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Variant : CV554439 (GRCh37/hg19 6q27(chr6:165190527-170919482)x1) Homo sapiens

Symbol: CV554439
Name: GRCh37/hg19 6q27(chr6:165190527-170919482)x1
Condition: not provided [RCV000682744]
Clinical Significance: pathogenic
Last Evaluated: 09/22/2017
Review Status: no assertion criteria provided
Related Genes: AFDN   C6orf118   C6orf120   CCR6   CEP43   DACT2   DLL1   ERMARD   FAM120B   FRMD1   GPR31   KIF25   LINC02487   MPC1   PDCD2   PDE10A   PHF10   PRR18   PSMB1   RNASET2   RPS6KA2   SDIM1   SFT2D1   SMOC2   TBP   TBXT   TCTE3   THBS2   TTLL2   UNC93A   WDR27  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh376165,190,527 - 170,919,482CLINVAR
Cytogenetic Map66q27CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 13795613
Created: 2018-10-09
Species: Homo sapiens
Last Modified: 2020-06-23
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.