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

Variant : CV555360 (GRCh37/hg19 15q13.1-13.3(chr15:29382884-32192467)x1) Homo sapiens

Symbol: CV555360
Name: GRCh37/hg19 15q13.1-13.3(chr15:29382884-32192467)x1
Condition: not provided [RCV000683665]
Clinical Significance: pathogenic
Last Evaluated: 08/31/2017
Review Status: no assertion criteria provided
Related Genes: APBA2   ARHGAP11B   CHRFAM7A   FAM189A1   FAN1   GOLGA8H   GOLGA8J   KLF13   MIR211   MTMR10   NSMCE3   OTUD7A   TJP1   TRPM1  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh371529,382,884 - 32,192,467CLINVAR
Cytogenetic Map1515q13.1-13.3CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 13797405
Created: 2018-10-09
Species: Homo sapiens
Last Modified: 2019-10-01
Status: ACTIVE



NHLBI Logo

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