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Variant : CV160852 (GRCh38/hg38 22q13.32-13.33(chr22:48955243-49606942)x3) Homo sapiens

Symbol: CV160852
Name: GRCh38/hg38 22q13.32-13.33(chr22:48955243-49606942)x3
Condition: See cases [RCV000139870]
Clinical Significance: uncertain significance
Last Evaluated: 12/22/2010
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: C22orf34   MIR3667  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000022.11:g.(?_48955243)_(49606942_?)dup
NC_000022.10:g.(?_49351055)_(50000590_?)dup
NC_000022.9:g.(?_47737059)_(48386594_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh382248,955,243 - 49,606,942CLINVAR
GRCh372249,351,055 - 50,000,590CLINVAR
Build 362247,737,059 - 48,386,594CLINVAR
Cytogenetic Map2222q13.32-13.33CLINVAR




Additional Information

 
CRRD Object Information
CRRD ID: 9487400
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2017-10-31
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.