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Variant : CV163457 (GRCh38/hg38 11p15.4(chr11:3685244-4414881)x3) Homo sapiens

Symbol: CV163457
Name: GRCh38/hg38 11p15.4(chr11:3685244-4414881)x3
Condition: See cases [RCV000141996]
Clinical Significance: uncertain significance
Last Evaluated: 08/19/2013
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: LINC02749   MIR4687   NUP98   OR52B4   PGAP2   RHOG   RRM1   STIM1   STIM1-AS1   TRIM21  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000011.10:g.(?_3685244)_(4414881_?)dup
NC_000011.9:g.(?_3706474)_(4436111_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh38113,685,244 - 4,414,881CLINVAR
GRCh37113,706,474 - 4,436,111CLINVAR
Build 36113,663,050 - 4,392,687CLINVAR
Cytogenetic Map1111p15.4CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9489516
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-07-28
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.