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Variant : CV155075 (GRCh38/hg38 5p15.33(chr5:369755-574780)x3) Homo sapiens

Symbol: CV155075
Name: GRCh38/hg38 5p15.33(chr5:369755-574780)x3
Condition: See cases [RCV000134721]
Clinical Significance: benign
Last Evaluated: 07/30/2010
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: AHRR   EXOC3   EXOC3-AS1   MIR4456   PDCD6-AHRR   SLC9A3   SLC9A3-AS1  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000005.10:g.(?_369755)_(574780_?)dup
NC_000005.9:g.(?_369870)_(574895_?)dup
NC_000005.8:g.(?_422870)_(627895_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh385369,755 - 574,780CLINVAR
GRCh375369,870 - 574,895CLINVAR
Build 365422,870 - 627,895CLINVAR
Cytogenetic Map55p15.33CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9482300
Created: 2014-09-09
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.