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

Variant : CV161061 (GRCh38/hg38 1q44(chr1:246202303-246759911)x3) Homo sapiens

Symbol: CV161061
Name: GRCh38/hg38 1q44(chr1:246202303-246759911)x3
Condition: See cases [RCV000140028]
Clinical Significance: likely benign
Last Evaluated: 04/30/2011
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: CNST   LINC01743   LOC110121251   SCCPDH   SMYD3   TFB2M  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000001.11:g.(?_246202303)_(246759911_?)dup
NC_000001.10:g.(?_246365605)_(246923213_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh381246,202,303 - 246,759,911CLINVAR
GRCh371246,365,605 - 246,923,213CLINVAR
Build 361244,432,228 - 244,989,836CLINVAR
Cytogenetic Map11q44CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9487558
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.