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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
DD3503
 
Resource Report
Resource Website
ECACC Cat# 00021515, RRID:CVCL_9P81 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 00021515 ECACC:00021515,
Wikidata:Q54830769
CVCL_9P81 2026-07-25 04:30:15 0
DD3555
 
Resource Report
Resource Website
RRID:CVCL_9N29 Homo sapiens (Human) Karyotypic information: 45,XY,der(14;21)(q10;q10)mat (ECACC=00062022)., Part of: ECACC chromosomal abnormality collection. Finite cell line Male ECACC:00062022,
Wikidata:Q54830804
CVCL_9N29 2026-07-25 04:30:16 0
DD3483
 
Resource Report
Resource Website
ECACC Cat# 99120702, RRID:CVCL_9N14 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 99120702 ECACC:99120702,
Wikidata:Q54830764
CVCL_9N14 2026-07-25 04:30:15 0
DD3506
 
Resource Report
Resource Website
RRID:CVCL_9P83 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC:00021518,
Wikidata:Q54830771
CVCL_9P83 2026-07-25 04:30:15 0
DD3517
 
Resource Report
Resource Website
ECACC Cat# 00030115, RRID:CVCL_9N17 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 00030115 ECACC:00030115,
Wikidata:Q54830778
CVCL_9N17 2026-07-25 04:30:15 0
DD3506
 
Resource Report
Resource Website
ECACC Cat# 00021518, RRID:CVCL_9P83 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 00021518 ECACC:00021518,
Wikidata:Q54830771
CVCL_9P83 2026-07-25 04:30:15 0
DD3521
 
Resource Report
Resource Website
ECACC Cat# 00031406, RRID:CVCL_9P90 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 00031406 ECACC:00031406,
Wikidata:Q54830785
CVCL_9P90 2026-07-25 04:30:16 0
DD3560
 
Resource Report
Resource Website
ECACC Cat# 00070601, RRID:CVCL_9N30 Homo sapiens (Human) Karyotypic information: 46,XY,inv(6)(p24;q16.2); de novo (ECACC=00070601)., Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 00070601 ECACC:00070601,
Wikidata:Q54830807
CVCL_9N30 2026-07-25 04:30:16 0
DD3522
 
Resource Report
Resource Website
RRID:CVCL_9N18 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC:00031407,
Wikidata:Q54830786
CVCL_9N18 2026-07-25 04:30:15 0
DD3536
 
Resource Report
Resource Website
RRID:CVCL_9N21 Homo sapiens (Human) Pulmonary stenosis Part of: ECACC chromosomal abnormality collection. Finite cell line Female ECACC:00042707,
Wikidata:Q54830792
CVCL_9N21 2026-07-25 04:30:16 0
DD3546
 
Resource Report
Resource Website
RRID:CVCL_9P94 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Finite cell line Female ECACC:00051011,
Wikidata:Q54830799
CVCL_9P94 2026-07-25 04:30:16 0
DD3556
 
Resource Report
Resource Website
RRID:CVCL_9P98 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC:00062234,
Wikidata:Q54830805
CVCL_9P98 2026-07-25 04:30:16 0
DD3513
 
Resource Report
Resource Website
ECACC Cat# 00022828, RRID:CVCL_9N16 Homo sapiens (Human) Karyotypic information: 46,XY,t(6;9)(q25.1;p24.1)mat (ECACC=00022828)., Part of: ECACC chromosomal abnormality collection. Finite cell line Male ECACC 00022828 ECACC:00022828,
Wikidata:Q54830776
CVCL_9N16 2026-07-25 04:30:15 0
DD3547
 
Resource Report
Resource Website
RRID:CVCL_9N28 Homo sapiens (Human) Karyotypic information: 46,XY,t(7;21)(q22.1;q21.2)pat (ECACC=00051012)., Part of: ECACC chromosomal abnormality collection. Finite cell line Male ECACC:00051012,
Wikidata:Q54830800
CVCL_9N28 2026-07-25 04:30:16 0
DD3545
 
Resource Report
Resource Website
ECACC Cat# 00050803, RRID:CVCL_9N27 Homo sapiens (Human) Karyotypic information: 46,XY,t(15;17)(p10;p10)mat (ECACC=00050803)., Part of: ECACC chromosomal abnormality collection. Finite cell line Male ECACC 00050803 ECACC:00050803,
Wikidata:Q54830798
CVCL_9N27 2026-07-25 04:30:16 0
DD3502
 
Resource Report
Resource Website
ECACC Cat# 00021514, RRID:CVCL_9P80 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 00021514 ECACC:00021514,
Wikidata:Q54830768
CVCL_9P80 2026-07-25 04:30:15 0
DD3508
 
Resource Report
Resource Website
ECACC Cat# 00021614, RRID:CVCL_9P84 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 00021614 ECACC:00021614,
Wikidata:Q54830772
CVCL_9P84 2026-07-25 04:30:15 0
DD3481
 
Resource Report
Resource Website
RRID:CVCL_9N12 Homo sapiens (Human) Turner syndrome Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC:99120302,
Wikidata:Q54830762
CVCL_9N12 2026-07-25 04:30:15 0
DD3517
 
Resource Report
Resource Website
RRID:CVCL_9N17 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC:00030115,
Wikidata:Q54830778
CVCL_9N17 2026-07-25 04:30:15 0
DD3466
 
Resource Report
Resource Website
RRID:CVCL_9P72 Homo sapiens (Human) Karyotypic information: 46,XX,t(10;11)(q24.?31;p15.5); de novo (ECACC=99092423)., Part of: ECACC chromosomal abnormality collection. Finite cell line Female ECACC:99092423,
Wikidata:Q54830755
CVCL_9P72 2026-07-25 04:30:15 0

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