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Search results: x Variables, w Analyses, x Documents, and z Datasets in x Studies
Clinical VariableDatasetVariable DescriptionVariable ID
Subject ID, consent group, subject source, source subject ID, and affection status of participants with or without different types of cancer and involved in the \"Use of Whole Genome Sequencing for Diagnosis and Discovery in the Cancer Genetics Clinic\" project.
Subject ID used in the Source Repositoryphv00251931.v1.p1
Subject ID, gender, year of birth, life status, race, medical history of participant with cancer #1, #2, #3, #4, medical history of other diagnosis, onset of cancer #1, #2, #3, #4, age at other diagnosis, and current age of participant with or without different types of cancer and involved in the \"Use of Whole Genome Sequencing for Diagnosis and Discovery in the Cancer Genetics Clinic\" project.
Other diagnosis [Colon polyposis, Hyperparathyroidism]phv00251947.v1.p1
Sample ID, body site where sample was obtained, analyte type, tumor status of sample, and sequencing center of participants with or without different types of cancer and involved in the \"Use of Whole Genome Sequencing for Diagnosis and Discovery in the Cancer Genetics Clinic\" project.
Analyte type [DNA]phv00251956.v1.p1
Subject ID, gender, year of birth, life status, race, medical history of participant with cancer #1, #2, #3, #4, medical history of other diagnosis, onset of cancer #1, #2, #3, #4, age at other diagnosis, and current age of participant with or without different types of cancer and involved in the \"Use of Whole Genome Sequencing for Diagnosis and Discovery in the Cancer Genetics Clinic\" project.
Disease onset cancer 3phv00251950.v1.p1
Subject ID, gender, year of birth, life status, race, medical history of participant with cancer #1, #2, #3, #4, medical history of other diagnosis, onset of cancer #1, #2, #3, #4, age at other diagnosis, and current age of participant with or without different types of cancer and involved in the \"Use of Whole Genome Sequencing for Diagnosis and Discovery in the Cancer Genetics Clinic\" project.
Current age of participantphv00251953.v1.p1
Subject ID, sample ID, sample source, source sample ID, and sample use variable of participants with or without different types of cancer and involved in the \"Use of Whole Genome Sequencing for Diagnosis and Discovery in the Cancer Genetics Clinic\" project.
Sample IDphv00251934.v1.p1
Subject ID, sample ID, sample source, source sample ID, and sample use variable of participants with or without different types of cancer and involved in the \"Use of Whole Genome Sequencing for Diagnosis and Discovery in the Cancer Genetics Clinic\" project.
Sample use Seq_DNA_SNP_CNV: SNP and CNV genotypes derived from sequence data Seq_DNA_WholeGenome: Whole genome sequencing phv00251937.v1.p1
Subject ID, gender, year of birth, life status, race, medical history of participant with cancer #1, #2, #3, #4, medical history of other diagnosis, onset of cancer #1, #2, #3, #4, age at other diagnosis, and current age of participant with or without different types of cancer and involved in the \"Use of Whole Genome Sequencing for Diagnosis and Discovery in the Cancer Genetics Clinic\" project.
Year of birth of participantphv00251940.v1.p1
Subject ID, gender, year of birth, life status, race, medical history of participant with cancer #1, #2, #3, #4, medical history of other diagnosis, onset of cancer #1, #2, #3, #4, age at other diagnosis, and current age of participant with or without different types of cancer and involved in the \"Use of Whole Genome Sequencing for Diagnosis and Discovery in the Cancer Genetics Clinic\" project.
Gender of participantphv00251939.v1.p1
Subject ID, gender, year of birth, life status, race, medical history of participant with cancer #1, #2, #3, #4, medical history of other diagnosis, onset of cancer #1, #2, #3, #4, age at other diagnosis, and current age of participant with or without different types of cancer and involved in the \"Use of Whole Genome Sequencing for Diagnosis and Discovery in the Cancer Genetics Clinic\" project.
Race of participant [African American, American Indian, Asian, Caucasian, Hispanic, Multiracial]phv00251942.v1.p1
Subject ID, gender, year of birth, life status, race, medical history of participant with cancer #1, #2, #3, #4, medical history of other diagnosis, onset of cancer #1, #2, #3, #4, age at other diagnosis, and current age of participant with or without different types of cancer and involved in the \"Use of Whole Genome Sequencing for Diagnosis and Discovery in the Cancer Genetics Clinic\" project.
Disease onset cancer 1phv00251948.v1.p1
Subject ID, gender, year of birth, life status, race, medical history of participant with cancer #1, #2, #3, #4, medical history of other diagnosis, onset of cancer #1, #2, #3, #4, age at other diagnosis, and current age of participant with or without different types of cancer and involved in the \"Use of Whole Genome Sequencing for Diagnosis and Discovery in the Cancer Genetics Clinic\" project.
History of cancer 3 [Breast, Ovarian, Pancreatic, Peritoneum, Skin]phv00251945.v1.p1
Subject ID, consent group, subject source, source subject ID, and affection status of participants with or without different types of cancer and involved in the \"Use of Whole Genome Sequencing for Diagnosis and Discovery in the Cancer Genetics Clinic\" project.
Case status of the subjectphv00251932.v1.p1
Subject ID, consent group, subject source, source subject ID, and affection status of participants with or without different types of cancer and involved in the \"Use of Whole Genome Sequencing for Diagnosis and Discovery in the Cancer Genetics Clinic\" project.
Consent group as determined by institutionphv00251929.v1.p1
Sample ID, body site where sample was obtained, analyte type, tumor status of sample, and sequencing center of participants with or without different types of cancer and involved in the \"Use of Whole Genome Sequencing for Diagnosis and Discovery in the Cancer Genetics Clinic\" project.
Body site where sample was collected [Peripheral Blood]phv00251955.v1.p1
Sample ID, body site where sample was obtained, analyte type, tumor status of sample, and sequencing center of participants with or without different types of cancer and involved in the \"Use of Whole Genome Sequencing for Diagnosis and Discovery in the Cancer Genetics Clinic\" project.
Name of the center which conducted sequencing [Complete Genomics, Inc.]phv00251958.v1.p1
Subject ID, sample ID, sample source, source sample ID, and sample use variable of participants with or without different types of cancer and involved in the \"Use of Whole Genome Sequencing for Diagnosis and Discovery in the Cancer Genetics Clinic\" project.
Subject IDphv00251933.v1.p1
Subject ID, sample ID, sample source, source sample ID, and sample use variable of participants with or without different types of cancer and involved in the \"Use of Whole Genome Sequencing for Diagnosis and Discovery in the Cancer Genetics Clinic\" project.
Sample ID used in the Source Repositoryphv00251936.v1.p1
Subject ID, consent group, subject source, source subject ID, and affection status of participants with or without different types of cancer and involved in the \"Use of Whole Genome Sequencing for Diagnosis and Discovery in the Cancer Genetics Clinic\" project.
Source repository where subjects originatephv00251930.v1.p1
Subject ID, gender, year of birth, life status, race, medical history of participant with cancer #1, #2, #3, #4, medical history of other diagnosis, onset of cancer #1, #2, #3, #4, age at other diagnosis, and current age of participant with or without different types of cancer and involved in the \"Use of Whole Genome Sequencing for Diagnosis and Discovery in the Cancer Genetics Clinic\" project.
Disease onset cancer 2phv00251949.v1.p1
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