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Variant : CV436446 (GRCh37/hg19 16q21-22.1(chr16:66537021-67369281)x3) Homo sapiens

Symbol: CV436446
Name: GRCh37/hg19 16q21-22.1(chr16:66537021-67369281)x3
Condition: See cases [RCV000510388]
Clinical Significance: uncertain significance
Last Evaluated: 02/01/2016
Review Status: no assertion criteria provided
Related Genes: B3GNT9   C16orf70   CA7   CBFB   CDH16   CES2   CES3   CES4A   CIAO2B   CKLF   CKLF-CMTM1   CMTM1   CMTM2   CMTM3   CMTM4   DYNC1LI2   E2F4   ELMO3   EXOC3L1   FBXL8   FHOD1   HSF4   KCTD19   KIAA0895L   LRRC29   LRRC36   MIR328   NAE1   NOL3   PDP2   PLEKHG4   RRAD   SLC9A5   TERB1   TK2   TMEM208   TRADD  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh371666,537,021 - 67,369,281CLINVAR
Cytogenetic Map1616q21-22.1CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 13443367
Created: 2017-11-07
Species: Homo sapiens
Last Modified: 2020-01-14
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.