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Variant : CV436669 (GRCh37/hg19 15q13.1-14(chr15:28828167-34509383)x3) Homo sapiens

Symbol: CV436669
Name: GRCh37/hg19 15q13.1-14(chr15:28828167-34509383)x3
Condition: See cases [RCV000512516]
Clinical Significance: uncertain significance
Last Evaluated: 06/22/2015
Review Status: no assertion criteria provided
Related Genes: APBA2   ARHGAP11A   ARHGAP11B   AVEN   CHRFAM7A   CHRM5   CHRNA7   EMC7   FAM189A1   FAN1   GOLGA8H   GOLGA8J   GOLGA8M   GOLGA8N   GOLGA8O   GREM1   KATNBL1   KLF13   MIR211   MTMR10   NSMCE3   OTUD7A   PGBD4   RYR3   SCG5   TJP1   TRPM1  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000015.9:g.(?_28828167)_(34509383_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh371528,828,167 - 34,509,383CLINVAR
Cytogenetic Map1515q13.1-14CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 13445478
Created: 2017-11-07
Species: Homo sapiens
Last Modified: 2019-08-06
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.