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Variant : CV156740 (GRCh38/hg38 8p23.1(chr8:7311998-7929893)x3) Homo sapiens

Symbol: CV156740
Name: GRCh38/hg38 8p23.1(chr8:7311998-7929893)x3
Condition: See cases [RCV000136210]
Clinical Significance: benign
Last Evaluated: 02/06/2013
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: DEFB103A   DEFB103B   DEFB104A   DEFB104B   DEFB105A   DEFB105B   DEFB106A   DEFB106B   DEFB107A   DEFB107B   DEFB109B   DEFB4A   DEFB4B   FAM66B   PRR23D1   PRR23D2   SPAG11A   SPAG11B   USP17L1   USP17L4   ZNF705B   ZNF705G  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000008.11:g.(?_7311998)_(7929893_?)dup
NC_000008.10:g.(?_7169520)_(7787415_?)dup
NC_000008.9:g.(?_7156930)_(7824825_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh3887,311,998 - 7,929,893CLINVAR
GRCh3787,169,520 - 7,787,415CLINVAR
Build 3687,156,930 - 7,824,825CLINVAR
Cytogenetic Map88p23.1CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9483771
Created: 2014-09-09
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.