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Variant : CV159891 (GRCh38/hg38 5p14.3(chr5:20893286-21454847)x1) Homo sapiens

Symbol: CV159891
Name: GRCh38/hg38 5p14.3(chr5:20893286-21454847)x1
Condition: See cases [RCV000139035]
Clinical Significance: uncertain significance
Last Evaluated: 05/07/2012
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: LINC02241  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000005.10:g.(?_20893286)_(21454847_?)del
NC_000005.9:g.(?_20893395)_(21454956_?)del
NC_000005.8:g.(?_20929152)_(21490713_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh38520,893,286 - 21,454,847CLINVAR
GRCh37520,893,395 - 21,454,956CLINVAR
Build 36520,929,152 - 21,490,713CLINVAR
Cytogenetic Map55p14.3CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9486567
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-02-20
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.