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Variant : CV73415 (GRCh38/hg38 10q26.13-26.2(chr10:122826743-126730948)x1) Homo sapiens

Symbol: CV73415
Name: GRCh38/hg38 10q26.13-26.2(chr10:122826743-126730948)x1
Condition: See cases [RCV000052609]
Clinical Significance: pathogenic
Last Evaluated: 08/12/2011
Review Status: classified by single submitter|criteria provided, single submitter|no assertion criteria provided
Related Genes: ABRAXAS2   AC073585.1   ACADSB   ADAM12   AL158835.1   AL589787.1   BCCIP   BUB3   C10orf88   C10orf90   CHST15   CPXM2   CTBP2   CUZD1   DHX32   EDRF1   EDRF1-AS1   EDRF1-DT   EEF1AKMT2   FAM24A   FAM24B   FAM53B   FAM53B-AS1   FANK1   FANK1-AS1   GPR26   HMX2   HMX3   IKZF5   LHPP   LINC00601   LINC02641   MIR4296   MIR4484   MMP21   NKX1-2   OAT   PSTK   TEX36   TEX36-AS1   UROS   ZRANB1  
Variant Type: copy number loss (SO:0001743)
Evidence: clinical testing
HGVS Name(s): NC_000010.11:g.(?_122826743)_(126730948_?)del
Human AssemblyChrPosition (strand)Source
GRCh3810122,826,743 - 126,730,948CLINVAR
GRCh3710124,586,259 - 128,419,517CLINVAR
Build 3610124,576,249 - 128,409,507CLINVAR
Cytogenetic Map1010q26.13-26.2CLINVAR

References - uncurated

Additional Information

External Database Links
CRRD Object Information
CRRD ID: 8619585
Created: 2014-05-13
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.