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

Variant : CV384065 (GRCh37/hg19 15q13.1-13.3(chr15:28659910-32446830)x4) Homo sapiens

Symbol: CV384065
Name: GRCh37/hg19 15q13.1-13.3(chr15:28659910-32446830)x4
Condition: See cases [RCV000448111]
Clinical Significance: likely pathogenic
Last Evaluated:
Review Status: no assertion criteria provided
Related Genes: APBA2   ARHGAP11B   CHRFAM7A   CHRNA7   FAM189A1   FAN1   GOLGA8H   GOLGA8J   GOLGA8M   KLF13   MIR211   MTMR10   NSMCE3   OTUD7A   TJP1   TRPM1  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh371528,659,910 - 32,446,830CLINVAR
Cytogenetic Map1515q13.1-13.3CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 12852821
Created: 2017-04-11
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.