Submit Data |  Help |  Video Tutorials |  News |  Publications |  FTP Download |  REST API |  Citing RGD |  Contact   

Variant : CV155590 (GRCh38/hg38 9q34.12(chr9:130600160-130655199)x3) Homo sapiens

Symbol: CV155590
Name: GRCh38/hg38 9q34.12(chr9:130600160-130655199)x3
Condition: See cases [RCV000135165]
Clinical Significance: likely benign
Last Evaluated: 11/30/2010
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: FUBP3   MIR6856  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000009.12:g.(?_130600160)_(130655199_?)dup
NC_000009.11:g.(?_133475547)_(133530586_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh389130,600,160 - 130,655,199CLINVAR
GRCh379133,475,547 - 133,530,586CLINVAR
Build 369132,465,368 - 132,520,407CLINVAR
Cytogenetic Map99q34.12CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9482738
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-03-17
Status: ACTIVE



NHLBI Logo

RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.