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Variant : CV608096 (GRCh37/hg19 Xp22.13(chrX:17637004-17638015)x0) Homo sapiens

Symbol: CV608096
Name: GRCh37/hg19 Xp22.13(chrX:17637004-17638015)x0
Condition: not provided [RCV000753396]
Clinical Significance: benign
Last Evaluated: 01/02/2013
Review Status: no assertion criteria provided
Related Genes: NHS  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37X17,637,004 - 17,638,015CLINVAR
Cytogenetic MapXXp22.13CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14350235
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2019-09-10
Status: ACTIVE



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