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Variant : CV159244 (GRCh38/hg38 15q13.2(chr15:30361656-30785793)x3) Homo sapiens

Symbol: CV159244
Name: GRCh38/hg38 15q13.2(chr15:30361656-30785793)x3
Condition: See cases [RCV000138507]
Clinical Significance: likely benign
Last Evaluated: 09/21/2012
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: ARHGAP11B   CHRFAM7A   GOLGA8H   GOLGA8Q   GOLGA8R  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000015.10:g.(?_30361656)_(30785793_?)dup
NC_000015.9:g.(?_30653859)_(31077996_?)dup
NC_000015.8:g.(?_28441151)_(28865288_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh381530,361,656 - 30,785,793CLINVAR
GRCh371530,653,859 - 31,077,996CLINVAR
Build 361528,441,151 - 28,865,288CLINVAR
Cytogenetic Map1515q13.2CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9486049
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2019-10-15
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.