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Variant : CV160545 (GRCh38/hg38 8p23.1(chr8:10379998-10970694)x3) Homo sapiens

Symbol: CV160545
Name: GRCh38/hg38 8p23.1(chr8:10379998-10970694)x3
Condition: See cases [RCV000139604]
Clinical Significance: uncertain significance
Last Evaluated: 09/21/2012
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: AC105001.1   C8orf74   LINCR-0001   MIR1322   MIR4286   MSRA   PINX1   PRSS51   PRSS55   RP1L1   SOX7   XKR6  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000008.11:g.(?_10379998)_(10970694_?)dup
NC_000008.10:g.(?_10237508)_(10828204_?)dup
NC_000008.9:g.(?_10274918)_(10865614_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh38810,379,998 - 10,970,694CLINVAR
GRCh37810,237,508 - 10,828,204CLINVAR
Build 36810,274,918 - 10,865,614CLINVAR
Cytogenetic Map88p23.1CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9487135
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-09-08
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.