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

Variant : CV164774 (GRCh38/hg38 1q44(chr1:245542908-246544740)x3) Homo sapiens

Symbol: CV164774
Name: GRCh38/hg38 1q44(chr1:245542908-246544740)x3
Condition: See cases [RCV000143087]
Clinical Significance: uncertain significance
Last Evaluated: 01/28/2013
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: KIF26B   LINC01743   LOC110121251   SMYD3   SMYD3-AS1   TFB2M  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000001.11:g.(?_245542908)_(246544740_?)dup
NC_000001.10:g.(?_245706210)_(246708042_?)dup
NC_000001.9:g.(?_243772833)_(244774665_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh381245,542,908 - 246,544,740CLINVAR
GRCh371245,706,210 - 246,708,042CLINVAR
Build 361243,772,833 - 244,774,665CLINVAR
Cytogenetic Map11q44CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9490685
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-09-29
Status: ACTIVE



NHLBI Logo

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