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

Variant : CV155880 (GRCh38/hg38 15q13.2-13.3(chr15:30438310-32607357)x3) Homo sapiens

Symbol: CV155880
Name: GRCh38/hg38 15q13.2-13.3(chr15:30438310-32607357)x3
Condition: See cases [RCV000135452]
Clinical Significance: conflicting interpretations of pathogenicity|conflicting data from submitters
Last Evaluated: 12/22/2010
Review Status: classified by multiple submitters|no assertion criteria provided
Related Genes: ARHGAP11B   CHRNA7   FAN1   GOLGA8H   GOLGA8K   GOLGA8N   GOLGA8O   GOLGA8Q   KLF13   LINC02256   LINC02352   MIR211   MTMR10   OTUD7A   TRPM1  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000015.10:g.(?_30438310)_(32607357_?)dup
NC_000015.9:g.(?_30730513)_(32899558_?)dup
NC_000015.8:g.(?_28517805)_(30686850_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh381530,438,310 - 32,607,357CLINVAR
GRCh371530,730,513 - 32,899,558CLINVAR
Build 361528,517,805 - 30,686,850CLINVAR
Cytogenetic Map1515q13.2-13.3CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9483025
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2019-10-08
Status: ACTIVE



NHLBI Logo

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