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Abbreviation: SNVs
Appearance Frequency: 1119 time(s)
Long forms: 11

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Long Form No. Long Form Research Area Co-occurring Abbreviation PubMed/MEDLINE Info. (Year, Title)
single nucleotide variants
(1103 times)
Genetics, Medical
(122 times)
CNVs (124 times)
NGS (107 times)
WES (62 times)
2002 High frequency of DAZ1/DAZ2 gene deletions in patients with severe oligozoospermia.
systemic necrotizing vasculitides
(5 times)
(2 times)
MPA (2 times)
PAN (2 times)
AAVs (1 time)
2011 Pregnancies in systemic necrotizing vasculitides: report on 12 women and their 20 pregnancies.
sequence variants
(2 times)
Medical Informatics
(1 time)
BMD (1 time)
CHARGE (1 time)
CNV (1 time)
2009 Inferring relative proportions of DNA variants from sequencing electropherograms.
spanlastic nanovesicles
(2 times)
Drug Therapy
(2 times)
AKBA (1 time)
DSC (1 time)
EA (1 time)
2019 Transdermal delivery of fluvastatin sodium via tailored spanlastic nanovesicles: mitigated Freund's adjuvant-induced rheumatoid arthritis in rats through suppressing p38 MAPK signaling pathway.
sequencing of identified variants
(1 time)
(1 time)
DNMBP (1 time)
2016 Whole Exome Sequencing and Segregation Analysis Confirms That a Mutation in COL17A1 Is the Cause of Epithelial Recurrent Erosion Dystrophy in a Large Dominant Pedigree Previously Mapped to Chromosome 10q23-q24.
Seven variations of a single nucleotide
(1 time)
(1 time)
INSL3 (1 time)
PCR (1 time)
UTR (1 time)
2019 Novel combined insulin-like 3 variations of a single nucleotide in cryptorchidism.
signature variation residues
(1 time)
(1 time)
SARS (1 time)
2005 Molecular evolution analysis and geographic investigation of severe acute respiratory syndrome coronavirus-like virus in palm civets at an animal market and on farms.
silicon nanovectors
(1 time)
(1 time)
Si (1 time)
2011 Size of the nanovectors determines the transplacental passage in pregnancy: study in rats.
single nt variants
(1 time)
Communicable Diseases
(1 time)
MLVA (1 time)
PCR (1 time)
PFGE (1 time)
2015 The utility of multiple molecular methods including whole genome sequencing as tools to differentiate Escherichia coli O157:H7 outbreaks.
10  specific mutations -single-nucleotide variations
(1 time)
Medical Informatics
(1 time)
SNPs (1 time)
SVs (1 time)
2018 Comparing the performance of selected variant callers using synthetic data and genome segmentation.
11  variations-single nucleotide variants
(1 time)
(1 time)
aCGH (1 time)
ASD (1 time)
CNVs (1 time)
2017 Integrative Variation Analysis Reveals that a Complex Genotype May Specify Phenotype in Siblings with Syndromic Autism Spectrum Disorder.