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Variant : CV672138 (Single allele) Homo sapiens

Symbol: CV672138
Name: Single allele
Condition: not provided [RCV000844963]
Clinical Significance: not provided
Last Evaluated:
Review Status: no assertion provided
Related Genes: PTCHD1  
Variant Type: duplication (SO:1000035)
Source: CLINVAR
Evidence: phenotyping only
Position
Human AssemblyChrPosition (strand)Source
GRCh37X23,351,116 - 23,530,035CLINVAR
Cytogenetic MapXXp22.11CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14746765
Created: 2019-09-06
Species: Homo sapiens
Last Modified: 2019-11-05
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.