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Variant : CV159020 (GRCh38/hg38 7p22.3(chr7:689554-2031521)x3) Homo sapiens

Symbol: CV159020
Name: GRCh38/hg38 7p22.3(chr7:689554-2031521)x3
Condition: See cases [RCV000138319]
Clinical Significance: uncertain significance
Last Evaluated: 04/16/2012
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: ADAP1   C7orf50   COX19   CYP2W1   DNAAF5   ELFN1   ELFN1-AS1   GET4   GPER1   GPR146   INTS1   LNCRI   MAD1L1   MAFK   MICALL2   MIR339   MIR4655   PRKAR1B   PSMG3   PSMG3-AS1   SUN1   TMEM184A   UNCX   ZFAND2A  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000007.14:g.(?_689554)_(2031521_?)dup
NC_000007.13:g.(?_729191)_(2071156_?)dup
NC_000007.12:g.(?_695717)_(2037682_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh387689,554 - 2,031,521CLINVAR
GRCh377729,191 - 2,071,156CLINVAR
Build 367695,717 - 2,037,682CLINVAR
Cytogenetic Map77p22.3CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9485868
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2019-11-12
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.