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Variant : CV164667 (GRCh38/hg38 10q25.3-26.11(chr10:117205385-118509587)x3) Homo sapiens

Symbol: CV164667
Name: GRCh38/hg38 10q25.3-26.11(chr10:117205385-118509587)x3
Condition: See cases [RCV000142980]
Clinical Significance: uncertain significance
Last Evaluated: 08/27/2012
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: CASC2   EMX2   EMX2OS   FAM204A   KCNK18   LINC00867   LINC02674   PDZD8   RAB11FIP2   SLC18A2  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000010.11:g.(?_117205385)_(118509587_?)dup
NC_000010.10:g.(?_118964896)_(120269099_?)dup
NC_000010.9:g.(?_118954886)_(120259089_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh3810117,205,385 - 118,509,587CLINVAR
GRCh3710118,964,896 - 120,269,099CLINVAR
Build 3610118,954,886 - 120,259,089CLINVAR
Cytogenetic Map1010q25.3-26.11CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9490578
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-08-04
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.