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Variant : CV672525 (GRCh37/hg19 Xq24(chrX:119173700-119583001)x2) Homo sapiens

Symbol: CV672525
Name: GRCh37/hg19 Xq24(chrX:119173700-119583001)x2
Condition: not provided [RCV000845641]
Clinical Significance: uncertain significance
Last Evaluated: 11/28/2017
Review Status: no assertion criteria provided
Related Genes: ATP1B4   LAMP2   RHOXF1   RHOXF2   RHOXF2B   TMEM255A   ZBTB33  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37X119,173,700 - 119,583,001CLINVAR
Cytogenetic MapXXq24CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14976094
Created: 2019-10-08
Species: Homo sapiens
Last Modified: 2019-11-12
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.