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Variant : CV592023 (GRCh37/hg19 10q26.2-26.3(chr10:129454892-135447971)x1) Homo sapiens

Symbol: CV592023
Name: GRCh37/hg19 10q26.2-26.3(chr10:129454892-135447971)x1
Condition: not provided [RCV000737323]
Clinical Significance: pathogenic
Last Evaluated: 05/01/2012
Review Status: no assertion criteria provided
Related Genes: ADAM8   ADGRA1   BNIP3   CALY   CFAP46   CLRN3   CYP2E1   DPYSL4   EBF3   ECHS1   FOXI2   FRG2B   FUOM   GLRX3   INPP5A   JAKMIP3   KNDC1   LINC01166   LINC02870   LRRC27   MGMT   MKI67   MTG1   NKX6-2   PAOX   PPP2R2D   PRAP1   PTPRE   PWWP2B   SPRN   STK32C   SYCE1   TCERG1L   TCERG1L-AS1   TUBGCP2   UTF1   VENTX   ZNF511  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh3710129,454,892 - 135,447,971CLINVAR
Cytogenetic Map1010q26.2-26.3CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14352626
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2020-05-26
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.