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Variant : CV161282 (GRCh38/hg38 4q24(chr4:100579010-101522050)x1) Homo sapiens

Symbol: CV161282
Name: GRCh38/hg38 4q24(chr4:100579010-101522050)x1
Condition: See cases [RCV000140237]
Clinical Significance: uncertain significance
Last Evaluated: 01/25/2013
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: LINC01216   LINC01218   MIR1255A   MIR8066   PPP3CA  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000004.12:g.(?_100579010)_(101522050_?)del
NC_000004.11:g.(?_101500167)_(102443207_?)del
NC_000004.10:g.(?_101719190)_(102662230_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh384100,579,010 - 101,522,050CLINVAR
GRCh374101,500,167 - 102,443,207CLINVAR
Build 364101,719,190 - 102,662,230CLINVAR
Cytogenetic Map44q24CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9487767
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2019-11-05
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.