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Variant : CV160597 (GRCh38/hg38 10q21.1(chr10:53308026-56420041)x3) Homo sapiens

Symbol: CV160597
Name: GRCh38/hg38 10q21.1(chr10:53308026-56420041)x3
Condition: See cases [RCV000139643]
Clinical Significance: likely benign
Last Evaluated: 10/24/2012
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.(?_53308026)_(56420041_?)dup
NC_000010.10:g.(?_55067786)_(58179802_?)dup
NC_000010.9:g.(?_54737792)_(57849808_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh381053,308,026 - 56,420,041CLINVAR
GRCh371055,067,786 - 58,179,802CLINVAR
Build 361054,737,792 - 57,849,808CLINVAR
Cytogenetic Map1010q21.1CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9487174
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-07-07
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.