 6,339,213-6,415,520 , GRCh38.p12 chr7: 6,299,582-6,375,889 RAC1, FAM220A, 1 more genes
    nsv3919826copy number variation1nstd102humanPathogenic GRCh37 chr7: 54,185-159,075,079 , GRCh38 chr7: 54,185-159,282,390 , NCBI36 chr7: 149,268-158,767,840 RAC1, RNU6-438P, 2682 more genes
    nsv6314715copy number variation1nstd102humanPathogenic GRCh37 chr14: 21,162,263-50,713,602 , GRCh38.p12 chr14: 20,694,104-50,246,884 HNRNPC, FOXG1, 616 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
    nsv3914603copy number variation1nstd102humanPathogenic GRCh37 chr7: 6,146,033-11,052,284 , NCBI36 chr7: 6,112,559-11,018,809 , GRCh38 chr7: 6,106,402-11,012,657 RAC1, LOC101154643, 69 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
    nsv3912217copy number variation1nstd102humanPathogenic GRCh38 chr7: 5,062,000-6,692,258 , GRCh37 chr7: 5,101,631-6,731,889 , NCBI36 chr7: 5,068,157-6,698,414 RAC1, RBAK-RBAKDN, 45 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
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Search details

    See more...

    Recent activity

    Clear Turn Off Turn On

    Your browsing activity is empty.

    Activity recording is turned off.

    Turn recording back on

    See more...
    You are here: NCBI > Variation > Database of Genomic Structural Variation (dbVar)
    Support Center