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evs.gs.washington.edu/CachedSimilar. lung and blood disorders by pioneering the application of next-generation
www.ncbi.nlm.nih.gov/pubmed/24174537SimilarOct 29, 2013 . Over the past decade, the Database of Genomic Variants (DGV; http://dgv.tcag.ca
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www.fiercebiotechresearch.com/. genomic-variants-database. /2013-09-25CachedSimilarSep 25, 2013 . NIH announced Wednesday that it is awarding three grants totaling more than
www.genenames.org/useful/genome-databases-and-browsersCachedSimilarHuman Genome Databases, Browsers and Variation Resources Other Vertebrate
www.openbioinformatics.org/annovar/CachedSimilarANNOVAR: Functional annotation of genetic variants from high-throughput .
https://www.eshg.org/. /www. /7.deLeeuw_data_interpretation.pdfCachedSimilarHealthy parents. ➢. Access database with all (potentially) pathogenic CNVs .
haemgen.haem.cam.ac.uk/lovd/variantsCachedLOVD - Leiden Open Variation Database. LOVD v.3.0 Build 09 [ Current LOVD
www.igvdb.res.in/CachedSimilarThe Indian Genome Variation initiative is a network program initiated in 2003 and
databib.org/repository/457CachedSimilarDescription: The Database of Genomic Variants (DGV) provides control data for
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www.ashg.org/2008meeting/abstracts/fulltext/f20900.htmCachedThe Database of Genomic Variants (DGV) - Annotating structural variation in the
gemini.readthedocs.org/CachedSimilarBy placing genetic variants, sample genotypes, and useful genome annotations
acronyms.thefreedictionary.com/Database+of+Genomic+VariantsCachedAcronym, Definition. DGV, Deutschen Golf Verbandes (German: German Golf
https://mseqdr.org/MITO/variantsCachedLOVD - Leiden Open Variation Database . Effect. Chr. Type. Ascending DNA
www.ncbi.nlm.nih.gov/dbvar/SimilardbVar is a database of large scale genomic variants. dbVar includes events such
tiara.gmi.ac.kr/CachedSimilarThis database improves the accuracy of detecting personal genomic variations,
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www.scivee.tv/node/36213CachedNov 8, 2011 . For more information about this resource, please see our blog post at URL http://
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ucscbrowser.genap.ca/cgi-bin/hgTables?db. CachedThis track displays copy number variants (CNVs), insertions/deletions (InDels),
https://thewinnower.com/. /proof-of-extensive-copy-number-variation-in-the -human-genomeCachedThe 0.1 per cent variation was attributed to some three million single nucleotide
gwas.biosciencedbc.jp/CachedNEWS 2013/Jul/02 Shizophrenia trio's case-control data were opened. 2013/Jun/
varianttools.sourceforge.net/Annotation/DGVCachedDatabase of Genomic Variants. Login · Home ▸ Annotation . genomic structural
https://groups.google.com/a/soe.ucsc.edu/d/. /genome/a6CfTefh0L0CachedGoogle Groups allows you to create and participate in online forums and email-
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