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Variant : CV554979 (GRCh37/hg19 10q23.1-23.32(chr10:83379241-93219169)x1) Homo sapiens

Symbol: CV554979
Name: GRCh37/hg19 10q23.1-23.32(chr10:83379241-93219169)x1
Condition: not provided [RCV000683284]
Clinical Significance: pathogenic
Last Evaluated: 03/09/2018
Review Status: no assertion criteria provided
Related Genes: ACTA2   ADIRF   ADIRF-AS1   AGAP11   ANKRD1   ANKRD22   ATAD1   BMPR1A   C10orf99   CCSER2   CDHR1   CH25H   FAM25A   FAS   FAS-AS1   GHITM   GLUD1   GRID1   HECTD2   HTR7   IFIT1   IFIT1B   IFIT2   IFIT3   IFIT5   KIF20B   KLLN   LDB3   LINC01520   LIPA   LIPF   LIPJ   LIPK   LIPM   LIPN   LRIT1   LRIT2   MINPP1   MIR107   MIR346   MMRN2   NRG3   NUTM2A   OPN4   PANK1   PAPSS2   PCGF5   PTEN   RGR   RNLS   RPP30   SHLD2   SLC16A12   SNCG   STAMBPL1   WAPL  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh371083,379,241 - 93,219,169CLINVAR
Cytogenetic Map1010q23.1-23.32CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 13796341
Created: 2018-10-09
Species: Homo sapiens
Last Modified: 2020-02-11
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.