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Variant : CV381886 (GRCh37/hg19 Xq28(chrX:152969516-153044721)x3) Homo sapiens

Symbol: CV381886
Name: GRCh37/hg19 Xq28(chrX:152969516-153044721)x3
Condition: See cases [RCV000447135]
Clinical Significance: likely benign
Last Evaluated:
Review Status: no assertion criteria provided
Related Genes: ABCD1   BCAP31   PLXNB3  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37X152,969,516 - 153,044,721CLINVAR
Cytogenetic MapXXq28CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 12851853
Created: 2017-04-11
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.