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Search Results for -
ATP-BINDING CASSETTE, SUBFAMILY C, MEMBER 7
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CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR
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Repository:
NIGMS Human Genetic Cell Repository
(6234)
NIA Aging Cell Culture Repository
(755)
NINDS Repository
(726)
NHGRI Sample Repository for Human Genetic Research
(386)
HD Community Biorepository
(95)
Allen Cell Collection
(34)
Autism
(34)
Centers for Disease Control and Prevention Repository
(21)
Orphan Disease Center
(13)
Collection:
Heritable Diseases
(5415)
Chromosome Abnormalities
(758)
PIGI Consented Sample
(732)
Lysosomal Storage Diseases
(448)
NHGRI Sample Repository for Human Genetic Research
(386)
CEPH
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GeT-RM Samples
(297)
Muscular Dystrophies
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Hereditary Cancers
(271)
dbGaP
(263)
Venezuelan Huntington Disease
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Epilepsy
(214)
CMD Specific
(200)
Motor Neuron Disease
(198)
Repository Linkage Families
(182)
Apparently Healthy Collection
(176)
Pharmacogenetics
(152)
Disorders of the Urea Cycle
(142)
Human Variation
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GRC
(122)
Hybrids
(118)
Tourette Syndrome
(116)
Retinitis Pigmentosa Foundation Collection
(114)
Animals
(106)
Alzheimer's Disease
(102)
Cerebrovascular Disease
(95)
Parkinsonism
(68)
FOXG1
(62)
Canadian Alzheimer Disease
(57)
Maturity-Onset Diabetes of the Young
(43)
"Intra-abdominal fat and risk of disease in children and adolescents" study
(38)
Italian Alzheimer Disease
(37)
German Alzheimer Disease
(27)
Nonhuman Primates
(27)
Dystonia
(24)
Control
(21)
Old Order Amish Major Affective Disorder
(15)
DGAP
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Gene-Edited hiPSC
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Alzheimer Disease With No Family History
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Engineered Cell Cultures
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Stem Cell Collection
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Ames Dwarf Mice
(5)
Specially Characterized Fibroblasts
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Whole-Genome Sequence
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LCL
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DNA
(2763)
Fibroblast
(1941)
iPSC
(159)
Plasmid
(75)
Somatic cell hybrid
(60)
High Molecular Weight DNA
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Smooth muscle
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Amniotic fluid-derived cell line
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Neuronally-derived
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Endothelial
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mESC
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Adipose stromal cell
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Protein
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96 well plate of DNA samples
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Chorionic villus-derived cell line
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FFPE
(1)
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Kidney-derived cell line
(1)
Microcell hybrid
(1)
hybrid regional mapping panel
(1)
Affected:
Yes
(4861)
No
(1488)
At Risk
(137)
Unknown
(27)
Mutation Data Available:
N
(4383)
Y
(3913)
No
(2)
Source:
B-Lymphocyte
(3202)
LCL
(1889)
Fibroblast
(682)
Skin, Arm
(294)
Skin, Unspecified
(261)
Whole Blood
(223)
Skin, Skin
(167)
Somatic cell hybrid
(58)
Skin, Thigh
(38)
Stem cell
(35)
Lung, Lung
(32)
Blood
(23)
Amniotic fluid
(15)
Aorta, thoracic
(12)
Brain striatum
(12)
Trachealis muscle
(12)
Skin, Ear
(6)
Skin, Back
(5)
Amniotic fluid-derived cell line
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Skin, Abdomen
(4)
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(4)
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(4)
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(4)
Skin, Thorax/abdomen
(4)
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Gonad, Gonad
(3)
Liver, Liver
(3)
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(3)
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(3)
Breast organoid
(2)
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(2)
Gonad, Ovary
(2)
Gonad, Testes
(2)
Leiomyoma
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Muscle, Unspecified
(2)
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Skin, Buttock
(2)
Skin, Fetal
(2)
Skin, Genital area
(2)
Skin, Hip
(2)
Smooth muscle
(2)
T-Lymphocyte
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Tumor-derived cell line
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Whole embryo, Embryo
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Amnion, Amnion
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Aorta, abdominal
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Artery, Aorta, thoracic
(1)
Bladder carcinoma
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Brain, Unspecified
(1)
Cartilage, Nasal
(1)
Cartilage, Unspecified
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(1)
Chorionic villus-derived cell line
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Ewing sarcoma
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Fetal, Arm
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Fetal, Unspecified
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Kidney
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Lens, Eye
(1)
Ligament, Teeth
(1)
Neuroepithelioma
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Peripheral Vein
(1)
Polyp, Nasal
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Retina of eye
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Skin, Calf
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Skin, Embryo
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Skin, Flank
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Skin, Labialscrotal fold
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Skin, Scalp
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(1)
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Tumor
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Tumor, Abdomen
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Tumor, Fibroma
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Tumor, Hepatoblastoma
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Umbilical Cord, Vein, umbilical
(1)
Vein, iliac
(1)
Vein, umbilical
(1)
Sex:
Female
(4034)
Male
(3965)
Other
(9)
Race:
White
(5802)
Black/African American
(323)
Asian
(146)
More than one race
(90)
Other
(62)
Hispanic/Latino
(55)
Asiatic Indian
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Unknown
(37)
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Caucasian
(29)
American Indian/Alaska Native
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Not Reported
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Asian, Other
(10)
Chinese
(7)
Filipino
(5)
Korean
(5)
Japanese
(2)
Vietnamese
(2)
Native Hawaiian/Other Pacific Islander
(1)
dbGap Data Available:
No
(8061)
Yes
(237)
Extended Clinical Data Available:
No
(7232)
Yes
(1066)
Age at Sampling (Years):
5-14
(1692)
0-4
(1044)
15-24
(883)
25-34
(833)
35-44
(822)
45-54
(592)
55-64
(525)
65-74
(248)
75-89
(147)
90-99
(22)
100+
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