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Variant : CV160566 (GRCh38/hg38 14q32.33(chr14:104872858-105605042)x3) Homo sapiens

Symbol: CV160566
Name: GRCh38/hg38 14q32.33(chr14:104872858-105605042)x3
Condition: See cases [RCV000139617]
Clinical Significance: uncertain significance
Last Evaluated: 09/18/2012
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: AHNAK2   BRF1   BTBD6   CDCA4   CEP170B   CLBA1   CRIP1   CRIP2   GPR132   IGH   IGHA2   IGHE   JAG2   LINC02298   MIR6765   MTA1   NUDT14   PACS2   PLD4   TEDC1   TEX22   TMEM121  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000014.9:g.(?_104872858)_(105605042_?)dup
NC_000014.8:g.(?_105339195)_(105803170_?)dup
NC_000014.7:g.(?_104410240)_(105239471_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh3814104,872,858 - 105,605,042 (+)CLINVAR
GRCh3714105,339,195 - 105,803,170 (+)CLINVAR
Build 3614104,410,240 - 105,239,471CLINVAR
Cytogenetic Map1414q32.33CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9487148
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2019-12-03
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.