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Variant : CV653463 (NC_000023.10:g.(?_5810858)_(6302039_?)dup) Homo sapiens

Symbol: CV653463
Name: NC_000023.10:g.(?_5810858)_(6302039_?)dup
Condition: not provided [RCV000794823]
Clinical Significance: uncertain significance
Last Evaluated: 09/12/2018
Review Status: criteria provided, single submitter
Related Genes: MIR4770   NLGN4X  
Variant Type: duplication (SO:1000035)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000023.10:g.(?_5810858)_(6302039_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh38X5,892,817 - 6,383,998CLINVAR
GRCh37X5,810,858 - 6,302,039CLINVAR
Cytogenetic MapXXp22.32-22.31CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14713995
Created: 2019-09-06
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.