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Product:
DNA
(18638)
LCL
(12452)
Fibroblast
(3890)
iPSC
(140)
Somatic cell hybrid
(94)
High Molecular Weight DNA
(46)
Smooth muscle
(32)
mESC
(32)
Endothelial
(29)
Amniotic fluid-derived cell line
(23)
Adipose stromal cell
(19)
Tumor-derived cell line
(8)
Epithelial
(6)
Keratinocyte
(6)
human variation panel
(6)
Melanocyte
(5)
Myeloma
(4)
96 well plate of DNA samples
(2)
Chorionic villus-derived cell line
(2)
Hybridoma
(2)
Kidney-derived cell line
(2)
Mesothelial
(2)
Neuronally-derived
(2)
hybrid mapping panel
(2)
Cytoplasmic transfer (cybrid)
(1)
Erythroleukemic cell line
(1)
FFPE
(1)
Microcell hybrid
(1)
Plasmid
(1)
gene mutation panel
(1)
hybrid regional mapping panel
(1)
Source:
B-Lymphocyte
(12491)
LCL
(9790)
Whole Blood
(7692)
Fibroblast
(1172)
Skin, Arm
(1007)
Skin, Unspecified
(393)
Skin, Skin
(205)
Somatic cell hybrid
(82)
Lung, Lung
(63)
Skin, Ear
(50)
Skin, Thigh
(45)
Aorta, thoracic
(39)
Skin, Foreskin
(26)
Skin, Abdomen
(24)
Amniotic fluid
(23)
Blood
(20)
Skin, Posterior iliac crest
(12)
Amniotic fluid-derived cell line
(9)
Skin, Thorax
(9)
Stem cell
(9)
Skin, Buttock
(8)
Skin, Leg
(8)
Skin, Back
(7)
Skin, Thorax/abdomen
(6)
Umbilical Cord, Umbilical cord
(6)
Artery, iliac
(5)
Liver, Liver
(5)
Muscle, Unspecified
(5)
Placental, Placenta
(5)
Skin, Buttock-thigh
(5)
Skin, Inguinal area
(5)
Skin, Sacrum
(5)
Vein, iliac
(5)
Gonad, Gonad
(4)
Skin, Hip
(4)
Artery, pulmonary
(3)
Breast organoid
(3)
Fetal, Unspecified
(3)
Gonad, Ovary
(3)
Kidney, Kidney
(3)
Skin, Right ischium
(3)
Tumor-derived cell line
(3)
Aorta, abdominal
(2)
Brain striatum
(2)
Chorionic villus
(2)
Conjunctiva, Conjunctiva
(2)
Gonad, Testes
(2)
Heart, Pericardium
(2)
Kidney
(2)
Leiomyoma
(2)
Retina of eye
(2)
Skin, Fetal
(2)
Skin, Genital area
(2)
Skin, Labialscrotal fold
(2)
Skin, Thoraco-lumbar junction
(2)
Skin, Toe
(2)
Smooth muscle
(2)
Tendon, Achilles tendon
(2)
Trachealis muscle
(2)
Tumor
(2)
Vein, umbilical
(2)
Adenocarcinoma
(1)
Adrenal cortex tumor
(1)
Amnion, Amnion
(1)
Aortic arch
(1)
Artery, Aorta, thoracic
(1)
Ascites fluid
(1)
Brain, Unspecified
(1)
Cartilage, Nasal
(1)
Cartilage, Unspecified
(1)
Cervix, Cerivix uteri
(1)
Chest
(1)
Chorionic villus-derived cell line
(1)
Cornea, Cornea
(1)
Endothelial
(1)
Epithelial
(1)
Ewing sarcoma
(1)
Eye
(1)
Fetal, Arm
(1)
Heart, Unspecified
(1)
Hydatidiform mole
(1)
Lens, Eye
(1)
Lung
(1)
Mesothelial
(1)
Peripheral Vein
(1)
Polyp, Nasal
(1)
Skin, Axilla
(1)
Skin, Breast
(1)
Skin, Calf
(1)
Skin, Embryo
(1)
Skin, Flank
(1)
Skin, Foot
(1)
Skin, Neck
(1)
Skin, Omentum
(1)
Skin, Scalp
(1)
Skin, Shoulder
(1)
Skin, Umbilical area
(1)
Spleen, Keloid
(1)
Tumor, Abdomen
(1)
Tumor, Adenoma
(1)
Repository:
NINDS Repository
(17878)
NIGMS Human Genetic Cell Repository
(12229)
NHGRI Sample Repository for Human Genetic Research
(2683)
NIA Aging Cell Culture Repository
(2534)
Autism
(86)
Centers for Disease Control and Prevention Repository
(15)
Orphan Disease Center
(13)
Allen Cell Collection
(8)
AREDS2
(3)
HD Community Biorepository
(3)
Sex:
Female
(18755)
Male
(16382)
Other
(17)
Race:
White
(25403)
Black/African American
(1563)
More than one race
(885)
Unknown
(499)
Asian
(453)
Other
(422)
Hispanic/Latino
(309)
Chinese
(215)
American Indian/Alaska Native
(83)
Caucasian
(74)
Asiatic Indian
(53)
East Indian
(47)
Not Reported
(35)
Asian, Other
(23)
Native Hawaiian/Other Pacific Islander
(22)
Filipino
(8)
Korean
(5)
Japanese
(3)
Vietnamese
(1)
Affected:
Yes
(19498)
No
(7744)
At Risk
(2634)
Unknown
(1306)
Mutation Data Available:
N
(30352)
Y
(5088)
No
(12)
Age at Sampling (Years):
45-54
(4279)
55-64
(4175)
35-44
(4139)
5-14
(3564)
25-34
(3420)
15-24
(3233)
65-74
(3139)
0-4
(2843)
75-89
(1699)
90-99
(177)
100+
(64)
Collection:
Heritable Diseases
(9070)
Epilepsy
(6695)
Motor Neuron Disease
(4810)
NHGRI Sample Repository for Human Genetic Research
(2683)
Cerebrovascular Disease
(2416)
Control
(2157)
Parkinsonism
(2153)
Chromosome Abnormalities
(1826)
Human Variation
(1079)
Old Order Amish Major Affective Disorder
(1009)
PIGI Consented Sample
(894)
dbGaP
(886)
Apparently Healthy Collection
(813)
Tourette Syndrome
(790)
GRC
(783)
Lysosomal Storage Diseases
(702)
CEPH
(546)
Muscular Dystrophies
(522)
Dystonia
(501)
GeT-RM Samples
(341)
Hereditary Cancers
(326)
Animals
(287)
Repository Linkage Families
(277)
CMD Specific
(260)
Canadian Alzheimer Disease
(226)
Maturity-Onset Diabetes of the Young
(222)
Hybrids
(176)
"Intra-abdominal fat and risk of disease in children and adolescents" study
(156)
Pharmacogenetics
(153)
Alzheimer's Disease
(148)
University of Georgia Centenarian Study
(144)
Venezuelan Huntington Disease
(127)
Disorders of the Urea Cycle
(118)
Italian Alzheimer Disease
(108)
FOXG1
(93)
German Alzheimer Disease
(93)
Nonhuman Primates
(66)
Retinitis Pigmentosa Foundation Collection
(60)
The 90+ Study
(51)
DGAP
(50)
Aged Sib Pairs
(48)
Ames Dwarf Mice
(44)
Stem Cell Collection
(32)
Whole-Genome Sequence
(24)
Alzheimer Disease With No Family History
(23)
Gene-Edited hiPSC
(12)
Non-Healing Wound Collection
(10)
Apparently healthy iPSCs
(6)
Engineered Cell Cultures
(6)
Specially Characterized Fibroblasts
(6)
Frontotemporal Degeneration
(2)
Prostate Cancer
(2)
dbGap Data Available:
No
(30882)
Yes
(4570)
Extended Clinical Data Available:
Yes
(18393)
No
(17059)
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LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 2
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