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Variant : CV679567 (GRCh37/hg19 Xq22.1-22.3(chrX:102436725-105520605)x1) Homo sapiens

Symbol: CV679567
Name: GRCh37/hg19 Xq22.1-22.3(chrX:102436725-105520605)x1
Condition: Early Onset Neurological Disease Trait [RCV000993773]
Clinical Significance: uncertain significance
Last Evaluated:
Review Status: no assertion criteria provided
Related Genes: BEX2   BEX3   BEX4   ESX1   FAM199X   H2BW1   H2BW2   IL1RAPL2   MORF4L2   NRK   PLP1   PWWP3B   RAB40A   RAB9B   SERPINA7   SLC25A53   TCEAL1   TCEAL3   TCEAL4   TCEAL5   TCEAL7   TCEAL8   TCEAL9   TEX13A   TMEM31   TMSB15B   ZCCHC18  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: research
Position
Human AssemblyChrPosition (strand)Source
GRCh37X102,436,725 - 105,520,605CLINVAR
Cytogenetic MapXXq22.1-22.3CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 21067579
Created: 2020-02-11
Species: Homo sapiens
Last Modified: 2020-03-24
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.