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Variant : CV592157 (GRCh37/hg19 11p14.3-12(chr11:24469451-37524085)x1) Homo sapiens

Symbol: CV592157
Name: GRCh37/hg19 11p14.3-12(chr11:24469451-37524085)x1
Condition: not provided [RCV000737457]
Clinical Significance: pathogenic
Last Evaluated: 11/24/2014
Review Status: no assertion criteria provided
Related Genes: ABTB2   ANO3   APIP   ARL14EP   BBOX1   BDNF   BDNF-AS   C11orf91   CAPRIN1   CAT   CCDC34   CCDC73   CD44   CD59   COMMD9   CSTF3   DCDC1   DEPDC7   DNAJC24   EHF   EIF3M   ELF5   ELP4   FBXO3   FIBIN   FJX1   FSHB   HIPK3   IFTAP   IMMP1L   KCNA4   KIAA1549L   KIF18A   LDLRAD3   LGR4   LIN7C   LINC00294   LMO2   LUZP2   METTL15   MIR610   MPPED2   MUC15   NAT10   PAMR1   PAX6   PDHX   PRR5L   PRRG4   QSER1   RAG1   RAG2   RCN1   SLC1A2   SLC5A12   TCP11L1   TRAF6   TRIM44   WT1   WT1-AS  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh371124,469,451 - 37,524,085CLINVAR
Cytogenetic Map1111p14.3-12CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 14352820
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2020-09-22
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.