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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
GM09214
 
Resource Report
Resource Website
Coriell Cat# GM09214, RRID:CVCL_4H96 Homo sapiens (Human) Population: Caucasian; Amish., Part of: Old Order Amish Major Affective Disorder cell line collection. Transformed cell line Male Coriell GM09214 CLO:CLO_0010689,
Coriell:GM09214,
Wikidata:Q54843616
CVCL_4H96 2026-07-25 04:34:04 0
GM09217
 
Resource Report
Resource Website
RRID:CVCL_AA70 Homo sapiens (Human) Crigler-Najjar syndrome Transformed cell line Female CLO:CLO_0010684,
BioSample:SAMN00798589,
Coriell:GM09217,
Wikidata:Q54843619
CVCL_AA70 2026-07-25 04:34:03 0
GM09238
 
Resource Report
Resource Website
Coriell Cat# GM09238, RRID:CVCL_AY31 Homo sapiens (Human) Population: African American. PMID:1672039 Transformed cell line Female GM9238 Coriell GM09238 CLO:CLO_0012040,
Coriell:GM09238,
Wikidata:Q54843631
CVCL_AY31 2026-07-25 04:34:03 0
GM09138
 
Resource Report
Resource Website
RRID:CVCL_4H91 Homo sapiens (Human) Manic bipolar affective disorder Population: Caucasian; Amish., Part of: Old Order Amish Major Affective Disorder cell line collection. Transformed cell line Male GM9138 CLO:CLO_0010630,
Coriell:GM09138,
Wikidata:Q54843597
CVCL_4H91 2026-07-25 04:34:02 0
GM09192
 
Resource Report
Resource Website
Coriell Cat# GM09192, RRID:CVCL_2T61 Homo sapiens (Human) Transformed cell line Female Coriell GM09192 CLO:CLO_0010633,
BioSample:SAMN00798577,
Coriell:GM09192,
Wikidata:Q54843604
CVCL_2T61 2026-07-25 04:34:03 0
GM09093
 
Resource Report
Resource Website
RRID:CVCL_4F61 Homo sapiens (Human) Very long-chain acyl-CoA dehydrogenase deficiency Population: Caucasian. Finite cell line Female CLO:CLO_0010652,
BioSample:SAMN00798541,
Coriell:GM09093,
Wikidata:Q54843582
CVCL_4F61 2026-07-25 04:34:02 0
GM09118
 
Resource Report
Resource Website
RRID:CVCL_CY63 Homo sapiens (Human) Gyrate atrophy Population: Caucasian. Finite cell line Female GM09118A CLO:CLO_0010621,
BioSample:SAMN00798561,
Coriell:GM09118,
Wikidata:Q54843594
CVCL_CY63 2026-07-25 04:34:02 0
GM09230
 
Resource Report
Resource Website
Coriell Cat# GM09230, RRID:CVCL_1L31 Homo sapiens (Human) Menkes disease Population: Caucasian. Finite cell line Male Coriell GM09230 CLO:CLO_0012009,
BioSample:SAMN00798595,
Coriell:GM09230,
Wikidata:Q54843622
CVCL_1L31 2026-07-25 04:34:03 0
GM09215
 
Resource Report
Resource Website
Coriell Cat# GM09215, RRID:CVCL_4H97 Homo sapiens (Human) Population: Caucasian; Amish., Part of: Old Order Amish Major Affective Disorder cell line collection. Transformed cell line Male Coriell GM09215 CLO:CLO_0010686,
Coriell:GM09215,
Wikidata:Q54843617
CVCL_4H97 2026-07-25 04:34:03 0
GM09195
 
Resource Report
Resource Website
RRID:CVCL_1L30 Homo sapiens (Human) Population: Caucasian. Transformed cell line Female CLO:CLO_0010638,
BioSample:SAMN00798581,
Coriell:GM09195,
Wikidata:Q54843607
CVCL_1L30 2026-07-25 04:34:02 0
GM09099
 
Resource Report
Resource Website
RRID:CVCL_N099 Homo sapiens (Human) Population: Caucasian., Part of: Human variation panel., Part of: Genetic Testing Reference Material (GeT-RM) samples. PMID:20889555
PMID:29959025
Transformed cell line Female GM17286 CLO:CLO_0010653,
CLO:CLO_0013086,
BioSample:SAMN00798543,
Coriell:GM09099,
Coriell:GM17286,
GEO:GSM569739,
GEO:GSM596350,
GEO:GSM596768,
GEO:GSM924888,
Wikidata:Q54843583
CVCL_N099 2026-07-25 04:34:02 0
GM09100
 
Resource Report
Resource Website
RRID:CVCL_AA69 Homo sapiens (Human) Multiple endocrine neoplasia type 2 Transformed cell line Female CLO:CLO_0010654,
BioSample:SAMN00798545,
Coriell:GM09100,
Wikidata:Q54843584
CVCL_AA69 2026-07-25 04:34:02 0
GM09099
 
Resource Report
Resource Website
Coriell Cat# GM09099, RRID:CVCL_N099 Homo sapiens (Human) Population: Caucasian., Part of: Human variation panel., Part of: Genetic Testing Reference Material (GeT-RM) samples. PMID:20889555
PMID:29959025
Transformed cell line Female GM17286 Coriell GM09099 CLO:CLO_0010653,
CLO:CLO_0013086,
BioSample:SAMN00798543,
Coriell:GM09099,
Coriell:GM17286,
GEO:GSM569739,
GEO:GSM596350,
GEO:GSM596768,
GEO:GSM924888,
Wikidata:Q54843583
CVCL_N099 2026-07-25 04:34:02 0
GM09189
 
Resource Report
Resource Website
RRID:CVCL_5N97 Homo sapiens (Human) Prader-Willi syndrome PMID:23665875 Transformed cell line Female CLO:CLO_0010631,
BioSample:SAMN00798575,
Coriell:GM09189,
Wikidata:Q54843603
CVCL_5N97 2026-07-25 04:34:03 0
GM09246
 
Resource Report
Resource Website
Coriell Cat# GM09246, RRID:CVCL_1L53 Homo sapiens (Human) Population: Caucasian; German/Swiss. Finite cell line Female GM09246A, GM09246B Coriell GM09246 CLO:CLO_0012033,
Coriell:GM09246,
Wikidata:Q54843633
CVCL_1L53 2026-07-25 04:34:03 0
GM09230
 
Resource Report
Resource Website
RRID:CVCL_1L31 Homo sapiens (Human) Menkes disease Population: Caucasian. Finite cell line Male CLO:CLO_0012009,
BioSample:SAMN00798595,
Coriell:GM09230,
Wikidata:Q54843622
CVCL_1L31 2026-07-25 04:34:04 0
GM09247
 
Resource Report
Resource Website
RRID:CVCL_1L54 Homo sapiens (Human) Population: Caucasian; German/Swiss. Finite cell line Male GM09247B CLO:CLO_0012031,
Coriell:GM09247,
Wikidata:Q54843634
CVCL_1L54 2026-07-25 04:34:03 0
GM09099
 
Resource Report
Resource Website
Coriell Cat# GM17286, RRID:CVCL_N099 Homo sapiens (Human) Population: Caucasian., Part of: Human variation panel., Part of: Genetic Testing Reference Material (GeT-RM) samples. PMID:20889555
PMID:29959025
Transformed cell line Female GM17286 Coriell GM17286 CLO:CLO_0010653,
CLO:CLO_0013086,
BioSample:SAMN00798543,
Coriell:GM09099,
Coriell:GM17286,
GEO:GSM569739,
GEO:GSM596350,
GEO:GSM596768,
GEO:GSM924888,
Wikidata:Q54843583
CVCL_N099 2026-07-25 04:34:02 0
GM09210
 
Resource Report
Resource Website
Coriell Cat# GM09210, RRID:CVCL_5U24 Homo sapiens (Human) Miller-Dieker syndrome Finite cell line Male Coriell GM09210 CLO:CLO_0010688,
Coriell:GM09210,
Wikidata:Q54843612
CVCL_5U24 2026-07-25 04:34:03 0
GM09154
 
Resource Report
Resource Website
RRID:CVCL_Y574 Homo sapiens (Human) Infantile neuroaxonal dystrophy Population: Hispanic. Finite cell line Female CLO:CLO_0010624,
BioSample:SAMN00798573,
Coriell:GM09154,
Wikidata:Q54843602
CVCL_Y574 2026-07-25 04:34:02 0

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