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Variant : CV165058 (GRCh38/hg38 10q24.32-25.3(chr10:102732173-114085105)x1) Homo sapiens

Symbol: CV165058
Name: GRCh38/hg38 10q24.32-25.3(chr10:102732173-114085105)x1
Condition: See cases [RCV000143371]
Clinical Significance: pathogenic
Last Evaluated: 04/23/2013
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: ACSL5   ADD3   ADD3-AS1   ADRA2A   ADRB1   AS3MT   ATP5MD   BBIP1   BORCS7   BORCS7-ASMT   CALHM1   CALHM2   CALHM3   CASP7   CFAP43   CFAP58   CFAP58-DT   CNNM2   COL17A1   CYP17A1   CYP17A1-AS1   DCLRE1A   DUSP5   GPAM   GSTO1   GSTO2   HABP2   INA   ITPRIP   ITPRIP-AS1   LINC01435   LINC02620   LINC02624   LINC02627   LINC02661   MIR1307   MIR4295   MIR4482   MIR4483   MIR4680   MIR548E   MIR609   MIR6715A   MIR6715B   MIR936   MXI1   NEURL1   NEURL1-AS1   NHLRC2   NRAP   NT5C2   PCGF6   PDCD11   PDCD4   PDCD4-AS1   PLEKHS1   RBM20   RPEL1   SFR1   SFXN2   SH3PXD2A   SH3PXD2A-AS1   SHOC2   SLK   SMC3   SMNDC1   SNORA87   SORCS1   SORCS3   SORCS3-AS1   STN1   TAF5   TCF7L2   TECTB   VTI1A   WBP1L   XPNPEP1   ZDHHC6  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000010.11:g.(?_102732173)_(114085105_?)del
NC_000010.10:g.(?_104491930)_(115844864_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh3810102,732,173 - 114,085,105CLINVAR
GRCh3710104,491,930 - 115,844,864CLINVAR
Build 3610104,481,920 - 115,834,854CLINVAR
Cytogenetic Map1010q24.32-25.3CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9490969
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-01-07
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.