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Variant : CV157829 (GRCh38/hg38 10q21.1(chr10:53366596-56420041)x4) Homo sapiens

Symbol: CV157829
Name: GRCh38/hg38 10q21.1(chr10:53366596-56420041)x4
Condition: See cases [RCV000137162]
Clinical Significance: uncertain significance
Last Evaluated: 12/22/2010
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: AL353784.1   MIR548F1   MTRNR2L5   PCDH15   ZWINT  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000010.11:g.(?_53366596)_(56420041_?)dup
NC_000010.10:g.(?_55126356)_(58179802_?)dup
NC_000010.9:g.(?_54796362)_(57849808_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh381053,366,596 - 56,420,041CLINVAR
GRCh371055,126,356 - 58,179,802CLINVAR
Build 361054,796,362 - 57,849,808CLINVAR
Cytogenetic Map1010q21.1CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9484721
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-06-30
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.