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Variant : CV164032 (GRCh38/hg38 3p12.3(chr3:75153221-76021659)x3) Homo sapiens

Symbol: CV164032
Name: GRCh38/hg38 3p12.3(chr3:75153221-76021659)x3
Condition: See cases [RCV000142357]
Clinical Significance: likely benign
Last Evaluated: 03/18/2014
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: FRG2C   LINC00960   LINC02018   MIR1324   MIR4273   MIR4444-2   ROBO2   ZNF717  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000003.12:g.(?_75153221)_(76021659_?)dup
NC_000003.11:g.(?_75202372)_(76070810_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh38375,153,221 - 76,021,659CLINVAR
GRCh37375,202,372 - 76,070,810CLINVAR
Build 36375,285,062 - 76,153,500CLINVAR
Cytogenetic Map33p12.3CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9489876
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2019-11-05
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.