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

Variant : CV158390 (GRCh38/hg38 17q11.2(chr17:31441351-32005206)x1) Homo sapiens

Symbol: CV158390
Name: GRCh38/hg38 17q11.2(chr17:31441351-32005206)x1
Condition: See cases [RCV000137707]
Clinical Significance: uncertain significance
Last Evaluated: 08/29/2012
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: COPRS   MIR193A   MIR365B   MIR4724   MIR4725   RAB11FIP4   SUZ12   TRT-CGT4-1   UTP6  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000017.11:g.(?_31441351)_(32005206_?)del
NC_000017.10:g.(?_29768369)_(30332225_?)del
NC_000017.9:g.(?_26792495)_(27356338_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh381731,441,351 - 32,005,206CLINVAR
GRCh371729,768,369 - 30,332,225CLINVAR
Build 361726,792,495 - 27,356,338CLINVAR
Cytogenetic Map1717q11.2CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9485259
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-07-28
Status: ACTIVE



NHLBI Logo

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