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6,967 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
DD3028
 
Resource Report
Resource Website
ECACC Cat# 97122203, RRID:CVCL_9N71 Homo sapiens (Human) Developmental delay Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 97122203 ECACC:97122203,
Wikidata:Q54830526
CVCL_9N71 2026-09-12 05:29:56 0
DD2998
 
Resource Report
Resource Website
ECACC Cat# 97102402, RRID:CVCL_AR42 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 97102402 ECACC:97102402,
Wikidata:Q54830507
CVCL_AR42 2026-09-12 05:29:56 0
DD3027
 
Resource Report
Resource Website
ECACC Cat# 97121905, RRID:CVCL_9N70 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 97121905 ECACC:97121905,
Wikidata:Q54830522
CVCL_9N70 2026-09-12 05:29:56 0
DD3044
 
Resource Report
Resource Website
ECACC Cat# 98011910, RRID:CVCL_9N73 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 98011910 ECACC:98011910,
Wikidata:Q54830534
CVCL_9N73 2026-09-12 05:29:57 0
DD3005
 
Resource Report
Resource Website
ECACC Cat# 97110613, RRID:CVCL_9N66 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 97110613 ECACC:97110613,
Wikidata:Q54830511
CVCL_9N66 2026-09-12 05:29:56 0
DD2973
 
Resource Report
Resource Website
ECACC Cat# 97090505, RRID:CVCL_9L77 Homo sapiens (Human) Turner syndrome Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 97090505 ECACC:97090505,
Wikidata:Q54830494
CVCL_9L77 2026-09-12 05:29:55 0
DD3025
 
Resource Report
Resource Website
ECACC Cat# 97121508, RRID:CVCL_9N68 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 97121508 ECACC:97121508,
Wikidata:Q54830520
CVCL_9N68 2026-09-12 05:29:56 0
DD0830
 
Resource Report
Resource Website
ECACC Cat# 92062586, RRID:CVCL_9C48 Homo sapiens (Human) 49,XXXXY syndrome Karyotypic information: 49,XXXXY (ECACC=92062586)., Part of: ECACC chromosomal abnormality collection. Finite cell line Male ECACC 92062586 ECACC:92062586,
Wikidata:Q54829357
CVCL_9C48 2026-09-12 05:29:26 0
DD0811
 
Resource Report
Resource Website
ECACC Cat# 92062302, RRID:CVCL_9C31 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 92062302 ECACC:92062302,
Wikidata:Q54829338
CVCL_9C31 2026-09-12 05:29:25 0
DD0818
 
Resource Report
Resource Website
ECACC Cat# 92062574, RRID:CVCL_9C36 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 92062574 ECACC:92062574,
Wikidata:Q54829344
CVCL_9C36 2026-09-12 05:29:25 0
DD0821
 
Resource Report
Resource Website
ECACC Cat# 92062577, RRID:CVCL_9C39 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 92062577 ECACC:92062577,
Wikidata:Q54829347
CVCL_9C39 2026-09-12 05:29:25 0
DD0841
 
Resource Report
Resource Website
ECACC Cat# 92070314, RRID:CVCL_9C55 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 92070314 ECACC:92070314,
Wikidata:Q54829379
CVCL_9C55 2026-09-12 05:29:26 0
DD0790
 
Resource Report
Resource Website
ECACC Cat# 92060528, RRID:CVCL_9C14 Homo sapiens (Human) Karyotypic information: 47,XX+?i(18p) (ECACC=92060528)., Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 92060528 ECACC:92060528,
Wikidata:Q54829317
CVCL_9C14 2026-09-12 05:29:25 0
DD0823
 
Resource Report
Resource Website
ECACC Cat# 92062579, RRID:CVCL_9C41 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 92062579 ECACC:92062579,
Wikidata:Q54829349
CVCL_9C41 2026-09-12 05:29:26 0
DD0836
 
Resource Report
Resource Website
ECACC Cat# 92070220, RRID:CVCL_9C52 Homo sapiens (Human) Trisomy 18 Karyotypic information: 47,XY,+18 (ECACC=92070220)., Part of: ECACC chromosomal abnormality collection. Finite cell line Female ECACC 92070220 ECACC:92070220,
Wikidata:Q54829376
CVCL_9C52 2026-09-12 05:29:26 0
DD0817
 
Resource Report
Resource Website
ECACC Cat# 92062572, RRID:CVCL_9C35 Homo sapiens (Human) Karyotypic information: 46,XX; 47,XY+mar(16); de novo (ECACC=92062572)., Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 92062572 ECACC:92062572,
Wikidata:Q54829342
CVCL_9C35 2026-09-12 05:29:25 0
DD0809
 
Resource Report
Resource Website
ECACC Cat# 92062201, RRID:CVCL_9C29 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 92062201 ECACC:92062201,
Wikidata:Q54829335
CVCL_9C29 2026-09-12 05:29:25 0
DD0796
 
Resource Report
Resource Website
ECACC Cat# 92061002, RRID:CVCL_9C18 Homo sapiens (Human) Karyotypic information: 46,XX,r(18)(p11;q23) (ECACC=92061002)., Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 92061002 ECACC:92061002,
Wikidata:Q54829322
CVCL_9C18 2026-09-12 05:29:25 0
DD0839
 
Resource Report
Resource Website
ECACC Cat# 92070312, RRID:CVCL_9C53 Homo sapiens (Human) Karyotypic information: 46,XY,t(12;13)(q24.31;q32.3); de novo (ECACC=92070312)., Part of: ECACC chromosomal abnormality collection. Finite cell line Male ECACC 92070312 ECACC:92070312,
Wikidata:Q54829377
CVCL_9C53 2026-09-12 05:29:26 0
DD0797
 
Resource Report
Resource Website
ECACC Cat# 92061213, RRID:CVCL_9C19 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 92061213 ECACC:92061213,
Wikidata:Q54829323
CVCL_9C19 2026-09-12 05:29:25 0

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