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

Variant : CV382573 (GRCh37/hg19 21q11.2-21.1(chr21:15442582-20723130)) Homo sapiens

Symbol: CV382573
Name: GRCh37/hg19 21q11.2-21.1(chr21:15442582-20723130)
Condition: See cases [RCV000447733]
Clinical Significance: pathogenic
Last Evaluated: 11/30/2010
Review Status: no assertion criteria provided
Related Genes: BTG3   C21orf91   CHODL   CXADR   HSPA13   LIPI   MIR125B2   MIR99A   MIRLET7C   NRIP1   RBM11   SAMSN1   TMPRSS15   USP25  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh372115,442,582 - 20,723,130CLINVAR
Cytogenetic Map2121q11.2-21.1CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 12852446
Created: 2017-04-11
Species: Homo sapiens
Last Modified: 2019-12-03
Status: ACTIVE



NHLBI Logo

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