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Variant : CV384191 (GRCh37/hg19 10q24.32-25.3(chr10:104030479-115410590)x1) Homo sapiens

Symbol: CV384191
Name: GRCh37/hg19 10q24.32-25.3(chr10:104030479-115410590)x1
Condition: See cases [RCV000448581]
Clinical Significance: pathogenic
Last Evaluated:
Review Status: no assertion criteria provided
Related Genes: ACSL5   ACTR1A   ADD3   ADRA2A   ARL3   AS3MT   ATP5MD   BBIP1   BORCS7   C10orf95   CALHM1   CALHM2   CALHM3   CFAP43   CFAP58   CNNM2   COL17A1   CUEDC2   CYP17A1   DUSP5   FBXL15   GBF1   GPAM   GSTO1   GSTO2   HABP2   INA   ITPRIP   MFSD13A   MIR146B   MXI1   NEURL1   NFKB2   NRAP   NT5C2   PCGF6   PDCD11   PDCD4   PSD   RBM20   SFR1   SFXN2   SH3PXD2A   SHOC2   SLK   SMC3   SMNDC1   SORCS1   SORCS3   STN1   SUFU   TAF5   TCF7L2   TECTB   TRIM8   VTI1A   WBP1L   XPNPEP1   ZDHHC6  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh3710104,030,479 - 115,410,590CLINVAR
Cytogenetic Map1010q24.32-25.3CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 12853287
Created: 2017-04-11
Species: Homo sapiens
Last Modified: 2020-01-14
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.