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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
GM10609
 
Resource Report
Resource Website
RRID:CVCL_0R05 Homo sapiens (Human) Greig syndrome PMID:23665875 Transformed cell line Female GM10609A CLO:CLO_0024279,
Coriell:GM10609,
Wikidata:Q54844552
CVCL_0R05 2026-08-15 04:31:07 0
GM10511
 
Resource Report
Resource Website
Coriell Cat# GM10511, RRID:CVCL_4J01 Homo sapiens (Human) Population: Caucasian; Amish., Part of: Old Order Amish Major Affective Disorder cell line collection. Transformed cell line Male Coriell GM10511 CLO:CLO_0024277,
Coriell:GM10511,
Wikidata:Q54844511
CVCL_4J01 2026-08-15 04:31:06 0
GM10614
 
Resource Report
Resource Website
Coriell Cat# GM10614, RRID:CVCL_0Q14 Homo sapiens (Human) Transformed cell line Female Coriell GM10614 CLO:CLO_0024542,
BioSample:SAMN00800103,
Coriell:GM10614,
Wikidata:Q54844554
CVCL_0Q14 2026-08-15 04:31:07 0
GM10636
 
Resource Report
Resource Website
RRID:CVCL_5P23 Homo sapiens (Human) PMID:23665875 Transformed cell line Female CLO:CLO_0024562,
BioSample:SAMN00800120,
Coriell:GM10636,
Wikidata:Q54844566
CVCL_5P23 2026-08-15 04:31:07 0
GM10634
 
Resource Report
Resource Website
RRID:CVCL_FA39 Homo sapiens (Human) D-glyceric aciduria Population: Caucasian. Finite cell line Male CLO:CLO_0024564,
BioSample:SAMN00800116,
Coriell:GM10634,
Wikidata:Q54844564
CVCL_FA39 2026-08-15 04:31:07 0
GM10565
 
Resource Report
Resource Website
Coriell Cat# GM10565, RRID:CVCL_5P19 Homo sapiens (Human) Hypogonadotropic hypogonadism with anosmia PMID:23665875 Transformed cell line Male Coriell GM10565 CLO:CLO_0024289,
BioSample:SAMN00800089,
Coriell:GM10565,
Wikidata:Q54844544
CVCL_5P19 2026-08-15 04:31:07 0
GM10647
 
Resource Report
Resource Website
RRID:CVCL_N152 Homo sapiens (Human) Population: Caucasian., Part of: Human variation panel., Part of: Genetic Testing Reference Material (GeT-RM) samples. PMID:1897572
PMID:20889555
PMID:29959025
Transformed cell line Male GM17295 CLO:CLO_0013127,
CLO:CLO_0024575,
BioSample:SAMN00800128,
Coriell:GM10647,
Coriell:GM17295,
GEO:GSM569743,
GEO:GSM596359,
GEO:GSM596816,
GEO:GSM924897,
Wikidata:Q54844570
CVCL_N152 2026-08-15 04:31:07 0
GM10534
 
Resource Report
Resource Website
RRID:CVCL_AM49 Homo sapiens (Human) Population: Caucasian., Part of: Retinitis Pigmentosa Foundation Collection. Transformed cell line Female GM10534A CLO:CLO_0024262,
BioSample:SAMN00800075,
Coriell:GM10534,
Wikidata:Q54844531
CVCL_AM49 2026-08-15 04:31:06 0
GM10525
 
Resource Report
Resource Website
RRID:CVCL_AM41 Homo sapiens (Human) Retinitis pigmentosa Population: Caucasian., Part of: Retinitis Pigmentosa Foundation Collection. Transformed cell line Male CLO:CLO_0024267,
BioSample:SAMN00800061,
Coriell:GM10525,
Wikidata:Q54844523
CVCL_AM41 2026-08-15 04:31:06 0
GM10624
 
Resource Report
Resource Website
Coriell Cat# GM10624, RRID:CVCL_DD84 Homo sapiens (Human) Hereditary optic atrophy Population: Jewish. Transformed cell line Male Coriell GM10624 CLO:CLO_0024550,
BioSample:SAMN00800107,
Coriell:GM10624,
Wikidata:Q54844560
CVCL_DD84 2026-08-15 04:31:07 0
GM10595
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_YP32 Homo sapiens (Human) Xeroderma pigmentosum, complementation group D PMID:1372108 Transformed cell line Male GM 10595 Coriell:GM10595,
Wikidata:Q93809863
cvcl_l754 CVCL_YP32 2026-08-15 04:31:07 0
GM10543
 
Resource Report
Resource Website
Coriell Cat# GM17391, RRID:CVCL_N150 Homo sapiens (Human) Population: Pacific., Part of: Yale-Stanford Collection from NIGMS Human Genetic Cell Repository., Part of: Human variation panel. Transformed cell line Female GM10543A, GM17391, JK975 Coriell GM17391 CLO:CLO_0012244,
CLO:CLO_0024292,
Coriell:GM10543,
Coriell:GM17391,
Wikidata:Q54844540
CVCL_N150 2026-08-15 04:31:06 0
GM10541
 
Resource Report
Resource Website
Coriell Cat# GM10541, RRID:CVCL_N148 Homo sapiens (Human) Population: Pacific., Part of: Yale-Stanford Collection from NIGMS Human Genetic Cell Repository., Part of: Human variation panel. PMID:14583597 Transformed cell line Male GM10541A, GM17389, JK971 Coriell GM10541 CLO:CLO_0012177,
CLO:CLO_0024294,
Coriell:GM10541,
Coriell:GM17389,
Wikidata:Q54844538
CVCL_N148 2026-08-15 04:31:06 0
GM10552
 
Resource Report
Resource Website
RRID:CVCL_V345 Homo sapiens (Human) Bernard-Soulier syndrome Transformed cell line Female CLO:CLO_0024293,
BioSample:SAMN00800083,
Coriell:GM10552,
Wikidata:Q54844541
CVCL_V345 2026-08-15 04:31:06 0
GM10535
 
Resource Report
Resource Website
RRID:CVCL_AM50 Homo sapiens (Human) Retinitis pigmentosa Population: Caucasian., Part of: Retinitis Pigmentosa Foundation Collection. Transformed cell line Female CLO:CLO_0024263,
BioSample:SAMN00800077,
Coriell:GM10535,
Wikidata:Q54844532
CVCL_AM50 2026-08-15 04:31:06 0
GM10559
 
Resource Report
Resource Website
RRID:CVCL_0Q12 Homo sapiens (Human) Marfan syndrome Transformed cell line Female CLO:CLO_0024291,
BioSample:SAMN00800087,
Coriell:GM10559,
Wikidata:Q54844543
CVCL_0Q12 2026-08-15 04:31:07 0
GM10568
 
Resource Report
Resource Website
RRID:CVCL_5P20 Homo sapiens (Human) Dyggve-Melchior-Clausen syndrome Population: Pakistani. Finite cell line Male CLO:CLO_0024287,
BioSample:SAMN00800093,
Coriell:GM10568,
Wikidata:Q54844546
CVCL_5P20 2026-08-15 04:31:07 0
GM10635
 
Resource Report
Resource Website
Coriell Cat# GM10635, RRID:CVCL_2T88 Homo sapiens (Human) Karyotypic information: 46,XY,t(15;19)(15pter->15q13::19q13.3->19qter;19pter->19q13.3::15q13->15qter) (Coriell=GM10635)., Population: Caucasian. Finite cell line Male Coriell GM10635 CLO:CLO_0024563,
BioSample:SAMN00800118,
Coriell:GM10635,
Wikidata:Q54844565
CVCL_2T88 2026-08-15 04:31:07 0
GM10628
 
Resource Report
Resource Website
RRID:CVCL_0Q16 Homo sapiens (Human) Transformed cell line Male GM10628A CLO:CLO_0024552,
BioSample:SAMN00800114,
Coriell:GM10628,
Wikidata:Q54844563
CVCL_0Q16 2026-08-15 04:31:07 0
GM10540
 
Resource Report
Resource Website
Coriell Cat# GM17388, RRID:CVCL_7502 Homo sapiens (Human) Population: Pacific., Part of: Yale-Stanford Collection from NIGMS Human Genetic Cell Repository., Part of: Human variation panel. PMID:14583597 Transformed cell line Male GM17388, JK965 Coriell GM17388 CLO:CLO_0012179,
CLO:CLO_0024297,
Coriell:GM10540,
Coriell:GM17388,
Wikidata:Q54844537
CVCL_7502 2026-08-15 04:31:06 0

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