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Variant : CV164451 (GRCh38/hg38 16q22.1(chr16:66921669-67312444)x3) Homo sapiens

Symbol: CV164451
Name: GRCh38/hg38 16q22.1(chr16:66921669-67312444)x3
Condition: See cases [RCV000142764]
Clinical Significance: uncertain significance
Last Evaluated: 12/22/2010
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: B3GNT9   C16orf70   CBFB   CES2   CES3   CES4A   CIAO2B   E2F4   ELMO3   EXOC3L1   FBXL8   FHOD1   HSF4   KCTD19   KIAA0895L   LRRC29   MIR328   NOL3   PLEKHG4   RRAD   SLC9A5   TMEM208   TRADD  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000016.10:g.(?_66921669)_(67312444_?)dup
NC_000016.9:g.(?_66955572)_(67346347_?)dup
NC_000016.8:g.(?_65513073)_(65903848_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh381666,921,669 - 67,312,444CLINVAR
GRCh371666,955,572 - 67,346,347CLINVAR
Build 361665,513,073 - 65,903,848CLINVAR
Cytogenetic Map1616q22.1CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9490362
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-01-21
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.