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Variant : CV157777 (GRCh38/hg38 5p15.33(chr5:435846-981479)x3) Homo sapiens

Symbol: CV157777
Name: GRCh38/hg38 5p15.33(chr5:435846-981479)x3
Condition: See cases [RCV000137119]
Clinical Significance: uncertain significance
Last Evaluated: 12/22/2010
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: AHRR   BRD9   CEP72   EXOC3   EXOC3-AS1   MIR4456   PDCD6-AHRR   SLC9A3   SLC9A3-AS1   TPPP   TRIP13   ZDHHC11   ZDHHC11B  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000005.10:g.(?_435846)_(981479_?)dup
NC_000005.9:g.(?_435961)_(981594_?)dup
NC_000005.8:g.(?_488961)_(1034594_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh385435,846 - 981,479CLINVAR
GRCh375435,961 - 981,594CLINVAR
Build 365488,961 - 1,034,594CLINVAR
Cytogenetic Map55p15.33CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9484678
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.