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Variant : CV165201 (GRCh38/hg38 8p23.1(chr8:9009853-10496260)x3) Homo sapiens

Symbol: CV165201
Name: GRCh38/hg38 8p23.1(chr8:9009853-10496260)x3
Condition: See cases [RCV000143514]
Clinical Significance: likely benign|uncertain significance
Last Evaluated: 06/22/2015
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: AC022784.1   AC104964.1   ERI1   MIR124-1   MIR124-1HG   MIR4660   MIR597   MSRA   PPP1R3B   SNORD3I   TNKS  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000008.11:g.(?_9009853)_(10496260_?)dup
NC_000008.10:g.(?_8867363)_(10353770_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh3889,009,853 - 10,496,260CLINVAR
GRCh3788,867,363 - 10,353,770CLINVAR
Build 3688,904,773 - 10,391,180CLINVAR
Cytogenetic Map88p23.1CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9491112
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-08-04
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.