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Variant : CV170732 (GRCh38/hg38 5p14.3(chr5:20895874-21402889)x1) Homo sapiens

Symbol: CV170732
Name: GRCh38/hg38 5p14.3(chr5:20895874-21402889)x1
Condition: See cases [RCV000148133]|See cases [RCV000509066]
Clinical Significance: uncertain significance
Last Evaluated: 08/12/2011
Review Status: classified by single submitter|criteria provided, 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.(?_20895874)_(21402889_?)del
NC_000005.9:g.(?_20895983)_(21402998_?)del
NC_000005.8:g.(?_20931740)_(21438755_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh38520,895,874 - 21,402,889CLINVAR
GRCh37520,895,983 - 21,402,998CLINVAR
Build 36520,931,740 - 21,438,755CLINVAR
Cytogenetic Map55p14.3CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9684682
Created: 2014-12-09
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.