Links from Gene
Items: 1 to 20 of 11430
1.
rs1491520272 [Homo sapiens]- Variant type:
- DEL
- Alleles:
- GT>-
[Show Flanks]
- Chromosome:
- 6:158872672
(GRCh38)
6:159293704
(GRCh37)
- Canonical SPDI:
- NC_000006.12:158872671:GT:
- Gene:
- LINC02901 (Varview)
- Functional Consequence:
- intron_variant,genic_upstream_transcript_variant
- Validated:
- by frequency,by alfa
- MAF:
-=0./0
(
ALFA)
-=0.000009/1
(GnomAD)
- HGVS:
2.
rs1491507153 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- CT>-
[Show Flanks]
- Chromosome:
- 6:158878850
(GRCh38)
6:159299882
(GRCh37)
- Canonical SPDI:
- NC_000006.12:158878846:TCTCT:TCT
- Gene:
- LINC02901 (Varview)
- Functional Consequence:
- intron_variant,genic_upstream_transcript_variant
- Validated:
- by frequency,by alfa
- MAF:
TCT=0./0
(
ALFA)
-=0.000026/7
(TOPMED)
- HGVS:
3.
rs1491498121 has merged into rs397885802 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- AAAAAAAA>-,A,AAA,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAAAAAA
[Show Flanks]
- Chromosome:
- 6:158882803
(GRCh38)
6:159303835
(GRCh37)
- Canonical SPDI:
- NC_000006.12:158882792:AAAAAAAAAAAAAAAAAA:AAAAAAAAAA,NC_000006.12:158882792:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000006.12:158882792:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000006.12:158882792:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000006.12:158882792:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000006.12:158882792:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000006.12:158882792:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000006.12:158882792:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000006.12:158882792:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000006.12:158882792:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000006.12:158882792:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA
- Gene:
- LINC02901 (Varview)
- Functional Consequence:
- genic_upstream_transcript_variant,intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
AAAAAAAAAAA=0./0
(
ALFA)
-=0.3055/1530
(1000Genomes)
- HGVS:
NC_000006.12:g.158882803_158882810del, NC_000006.12:g.158882804_158882810del, NC_000006.12:g.158882806_158882810del, NC_000006.12:g.158882807_158882810del, NC_000006.12:g.158882808_158882810del, NC_000006.12:g.158882809_158882810del, NC_000006.12:g.158882810del, NC_000006.12:g.158882810dup, NC_000006.12:g.158882809_158882810dup, NC_000006.12:g.158882808_158882810dup, NC_000006.12:g.158882803_158882810dup, NC_000006.11:g.159303835_159303842del, NC_000006.11:g.159303836_159303842del, NC_000006.11:g.159303838_159303842del, NC_000006.11:g.159303839_159303842del, NC_000006.11:g.159303840_159303842del, NC_000006.11:g.159303841_159303842del, NC_000006.11:g.159303842del, NC_000006.11:g.159303842dup, NC_000006.11:g.159303841_159303842dup, NC_000006.11:g.159303840_159303842dup, NC_000006.11:g.159303835_159303842dup
4.
rs1491449194 has merged into rs545734114 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- TTTTTTTTTTT>-,TT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT
[Show Flanks]
- Chromosome:
- 6:158913316
(GRCh38)
6:159334348
(GRCh37)
- Canonical SPDI:
- NC_000006.12:158913307:TTTTTTTTTTTTTTTTTTT:TTTTTTTT,NC_000006.12:158913307:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000006.12:158913307:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000006.12:158913307:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000006.12:158913307:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000006.12:158913307:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000006.12:158913307:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000006.12:158913307:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000006.12:158913307:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000006.12:158913307:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000006.12:158913307:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000006.12:158913307:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:158913307:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:158913307:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:158913307:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:158913307:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:158913307:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:158913307:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:158913307:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- Validated:
- by frequency,by alfa,by cluster
- MAF:
TTTTTTTTTT=0./0
(
ALFA)
-=0.025/1
(GENOME_DK)
-=0.1893/948
(1000Genomes)
- HGVS:
NC_000006.12:g.158913316_158913326del, NC_000006.12:g.158913318_158913326del, NC_000006.12:g.158913320_158913326del, NC_000006.12:g.158913321_158913326del, NC_000006.12:g.158913322_158913326del, NC_000006.12:g.158913323_158913326del, NC_000006.12:g.158913324_158913326del, NC_000006.12:g.158913325_158913326del, NC_000006.12:g.158913326del, NC_000006.12:g.158913326dup, NC_000006.12:g.158913325_158913326dup, NC_000006.12:g.158913324_158913326dup, NC_000006.12:g.158913323_158913326dup, NC_000006.12:g.158913322_158913326dup, NC_000006.12:g.158913321_158913326dup, NC_000006.12:g.158913320_158913326dup, NC_000006.12:g.158913319_158913326dup, NC_000006.12:g.158913318_158913326dup, NC_000006.12:g.158913315_158913326dup, NC_000006.11:g.159334348_159334358del, NC_000006.11:g.159334350_159334358del, NC_000006.11:g.159334352_159334358del, NC_000006.11:g.159334353_159334358del, NC_000006.11:g.159334354_159334358del, NC_000006.11:g.159334355_159334358del, NC_000006.11:g.159334356_159334358del, NC_000006.11:g.159334357_159334358del, NC_000006.11:g.159334358del, NC_000006.11:g.159334358dup, NC_000006.11:g.159334357_159334358dup, NC_000006.11:g.159334356_159334358dup, NC_000006.11:g.159334355_159334358dup, NC_000006.11:g.159334354_159334358dup, NC_000006.11:g.159334353_159334358dup, NC_000006.11:g.159334352_159334358dup, NC_000006.11:g.159334351_159334358dup, NC_000006.11:g.159334350_159334358dup, NC_000006.11:g.159334347_159334358dup
5.
rs1491415627 has merged into rs544283626 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- TTTTTTT>-,T,TTT,TTTT,TTTTT,TTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
[Show Flanks]
- Chromosome:
- 6:158872686
(GRCh38)
6:159293718
(GRCh37)
- Canonical SPDI:
- NC_000006.12:158872672:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000006.12:158872672:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000006.12:158872672:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000006.12:158872672:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000006.12:158872672:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000006.12:158872672:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000006.12:158872672:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000006.12:158872672:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:158872672:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:158872672:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:158872672:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- Gene:
- LINC02901 (Varview)
- Functional Consequence:
- genic_upstream_transcript_variant,intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
TTTTTTTTTTTTTTTT=0./0
(
ALFA)
-=0.4944/2476
(1000Genomes)
- HGVS:
NC_000006.12:g.158872686_158872692del, NC_000006.12:g.158872687_158872692del, NC_000006.12:g.158872689_158872692del, NC_000006.12:g.158872690_158872692del, NC_000006.12:g.158872691_158872692del, NC_000006.12:g.158872692del, NC_000006.12:g.158872692dup, NC_000006.12:g.158872691_158872692dup, NC_000006.12:g.158872690_158872692dup, NC_000006.12:g.158872689_158872692dup, NC_000006.12:g.158872692_158872693insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000006.11:g.159293718_159293724del, NC_000006.11:g.159293719_159293724del, NC_000006.11:g.159293721_159293724del, NC_000006.11:g.159293722_159293724del, NC_000006.11:g.159293723_159293724del, NC_000006.11:g.159293724del, NC_000006.11:g.159293724dup, NC_000006.11:g.159293723_159293724dup, NC_000006.11:g.159293722_159293724dup, NC_000006.11:g.159293721_159293724dup, NC_000006.11:g.159293724_159293725insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
6.
rs1491329500 [Homo sapiens]- Variant type:
- DEL
- Alleles:
- CT>-
[Show Flanks]
- Chromosome:
- 6:158917148
(GRCh38)
6:159338180
(GRCh37)
- Canonical SPDI:
- NC_000006.12:158917147:CT:
- Validated:
- by frequency,by alfa
- MAF:
-=0./0
(
ALFA)
-=0.000004/1
(TOPMED)
- HGVS:
9.
rs1491080332 has merged into rs67217647 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- TTT>-,T,TT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTTTTTTTTTTTTTTTT
[Show Flanks]
- Chromosome:
- 6:158895960
(GRCh38)
6:159316992
(GRCh37)
- Canonical SPDI:
- NC_000006.12:158895949:TTTTTTTTTTTTT:TTTTTTTTTT,NC_000006.12:158895949:TTTTTTTTTTTTT:TTTTTTTTTTT,NC_000006.12:158895949:TTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000006.12:158895949:TTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000006.12:158895949:TTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000006.12:158895949:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000006.12:158895949:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000006.12:158895949:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- Gene:
- LINC02901 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
TTTTTTTTTTT=0./0
(
ALFA)
-=0.2003/1003
(1000Genomes)
- HGVS:
NC_000006.12:g.158895960_158895962del, NC_000006.12:g.158895961_158895962del, NC_000006.12:g.158895962del, NC_000006.12:g.158895962dup, NC_000006.12:g.158895961_158895962dup, NC_000006.12:g.158895960_158895962dup, NC_000006.12:g.158895959_158895962dup, NC_000006.12:g.158895962_158895963insTTTTTTTTTTTTTTTTTTT, NC_000006.11:g.159316992_159316994del, NC_000006.11:g.159316993_159316994del, NC_000006.11:g.159316994del, NC_000006.11:g.159316994dup, NC_000006.11:g.159316993_159316994dup, NC_000006.11:g.159316992_159316994dup, NC_000006.11:g.159316991_159316994dup, NC_000006.11:g.159316994_159316995insTTTTTTTTTTTTTTTTTTT
10.
rs1490851334 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- G>T
[Show Flanks]
- Chromosome:
- 6:158868010
(GRCh38)
6:159289042
(GRCh37)
- Canonical SPDI:
- NC_000006.12:158868009:G:T
- Gene:
- LINC02901 (Varview)
- Functional Consequence:
- 2KB_upstream_variant,upstream_transcript_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
T=0.000071/1
(
ALFA)
T=0.000011/3
(TOPMED)
T=0.000014/2
(GnomAD)
- HGVS:
11.
rs1490756853 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- T>C
[Show Flanks]
- Chromosome:
- 6:158888901
(GRCh38)
6:159309933
(GRCh37)
- Canonical SPDI:
- NC_000006.12:158888900:T:C
- Gene:
- LINC02901 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
C=0./0
(
ALFA)
C=0.000014/2
(GnomAD)
C=0.000015/4
(TOPMED)
- HGVS:
12.
rs1490702564 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- G>A
[Show Flanks]
- Chromosome:
- 6:158904240
(GRCh38)
6:159325272
(GRCh37)
- Canonical SPDI:
- NC_000006.12:158904239:G:A
- Gene:
- LINC02901 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
A=0./0
(
ALFA)
A=0.000004/1
(TOPMED)
A=0.000007/1
(GnomAD)
- HGVS:
13.
rs1490684074 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- G>T
[Show Flanks]
- Chromosome:
- 6:158889978
(GRCh38)
6:159311010
(GRCh37)
- Canonical SPDI:
- NC_000006.12:158889977:G:T
- Gene:
- LINC02901 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
T=0./0
(
ALFA)
T=0.000015/4
(TOPMED)
T=0.000043/6
(GnomAD)
- HGVS:
14.
rs1490557940 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- T>C
[Show Flanks]
- Chromosome:
- 6:158875672
(GRCh38)
6:159296704
(GRCh37)
- Canonical SPDI:
- NC_000006.12:158875671:T:C
- Gene:
- LINC02901 (Varview)
- Functional Consequence:
- genic_upstream_transcript_variant,intron_variant
- Validated:
- by frequency,by alfa
- MAF:
C=0./0
(
ALFA)
C=0.000004/1
(TOPMED)
- HGVS:
15.
rs1490434612 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- ->GGG
[Show Flanks]
- Chromosome:
- 6:158883019
(GRCh38)
6:159304052
(GRCh37)
- Canonical SPDI:
- NC_000006.12:158883019:GG:GGGGG
- Gene:
- LINC02901 (Varview)
- Functional Consequence:
- genic_upstream_transcript_variant,intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
GGGGG=0./0
(
ALFA)
GGG=0.000007/1
(GnomAD)
GGG=0.000011/3
(TOPMED)
- HGVS:
17.
rs1490265780 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- C>G
[Show Flanks]
- Chromosome:
- 6:158888439
(GRCh38)
6:159309471
(GRCh37)
- Canonical SPDI:
- NC_000006.12:158888438:C:G
- Gene:
- LINC02901 (Varview)
- Functional Consequence:
- genic_upstream_transcript_variant,upstream_transcript_variant,intron_variant
- Validated:
- by frequency,by alfa
- MAF:
G=0./0
(
ALFA)
G=0.000008/2
(TOPMED)
- HGVS:
18.
rs1490242827 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- T>C
[Show Flanks]
- Chromosome:
- 6:158874490
(GRCh38)
6:159295522
(GRCh37)
- Canonical SPDI:
- NC_000006.12:158874489:T:C
- Gene:
- LINC02901 (Varview)
- Functional Consequence:
- genic_upstream_transcript_variant,intron_variant
- Validated:
- by frequency,by alfa
- MAF:
C=0./0
(
ALFA)
C=0.000004/1
(TOPMED)
- HGVS:
19.
rs1490181249 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- C>T
[Show Flanks]
- Chromosome:
- 6:158868723
(GRCh38)
6:159289755
(GRCh37)
- Canonical SPDI:
- NC_000006.12:158868722:C:T
- Gene:
- LINC02901 (Varview)
- Functional Consequence:
- 2KB_upstream_variant,upstream_transcript_variant
- Validated:
- by frequency,by alfa
- MAF:
T=0.000084/1
(
ALFA)
T=0.000021/3
(GnomAD)
- HGVS:
20.
rs1490086944 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- T>G
[Show Flanks]
- Chromosome:
- 6:158905054
(GRCh38)
6:159326086
(GRCh37)
- Canonical SPDI:
- NC_000006.12:158905053:T:G
- Gene:
- LINC02901 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
G=0./0
(
ALFA)
G=0.000004/1
(TOPMED)
G=0.000007/1
(GnomAD)
- HGVS: