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Variant : CV383775 (GRCh37/hg19 10q23.1-23.31(chr10:86766571-92609514)x1) Homo sapiens

Symbol: CV383775
Name: GRCh37/hg19 10q23.1-23.31(chr10:86766571-92609514)x1
Condition: See cases [RCV000447104]
Clinical Significance: pathogenic
Last Evaluated:
Review Status: no assertion criteria provided
Related Genes: ACTA2   ADIRF   ADIRF-AS1   AGAP11   ANKRD22   ATAD1   BMPR1A   CH25H   FAM25A   FAS   FAS-AS1   GLUD1   GRID1   HTR7   IFIT1   IFIT1B   IFIT2   IFIT3   IFIT5   KIF20B   KLLN   LDB3   LINC01520   LIPA   LIPF   LIPJ   LIPK   LIPM   LIPN   MINPP1   MIR107   MIR346   MMRN2   NUTM2A   OPN4   PANK1   PAPSS2   PTEN   RNLS   SHLD2   SLC16A12   SNCG   STAMBPL1   WAPL  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh371086,766,571 - 92,609,514CLINVAR
Cytogenetic Map1010q23.1-23.31CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 12851822
Created: 2017-04-11
Species: Homo sapiens
Last Modified: 2020-02-20
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.