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Repository:
NIGMS Human Genetic Cell Repository
(1154)
NIA Aging Cell Culture Repository
(490)
NINDS Repository
(416)
NHGRI Sample Repository for Human Genetic Research
(39)
Autism
(10)
Centers for Disease Control and Prevention Repository
(5)
HD Community Biorepository
(5)
Orphan Disease Center
(4)
Collection:
Heritable Diseases
(737)
Tourette Syndrome
(212)
Chromosome Abnormalities
(205)
Apparently Healthy Collection
(172)
CEPH
(159)
Epilepsy
(139)
PIGI Consented Sample
(121)
GRC
(120)
Hybrids
(110)
Lysosomal Storage Diseases
(83)
Repository Linkage Families
(79)
dbGaP
(70)
"Intra-abdominal fat and risk of disease in children and adolescents" study
(66)
Animals
(60)
Muscular Dystrophies
(58)
Alzheimer's Disease
(43)
Human Variation
(42)
GeT-RM Samples
(39)
NHGRI Sample Repository for Human Genetic Research
(39)
Hereditary Cancers
(38)
CMD Specific
(36)
Cerebrovascular Disease
(35)
Pharmacogenetics
(34)
Canadian Alzheimer Disease
(29)
Old Order Amish Major Affective Disorder
(24)
Ames Dwarf Mice
(18)
Italian Alzheimer Disease
(17)
Aged Sib Pairs
(13)
German Alzheimer Disease
(13)
Parkinsonism
(13)
Nonhuman Primates
(12)
Disorders of the Urea Cycle
(10)
DGAP
(7)
Maturity-Onset Diabetes of the Young
(7)
Control
(6)
Motor Neuron Disease
(6)
Stem Cell Collection
(6)
Dystonia
(5)
Venezuelan Huntington Disease
(4)
Engineered Cell Cultures
(3)
FOXG1
(3)
Specially Characterized Fibroblasts
(3)
Alzheimer Disease With No Family History
(2)
University of Georgia Centenarian Study
(2)
Whole-Genome Sequence
(2)
Apparently healthy iPSCs
(1)
Prostate Cancer
(1)
Retinitis Pigmentosa Foundation Collection
(1)
Product:
DNA
(892)
LCL
(609)
Fibroblast
(498)
Somatic cell hybrid
(58)
iPSC
(22)
Smooth muscle
(11)
Endothelial
(8)
mESC
(6)
Amniotic fluid-derived cell line
(4)
High Molecular Weight DNA
(3)
Chorionic villus-derived cell line
(2)
Neuronally-derived
(2)
Plasmid
(2)
Antibodies
(1)
CEPH family kit
(1)
Epithelial
(1)
Mesothelial
(1)
Tumor-derived cell line
(1)
hybrid regional mapping panel
(1)
Affected:
Yes
(1064)
No
(514)
At Risk
(28)
Unknown
(5)
Mutation Data Available:
N
(1670)
Y
(451)
No
(2)
Source:
B-Lymphocyte
(611)
LCL
(391)
Whole Blood
(294)
Fibroblast
(168)
Skin, Arm
(153)
Somatic cell hybrid
(52)
Skin, Skin
(38)
Skin, Unspecified
(37)
Lung, Lung
(22)
Skin, Ear
(18)
Aorta, thoracic
(10)
Skin, Foreskin
(6)
Skin, Thigh
(6)
Blood
(5)
Amniotic fluid
(4)
Leiomyoma
(3)
Skin, Abdomen
(3)
Artery, iliac
(2)
Brain striatum
(2)
Chorionic villus
(2)
Skin, Buttock-thigh
(2)
Skin, Sacrum
(2)
Skin, Thorax/abdomen
(2)
Smooth muscle
(2)
Vein, iliac
(2)
Adenocarcinoma
(1)
Amniotic fluid-derived cell line
(1)
Aorta, abdominal
(1)
Artery, Aorta, thoracic
(1)
Artery, pulmonary
(1)
Breast organoid
(1)
Cartilage, Nasal
(1)
Chorionic villus-derived cell line
(1)
Fetal, Unspecified
(1)
Gonad, Gonad
(1)
Ligament, Teeth
(1)
Lung
(1)
Skin, Buttock
(1)
Skin, Embryo
(1)
Skin, Hip
(1)
Skin, Leg
(1)
Skin, Posterior iliac crest
(1)
Skin, Thoraco-lumbar junction
(1)
Skin, Thorax
(1)
Sex:
Male
(1073)
Female
(912)
Other
(2)
Race:
White
(1457)
Black/African American
(126)
More than one race
(44)
Asian
(32)
Unknown
(21)
Hispanic/Latino
(15)
Other
(12)
Caucasian
(11)
East Indian
(6)
American Indian/Alaska Native
(5)
Chinese
(4)
Asian, Other
(3)
Not Reported
(2)
dbGap Data Available:
No
(1960)
Yes
(163)
Extended Clinical Data Available:
No
(1650)
Yes
(473)
Age at Sampling (Years):
5-14
(783)
0-4
(254)
15-24
(134)
25-34
(133)
55-64
(109)
35-44
(102)
45-54
(94)
75-89
(63)
65-74
(44)
90-99
(14)
100+
(3)
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