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Variant : CV73915 (GRCh38/hg38 7q11.23(chr7:73352104-74719154)x3) Homo sapiens

Symbol: CV73915
Name: GRCh38/hg38 7q11.23(chr7:73352104-74719154)x3
Condition: See cases [RCV000053151]
Clinical Significance: pathogenic
Last Evaluated: 08/12/2011
Review Status: classified by single submitter|criteria provided, single submitter|no assertion criteria provided
Related Genes: ABHD11   ABHD11-AS1   AC211433.1   BAZ1B   BCL7B   BUD23   CLDN3   CLDN4   CLIP2   DNAJC30   EIF4H   ELN   FKBP6   FZD9   GTF2I   GTF2IRD1   LAT2   LIMK1   METTL27   MIR10525   MIR4284   MIR590   MLXIPL   RFC2   STX1A   TBL2   TMEM270   VPS37D  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000007.14:g.(?_73352104)_(74719154_?)dup
NC_000007.13:g.(?_72766113)_(74133473_?)dup
NC_000007.12:g.(?_72404049)_(73771409_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh38773,352,104 - 74,719,154CLINVAR
GRCh37772,766,113 - 74,133,473CLINVAR
Build 36772,404,049 - 73,771,409CLINVAR
Cytogenetic Map77q11.23CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 8620093
Created: 2014-05-13
Species: Homo sapiens
Last Modified: 2020-08-04
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.