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

Variant : CV164793 (GRCh38/hg38 Xq21.1-21.2(chrX:85089622-85949735)x2) Homo sapiens

Symbol: CV164793
Name: GRCh38/hg38 Xq21.1-21.2(chrX:85089622-85949735)x2
Condition: See cases [RCV000143106]
Clinical Significance: uncertain significance
Last Evaluated: 02/25/2013
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: APOOL   CHM   MIR1321   MIR361   POF1B   SATL1   ZNF711  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000023.11:g.(?_85089622)_(85949735_?)dup
NC_000023.10:g.(?_84344628)_(85204740_?)dup
NC_000023.9:g.(?_84231284)_(85091396_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh38X85,089,622 - 85,949,735CLINVAR
GRCh37X84,344,628 - 85,204,740CLINVAR
Build 36X84,231,284 - 85,091,396CLINVAR
Cytogenetic MapXXq21.1-21.2CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9490704
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2019-09-10
Status: ACTIVE



NHLBI Logo

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