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Variant : CV156525 (GRCh38/hg38 7q11.23(chr7:73352303-74779051)x1) Homo sapiens

Symbol: CV156525
Name: GRCh38/hg38 7q11.23(chr7:73352303-74779051)x1
Condition: See cases [RCV000136014]
Clinical Significance: pathogenic
Last Evaluated: 09/21/2012
Review Status: classified by 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   NCF1   RFC2   STX1A   TBL2   TMEM270   VPS37D  
Variant Type: copy number loss (SO:0001743)
Evidence: clinical testing
HGVS Name(s): NC_000007.14:g.(?_73352303)_(74779051_?)del
Human AssemblyChrPosition (strand)Source
GRCh38773,352,303 - 74,779,051CLINVAR
GRCh37772,766,312 - 74,193,397CLINVAR
Build 36772,404,248 - 73,831,333CLINVAR
Cytogenetic Map77q11.23CLINVAR

References - uncurated

Additional Information

External Database Links
RGD Object Information
RGD ID: 9483577
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-08-04
Status: ACTIVE


RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.