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256,031 Results - per page

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Name Proper Citation Organism Disease Comments Defining Citation Category Sex Synonyms Vendor Catalog Number Cross References Hierarchy Originate from Same Individual ID Record Last Update Mentions Count
GM01604
 
Resource Report
Resource Website
RRID:CVCL_7325 Homo sapiens (Human) Population: African American. PMID:3374507
PMID:10655550
Finite cell line Male GM1604, GM-1604, GM 1604, GM01604A CLO:CLO_0031549,
BioSample:SAMN00806965,
Coriell:GM01604,
Wikidata:Q54836941
CVCL_7325 2026-07-25 04:32:19 0
GM01612
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# GM01612, RRID:CVCL_JB63 Homo sapiens (Human) Niemann-Pick disease Finite cell line Male GM-1612 Coriell GM01612 Coriell:GM01612,
Wikidata:Q54836948
CVCL_JB63 2026-07-25 04:32:22 0
GM01643
 
Resource Report
Resource Website
Coriell Cat# GM01643, RRID:CVCL_5L43 Homo sapiens (Human) Tuberous sclerosis 1 Population: African American. Finite cell line Male GM-1643 Coriell GM01643 CLO:CLO_0031524,
BioSample:SAMN00807015,
Coriell:GM01643,
Wikidata:Q54836976
CVCL_5L43 2026-07-25 04:32:22 0
GM01578
 
Resource Report
Resource Website
Coriell Cat# GM01578, RRID:CVCL_2Z66 Homo sapiens (Human) Nevoid basal cell carcinoma syndrome Population: Caucasian. Transformed cell line Male GM-1578 Coriell GM01578 CLO:CLO_0031466,
BioSample:SAMN00806933,
Coriell:GM01578,
Wikidata:Q54836922
CVCL_2Z66 2026-07-25 04:32:21 0
GM01636
 
Resource Report
Resource Website
Coriell Cat# GM01636, RRID:CVCL_5L40 Homo sapiens (Human) Tuberous sclerosis 1 Population: African American. Transformed cell line Male GM-1636 Coriell GM01636 CLO:CLO_0031506,
BioSample:SAMN00807005,
Coriell:GM01636,
Wikidata:Q54836971
CVCL_5L40 2026-07-25 04:32:20 0
GM01606
 
Resource Report
Resource Website
RRID:CVCL_F266 Homo sapiens (Human) Wolman disease PMID:6782865 Finite cell line Female GM-1606, GM 1606, GM01606A CLO:CLO_0003520,
CLO:CLO_0031564,
CLDB:cl1487,
Coriell:GM01606,
Wikidata:Q54836943
CVCL_F266 2026-07-25 04:32:21 0
GM01609
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# GM01609, RRID:CVCL_JB87 Homo sapiens (Human) Wolfram syndrome Finite cell line Female GM-1609 Coriell GM01609 Coriell:GM01609,
Wikidata:Q54836945
CVCL_JB87 2026-07-25 04:32:20 0
GM01680
 
Resource Report
Resource Website
RRID:CVCL_7332 Homo sapiens (Human) Population: Caucasian. PMID:3860870
PMID:19896956
PMID:30567591
Finite cell line Female GM1680, GM-1680, GM 1680, GM01680A CLO:CLO_0030963,
BioSample:SAMN00807069,
Coriell:GM01680,
GEO:GSM3124666,
Wikidata:Q54837012
CVCL_7332 2026-07-25 04:32:23 0
GM01701
 
Resource Report
Resource Website
Coriell Cat# GM01701, RRID:CVCL_1D25 Homo sapiens (Human) Population: Caucasian. Finite cell line Male GM-1701 Coriell GM01701 CLO:CLO_0030972,
BioSample:SAMN00807085,
Coriell:GM01701,
Wikidata:Q54837021
CVCL_1D25 2026-07-25 04:32:22 0
GM01700
 
Resource Report
Resource Website
Coriell Cat# GM01700, RRID:CVCL_1D22 Homo sapiens (Human) Karyotypic information: 46,XY,t(21;22)(p12;2q11.2).arr(1-22)x2,(XY)x1 (Coriell=GM01700). PMID:23665875 Finite cell line Male GM-1700 Coriell GM01700 CLO:CLO_0030973,
Coriell:GM01700,
Wikidata:Q54837020
CVCL_1D22 2026-07-25 04:32:21 0
GM01672
 
Resource Report
Resource Website
Coriell Cat# GM01672, RRID:CVCL_1R60 Homo sapiens (Human) Triploidy syndrome Karyotypic information: 69,XXY (Coriell=GM01672)., Population: Caucasian. PMID:6156493 Finite cell line Male GM-1672, GM 1672 Coriell GM01672 CLO:CLO_0030952,
BioSample:SAMN00807057,
Coriell:GM01672,
Wikidata:Q54837002
CVCL_1R60 2026-07-25 04:32:21 0
GM01708
 
Resource Report
Resource Website
Discontinued
RRID:CVCL_L959 Homo sapiens (Human) Population: Caucasian. Finite cell line Male GM-1708, GM-1010, GM01010 CLO:CLO_0030974,
BioSample:SAMN00807095,
Coriell:GM01010,
Coriell:GM01708,
Wikidata:Q54837027
CVCL_L959 2026-07-25 04:32:22 0
GM01665
 
Resource Report
Resource Website
Coriell Cat# GM01665, RRID:CVCL_0Q01 Homo sapiens (Human) Karyotypic information: 46,XX,t(12;21)(12qter->12p11::21p11->21pter;21qter->21p11::12p11->12pter) (Coriell=GM01665)., Population: Caucasian. Finite cell line Female GM-1665 Coriell GM01665 CLO:CLO_0030955,
BioSample:SAMN00807053,
Coriell:GM01665,
Wikidata:Q54836998
CVCL_0Q01 2026-07-25 04:32:21 0
GM01657
 
Resource Report
Resource Website
Coriell Cat# GM01657, RRID:CVCL_2Z68 Homo sapiens (Human) Nevoid basal cell carcinoma syndrome Population: Caucasian. Finite cell line Male GM-1657 Coriell GM01657 CLO:CLO_0030945,
BioSample:SAMN00807037,
Coriell:GM01657,
Wikidata:Q54836989
CVCL_2Z68 2026-07-25 04:32:22 0
GM01718
 
Resource Report
Resource Website
RRID:CVCL_9R63 Homo sapiens (Human) Neuraminidase deficiency PMID:9054950 Finite cell line Female GM-1718, GM01718A, GM1718A CLO:CLO_0030984,
BioSample:SAMN00807105,
Coriell:GM01718,
Wikidata:Q54837032
CVCL_9R63 2026-07-25 04:32:22 0
GM01709
 
Resource Report
Resource Website
RRID:CVCL_X252 Homo sapiens (Human) Gonadal dysgenesis Population: Caucasian. PMID:6661932
PMID:23665875
Finite cell line Sex ambiguous GM-1709, GM 1709 CLO:CLO_0030969,
BioSample:SAMN00807097,
Coriell:GM01709,
Wikidata:Q54837028
CVCL_X252 2026-07-25 04:32:22 0
GM01727
 
Resource Report
Resource Website
Coriell Cat# GM01727, RRID:CVCL_X083 Homo sapiens (Human) Karyotypic information: 46,XY,del(18)(qter>p11) (Coriell=GM01727)., Population: Caucasian. PMID:6617268
PMID:6661932
Finite cell line Male GM-1727, GM 1727 Coriell GM01727 CLO:CLO_0030998,
BioSample:SAMN00807119,
Coriell:GM01727,
Wikidata:Q54837041
CVCL_X083 2026-07-25 04:32:22 0
GM01736
 
Resource Report
Resource Website
Coriell Cat# GM01736, RRID:CVCL_1F09 Homo sapiens (Human) Xeroderma pigmentosum, complementation group C Population: Caucasian. Finite cell line Female GM-1736, GM1736 Coriell GM01736 CLO:CLO_0030994,
BioSample:SAMN00807123,
Coriell:GM01736,
Wikidata:Q54837044
CVCL_1F09 2026-07-25 04:32:22 0
GM01706
 
Resource Report
Resource Website
Discontinued
Coriell Cat# GM01706, RRID:CVCL_7334 Homo sapiens (Human) Population: Caucasian. PMID:30567591 Finite cell line Female GM1706, GM-1706, GM 1706, GM01706A, GM1706A, GM00237, GM0237 Coriell GM01706 CLO:CLO_0030976,
BioSample:SAMN00807091,
Coriell:GM00237,
Coriell:GM01706,
GEO:GSM3124688,
Wikidata:Q54837025
CVCL_7334 2026-07-25 04:32:22 0
GM01742
 
Resource Report
Resource Website
Discontinued
RRID:CVCL_CX27 Homo sapiens (Human) I-cell disease Finite cell line Female GM-1742 Coriell:GM01742,
Wikidata:Q54837054
CVCL_CX27 2026-07-25 04:32:25 0

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