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Variant : CV72087 (GRCh38/hg38 3q29(chr3:196077857-197165715)x1) Homo sapiens

Symbol: CV72087
Name: GRCh38/hg38 3q29(chr3:196077857-197165715)x1
Condition: Intellectual functioning disability [RCV000051202]|See cases [RCV000051202]
Clinical Significance: pathogenic
Last Evaluated: 08/12/2011
Review Status: classified by single submitter|criteria provided, single submitter|no assertion criteria provided
Related Genes: CEP19   DLG1   FBXO45   LINC00885   LINC01063   MELTF   MELTF-AS1   NCBP2   NCBP2-AS1   NCBP2AS2   NRROS   PAK2   PCYT1A   PIGX   PIGZ   RNF168   SENP5   SLC51A   SMCO1   TCTEX1D2   TFRC   TM4SF19   TM4SF19-AS1   TM4SF19-TCTEX1D2   UBXN7   UBXN7-AS1   WDR53   ZDHHC19  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000003.12:g.(?_196077857)_(197165715_?)del
NC_000003.11:g.(?_195804728)_(196892586_?)del
NC_000003.10:g.(?_197289125)_(198376983_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh383196,077,857 - 197,165,715CLINVAR
GRCh373195,804,728 - 196,892,586CLINVAR
Build 363197,289,125 - 198,376,983CLINVAR
Cytogenetic Map33q29CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 8618242
Created: 2014-05-13
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.