最新の情報は下記 URL でご確認いただけます (外部サイトへ移動します) 。
https://ftp.ncbi.nlm.nih.gov/pub/clinvar/tab_delimited/archive/
表のタイトル行が青色の項目は、クリックすることでソートすることができます。
| Type | Name | Gene Symbol | Clinical Significance | Chromosome | Start | Stop | Reference Allele | Alternate Allele | Review Status | Other IDs |
|---|---|---|---|---|---|---|---|---|---|---|
| (GRCh37) | ||||||||||
| single nucleotide variant | NM_000384.3(APOB):c.1830-1G>A | APOB | Pathogenic | 2 | 21250938 | 21250938 | C | T | criteria provided, multiple submitters, no conflicts | ClinGen:CA346013946 |
| Deletion | NC_000019.10:g.(?_11100203)_(11102806_?)del | LDLR | Pathogenic | 19 | 11210879 | 11213482 | na | na | criteria provided, single submitter | - |
| Duplication | NC_000019.9:g.(?_11215876)_(11222335_?)dup | LDLR | Likely pathogenic | 19 | 11215876 | 11222335 | na | na | criteria provided, single submitter | - |
| Duplication | NC_000019.9:g.(?_11210879)_(11222335_?)dup | LDLR | Pathogenic | 19 | 11210879 | 11222335 | na | na | criteria provided, single submitter | - |
| Indel | NM_000527.5(LDLR):c.1811delinsCT (p.Arg604fs) | LDLR | Pathogenic | 19 | 11227640 | 11227640 | G | CT | criteria provided, single submitter | ClinGen:CA658658768 |
| single nucleotide variant | NM_000384.3(APOB):c.9176G>A (p.Arg3059His) | APOB | Pathogenic | 2 | 21230564 | 21230564 | C | T | criteria provided, single submitter | ClinGen:CA066340 |
| single nucleotide variant | NM_000163.5(GHR):c.945G>A (p.Lys315=) | GHR | Pathogenic | 5 | 42718223 | 42718223 | G | A | criteria provided, single submitter | ClinGen:CA443805565 |
| single nucleotide variant | NM_000527.5(LDLR):c.1186+2T>G | LDLR | Likely pathogenic | 19 | 11222317 | 11222317 | T | G | criteria provided, single submitter | ClinGen:CA032579 |
| Duplication | NM_000527.5(LDLR):c.1867dup (p.Ile623fs) | LDLR | Pathogenic/Likely pathogenic | 19 | 11230788 | 11230789 | T | TA | criteria provided, multiple submitters, no conflicts | ClinGen:CA658684220 |
| Deletion | NM_000527.5(LDLR):c.2233_2291del (p.Pro745fs) | LDLR | Pathogenic/Likely pathogenic | 19 | 11233942 | 11234000 | ACCTGTTCCCGACACCTCCCGGCTGCCTGGGGCCACCCCTGGGCTCACCACGGTGGAGAT | A | criteria provided, multiple submitters, no conflicts | ClinGen:CA658799127 |