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Variant : CV159867 (GRCh38/hg38 9p24.3-13.3(chr9:204104-34151476)x3) Homo sapiens

Symbol: CV159867
Name: GRCh38/hg38 9p24.3-13.3(chr9:204104-34151476)x3
Condition: See cases [RCV000139015]
Clinical Significance: pathogenic|likely benign
Last Evaluated: 08/02/2012
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: ACER2   ACO1   ADAMTSL1   AK3   ANKRD18B   APTX   AQP3   AQP7   B4GALT1   B4GALT1-AS1   BAG1   BNC2   BNC2-AS1   C9orf72   C9orf92   CAAP1   CCDC171   CD274   CDC37L1   CDC37L1-DT   CDKN2A   CDKN2A-DT   CDKN2B   CDKN2B-AS1   CER1   CHMP5   CNTLN   DCAF12   DDX58   DENND4C   DMAC1   DMRT1   DMRT2   DMRT3   DMRTA1   DNAJA1   DOCK8   DOCK8-AS1   ELAVL2   EQTN   ERMP1   ERVFRD-3   FOCAD   FOCAD-AS1   FREM1   GLDC   GLIS3   GLIS3-AS1   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   KANK1   KCNV2   KDM4C   KIAA2026   KLHL9   LINC00032   LINC00583   LINC01230   LINC01231   LINC01235   LINC01239   LINC01241   LINC01242   LINC01243   LINC01251   LINC02851   LINGO2   LRRC19   LURAP1L   LURAP1L-AS1   MIR101-2   MIR12117   MIR31   MIR3152   MIR31HG   MIR4473   MIR4474   MIR4665   MIR491   MIR6851   MIR873   MIR876   MLANA   MLLT3   MOB3B   MPDZ   MTAP   NDUFB6   NFIB   NFX1   NOL6   PDCD1LG2   PLAA   PLGRKT   PLIN2   PLPP6   PRSS3   PSIP1   PTENP1-AS   PTPRD   PTPRD-AS1   PTPRD-AS2   PUM3   RANBP6   RCL1   RFX3   RFX3-AS1   RIC1   RLN1   RLN2   RPS6   RRAGA   SAXO1   SCARNA8   SH3GL2   SLC1A1   SLC24A2   SMARCA2   SMIM27   SMU1   SNAPC3   SNORA30B   SNORD121A   SNORD121B   SNORD137   SPATA6L   SPINK4   TAF1L   TEK   TMEM215   TOPORS   TPD52L3   TRH-GTG1-6   TTC39B   TUSC1   TYRP1   UBAP2   UBE2R2   UBE2R2-AS1   UHRF2   VLDLR   VLDLR-AS1   ZDHHC21  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000009.12:g.(?_204104)_(34151476_?)dup
NC_000009.11:g.(?_204104)_(34151474_?)dup
NC_000009.10:g.(?_194104)_(34141474_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh389204,104 - 34,151,476CLINVAR
GRCh379204,104 - 34,151,474CLINVAR
Build 369194,104 - 34,141,474CLINVAR
Cytogenetic Map99p24.3-13.3CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9486547
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-01-14
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.