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Variant : CV163729 (GRCh38/hg38 7q11.23(chr7:73286522-74727156)x1) Homo sapiens

Symbol: CV163729
Name: GRCh38/hg38 7q11.23(chr7:73286522-74727156)x1
Condition: See cases [RCV000142159]
Clinical Significance: pathogenic
Last Evaluated: 11/05/2013
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: ABHD11   ABHD11-AS1   BAZ1B   BCL7B   BUD23   CLDN3   CLDN4   CLIP2   DNAJC30   EIF4H   ELN   FKBP6   FZD9   GTF2I   GTF2IRD1   LAT2   LIMK1   METTL27   MIR10525   MIR4284   MIR590   MLXIPL   NSUN5   RFC2   STX1A   TBL2   TMEM270   TRIM50   VPS37D  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000007.14:g.(?_73286522)_(74727156_?)del
NC_000007.13:g.(?_72700524)_(74141494_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh38773,286,522 - 74,727,156CLINVAR
GRCh37772,700,524 - 74,141,494CLINVAR
Build 36772,338,460 - 73,779,430CLINVAR
Cytogenetic Map77q11.23CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9489678
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2019-11-05
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.