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Variant : CV154718 (GRCh38/hg38 9p24.2(chr9:2413996-2711186)x3) Homo sapiens

Symbol: CV154718
Name: GRCh38/hg38 9p24.2(chr9:2413996-2711186)x3
Condition: See cases [RCV000134371]
Clinical Significance: benign
Last Evaluated: 11/30/2010
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: VLDLR   VLDLR-AS1  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000009.12:g.(?_2413996)_(2711186_?)dup
NC_000009.11:g.(?_2413996)_(2711186_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh3892,413,996 - 2,711,186CLINVAR
GRCh3792,413,996 - 2,711,186CLINVAR
Build 3692,403,996 - 2,701,186CLINVAR
Cytogenetic Map99p24.2CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9481951
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-03-24
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.