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2,880 results for “variant”

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ClinicalTrials.gov24/100

Characterization and Natural History of Williams Syndrome and Other Chromosome 7q11.23 Variants

ClinicalTrials.gov study NCT06930417. IPD Sharing: YES. Countries: 1. Publications: 0.

controlledIPD-YESFeb 2026View details →
ClinicalTrials.gov24/100

Study on Fertility Parameters in Women With Germline Variants in BRCA1 and BRCA2

ClinicalTrials.gov study NCT06710015. IPD Sharing: NO. Countries: 1. Publications: 0.

closedIPD-NOFeb 2026View details →
ClinicalTrials.gov24/100

Impact of Different BRCA1/2 Gene Variants on Response to Therapy and Prognosis of Ovarian Cancer

ClinicalTrials.gov study NCT06775470. IPD Sharing: NO. Countries: 1. Publications: 0.

closedIPD-NOFeb 2026View details →
ClinicalTrials.gov24/100

Correlation Study of Isotype Switching and Neutralizing Capacity to the COVID-19 Variants Strain

ClinicalTrials.gov study NCT05087277. IPD Sharing: Not stated. Countries: 1. Publications: 0.

restrictedIPD-UNDECIDEDFeb 2026View details →
ClinicalTrials.gov24/100

Acoramidis Transthyretin Amyloidosis Prevention Trial in the Young (ACT-EARLY) Study in Asymptomatic Carriers of a Pathogenic TTR Variant

ClinicalTrials.gov study NCT06563895. IPD Sharing: Not stated. Countries: 23. Publications: 0.

restrictedIPD-UNDECIDEDFeb 2026View details →
ClinicalTrials.gov24/100

Prospective Follow-up of the Prevision Hip Stem With Comparison of Different Implant Variants

ClinicalTrials.gov study NCT06626490. IPD Sharing: Not stated. Countries: 1. Publications: 0.

restrictedIPD-UNDECIDEDFeb 2026View details →
ClinicalTrials.gov24/100

PLIN1 Variants in Precocious ACS (SCAPLIN)

ClinicalTrials.gov study NCT04904432. IPD Sharing: Not stated. Countries: 1. Publications: 0.

restrictedIPD-UNDECIDEDFeb 2026View details →
ClinicalTrials.gov24/100

New Variants Involved in Taybi-Linder Syndrome

ClinicalTrials.gov study NCT03222947. IPD Sharing: NO. Countries: 1. Publications: 0.

closedIPD-NOFeb 2026View details →
ClinicalTrials.gov24/100

Follow-up Gene Therapy Trial for the Treatment of X-linked Retinitis Pigmentosa Associated With Variants in the RPGR Gene

ClinicalTrials.gov study NCT04794101. IPD Sharing: NO. Countries: 11. Publications: 0.

closedIPD-NOFeb 2026View details →
ClinicalTrials.gov24/100

Whole Exome Sequencing in Finding Causative Variants in Germline DNA Samples From Patients With Congestive Heart Failure Receiving Therapy for Breast Cancer

ClinicalTrials.gov study NCT02610426. IPD Sharing: Not stated. Countries: 1. Publications: 0.

restrictedIPD-UNDECIDEDFeb 2026View details →
ClinicalTrials.gov24/100

Clock and Narcolepsy Genetic Variants and the Effects of Stalevo® (Levodopa/Carbidopa/Entacapone) on Sleep Disorders in Parkinson's Disease

ClinicalTrials.gov study NCT02452606. IPD Sharing: Not stated. Countries: 1. Publications: 0.

restrictedIPD-UNDECIDEDFeb 2026View details →
ClinicalTrials.gov24/100

Cognitive, Behavioral, and Functional Change in Behavioral Variant Frontotemporal Dementia (bvFTD)

ClinicalTrials.gov study NCT03088956. IPD Sharing: Not stated. Countries: 1. Publications: 0.

restrictedIPD-UNDECIDEDFeb 2026View details →
ClinicalTrials.gov24/100

Surveillance for Antiviral Resistant Variants in Chronic Hepatitis C Patients

ClinicalTrials.gov study NCT02065999. IPD Sharing: Not stated. Countries: 1. Publications: 0.

restrictedIPD-UNDECIDEDFeb 2026View details →
geo24/100

Transcriptome data of compatible soybean host inoculated with Sinorhizobium fredii with variants of NopP and NopI

GEO Series GSE274768. Glycine max. 45 samples. Type: Expression profiling by high throughput sequencing.

openGEO-OpenAug 2024View details →
geo24/100

Mapping cis-regulatory chromatin contacts in neural cells links neuropsychiatric disorder risk variants to target genes [PCHiC]

GEO Series GSE113481. Homo sapiens. 12 samples. Type: Other.

openGEO-OpenJun 2019View details →
geo24/100

Loss-of-function variants in ciliary genes confer high risk for Tetralogy of Fallot

GEO Series GSE295521. Mus musculus. 7 samples. Type: Expression profiling by high throughput sequencing.

openGEO-OpenSep 2025View details →
geo24/100

Genetic Copy Number Variants in Sib Pairs Both Affected with Schizophrenia

GEO Series GSE16930. Homo sapiens. 20 samples. Type: Genome variation profiling by array.

openGEO-OpenJun 2010View details →
geo24/100

The CD33 short isoform is a gain-of-function variant that enhances Aß1-42 phagocytosis in microglia II

GEO Series GSE172527. Mus musculus. 3 samples. Type: Expression profiling by high throughput sequencing.

openGEO-OpenApr 2021View details →
geo24/100

Identification of introduced and stably inherited DNA methylation variants in soybean associated with soybean cyst nematode parasitism

GEO Series GSE130139. Glycine max. 30 samples. Type: Methylation profiling by high throughput sequencing; Expression profiling by high throughput sequencing.

openGEO-OpenJan 2020View details →
geo24/100

Pooled scanning of protein variants identifies novel RNA-binding mutants

GEO Series GSE293492. Escherichia coli. 4 samples. Type: Other.

openGEO-OpenJun 2025View details →

ScienceDex guides

Understand access before you commit

These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.

Compare curated datasets

Allen Brain Atlas

Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.

allen-brain-atlas
neuroscienceopenDocumentation, web resources, and API references are available online.
Last verified 2026-04-30Open record

Annotated Behaviour and Observability Dataset (ABODe)

ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.

abode-home-cage
behavioral-neuroscienceopenThe DataShare record exposes download links for annotations, documentation, license text, and the zipped per-snippet data directory.
Last verified 2026-04-30Open record

DANDI Archive for NWB datasets

DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.

dandi-nwb
electrophysiologyopenPublished Dandiset metadata and archive endpoints are available through the production DANDI API.
Last verified 2026-04-30Open record

International Brain Laboratory public data

The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.

ibl
behavioral-neuroscienceopenPublic sessions can be searched and loaded from the IBL public data server through ONE.
Last verified 2026-04-29Open record

OpenNeuro

OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.

openneuro
neuroscienceopenPublished datasets are available on demand over the internet.
Last verified 2026-04-29Open record

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