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Variant : CV162920 (GRCh38/hg38 15q13.2-13.3(chr15:30094195-32151843)x3) Homo sapiens

Symbol: CV162920
Name: GRCh38/hg38 15q13.2-13.3(chr15:30094195-32151843)x3
Condition: See cases [RCV000141654]
Clinical Significance: uncertain significance
Last Evaluated: 04/23/2013
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: ARHGAP11B   CHRFAM7A   CHRNA7   FAN1   GOLGA8H   GOLGA8J   GOLGA8Q   GOLGA8R   GOLGA8T   KLF13   LINC02249   LINC02352   MIR211   MTMR10   OTUD7A   TRPM1  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000015.10:g.(?_30094195)_(32151843_?)dup
NC_000015.9:g.(?_30386398)_(32444044_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh381530,094,195 - 32,151,843CLINVAR
GRCh371530,386,398 - 32,444,044CLINVAR
Build 361528,173,690 - 30,231,336CLINVAR
Cytogenetic Map1515q13.2-13.3CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9489179
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2019-10-08
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.