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Variant : CV554244 (GRCh37/hg19 5p13.1-12(chr5:41879642-42911463)x1) Homo sapiens

Symbol: CV554244
Name: GRCh37/hg19 5p13.1-12(chr5:41879642-42911463)x1
Condition: not provided [RCV000682549]
Clinical Significance: uncertain significance
Last Evaluated: 01/04/2018
Review Status: no assertion criteria provided
Related Genes: C5orf51   CCDC152   FBXO4   GHR   SELENOP  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37541,879,642 - 42,911,463CLINVAR
Cytogenetic Map55p13.1-12CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 13795400
Created: 2018-10-09
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.