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Variant : CV164862 (GRCh38/hg38 7p22.3-22.2(chr7:45130-3406236)x3) Homo sapiens

Symbol: CV164862
Name: GRCh38/hg38 7p22.3-22.2(chr7:45130-3406236)x3
Condition: See cases [RCV000143175]
Clinical Significance: uncertain significance
Last Evaluated: 12/10/2012
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: ADAP1   AMZ1   BRAT1   C7orf50   CARD11   CARD11-AS1   CHST12   COX19   CYP2W1   DNAAF5   EIF3B   ELFN1   ELFN1-AS1   FAM20C   GET4   GNA12   GPER1   GPR146   GRIFIN   INTS1   IQCE   LFNG   LNCRI   MAD1L1   MAFK   MICALL2   MIR339   MIR4648   MIR4655   MIR6836   MRM2   NUDT1   PDGFA   PRKAR1B   PRKAR1B-AS1   PRKAR1B-AS2   PSMG3   PSMG3-AS1   SDK1   SNORA114   SNX8   SUN1   TMEM184A   TTYH3   UNCX   ZFAND2A  
Variant Type: copy number gain (SO:0001742)
Evidence: clinical testing
HGVS Name(s): NC_000007.13:g.(?_45130)_(3445868_?)dup
Human AssemblyChrPosition (strand)Source
GRCh38745,130 - 3,406,236CLINVAR
GRCh37745,130 - 3,445,868CLINVAR
Build 367140,213 - 3,412,394CLINVAR
Cytogenetic Map77p22.3-22.2CLINVAR

References - uncurated

Additional Information

External Database Links
CRRD Object Information
CRRD ID: 9490773
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2019-11-05
Status: ACTIVE


RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.