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Variant : CV165422 (GRCh38/hg38 Xp22.31(chrX:6209399-6531518)x3) Homo sapiens

Symbol: CV165422
Name: GRCh38/hg38 Xp22.31(chrX:6209399-6531518)x3
Condition: See cases [RCV000143735]
Clinical Significance: uncertain significance
Last Evaluated: 03/10/2014
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: MIR4770   NLGN4X  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000023.11:g.(?_6209399)_(6531518_?)dup
NC_000023.10:g.(?_6127440)_(6449559_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh38X6,209,399 - 6,531,518CLINVAR
GRCh37X6,127,440 - 6,449,559CLINVAR
Build 36X6,137,440 - 6,459,559CLINVAR
Cytogenetic MapXXp22.31CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9491333
Created: 2014-09-09
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.