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Variant : CV160094 (GRCh38/hg38 4p16.1(chr4:7237156-7730219)x3) Homo sapiens

Symbol: CV160094
Name: GRCh38/hg38 4p16.1(chr4:7237156-7730219)x3
Condition: See cases [RCV000139210]
Clinical Significance: likely benign
Last Evaluated: 09/21/2012
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: LOC112978667   MIR4274   MIR4798   PSAPL1   SORCS2  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000004.12:g.(?_7237156)_(7730219_?)dup
NC_000004.11:g.(?_7238883)_(7731946_?)dup
NC_000004.10:g.(?_7289784)_(7782846_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh3847,237,156 - 7,730,219CLINVAR
GRCh3747,238,883 - 7,731,946CLINVAR
Build 3647,289,784 - 7,782,846CLINVAR
Cytogenetic Map44p16.1CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9486741
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-09-22
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.