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Variant : CV157252 (GRCh38/hg38 9p24.1-21.2(chr9:4661872-27661572)x3) Homo sapiens

Symbol: CV157252
Name: GRCh38/hg38 9p24.1-21.2(chr9:4661872-27661572)x3
Condition: See cases [RCV000136680]
Clinical Significance: pathogenic
Last Evaluated: 12/22/2010
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: ACER2   ADAMTSL1   AK3   AL353753.1   AL445623.2   AL513422.1   BNC2   BNC2-AS1   C9orf72   C9orf92   CAAP1   CCDC171   CD274   CDC37L1   CDC37L1-DT   CDKN2A   CDKN2A-DT   CDKN2B   CDKN2B-AS1   CER1   CNTLN   DENND4C   DMAC1   DMRTA1   ELAVL2   EQTN   ERMP1   ERVFRD-3   FOCAD   FOCAD-AS1   FREM1   GLDC   HACD4   HAUS6   IFNA1   IFNA10   IFNA13   IFNA14   IFNA16   IFNA17   IFNA2   IFNA21   IFNA4   IFNA5   IFNA6   IFNA7   IFNA8   IFNB1   IFNE   IFNK   IFNW1   IFT74   IFT74-AS1   IL33   INSL4   INSL6   IZUMO3   JAK2   KDM4C   KIAA2026   KLHL9   LINC00032   LINC00583   LINC01235   LINC01239   LINC01241   LINC02851   LRRC19   LURAP1L   LURAP1L-AS1   MIR101-2   MIR31   MIR3152   MIR31HG   MIR4473   MIR4474   MIR4665   MIR491   MLANA   MLLT3   MOB3B   MPDZ   MTAP   NFIB   PDCD1LG2   PLAA   PLGRKT   PLIN2   PLPP6   PSIP1   PTPRD   PTPRD-AS1   PTPRD-AS2   RANBP6   RCL1   RIC1   RLN1   RLN2   RPS6   RRAGA   SAXO1   SCARNA8   SH3GL2   SLC24A2   SNAPC3   SNORA30B   SNORD137   SPATA6L   TEK   TPD52L3   TRH-GTG1-6   TTC39B   TUSC1   TYRP1   UHRF2   ZDHHC21  
Variant Type: copy number gain (SO:0001742)
Evidence: clinical testing
HGVS Name(s): NC_000009.12:g.(?_4661872)_(27661572_?)dup
Human AssemblyChrPosition (strand)Source
GRCh3894,661,872 - 27,661,572CLINVAR
GRCh3794,661,872 - 27,661,570CLINVAR
Build 3694,651,872 - 27,651,570CLINVAR
Cytogenetic Map99p24.1-21.2CLINVAR

References - uncurated

Additional Information

External Database Links
RGD Object Information
RGD ID: 9484241
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-06-23
Status: ACTIVE


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