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Variant : CV158859 (GRCh38/hg38 5p15.33(chr5:22149-946680)x1) Homo sapiens

Symbol: CV158859
Name: GRCh38/hg38 5p15.33(chr5:22149-946680)x1
Condition: See cases [RCV000138166]
Clinical Significance: uncertain significance
Last Evaluated: 06/01/2012
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: AHRR   BRD9   CCDC127   CEP72   EXOC3   EXOC3-AS1   LRRC14B   MIR4456   PDCD6   PDCD6-AHRR   PLEKHG4B   SDHA   SLC9A3   SLC9A3-AS1   TPPP   TRIP13   ZDHHC11   ZDHHC11B  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000005.10:g.(?_22149)_(946680_?)del
NC_000005.9:g.(?_22149)_(946795_?)del
NC_000005.8:g.(?_75149)_(999795_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh38522,149 - 946,680CLINVAR
GRCh37522,149 - 946,795CLINVAR
Build 36575,149 - 999,795CLINVAR
Cytogenetic Map55p15.33CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9485715
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-05-26
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.