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Variant : CV156269 (GRCh38/hg38 4q21.21-21.22(chr4:79742612-83153725)x1) Homo sapiens

Symbol: CV156269
Name: GRCh38/hg38 4q21.21-21.22(chr4:79742612-83153725)x1
Condition: See cases [RCV000135797]
Clinical Significance: uncertain significance
Last Evaluated: 12/22/2010
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: ANTXR2   BMP3   CFAP299   COPS4   ENOPH1   FGF5   HNRNPD   HNRNPDL   LIN54   LINC00575   MIR575   PCAT4   PLAC8   PRDM8   PRKG2   RASGEF1B   SCD5   SEC31A   SNORD143   SNORD144   THAP9   THAP9-AS1   TMEM150C  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000004.12:g.(?_79742612)_(83153725_?)del
NC_000004.11:g.(?_80663766)_(84074878_?)del
NC_000004.10:g.(?_80882790)_(84293902_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh38479,742,612 - 83,153,725CLINVAR
GRCh37480,663,766 - 84,074,878CLINVAR
Build 36480,882,790 - 84,293,902CLINVAR
Cytogenetic Map44q21.21-21.22CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9483363
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-01-21
Status: ACTIVE



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