SNP Links for Gene (Select 401164) - SNP

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Select item 14915530131.

rs1491553013 [Homo sapiens]

Variant type:: INS
Alleles:: ->A [Show Flanks]
Chromosome:: 4:188507087 (GRCh38)
4:189428242 (GRCh37)
Canonical SPDI:: NC_000004.12:188507087::A
Gene:: LINC01060 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.00134/6 (ALFA)
A=0.00237/67 (TOMMO)
HGVS:: NC_000004.12:g.188507087_188507088insA, NC_000004.11:g.189428241_189428242insA, NT_187545.1:g.165600dup

Select item 14915330412.

rs1491533041 has merged into rs769066427 [Homo sapiens]

Variant type:: DELINS
Alleles:: CACACACACACACACA>-,CA,CACACACA,CACACACACACA,CACACACACACACA,CACACACACACACACACA,CACACACACACACACACACA [Show Flanks]
Chromosome:: 4:188454514 (GRCh38)
4:189375668 (GRCh37)
Canonical SPDI:: NC_000004.12:188454508:ACACACACACACACACACACA:ACACA,NC_000004.12:188454508:ACACACACACACACACACACA:ACACACA,NC_000004.12:188454508:ACACACACACACACACACACA:ACACACACACACA,NC_000004.12:188454508:ACACACACACACACACACACA:ACACACACACACACACA,NC_000004.12:188454508:ACACACACACACACACACACA:ACACACACACACACACACA,NC_000004.12:188454508:ACACACACACACACACACACA:ACACACACACACACACACACACA,NC_000004.12:188454508:ACACACACACACACACACACA:ACACACACACACACACACACACACA
Gene:: LINC01060 (Varview), LOC105377609 (Varview)
Functional Consequence:: 2KB_upstream_variant,intron_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: ACACACACACACACACA=0./0 (ALFA)
-=0.0667/40 (NorthernSweden)
-=0.175/7 (GENOME_DK)
HGVS:: NC_000004.12:g.188454510CA[2], NC_000004.12:g.188454510CA[3], NC_000004.12:g.188454510CA[6], NC_000004.12:g.188454510CA[8], NC_000004.12:g.188454510CA[9], NC_000004.12:g.188454510CA[11], NC_000004.12:g.188454510CA[12], NC_000004.11:g.189375664CA[2], NC_000004.11:g.189375664CA[3], NC_000004.11:g.189375664CA[6], NC_000004.11:g.189375664CA[8], NC_000004.11:g.189375664CA[9], NC_000004.11:g.189375664CA[11], NC_000004.11:g.189375664CA[12], NT_187545.1:g.113088CA[2], NT_187545.1:g.113088CA[3], NT_187545.1:g.113088CA[6], NT_187545.1:g.113088CA[8], NT_187545.1:g.113088CA[9], NT_187545.1:g.113088CA[11], NT_187545.1:g.113088CA[12]

Select item 14915269443.

rs1491526944 has merged into rs11298038 [Homo sapiens]

Variant type:: DELINS
Alleles:: TT>-,T,TTT [Show Flanks]
Chromosome:: 4:188586662 (GRCh38)
4:189507816 (GRCh37)
Canonical SPDI:: NC_000004.12:188586652:TTTTTTTTTTT:TTTTTTTTT,NC_000004.12:188586652:TTTTTTTTTTT:TTTTTTTTTT,NC_000004.12:188586652:TTTTTTTTTTT:TTTTTTTTTTTT
Gene:: LINC01060 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTTT=0./0 (ALFA)
T=0./0 (GENOME_DK)
T=0.0316/117 (TWINSUK)
T=0.0353/136 (ALSPAC)
T=0.0381/38 (GoNL)
T=0.0787/394 (1000Genomes)
HGVS:: NC_000004.12:g.188586662_188586663del, NC_000004.12:g.188586663del, NC_000004.12:g.188586663dup, NC_000004.11:g.189507816_189507817del, NC_000004.11:g.189507817del, NC_000004.11:g.189507817dup

Select item 14915150224.

rs1491515022 [Homo sapiens]

Variant type:: DEL
Alleles:: GT>- [Show Flanks]
Chromosome:: 4:188566904 (GRCh38)
4:189488058 (GRCh37)
Canonical SPDI:: NC_000004.12:188566903:GT:
Gene:: LINC01060 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
-=0.00002/2 (GnomAD)
HGVS:: NC_000004.12:g.188566904_188566905del, NC_000004.11:g.189488058_189488059del

Select item 14915138025.

rs1491513802 [Homo sapiens]

Variant type:: DEL
Alleles:: GA>- [Show Flanks]
Chromosome:: 4:188571813 (GRCh38)
4:189492967 (GRCh37)
Canonical SPDI:: NC_000004.12:188571812:GA:
Gene:: LINC01060 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0.03052/362 (ALFA)
HGVS:: NC_000004.12:g.188571813_188571814del, NC_000004.11:g.189492967_189492968del

Select item 14915001646.

rs1491500164 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->GT [Show Flanks]
Chromosome:: 4:188590486 (GRCh38)
4:189511641 (GRCh37)
Canonical SPDI:: NC_000004.12:188590486:T:TGT
Gene:: LINC01060 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TGT=0./0 (ALFA)
TG=0.00049/2 (Estonian)
TG=0.00424/239 (GnomAD)
TG=0.00883/5 (NorthernSweden)
HGVS:: NC_000004.12:g.188590487_188590488insGT, NC_000004.11:g.189511641_189511642insGT

Select item 14914624257.

rs1491462425 [Homo sapiens]

Variant type:: SNV:
Alleles:: ->TAAAAAA
Chromosome:: no mapping
Canonical SPDI:

Select item 14914619008.

rs1491461900 has merged into rs34170231 [Homo sapiens]

Variant type:: DELINS
Alleles:: TT>-,T,TTT,TTTT,TTTTT [Show Flanks]
Chromosome:: 4:188566915 (GRCh38)
4:189488069 (GRCh37)
Canonical SPDI:: NC_000004.12:188566904:TTTTTTTTTTTT:TTTTTTTTTT,NC_000004.12:188566904:TTTTTTTTTTTT:TTTTTTTTTTT,NC_000004.12:188566904:TTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000004.12:188566904:TTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000004.12:188566904:TTTTTTTTTTTT:TTTTTTTTTTTTTTT
Gene:: LINC01060 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTTTTTT=0./0 (ALFA)
-=0.3185/1351 (1000Genomes)
HGVS:: NC_000004.12:g.188566915_188566916del, NC_000004.12:g.188566916del, NC_000004.12:g.188566916dup, NC_000004.12:g.188566915_188566916dup, NC_000004.12:g.188566914_188566916dup, NC_000004.11:g.189488069_189488070del, NC_000004.11:g.189488070del, NC_000004.11:g.189488070dup, NC_000004.11:g.189488069_189488070dup, NC_000004.11:g.189488068_189488070dup

Select item 14914253989.

rs1491425398 [Homo sapiens]

Variant type:: DEL
Alleles:: AT>- [Show Flanks]
Chromosome:: 4:188479103 (GRCh38)
4:189400257 (GRCh37)
Canonical SPDI:: NC_000004.12:188479102:AT:
Gene:: LINC01060 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
-=0.00003/2 (GnomAD)
HGVS:: NC_000004.12:g.188479103_188479104del, NC_000004.11:g.189400257_189400258del

Select item 149138305410.

rs1491383054 [Homo sapiens]

Variant type:: DELINS
Alleles:: TA>- [Show Flanks]
Chromosome:: 4:188498227 (GRCh38)
4:189419381 (GRCh37)
Canonical SPDI:: NC_000004.12:188498225:ATA:A
Gene:: LINC01060 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
-=0.000004/1 (TOPMED)
-=0.000007/1 (GnomAD)
HGVS:: NC_000004.12:g.188498227_188498228del, NC_000004.11:g.189419381_189419382del, NT_187545.1:g.156752_156753del

Select item 149138032111.

rs1491380321 has merged into rs59318611 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAA>-,AAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 4:188499408 (GRCh38)
4:189420562 (GRCh37)
Canonical SPDI:: NC_000004.12:188499398:AAAAAAAAAAAAAAAAAA:AAAAAAAAA,NC_000004.12:188499398:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000004.12:188499398:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000004.12:188499398:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000004.12:188499398:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000004.12:188499398:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000004.12:188499398:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000004.12:188499398:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000004.12:188499398:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000004.12:188499398:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:188499398:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: LINC01060 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAAA=0./0 (ALFA)
-=0.4862/2435 (1000Genomes)
HGVS:: NC_000004.12:g.188499408_188499416del, NC_000004.12:g.188499411_188499416del, NC_000004.12:g.188499413_188499416del, NC_000004.12:g.188499414_188499416del, NC_000004.12:g.188499415_188499416del, NC_000004.12:g.188499416del, NC_000004.12:g.188499416dup, NC_000004.12:g.188499415_188499416dup, NC_000004.12:g.188499414_188499416dup, NC_000004.12:g.188499413_188499416dup, NC_000004.12:g.188499410_188499416dup, NC_000004.11:g.189420562_189420570del, NC_000004.11:g.189420565_189420570del, NC_000004.11:g.189420567_189420570del, NC_000004.11:g.189420568_189420570del, NC_000004.11:g.189420569_189420570del, NC_000004.11:g.189420570del, NC_000004.11:g.189420570dup, NC_000004.11:g.189420569_189420570dup, NC_000004.11:g.189420568_189420570dup, NC_000004.11:g.189420567_189420570dup, NC_000004.11:g.189420564_189420570dup, NT_187545.1:g.157933_157941del, NT_187545.1:g.157936_157941del, NT_187545.1:g.157938_157941del, NT_187545.1:g.157939_157941del, NT_187545.1:g.157940_157941del, NT_187545.1:g.157941del, NT_187545.1:g.157941dup, NT_187545.1:g.157940_157941dup, NT_187545.1:g.157939_157941dup, NT_187545.1:g.157938_157941dup, NT_187545.1:g.157935_157941dup

Select item 149137682712.

rs1491376827 [Homo sapiens]

Variant type:: DELINS
Alleles:: AA>-,A,AAGAAAA [Show Flanks]
Chromosome:: 4:188529794 (GRCh38)
4:189450948 (GRCh37)
Canonical SPDI:: NC_000004.12:188529791:AAAA:AA,NC_000004.12:188529791:AAAA:AAA,NC_000004.12:188529791:AAAA:AAAAGAAAA
Gene:: LINC01060 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAA=0./0 (ALFA)
-=0.000004/1 (TOPMED)
AAAAG=0.000008/1 (GnomAD)
HGVS:: NC_000004.12:g.188529794_188529795del, NC_000004.12:g.188529795del, NC_000004.12:g.188529792_188529795A[4]GAAAA[1], NC_000004.11:g.189450948_189450949del, NC_000004.11:g.189450949del, NC_000004.11:g.189450946_189450949A[4]GAAAA[1], NT_187545.1:g.193379_193380del, NT_187545.1:g.193380del, NT_187545.1:g.193377_193380A[4]GAAAA[1]

Select item 149136591013.

rs1491365910 has merged into rs70940998 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAAAAAAAA>-,A,AA,AAA,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 4:188595023 (GRCh38)
4:189516177 (GRCh37)
Canonical SPDI:: NC_000004.12:188595013:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA,NC_000004.12:188595013:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA,NC_000004.12:188595013:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000004.12:188595013:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000004.12:188595013:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000004.12:188595013:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000004.12:188595013:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000004.12:188595013:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000004.12:188595013:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000004.12:188595013:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000004.12:188595013:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000004.12:188595013:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000004.12:188595013:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000004.12:188595013:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:188595013:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:188595013:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:188595013:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:188595013:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:188595013:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:188595013:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:188595013:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:188595013:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:188595013:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:188595013:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:188595013:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:188595013:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:188595013:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:188595013:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:188595013:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:188595013:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:188595013:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:188595013:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:188595013:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:188595013:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:188595013:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:188595013:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:188595013:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:188595013:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:188595013:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:188595013:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:188595013:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:188595013:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:188595013:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: LINC01060 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAA=0./0 (ALFA)
AAAAAAAAAAAAA=0.05/2 (GENOME_DK)
-=0.3668/1837 (1000Genomes)
HGVS:: NC_000004.12:g.188595023_188595037del, NC_000004.12:g.188595024_188595037del, NC_000004.12:g.188595025_188595037del, NC_000004.12:g.188595026_188595037del, NC_000004.12:g.188595027_188595037del, NC_000004.12:g.188595028_188595037del, NC_000004.12:g.188595029_188595037del, NC_000004.12:g.188595030_188595037del, NC_000004.12:g.188595031_188595037del, NC_000004.12:g.188595032_188595037del, NC_000004.12:g.188595033_188595037del, NC_000004.12:g.188595034_188595037del, NC_000004.12:g.188595035_188595037del, NC_000004.12:g.188595036_188595037del, NC_000004.12:g.188595037del, NC_000004.12:g.188595037dup, NC_000004.12:g.188595036_188595037dup, NC_000004.12:g.188595035_188595037dup, NC_000004.12:g.188595034_188595037dup, NC_000004.12:g.188595033_188595037dup, NC_000004.12:g.188595032_188595037dup, NC_000004.12:g.188595031_188595037dup, NC_000004.12:g.188595030_188595037dup, NC_000004.12:g.188595029_188595037dup, NC_000004.12:g.188595028_188595037dup, NC_000004.12:g.188595027_188595037dup, NC_000004.12:g.188595026_188595037dup, NC_000004.12:g.188595025_188595037dup, NC_000004.12:g.188595024_188595037dup, NC_000004.12:g.188595022_188595037dup, NC_000004.12:g.188595021_188595037dup, NC_000004.12:g.188595018_188595037dup, NC_000004.12:g.188595015_188595037dup, NC_000004.12:g.188595037_188595038insAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000004.12:g.188595037_188595038insAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000004.12:g.188595037_188595038insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000004.12:g.188595037_188595038insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000004.12:g.188595037_188595038insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000004.12:g.188595037_188595038insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000004.12:g.188595037_188595038insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000004.12:g.188595037_188595038insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000004.12:g.188595037_188595038insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000004.12:g.188595037_188595038insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000004.11:g.189516177_189516191del, NC_000004.11:g.189516178_189516191del, NC_000004.11:g.189516179_189516191del, NC_000004.11:g.189516180_189516191del, NC_000004.11:g.189516181_189516191del, NC_000004.11:g.189516182_189516191del, NC_000004.11:g.189516183_189516191del, NC_000004.11:g.189516184_189516191del, NC_000004.11:g.189516185_189516191del, NC_000004.11:g.189516186_189516191del, NC_000004.11:g.189516187_189516191del, NC_000004.11:g.189516188_189516191del, NC_000004.11:g.189516189_189516191del, NC_000004.11:g.189516190_189516191del, NC_000004.11:g.189516191del, NC_000004.11:g.189516191dup, NC_000004.11:g.189516190_189516191dup, NC_000004.11:g.189516189_189516191dup, NC_000004.11:g.189516188_189516191dup, NC_000004.11:g.189516187_189516191dup, NC_000004.11:g.189516186_189516191dup, NC_000004.11:g.189516185_189516191dup, NC_000004.11:g.189516184_189516191dup, NC_000004.11:g.189516183_189516191dup, NC_000004.11:g.189516182_189516191dup, NC_000004.11:g.189516181_189516191dup, NC_000004.11:g.189516180_189516191dup, NC_000004.11:g.189516179_189516191dup, NC_000004.11:g.189516178_189516191dup, NC_000004.11:g.189516176_189516191dup, NC_000004.11:g.189516175_189516191dup, NC_000004.11:g.189516172_189516191dup, NC_000004.11:g.189516169_189516191dup, NC_000004.11:g.189516191_189516192insAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000004.11:g.189516191_189516192insAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000004.11:g.189516191_189516192insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000004.11:g.189516191_189516192insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000004.11:g.189516191_189516192insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000004.11:g.189516191_189516192insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000004.11:g.189516191_189516192insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000004.11:g.189516191_189516192insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000004.11:g.189516191_189516192insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000004.11:g.189516191_189516192insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

Select item 149136543014.

rs1491365430 has merged into rs1247005261 [Homo sapiens]

Variant type:: DELINS
Alleles:: A>-,AA [Show Flanks]
Chromosome:: 4:188463792 (GRCh38)
4:189384946 (GRCh37)
Canonical SPDI:: NC_000004.12:188463791:AAAAAAAA:AAAAAAA,NC_000004.12:188463791:AAAAAAAA:AAAAAAAAA
Gene:: LINC01060 (Varview), LOC105377609 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAA=0./0 (ALFA)
-=0.000019/5 (TOPMED)
-=0.000035/1 (TOMMO)
-=0.000043/6 (GnomAD)
HGVS:: NC_000004.12:g.188463799del, NC_000004.12:g.188463799dup, NC_000004.11:g.189384953del, NC_000004.11:g.189384953dup, NT_187545.1:g.122377del, NT_187545.1:g.122377dup

Select item 149135925815.

rs1491359258 [Homo sapiens]

Variant type:: DEL
Alleles:: AC>- [Show Flanks]
Chromosome:: 4:188571834 (GRCh38)
4:189492988 (GRCh37)
Canonical SPDI:: NC_000004.12:188571833:AC:
Gene:: LINC01060 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
-=0.000007/1 (GnomAD)
HGVS:: NC_000004.12:g.188571834_188571835del, NC_000004.11:g.189492988_189492989del

Select item 149135698316.

rs1491356983 has merged into rs10543937 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAA>-,A,AA,AAA,AAAA,AAAAA,AAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 4:188581428 (GRCh38)
4:189502582 (GRCh37)
Canonical SPDI:: NC_000004.12:188581417:AAAAAAAAAAAAAAAAA:AAAAAAAAAA,NC_000004.12:188581417:AAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000004.12:188581417:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000004.12:188581417:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000004.12:188581417:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000004.12:188581417:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000004.12:188581417:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000004.12:188581417:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000004.12:188581417:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000004.12:188581417:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: LINC01060 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAA=0./0 (ALFA)
-=0.0882/340 (ALSPAC)
A=0.2839/1422 (1000Genomes)
HGVS:: NC_000004.12:g.188581428_188581434del, NC_000004.12:g.188581429_188581434del, NC_000004.12:g.188581430_188581434del, NC_000004.12:g.188581431_188581434del, NC_000004.12:g.188581432_188581434del, NC_000004.12:g.188581433_188581434del, NC_000004.12:g.188581434del, NC_000004.12:g.188581434dup, NC_000004.12:g.188581433_188581434dup, NC_000004.12:g.188581425_188581434dup, NC_000004.11:g.189502582_189502588del, NC_000004.11:g.189502583_189502588del, NC_000004.11:g.189502584_189502588del, NC_000004.11:g.189502585_189502588del, NC_000004.11:g.189502586_189502588del, NC_000004.11:g.189502587_189502588del, NC_000004.11:g.189502588del, NC_000004.11:g.189502588dup, NC_000004.11:g.189502587_189502588dup, NC_000004.11:g.189502579_189502588dup

Select item 149134262217.

rs1491342622 has merged into rs754665666 [Homo sapiens]

Variant type:: DELINS
Alleles:: CACACACACA>-,CA,CACA,CACACA,CACACACA,CACACACACACA,CACACACACACACA,CACACACACACACACA,CACACACACACACACACA,CACACACACACACACACACA,CACACACACACACACACACACA,CACACACACACACACACACACACA,CACACACACACACACACACACACACA,CACACACACACACACACACACACACACA,CACACACACACACACACACACACACACACA,CACACACACACACACACACACACACACACACA,CACACACACACACACACACACACACACACACACA,CACACACACACACACACACACACACACACACACACA,CACACACACACACACACACACACACACACACACACACA [Show Flanks]
Chromosome:: 4:188454548 (GRCh38)
4:189375702 (GRCh37)
Canonical SPDI:: NC_000004.12:188454530:ACACACACACACACACACACACACACA:ACACACACACACACACA,NC_000004.12:188454530:ACACACACACACACACACACACACACA:ACACACACACACACACACA,NC_000004.12:188454530:ACACACACACACACACACACACACACA:ACACACACACACACACACACA,NC_000004.12:188454530:ACACACACACACACACACACACACACA:ACACACACACACACACACACACA,NC_000004.12:188454530:ACACACACACACACACACACACACACA:ACACACACACACACACACACACACA,NC_000004.12:188454530:ACACACACACACACACACACACACACA:ACACACACACACACACACACACACACACA,NC_000004.12:188454530:ACACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACA,NC_000004.12:188454530:ACACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACA,NC_000004.12:188454530:ACACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACACA,NC_000004.12:188454530:ACACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACACACA,NC_000004.12:188454530:ACACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACACACACA,NC_000004.12:188454530:ACACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACACACACACA,NC_000004.12:188454530:ACACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACACACACACACA,NC_000004.12:188454530:ACACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACACACACACACACA,NC_000004.12:188454530:ACACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACACACACACACACACA,NC_000004.12:188454530:ACACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACACACACACACACACACA,NC_000004.12:188454530:ACACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACACACACACACACACACACA,NC_000004.12:188454530:ACACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACACACACACACACACACACACA,NC_000004.12:188454530:ACACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACACACACACACACACACACACACA
Gene:: LINC01060 (Varview), LOC105377609 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: ACACACACACACACACACACACA=0./0 (ALFA)
HGVS:: NC_000004.12:g.188454532CA[8], NC_000004.12:g.188454532CA[9], NC_000004.12:g.188454532CA[10], NC_000004.12:g.188454532CA[11], NC_000004.12:g.188454532CA[12], NC_000004.12:g.188454532CA[14], NC_000004.12:g.188454532CA[15], NC_000004.12:g.188454532CA[16], NC_000004.12:g.188454532CA[17], NC_000004.12:g.188454532CA[18], NC_000004.12:g.188454532CA[19], NC_000004.12:g.188454532CA[20], NC_000004.12:g.188454532CA[21], NC_000004.12:g.188454532CA[22], NC_000004.12:g.188454532CA[23], NC_000004.12:g.188454532CA[24], NC_000004.12:g.188454532CA[25], NC_000004.12:g.188454532CA[26], NC_000004.12:g.188454532CA[27], NC_000004.11:g.189375686CA[8], NC_000004.11:g.189375686CA[9], NC_000004.11:g.189375686CA[10], NC_000004.11:g.189375686CA[11], NC_000004.11:g.189375686CA[12], NC_000004.11:g.189375686CA[14], NC_000004.11:g.189375686CA[15], NC_000004.11:g.189375686CA[16], NC_000004.11:g.189375686CA[17], NC_000004.11:g.189375686CA[18], NC_000004.11:g.189375686CA[19], NC_000004.11:g.189375686CA[20], NC_000004.11:g.189375686CA[21], NC_000004.11:g.189375686CA[22], NC_000004.11:g.189375686CA[23], NC_000004.11:g.189375686CA[24], NC_000004.11:g.189375686CA[25], NC_000004.11:g.189375686CA[26], NC_000004.11:g.189375686CA[27], NT_187545.1:g.113110CA[8], NT_187545.1:g.113110CA[9], NT_187545.1:g.113110CA[10], NT_187545.1:g.113110CA[11], NT_187545.1:g.113110CA[12], NT_187545.1:g.113110CA[14], NT_187545.1:g.113110CA[15], NT_187545.1:g.113110CA[16], NT_187545.1:g.113110CA[17], NT_187545.1:g.113110CA[18], NT_187545.1:g.113110CA[19], NT_187545.1:g.113110CA[20], NT_187545.1:g.113110CA[21], NT_187545.1:g.113110CA[22], NT_187545.1:g.113110CA[23], NT_187545.1:g.113110CA[24], NT_187545.1:g.113110CA[25], NT_187545.1:g.113110CA[26], NT_187545.1:g.113110CA[27]

Select item 149131726918.

rs1491317269 has merged into rs70940986 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTT>-,T,TT,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 4:188479117 (GRCh38)
4:189400271 (GRCh37)
Canonical SPDI:: NC_000004.12:188479103:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000004.12:188479103:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000004.12:188479103:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000004.12:188479103:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000004.12:188479103:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000004.12:188479103:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000004.12:188479103:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000004.12:188479103:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000004.12:188479103:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000004.12:188479103:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:188479103:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:188479103:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:188479103:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:188479103:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:188479103:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:188479103:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:188479103:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:188479103:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:188479103:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:188479103:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:188479103:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:188479103:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:188479103:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:188479103:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:188479103:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:188479103:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:188479103:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:188479103:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:188479103:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:188479103:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:188479103:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:188479103:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:188479103:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:188479103:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:188479103:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:188479103:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:188479103:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:188479103:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:188479103:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:188479103:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: LINC01060 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTTTTT=0./0 (ALFA)
-=0.0182/13 (Korea1K)
HGVS:: NC_000004.12:g.188479117_188479125del, NC_000004.12:g.188479118_188479125del, NC_000004.12:g.188479119_188479125del, NC_000004.12:g.188479120_188479125del, NC_000004.12:g.188479121_188479125del, NC_000004.12:g.188479122_188479125del, NC_000004.12:g.188479123_188479125del, NC_000004.12:g.188479124_188479125del, NC_000004.12:g.188479125del, NC_000004.12:g.188479125dup, NC_000004.12:g.188479124_188479125dup, NC_000004.12:g.188479123_188479125dup, NC_000004.12:g.188479122_188479125dup, NC_000004.12:g.188479121_188479125dup, NC_000004.12:g.188479120_188479125dup, NC_000004.12:g.188479119_188479125dup, NC_000004.12:g.188479118_188479125dup, NC_000004.12:g.188479117_188479125dup, NC_000004.12:g.188479116_188479125dup, NC_000004.12:g.188479115_188479125dup, NC_000004.12:g.188479114_188479125dup, NC_000004.12:g.188479113_188479125dup, NC_000004.12:g.188479112_188479125dup, NC_000004.12:g.188479111_188479125dup, NC_000004.12:g.188479110_188479125dup, NC_000004.12:g.188479109_188479125dup, NC_000004.12:g.188479108_188479125dup, NC_000004.12:g.188479107_188479125dup, NC_000004.12:g.188479106_188479125dup, NC_000004.12:g.188479105_188479125dup, NC_000004.12:g.188479104_188479125dup, NC_000004.12:g.188479125_188479126insTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.12:g.188479125_188479126insTTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.12:g.188479125_188479126insTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.12:g.188479125_188479126insTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.12:g.188479125_188479126insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.12:g.188479125_188479126insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.12:g.188479125_188479126insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.12:g.188479125_188479126insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.12:g.188479125_188479126insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.11:g.189400271_189400279del, NC_000004.11:g.189400272_189400279del, NC_000004.11:g.189400273_189400279del, NC_000004.11:g.189400274_189400279del, NC_000004.11:g.189400275_189400279del, NC_000004.11:g.189400276_189400279del, NC_000004.11:g.189400277_189400279del, NC_000004.11:g.189400278_189400279del, NC_000004.11:g.189400279del, NC_000004.11:g.189400279dup, NC_000004.11:g.189400278_189400279dup, NC_000004.11:g.189400277_189400279dup, NC_000004.11:g.189400276_189400279dup, NC_000004.11:g.189400275_189400279dup, NC_000004.11:g.189400274_189400279dup, NC_000004.11:g.189400273_189400279dup, NC_000004.11:g.189400272_189400279dup, NC_000004.11:g.189400271_189400279dup, NC_000004.11:g.189400270_189400279dup, NC_000004.11:g.189400269_189400279dup, NC_000004.11:g.189400268_189400279dup, NC_000004.11:g.189400267_189400279dup, NC_000004.11:g.189400266_189400279dup, NC_000004.11:g.189400265_189400279dup, NC_000004.11:g.189400264_189400279dup, NC_000004.11:g.189400263_189400279dup, NC_000004.11:g.189400262_189400279dup, NC_000004.11:g.189400261_189400279dup, NC_000004.11:g.189400260_189400279dup, NC_000004.11:g.189400259_189400279dup, NC_000004.11:g.189400258_189400279dup, NC_000004.11:g.189400279_189400280insTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.11:g.189400279_189400280insTTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.11:g.189400279_189400280insTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.11:g.189400279_189400280insTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.11:g.189400279_189400280insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.11:g.189400279_189400280insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.11:g.189400279_189400280insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.11:g.189400279_189400280insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.11:g.189400279_189400280insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_187545.1:g.137693_137701del, NT_187545.1:g.137694_137701del, NT_187545.1:g.137695_137701del, NT_187545.1:g.137696_137701del, NT_187545.1:g.137697_137701del, NT_187545.1:g.137698_137701del, NT_187545.1:g.137699_137701del, NT_187545.1:g.137700_137701del, NT_187545.1:g.137701del, NT_187545.1:g.137701dup, NT_187545.1:g.137700_137701dup, NT_187545.1:g.137699_137701dup, NT_187545.1:g.137698_137701dup, NT_187545.1:g.137697_137701dup, NT_187545.1:g.137696_137701dup, NT_187545.1:g.137695_137701dup, NT_187545.1:g.137694_137701dup, NT_187545.1:g.137693_137701dup, NT_187545.1:g.137692_137701dup, NT_187545.1:g.137691_137701dup, NT_187545.1:g.137690_137701dup, NT_187545.1:g.137689_137701dup, NT_187545.1:g.137688_137701dup, NT_187545.1:g.137687_137701dup, NT_187545.1:g.137686_137701dup, NT_187545.1:g.137685_137701dup, NT_187545.1:g.137684_137701dup, NT_187545.1:g.137683_137701dup, NT_187545.1:g.137682_137701dup, NT_187545.1:g.137681_137701dup, NT_187545.1:g.137680_137701dup, NT_187545.1:g.137679_137701dup, NT_187545.1:g.137678_137701dup, NT_187545.1:g.137701_137702insTTTTTTTTTTTTTTTTTTTTTTTTT, NT_187545.1:g.137701_137702insTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_187545.1:g.137701_137702insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_187545.1:g.137701_137702insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_187545.1:g.137701_137702insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_187545.1:g.137701_137702insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_187545.1:g.137701_137702insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Select item 149126438619.

rs1491264386 [Homo sapiens]

Variant type:: DELINS
Alleles:: CG>- [Show Flanks]
Chromosome:: 4:188507088 (GRCh38)
4:189428242 (GRCh37)
Canonical SPDI:: NC_000004.12:188507086:GCG:G
Gene:: LINC01060 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
-=0.00375/106 (TOMMO)
HGVS:: NC_000004.12:g.188507088_188507089del, NC_000004.11:g.189428242_189428243del, NT_187545.1:g.165600A>C, NT_187545.1:g.165598AG[3]

Select item 149124486720.

rs1491244867 [Homo sapiens]

Variant type:: DEL
Alleles:: GT>- [Show Flanks]
Chromosome:: 4:188510183 (GRCh38)
4:189431337 (GRCh37)
Canonical SPDI:: NC_000004.12:188510182:GT:
Gene:: LINC01060 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
-=0.000008/2 (TOPMED)
HGVS:: NC_000004.12:g.188510183_188510184del, NC_000004.11:g.189431337_189431338del, NT_187545.1:g.173768_173769del

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