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Variant : CV156145 (GRCh38/hg38 9p24.3-22.1(chr9:204104-18882281)x1) Homo sapiens

Symbol: CV156145
Name: GRCh38/hg38 9p24.3-22.1(chr9:204104-18882281)x1
Condition: See cases [RCV000135694]
Clinical Significance: pathogenic
Last Evaluated: 02/25/2011
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: ADAMTSL1   AK3   AL513422.1   BNC2   BNC2-AS1   C9orf92   CCDC171   CD274   CDC37L1   CDC37L1-DT   CER1   CNTLN   DMAC1   DMRT1   DMRT2   DMRT3   DOCK8   DOCK8-AS1   ERMP1   FREM1   GLDC   GLIS3   GLIS3-AS1   IL33   INSL4   INSL6   JAK2   KANK1   KCNV2   KDM4C   KIAA2026   LINC00583   LINC01230   LINC01231   LINC01235   LINC02851   LURAP1L   LURAP1L-AS1   MIR101-2   MIR3152   MIR4665   MLANA   MPDZ   NFIB   PDCD1LG2   PLGRKT   PLPP6   PSIP1   PTPRD   PTPRD-AS1   PTPRD-AS2   PUM3   RANBP6   RCL1   RFX3   RFX3-AS1   RIC1   RLN1   RLN2   SH3GL2   SLC1A1   SMARCA2   SNAPC3   SNORD137   SPATA6L   TPD52L3   TRH-GTG1-6   TTC39B   TYRP1   UHRF2   VLDLR   VLDLR-AS1   ZDHHC21  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000009.12:g.(?_204104)_(18882281_?)del
NC_000009.11:g.(?_204104)_(18882279_?)del
NC_000009.10:g.(?_194104)_(18872279_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh389204,104 - 18,882,281CLINVAR
GRCh379204,104 - 18,882,279CLINVAR
Build 369194,104 - 18,872,279CLINVAR
Cytogenetic Map99p24.3-22.1CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9483265
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-06-30
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.