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Variant : CV556065 (GRCh37/hg19 Xq22.3(chrX:104552572-104723419)x0) Homo sapiens

Symbol: CV556065
Name: GRCh37/hg19 Xq22.3(chrX:104552572-104723419)x0
Condition: not provided [RCV000684370]
Clinical Significance: uncertain significance
Last Evaluated: 01/17/2018
Review Status: no assertion criteria provided
Related Genes: IL1RAPL2  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37X104,552,572 - 104,723,419CLINVAR
Cytogenetic MapXXq22.3CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 13798656
Created: 2018-10-09
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.