Submit Data |  Help |  Video Tutorials |  News |  Publications |  FTP Download |  REST API |  Citing RGD |  Contact   

Variant : CV154692 (GRCh38/hg38 8q24.13(chr8:124895891-125399814)x3) Homo sapiens

Symbol: CV154692
Name: GRCh38/hg38 8q24.13(chr8:124895891-125399814)x3
Condition: See cases [RCV000134345]
Clinical Significance: uncertain significance
Last Evaluated: 11/30/2010
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: LINC00964   NSMCE2   SQLE   WASHC5   ZNF572  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000008.11:g.(?_124895891)_(125399814_?)dup
NC_000008.10:g.(?_125908133)_(126412056_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh388124,895,891 - 125,399,814CLINVAR
GRCh378125,908,133 - 126,412,056CLINVAR
Build 368125,977,314 - 126,481,238CLINVAR
Cytogenetic Map88q24.13CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9481925
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-03-24
Status: ACTIVE



NHLBI Logo

RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.