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Variant : CV160638 (GRCh38/hg38 8p23.1(chr8:7205665-7948701)x3) Homo sapiens

Symbol: CV160638
Name: GRCh38/hg38 8p23.1(chr8:7205665-7948701)x3
Condition: See cases [RCV000139683]
Clinical Significance: benign
Last Evaluated: 09/21/2012
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   LINC00965   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.(?_7205665)_(7948701_?)dup
NC_000008.10:g.(?_7063187)_(7806223_?)dup
NC_000008.9:g.(?_7050597)_(7843633_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh3887,205,665 - 7,948,701CLINVAR
GRCh3787,063,187 - 7,806,223CLINVAR
Build 3687,050,597 - 7,843,633CLINVAR
Cytogenetic Map88p23.1CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9487213
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.