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Variant : CV613860 (GRCh37/hg19 10q25.3-26.13(chr10:117024753-124942806)) Homo sapiens

Symbol: CV613860
Name: GRCh37/hg19 10q25.3-26.13(chr10:117024753-124942806)
Condition: Chromosome 10q26 deletion syndrome [RCV000767564]
Clinical Significance: pathogenic
Last Evaluated: 11/01/2018
Review Status: criteria provided, single submitter
Related Genes: ACADSB   ARMS2   ATE1   ATRNL1   BAG3   BTBD16   BUB3   C10orf120   C10orf82   C10orf88   CACUL1   CASC2   CCDC172   CUZD1   DENND10   DMBT1   EIF3A   EMX2   EMX2OS   ENO4   FAM204A   FAM24A   FAM24B   FGFR2   GFRA1   GRK5   HMX2   HMX3   HSPA12A   HTRA1   IKZF5   INPP5F   KCNK18   MCMBP   NANOS1   NSMCE4A   PDZD8   PLEKHA1   PLPP4   PNLIP   PNLIPRP1   PNLIPRP2   PNLIPRP3   PRDX3   PRLHR   PSTK   RAB11FIP2   RGS10   SEC23IP   SFXN4   SHTN1   SLC18A2   TACC2   TIAL1   VAX1   WDR11  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh3710117,024,753 - 124,942,806CLINVAR
Cytogenetic Map1010q25.3-26.13CLINVAR
Trait Synonyms: TERMINAL CHROMOSOME 10q26 DELETION SYNDROME



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14399531
Created: 2019-05-07
Species: Homo sapiens
Last Modified: 2020-07-28
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.