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Variant : CV155818 (GRCh38/hg38 5p15.33(chr5:22149-1278576)x3) Homo sapiens

Symbol: CV155818
Name: GRCh38/hg38 5p15.33(chr5:22149-1278576)x3
Condition: See cases [RCV000135393]
Clinical Significance: uncertain significance
Last Evaluated: 11/30/2010
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: AHRR   BRD9   CCDC127   CEP72   EXOC3   EXOC3-AS1   LRRC14B   MIR4456   MIR4635   NKD2   PDCD6   PLEKHG4B   SDHA   SLC12A7   SLC6A18   SLC6A19   SLC9A3   SLC9A3-AS1   TERT   TPPP   TRIP13   ZDHHC11   ZDHHC11B  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000005.10:g.(?_22149)_(1278576_?)dup
NC_000005.9:g.(?_22149)_(1278691_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh38522,149 - 1,278,576CLINVAR
GRCh37522,149 - 1,278,691CLINVAR
Build 36575,149 - 1,331,691CLINVAR
Cytogenetic Map55p15.33CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9482966
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-02-11
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.