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Variant : CV383441 (GRCh37/hg19 11p14.1-13(chr11:27895487-34494489)x1) Homo sapiens

Symbol: CV383441
Name: GRCh37/hg19 11p14.1-13(chr11:27895487-34494489)x1
Condition: See cases [RCV000448524]
Clinical Significance: pathogenic
Last Evaluated:
Review Status: no assertion criteria provided
Related Genes: ABTB2   ARL14EP   C11orf91   CAPRIN1   CAT   CCDC73   CD59   CSTF3   DCDC1   DEPDC7   DNAJC24   EIF3M   ELP4   FBXO3   FSHB   HIPK3   IMMP1L   KCNA4   KIAA1549L   KIF18A   LINC00294   LMO2   METTL15   MIR610   MPPED2   NAT10   PAX6   PRRG4   QSER1   RCN1   TCP11L1   WT1   WT1-AS  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh371127,895,487 - 34,494,489CLINVAR
Cytogenetic Map1111p14.1-13CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 12853231
Created: 2017-04-11
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.