Submit Data |  Help |  Video Tutorials |  News |  Publications |  FTP Download |  REST API |  Citing RGD |  Contact   

Variant : CV73983 (GRCh38/hg38 15q26.2-26.3(chr15:96069425-101849578)x1) Homo sapiens

Symbol: CV73983
Name: GRCh38/hg38 15q26.2-26.3(chr15:96069425-101849578)x1
Condition: Intrauterine growth retardation [RCV000053228]|See cases [RCV000053228]
Clinical Significance: pathogenic
Last Evaluated: 08/12/2011
Review Status: classified by single submitter|criteria provided, single submitter|no assertion criteria provided
Related Genes: ADAMTS17   ALDH1A3   ARRDC4   ASB7   CERS3   CERS3-AS1   CHSY1   FAM169B   IGF1R   IRAIN   LINC00923   LINC01582   LINC02244   LINC02251   LINC02254   LINC02348   LINC02351   LINS1   LRRC28   LRRK1   LUNAR1   LYSMD4   MEF2A   MIR1469   MIR4714   NR2F2   NR2F2-AS1   OR4F15   OR4F6   PCSK6   PCSK6-AS1   PGPEP1L   SELENOS   SNRPA1   SPATA41   SPATA8   SPATA8-AS1   SYNM   TARS3   TM2D3   TTC23  
Variant Type: copy number loss (SO:0001743)
Evidence: clinical testing
HGVS Name(s): NC_000015.10:g.(?_96069425)_(101849578_?)del
Human AssemblyChrPosition (strand)Source
GRCh381596,069,425 - 101,849,578CLINVAR
GRCh371596,612,654 - 102,389,781CLINVAR
Build 361594,413,658 - 100,207,304CLINVAR
Cytogenetic Map1515q26.2-26.3CLINVAR

References - uncurated

Additional Information

External Database Links
RGD Object Information
RGD ID: 8620165
Created: 2014-05-13
Species: Homo sapiens
Last Modified: 2019-10-08
Status: ACTIVE


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