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Variant : CV157486 (GRCh38/hg38 10q26.13-26.2(chr10:124032888-127368827)x3) Homo sapiens

Symbol: CV157486
Name: GRCh38/hg38 10q26.13-26.2(chr10:124032888-127368827)x3
Condition: See cases [RCV000136887]
Clinical Significance: pathogenic
Last Evaluated: 10/19/2010
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: ABRAXAS2   ADAM12   AL158835.1   AL589787.1   BCCIP   C10orf90   CHST15   CTBP2   DHX32   DOCK1   EDRF1   EDRF1-AS1   EDRF1-DT   EEF1AKMT2   FAM53B   FAM53B-AS1   FANK1   FANK1-AS1   INSYN2A   LHPP   LINC00601   MIR4296   MIR4484   MMP21   NKX1-2   OAT   TEX36   TEX36-AS1   UROS   ZRANB1  
Variant Type: copy number gain (SO:0001742)
Evidence: clinical testing
HGVS Name(s): NC_000010.11:g.(?_124032888)_(127368827_?)dup
Human AssemblyChrPosition (strand)Source
GRCh3810124,032,888 - 127,368,827CLINVAR
GRCh3710125,792,404 - 129,167,091CLINVAR
Build 3610125,782,394 - 129,057,081CLINVAR
Cytogenetic Map1010q26.13-26.2CLINVAR

References - uncurated

Additional Information

External Database Links
CRRD Object Information
CRRD ID: 9484448
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-07-28
Status: ACTIVE


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