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Variant : CV436194 (GRCh37/hg19 5q32(chr5:147713457-147774708)x3) Homo sapiens

Symbol: CV436194
Name: GRCh37/hg19 5q32(chr5:147713457-147774708)x3
Condition: See cases [RCV000510168]
Clinical Significance: uncertain significance
Last Evaluated: 04/22/2014
Review Status: no assertion criteria provided
Related Genes: FBXO38   SPINK9  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh375147,713,457 - 147,774,708CLINVAR
Cytogenetic Map55q32CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 13443149
Created: 2017-11-07
Species: Homo sapiens
Last Modified: 2020-05-19
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.