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Variant : CV383671 (GRCh37/hg19 11p14.1-11.2(chr11:29238811-45494063)x1) Homo sapiens

Symbol: CV383671
Name: GRCh37/hg19 11p14.1-11.2(chr11:29238811-45494063)x1
Condition: See cases [RCV000445800]
Clinical Significance: pathogenic
Last Evaluated:
Review Status: no assertion criteria provided
Related Genes: ABTB2   ACCS   ACCSL   ALKBH3   ALX4   API5   APIP   ARL14EP   C11orf91   C11orf96   CAPRIN1   CAT   CCDC73   CD44   CD59   CD82   COMMD9   CSTF3   DCDC1   DEPDC7   DNAJC24   EHF   EIF3M   ELF5   ELP4   EXT2   FBXO3   FJX1   FSHB   HIPK3   HSD17B12   IFTAP   IMMP1L   KCNA4   KIAA1549L   LDLRAD3   LINC00294   LMO2   LRRC4C   MPPED2   NAT10   PAMR1   PAX6   PDHX   PRDM11   PRR5L   PRRG4   QSER1   RAG1   RAG2   RCN1   SLC1A2   SYT13   TCP11L1   TP53I11   TRAF6   TRIM44   TSPAN18   TTC17   WT1   WT1-AS  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh371129,238,811 - 45,494,063CLINVAR
Cytogenetic Map1111p14.1-11.2CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 12850533
Created: 2017-04-11
Species: Homo sapiens
Last Modified: 2020-02-20
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.