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Variant : CV676490 (GRCh37/hg19 11p14.3-13(chr11:22079154-35597645)x1) Homo sapiens

Symbol: CV676490
Name: GRCh37/hg19 11p14.3-13(chr11:22079154-35597645)x1
Condition: not provided [RCV000849589]
Clinical Significance: pathogenic
Last Evaluated: 06/30/2017
Review Status: no assertion criteria provided
Related Genes: ABTB2   ANO3   ANO5   APIP   ARL14EP   BBOX1   BDNF   BDNF-AS   C11orf91   CAPRIN1   CAT   CCDC179   CCDC34   CCDC73   CD44   CD59   CSTF3   DCDC1   DEPDC7   DNAJC24   EHF   EIF3M   ELF5   ELP4   FANCF   FBXO3   FIBIN   FSHB   GAS2   HIPK3   IMMP1L   KCNA4   KIAA1549L   KIF18A   LGR4   LIN7C   LINC00294   LMO2   LUZP2   METTL15   MIR610   MPPED2   MUC15   NAT10   PAMR1   PAX6   PDHX   PRRG4   QSER1   RCN1   SLC17A6   SLC1A2   SLC5A12   SVIP   TCP11L1   WT1   WT1-AS  
Variant Type: copy number loss (SO:0001743)
Evidence: clinical testing
Human AssemblyChrPosition (strand)Source
GRCh371122,079,154 - 35,597,645CLINVAR
Cytogenetic Map1111p14.3-13CLINVAR

Additional Information

External Database Links
RGD Object Information
RGD ID: 14976634
Created: 2019-10-08
Species: Homo sapiens
Last Modified: 2020-09-08
Status: ACTIVE


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