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Variant : CV554429 (GRCh37/hg19 6q25.3-27(chr6:159844762-170919482)x3) Homo sapiens

Symbol: CV554429
Name: GRCh37/hg19 6q25.3-27(chr6:159844762-170919482)x3
Condition: not provided [RCV000682734]
Clinical Significance: pathogenic
Last Evaluated: 09/05/2017
Review Status: no assertion criteria provided
Related Genes: ACAT2   AFDN   AGPAT4   AIRN   C6orf118   C6orf120   CCR6   CEP43   DACT2   DLL1   ERMARD   FAM120B   FRMD1   GPR31   IGF2R   KIF25   LINC02487   LPA   MAP3K4   MAS1   MPC1   MRPL18   PACRG   PDCD2   PDE10A   PHF10   PLG   PNLDC1   PRKN   PRR18   PSMB1   QKI   RNASET2   RPS6KA2   SDIM1   SFT2D1   SLC22A1   SLC22A2   SLC22A3   SMOC2   SOD2   TBP   TBXT   TCP1   TCTE3   THBS2   TTLL2   UNC93A   WDR27   WTAP  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh376159,844,762 - 170,919,482CLINVAR
Cytogenetic Map66q25.3-27CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 13795603
Created: 2018-10-09
Species: Homo sapiens
Last Modified: 2020-06-30
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.