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Variant : CV158957 (GRCh38/hg38 7p15.3-15.2(chr7:23765383-26136158)x1) Homo sapiens

Symbol: CV158957
Name: GRCh38/hg38 7p15.3-15.2(chr7:23765383-26136158)x1
Condition: See cases [RCV000138258]
Clinical Significance: likely pathogenic|uncertain significance
Last Evaluated: 06/22/2015
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: C7orf31   CYCS   GSDME   MIR148A   MPP6   NPVF   NPY   OSBPL3   STK31  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000007.14:g.(?_23765383)_(26136158_?)del
NC_000007.13:g.(?_23805002)_(26175778_?)del
NC_000007.12:g.(?_23771527)_(26142303_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh38723,765,383 - 26,136,158CLINVAR
GRCh37723,805,002 - 26,175,778CLINVAR
Build 36723,771,527 - 26,142,303CLINVAR
Cytogenetic Map77p15.3-15.2CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9485807
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-01-21
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.