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Variant : CV156433 (GRCh38/hg38 5p15.33(chr5:924086-1544344)x3) Homo sapiens

Symbol: CV156433
Name: GRCh38/hg38 5p15.33(chr5:924086-1544344)x3
Condition: See cases [RCV000135933]
Clinical Significance: uncertain significance
Last Evaluated: 02/25/2011
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: CLPTM1L   LINC01511   LPCAT1   MIR4457   MIR4635   MIR6075   NKD2   SLC12A7   SLC6A18   SLC6A19   SLC6A3   TERT  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000005.10:g.(?_924086)_(1544344_?)dup
NC_000005.9:g.(?_924201)_(1544459_?)dup
NC_000005.8:g.(?_977201)_(1597459_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh385924,086 - 1,544,344CLINVAR
GRCh375924,201 - 1,544,459CLINVAR
Build 365977,201 - 1,597,459CLINVAR
Cytogenetic Map55p15.33CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9483499
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.