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Variant : CV163329 (GRCh38/hg38 5p13.1-12(chr5:41876210-42913877)x1) Homo sapiens

Symbol: CV163329
Name: GRCh38/hg38 5p13.1-12(chr5:41876210-42913877)x1
Condition: See cases [RCV000141916]
Clinical Significance: uncertain significance
Last Evaluated: 07/16/2013
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: C5orf51   CCDC152   FBXO4   GHR   SELENOP  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000005.10:g.(?_41876210)_(42913877_?)del
NC_000005.9:g.(?_41876312)_(42913979_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh38541,876,210 - 42,913,877CLINVAR
GRCh37541,876,312 - 42,913,979CLINVAR
Build 36541,912,069 - 42,949,736CLINVAR
Cytogenetic Map55p13.1-12CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9489438
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.