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Variant : CV161866 (GRCh38/hg38 9p24.3-24.2(chr9:1845513-3022547)x3) Homo sapiens

Symbol: CV161866
Name: GRCh38/hg38 9p24.3-24.2(chr9:1845513-3022547)x3
Condition: See cases [RCV000140756]
Clinical Significance: uncertain significance
Last Evaluated: 01/28/2013
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: KCNV2   PUM3   SMARCA2   VLDLR   VLDLR-AS1  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000009.12:g.(?_1845513)_(3022547_?)dup
NC_000009.11:g.(?_1845513)_(3022547_?)dup
NC_000009.10:g.(?_1835513)_(3012547_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh3891,845,513 - 3,022,547CLINVAR
GRCh3791,845,513 - 3,022,547CLINVAR
Build 3691,835,513 - 3,012,547CLINVAR
Cytogenetic Map99p24.3-24.2CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9488285
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.