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Variant : CV604562 (GRCh37/hg19 10q26.3(chr10:134777671-135434303)x1) Homo sapiens

Symbol: CV604562
Name: GRCh37/hg19 10q26.3(chr10:134777671-135434303)x1
Condition: not provided [RCV000749862]
Clinical Significance: benign
Last Evaluated: 11/17/2010
Review Status: no assertion criteria provided
Related Genes: ADAM8   ADGRA1   CALY   CYP2E1   ECHS1   FUOM   KNDC1   LINC01166   MTG1   PAOX   PRAP1   SPRN   SYCE1   TUBGCP2   UTF1   VENTX   ZNF511  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh3710134,777,671 - 135,434,303CLINVAR
Cytogenetic Map1010q26.3CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14365191
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2020-05-19
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.