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Select item 14915256111.

rs1491525611 has merged into rs61261486 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTTTT>-,TT,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 1:236528559 (GRCh38)
1:236691859 (GRCh37)
Canonical SPDI:: NC_000001.11:236528546:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000001.11:236528546:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000001.11:236528546:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000001.11:236528546:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000001.11:236528546:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000001.11:236528546:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000001.11:236528546:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000001.11:236528546:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000001.11:236528546:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000001.11:236528546:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:236528546:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:236528546:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:236528546:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:236528546:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:236528546:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:236528546:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:236528546:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:236528546:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:236528546:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:236528546:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:236528546:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:236528546:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:236528546:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:236528546:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:236528546:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:236528546:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:236528546:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:236528546:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:236528546:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:236528546:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:236528546:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:236528546:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: LGALS8 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTTTTT=0./0 (ALFA)
TTT=0.1819/911 (1000Genomes)
HGVS:: NC_000001.11:g.236528559_236528569del, NC_000001.11:g.236528561_236528569del, NC_000001.11:g.236528562_236528569del, NC_000001.11:g.236528563_236528569del, NC_000001.11:g.236528564_236528569del, NC_000001.11:g.236528565_236528569del, NC_000001.11:g.236528566_236528569del, NC_000001.11:g.236528567_236528569del, NC_000001.11:g.236528568_236528569del, NC_000001.11:g.236528569del, NC_000001.11:g.236528569dup, NC_000001.11:g.236528568_236528569dup, NC_000001.11:g.236528567_236528569dup, NC_000001.11:g.236528566_236528569dup, NC_000001.11:g.236528565_236528569dup, NC_000001.11:g.236528564_236528569dup, NC_000001.11:g.236528563_236528569dup, NC_000001.11:g.236528562_236528569dup, NC_000001.11:g.236528561_236528569dup, NC_000001.11:g.236528560_236528569dup, NC_000001.11:g.236528559_236528569dup, NC_000001.11:g.236528558_236528569dup, NC_000001.11:g.236528557_236528569dup, NC_000001.11:g.236528556_236528569dup, NC_000001.11:g.236528555_236528569dup, NC_000001.11:g.236528554_236528569dup, NC_000001.11:g.236528553_236528569dup, NC_000001.11:g.236528550_236528569dup, NC_000001.11:g.236528548_236528569dup, NC_000001.11:g.236528547_236528569dup, NC_000001.11:g.236528569_236528570insTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000001.11:g.236528569_236528570insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000001.10:g.236691859_236691869del, NC_000001.10:g.236691861_236691869del, NC_000001.10:g.236691862_236691869del, NC_000001.10:g.236691863_236691869del, NC_000001.10:g.236691864_236691869del, NC_000001.10:g.236691865_236691869del, NC_000001.10:g.236691866_236691869del, NC_000001.10:g.236691867_236691869del, NC_000001.10:g.236691868_236691869del, NC_000001.10:g.236691869del, NC_000001.10:g.236691869dup, NC_000001.10:g.236691868_236691869dup, NC_000001.10:g.236691867_236691869dup, NC_000001.10:g.236691866_236691869dup, NC_000001.10:g.236691865_236691869dup, NC_000001.10:g.236691864_236691869dup, NC_000001.10:g.236691863_236691869dup, NC_000001.10:g.236691862_236691869dup, NC_000001.10:g.236691861_236691869dup, NC_000001.10:g.236691860_236691869dup, NC_000001.10:g.236691859_236691869dup, NC_000001.10:g.236691858_236691869dup, NC_000001.10:g.236691857_236691869dup, NC_000001.10:g.236691856_236691869dup, NC_000001.10:g.236691855_236691869dup, NC_000001.10:g.236691854_236691869dup, NC_000001.10:g.236691853_236691869dup, NC_000001.10:g.236691850_236691869dup, NC_000001.10:g.236691848_236691869dup, NC_000001.10:g.236691847_236691869dup, NC_000001.10:g.236691869_236691870insTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000001.10:g.236691869_236691870insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Select item 14915249532.

rs1491524953 has merged into rs5781896 [Homo sapiens]

Variant type:: DELINS
Alleles:: TT>-,T,TTT,TTTT,TTTTT,TTTTTT [Show Flanks]
Chromosome:: 1:236544732 (GRCh38)
1:236708032 (GRCh37)
Canonical SPDI:: NC_000001.11:236544722:TTTTTTTTTTT:TTTTTTTTT,NC_000001.11:236544722:TTTTTTTTTTT:TTTTTTTTTT,NC_000001.11:236544722:TTTTTTTTTTT:TTTTTTTTTTTT,NC_000001.11:236544722:TTTTTTTTTTT:TTTTTTTTTTTTT,NC_000001.11:236544722:TTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000001.11:236544722:TTTTTTTTTTT:TTTTTTTTTTTTTTT
Gene:: LGALS8 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTTTTTT=0.00068/10 (ALFA)
T=0.225/9 (GENOME_DK)
-=0.24342/37 (1000Genomes)
HGVS:: NC_000001.11:g.236544732_236544733del, NC_000001.11:g.236544733del, NC_000001.11:g.236544733dup, NC_000001.11:g.236544732_236544733dup, NC_000001.11:g.236544731_236544733dup, NC_000001.11:g.236544730_236544733dup, NC_000001.10:g.236708032_236708033del, NC_000001.10:g.236708033del, NC_000001.10:g.236708033dup, NC_000001.10:g.236708032_236708033dup, NC_000001.10:g.236708031_236708033dup, NC_000001.10:g.236708030_236708033dup

Select item 14914973303.

rs1491497330 [Homo sapiens]

Variant type:: DEL
Alleles:: CC>- [Show Flanks]
Chromosome:: 1:236527688 (GRCh38)
1:236690988 (GRCh37)
Canonical SPDI:: NC_000001.11:236527687:CC:
Gene:: LGALS8 (Varview)
Functional Consequence:: intron_variant
HGVS:: NC_000001.11:g.236527688_236527689del, NC_000001.10:g.236690988_236690989del

Select item 14913918154.

rs1491391815 [Homo sapiens]

Variant type:: DELINS
Alleles:: AA>-,AAA [Show Flanks]
Chromosome:: 1:236538109 (GRCh38)
1:236701409 (GRCh37)
Canonical SPDI:: NC_000001.11:236538105:AAAAA:AAA,NC_000001.11:236538105:AAAAA:AAAAAA
Gene:: LGALS8 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: AAAAAA=0./0 (ALFA)
A=0.00002/1 (GnomAD)
HGVS:: NC_000001.11:g.236538109_236538110del, NC_000001.11:g.236538110dup, NC_000001.10:g.236701409_236701410del, NC_000001.10:g.236701410dup

Select item 14913832885.

rs1491383288 has merged into rs57058408 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTT>-,T,TT,TTT,TTTT,TTTTTT,TTTTTTT [Show Flanks]
Chromosome:: 1:236533647 (GRCh38)
1:236696947 (GRCh37)
Canonical SPDI:: NC_000001.11:236533637:TTTTTTTTTTTTTT:TTTTTTTTT,NC_000001.11:236533637:TTTTTTTTTTTTTT:TTTTTTTTTT,NC_000001.11:236533637:TTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000001.11:236533637:TTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000001.11:236533637:TTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000001.11:236533637:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000001.11:236533637:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT
Gene:: LGALS8 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTT=0./0 (ALFA)
-=0.4972/2490 (1000Genomes)
HGVS:: NC_000001.11:g.236533647_236533651del, NC_000001.11:g.236533648_236533651del, NC_000001.11:g.236533649_236533651del, NC_000001.11:g.236533650_236533651del, NC_000001.11:g.236533651del, NC_000001.11:g.236533651dup, NC_000001.11:g.236533650_236533651dup, NC_000001.10:g.236696947_236696951del, NC_000001.10:g.236696948_236696951del, NC_000001.10:g.236696949_236696951del, NC_000001.10:g.236696950_236696951del, NC_000001.10:g.236696951del, NC_000001.10:g.236696951dup, NC_000001.10:g.236696950_236696951dup

Select item 14913284646.

rs1491328464 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->GTTTTTTT [Show Flanks]
Chromosome:: 1:236537022 (GRCh38)
1:236700323 (GRCh37)
Canonical SPDI:: NC_000001.11:236537022:TTTTTTT:TTTTTTTGTTTTTTT
Gene:: LGALS8 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by cluster
MAF:: TTTTTTTG=0.00014/4 (TOMMO)
TTTTTTTG=0.00502/3 (NorthernSweden)
HGVS:: NC_000001.11:g.236537023_236537029T[7]GTTTTTTT[1], NC_000001.10:g.236700323_236700329T[7]GTTTTTTT[1]

Select item 14913071857.

rs1491307185 [Homo sapiens]

Variant type:: DELINS
Alleles:: CT>- [Show Flanks]
Chromosome:: 1:236544734 (GRCh38)
1:236708034 (GRCh37)
Canonical SPDI:: NC_000001.11:236544732:TCT:T
Gene:: LGALS8 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by cluster
MAF:: -=0.000008/1 (ExAC)
HGVS:: NC_000001.11:g.236544734_236544735del, NC_000001.10:g.236708034_236708035del

Select item 14913059998.

rs1491305999 [Homo sapiens]

Variant type:: INS
Alleles:: ->AA,AAA,AAAA [Show Flanks]
Chromosome:: 1:236527688 (GRCh38)
1:236690989 (GRCh37)
Canonical SPDI:: NC_000001.11:236527688::AA,NC_000001.11:236527688::AAA,NC_000001.11:236527688::AAAA
Gene:: LGALS8 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: AAAA=0./0 (ALFA)
HGVS:: NC_000001.11:g.236527688_236527689insAA, NC_000001.11:g.236527688_236527689insAAA, NC_000001.11:g.236527688_236527689insAAAA, NC_000001.10:g.236690988_236690989insAA, NC_000001.10:g.236690988_236690989insAAA, NC_000001.10:g.236690988_236690989insAAAA

Select item 14912992409.

rs1491299240 [Homo sapiens]

Variant type:: DEL
Alleles:: CA>- [Show Flanks]
Chromosome:: 1:236535060 (GRCh38)
1:236698360 (GRCh37)
Canonical SPDI:: NC_000001.11:236535059:CA:
Gene:: LGALS8 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: -=0.0011/13 (ALFA)
HGVS:: NC_000001.11:g.236535060_236535061del, NC_000001.10:g.236698360_236698361del

Select item 149129159710.

rs1491291597 [Homo sapiens]

Variant type:: DEL
Alleles:: GA>- [Show Flanks]
Chromosome:: 1:236531684 (GRCh38)
1:236694984 (GRCh37)
Canonical SPDI:: NC_000001.11:236531683:GA:
Gene:: LGALS8 (Varview)
Functional Consequence:: intron_variant
Validated:: by cluster
HGVS:: NC_000001.11:g.236531684_236531685del, NC_000001.10:g.236694984_236694985del

Select item 149127243611.

rs1491272436 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->AAAAAAAAGAAAGAAAA [Show Flanks]
Chromosome:: 1:236538106 (GRCh38)
1:236701407 (GRCh37)
Canonical SPDI:: NC_000001.11:236538106:AAAA:AAAAAAAAAAAAGAAAGAAAA
Gene:: LGALS8 (Varview)
Functional Consequence:: intron_variant
HGVS:: NC_000001.11:g.236538107_236538110A[12]GAAA[2]A[1], NC_000001.10:g.236701407_236701410A[12]GAAA[2]A[1]

Select item 149124728712.

rs1491247287 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->CTTT [Show Flanks]
Chromosome:: 1:236528547 (GRCh38)
1:236691848 (GRCh37)
Canonical SPDI:: NC_000001.11:236528547:TTT:TTTCTTT
Gene:: LGALS8 (Varview)
Functional Consequence:: intron_variant
HGVS:: NC_000001.11:g.236528550_236528551insCTTT, NC_000001.10:g.236691850_236691851insCTTT

Select item 149121521813.

rs1491215218 has merged into rs61261486 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTTTT>-,TT,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 1:236528559 (GRCh38)
1:236691859 (GRCh37)
Canonical SPDI:: NC_000001.11:236528546:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000001.11:236528546:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000001.11:236528546:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000001.11:236528546:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000001.11:236528546:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000001.11:236528546:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000001.11:236528546:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000001.11:236528546:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000001.11:236528546:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000001.11:236528546:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:236528546:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:236528546:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:236528546:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:236528546:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:236528546:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:236528546:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:236528546:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:236528546:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:236528546:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:236528546:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:236528546:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:236528546:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:236528546:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:236528546:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:236528546:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:236528546:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:236528546:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:236528546:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:236528546:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:236528546:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:236528546:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:236528546:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: LGALS8 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTTTTT=0./0 (ALFA)
TTT=0.1819/911 (1000Genomes)
HGVS:: NC_000001.11:g.236528559_236528569del, NC_000001.11:g.236528561_236528569del, NC_000001.11:g.236528562_236528569del, NC_000001.11:g.236528563_236528569del, NC_000001.11:g.236528564_236528569del, NC_000001.11:g.236528565_236528569del, NC_000001.11:g.236528566_236528569del, NC_000001.11:g.236528567_236528569del, NC_000001.11:g.236528568_236528569del, NC_000001.11:g.236528569del, NC_000001.11:g.236528569dup, NC_000001.11:g.236528568_236528569dup, NC_000001.11:g.236528567_236528569dup, NC_000001.11:g.236528566_236528569dup, NC_000001.11:g.236528565_236528569dup, NC_000001.11:g.236528564_236528569dup, NC_000001.11:g.236528563_236528569dup, NC_000001.11:g.236528562_236528569dup, NC_000001.11:g.236528561_236528569dup, NC_000001.11:g.236528560_236528569dup, NC_000001.11:g.236528559_236528569dup, NC_000001.11:g.236528558_236528569dup, NC_000001.11:g.236528557_236528569dup, NC_000001.11:g.236528556_236528569dup, NC_000001.11:g.236528555_236528569dup, NC_000001.11:g.236528554_236528569dup, NC_000001.11:g.236528553_236528569dup, NC_000001.11:g.236528550_236528569dup, NC_000001.11:g.236528548_236528569dup, NC_000001.11:g.236528547_236528569dup, NC_000001.11:g.236528569_236528570insTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000001.11:g.236528569_236528570insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000001.10:g.236691859_236691869del, NC_000001.10:g.236691861_236691869del, NC_000001.10:g.236691862_236691869del, NC_000001.10:g.236691863_236691869del, NC_000001.10:g.236691864_236691869del, NC_000001.10:g.236691865_236691869del, NC_000001.10:g.236691866_236691869del, NC_000001.10:g.236691867_236691869del, NC_000001.10:g.236691868_236691869del, NC_000001.10:g.236691869del, NC_000001.10:g.236691869dup, NC_000001.10:g.236691868_236691869dup, NC_000001.10:g.236691867_236691869dup, NC_000001.10:g.236691866_236691869dup, NC_000001.10:g.236691865_236691869dup, NC_000001.10:g.236691864_236691869dup, NC_000001.10:g.236691863_236691869dup, NC_000001.10:g.236691862_236691869dup, NC_000001.10:g.236691861_236691869dup, NC_000001.10:g.236691860_236691869dup, NC_000001.10:g.236691859_236691869dup, NC_000001.10:g.236691858_236691869dup, NC_000001.10:g.236691857_236691869dup, NC_000001.10:g.236691856_236691869dup, NC_000001.10:g.236691855_236691869dup, NC_000001.10:g.236691854_236691869dup, NC_000001.10:g.236691853_236691869dup, NC_000001.10:g.236691850_236691869dup, NC_000001.10:g.236691848_236691869dup, NC_000001.10:g.236691847_236691869dup, NC_000001.10:g.236691869_236691870insTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000001.10:g.236691869_236691870insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Select item 149118022014.

rs1491180220 [Homo sapiens]

Variant type:: DEL
Alleles:: AT>- [Show Flanks]
Chromosome:: 1:236533637 (GRCh38)
1:236696937 (GRCh37)
Canonical SPDI:: NC_000001.11:236533636:AT:
Gene:: LGALS8 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0.000084/1 (ALFA)
-=0.000104/12 (GnomAD)
-=0.005202/85 (TOMMO)
-=0.006726/12 (Korea1K)
HGVS:: NC_000001.11:g.236533637_236533638del, NC_000001.10:g.236696937_236696938del

Select item 149112353415.

rs1491123534 [Homo sapiens]

Variant type:: DEL
Alleles:: AT>- [Show Flanks]
Chromosome:: 1:236528546 (GRCh38)
1:236691846 (GRCh37)
Canonical SPDI:: NC_000001.11:236528545:AT:
Gene:: LGALS8 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0.00051/6 (ALFA)
-=0.00062/4 (1000Genomes)
-=0.00108/68 (GnomAD)
HGVS:: NC_000001.11:g.236528546_236528547del, NC_000001.10:g.236691846_236691847del

Select item 149112084216.

rs1491120842 has merged into rs60024224 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTT>-,TT,TTTT,TTTTT,TTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 1:236537029 (GRCh38)
1:236700329 (GRCh37)
Canonical SPDI:: NC_000001.11:236537021:TTTTTTTTTTTTT:TTTTTTT,NC_000001.11:236537021:TTTTTTTTTTTTT:TTTTTTTTT,NC_000001.11:236537021:TTTTTTTTTTTTT:TTTTTTTTTTT,NC_000001.11:236537021:TTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000001.11:236537021:TTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000001.11:236537021:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000001.11:236537021:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000001.11:236537021:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000001.11:236537021:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000001.11:236537021:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000001.11:236537021:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000001.11:236537021:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:236537021:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:236537021:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:236537021:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:236537021:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:236537021:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:236537021:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:236537021:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:236537021:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:236537021:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:236537021:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:236537021:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:236537021:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:236537021:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:236537021:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:236537021:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:236537021:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:236537021:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:236537021:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:236537021:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: LGALS8 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTT=0./0 (ALFA)
-=0.2899/1452 (1000Genomes)
HGVS:: NC_000001.11:g.236537029_236537034del, NC_000001.11:g.236537031_236537034del, NC_000001.11:g.236537033_236537034del, NC_000001.11:g.236537034del, NC_000001.11:g.236537034dup, NC_000001.11:g.236537032_236537034dup, NC_000001.11:g.236537031_236537034dup, NC_000001.11:g.236537030_236537034dup, NC_000001.11:g.236537029_236537034dup, NC_000001.11:g.236537028_236537034dup, NC_000001.11:g.236537027_236537034dup, NC_000001.11:g.236537026_236537034dup, NC_000001.11:g.236537025_236537034dup, NC_000001.11:g.236537024_236537034dup, NC_000001.11:g.236537023_236537034dup, NC_000001.11:g.236537022_236537034dup, NC_000001.11:g.236537034_236537035insTTTTTTTTTTTTTT, NC_000001.11:g.236537034_236537035insTTTTTTTTTTTTTTT, NC_000001.11:g.236537034_236537035insTTTTTTTTTTTTTTTT, NC_000001.11:g.236537034_236537035insTTTTTTTTTTTTTTTTT, NC_000001.11:g.236537034_236537035insTTTTTTTTTTTTTTTTTT, NC_000001.11:g.236537034_236537035insTTTTTTTTTTTTTTTTTTT, NC_000001.11:g.236537034_236537035insTTTTTTTTTTTTTTTTTTTT, NC_000001.11:g.236537034_236537035insTTTTTTTTTTTTTTTTTTTTT, NC_000001.11:g.236537034_236537035insTTTTTTTTTTTTTTTTTTTTTT, NC_000001.11:g.236537034_236537035insTTTTTTTTTTTTTTTTTTTTTTT, NC_000001.11:g.236537034_236537035insTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000001.11:g.236537034_236537035insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000001.11:g.236537034_236537035insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000001.11:g.236537034_236537035insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000001.11:g.236537034_236537035insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000001.10:g.236700329_236700334del, NC_000001.10:g.236700331_236700334del, NC_000001.10:g.236700333_236700334del, NC_000001.10:g.236700334del, NC_000001.10:g.236700334dup, NC_000001.10:g.236700332_236700334dup, NC_000001.10:g.236700331_236700334dup, NC_000001.10:g.236700330_236700334dup, NC_000001.10:g.236700329_236700334dup, NC_000001.10:g.236700328_236700334dup, NC_000001.10:g.236700327_236700334dup, NC_000001.10:g.236700326_236700334dup, NC_000001.10:g.236700325_236700334dup, NC_000001.10:g.236700324_236700334dup, NC_000001.10:g.236700323_236700334dup, NC_000001.10:g.236700322_236700334dup, NC_000001.10:g.236700334_236700335insTTTTTTTTTTTTTT, NC_000001.10:g.236700334_236700335insTTTTTTTTTTTTTTT, NC_000001.10:g.236700334_236700335insTTTTTTTTTTTTTTTT, NC_000001.10:g.236700334_236700335insTTTTTTTTTTTTTTTTT, NC_000001.10:g.236700334_236700335insTTTTTTTTTTTTTTTTTT, NC_000001.10:g.236700334_236700335insTTTTTTTTTTTTTTTTTTT, NC_000001.10:g.236700334_236700335insTTTTTTTTTTTTTTTTTTTT, NC_000001.10:g.236700334_236700335insTTTTTTTTTTTTTTTTTTTTT, NC_000001.10:g.236700334_236700335insTTTTTTTTTTTTTTTTTTTTTT, NC_000001.10:g.236700334_236700335insTTTTTTTTTTTTTTTTTTTTTTT, NC_000001.10:g.236700334_236700335insTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000001.10:g.236700334_236700335insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000001.10:g.236700334_236700335insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000001.10:g.236700334_236700335insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000001.10:g.236700334_236700335insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Select item 149111057917.

rs1491110579 [Homo sapiens]

Variant type:: DEL
Alleles:: CT>- [Show Flanks]
Chromosome:: 1:236533970 (GRCh38)
1:236697270 (GRCh37)
Canonical SPDI:: NC_000001.11:236533969:CT:
Gene:: LGALS8 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0./0 (ALFA)
-=0.000011/3 (TOPMED)
-=0.00002/1 (GnomAD)
HGVS:: NC_000001.11:g.236533970_236533971del, NC_000001.10:g.236697270_236697271del

Select item 149107680218.

rs1491076802 has merged into rs74680187 [Homo sapiens]

Variant type:: DELINS
Alleles:: AA>-,A,AAA,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA [Show Flanks]
Chromosome:: 1:236527697 (GRCh38)
1:236690997 (GRCh37)
Canonical SPDI:: NC_000001.11:236527689:AAAAAAAAA:AAAAAAA,NC_000001.11:236527689:AAAAAAAAA:AAAAAAAA,NC_000001.11:236527689:AAAAAAAAA:AAAAAAAAAA,NC_000001.11:236527689:AAAAAAAAA:AAAAAAAAAAA,NC_000001.11:236527689:AAAAAAAAA:AAAAAAAAAAAA,NC_000001.11:236527689:AAAAAAAAA:AAAAAAAAAAAAA,NC_000001.11:236527689:AAAAAAAAA:AAAAAAAAAAAAAA,NC_000001.11:236527689:AAAAAAAAA:AAAAAAAAAAAAAAA
Gene:: LGALS8 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAA=0./0 (ALFA)
A=0.1725/530 (1000Genomes)
HGVS:: NC_000001.11:g.236527697_236527698del, NC_000001.11:g.236527698del, NC_000001.11:g.236527698dup, NC_000001.11:g.236527697_236527698dup, NC_000001.11:g.236527696_236527698dup, NC_000001.11:g.236527695_236527698dup, NC_000001.11:g.236527694_236527698dup, NC_000001.11:g.236527693_236527698dup, NC_000001.10:g.236690997_236690998del, NC_000001.10:g.236690998del, NC_000001.10:g.236690998dup, NC_000001.10:g.236690997_236690998dup, NC_000001.10:g.236690996_236690998dup, NC_000001.10:g.236690995_236690998dup, NC_000001.10:g.236690994_236690998dup, NC_000001.10:g.236690993_236690998dup

Select item 149107058719.

rs1491070587 [Homo sapiens]

Variant type:: DELINS
Alleles:: GAGA>-,GA [Show Flanks]
Chromosome:: 1:236516615 (GRCh38)
1:236679915 (GRCh37)
Canonical SPDI:: NC_000001.11:236516613:AGAGA:A,NC_000001.11:236516613:AGAGA:AGA
Gene:: LGALS8 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AGA=0./0 (ALFA)
-=0.000008/1 (GnomAD)
-=0.000034/9 (TOPMED)
HGVS:: NC_000001.11:g.236516615_236516618del, NC_000001.11:g.236516615GA[1], NC_000001.10:g.236679915_236679918del, NC_000001.10:g.236679915GA[1]

Select item 149104122220.

rs1491041222 has merged into rs55866014 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAA>-,A,AA,AAAAAAA,AAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 1:236551002 (GRCh38)
1:236714302 (GRCh37)
Canonical SPDI:: NC_000001.11:236550992:AAAAAAAAAAAAAAAAAA:AAAAAAAAA,NC_000001.11:236550992:AAAAAAAAAAAAAAAAAA:AAAAAAAAAA,NC_000001.11:236550992:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000001.11:236550992:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000001.11:236550992:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000001.11:236550992:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000001.11:236550992:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000001.11:236550992:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000001.11:236550992:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:236550992:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:236550992:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:236550992:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:236550992:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:236550992:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:236550992:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:236550992:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: LGALS8 (Varview), HEATR1 (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant,3_prime_UTR_variant
Clinical significance:: benign
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAA=0./0 (ALFA)
HGVS:: NC_000001.11:g.236551002_236551010del, NC_000001.11:g.236551003_236551010del, NC_000001.11:g.236551004_236551010del, NC_000001.11:g.236551009_236551010del, NC_000001.11:g.236551010del, NC_000001.11:g.236551010dup, NC_000001.11:g.236551009_236551010dup, NC_000001.11:g.236551008_236551010dup, NC_000001.11:g.236551007_236551010dup, NC_000001.11:g.236551006_236551010dup, NC_000001.11:g.236551005_236551010dup, NC_000001.11:g.236551004_236551010dup, NC_000001.11:g.236551003_236551010dup, NC_000001.11:g.236551002_236551010dup, NC_000001.11:g.236550998_236551010dup, NC_000001.11:g.236550997_236551010dup, NC_000001.10:g.236714302_236714310del, NC_000001.10:g.236714303_236714310del, NC_000001.10:g.236714304_236714310del, NC_000001.10:g.236714309_236714310del, NC_000001.10:g.236714310del, NC_000001.10:g.236714310dup, NC_000001.10:g.236714309_236714310dup, NC_000001.10:g.236714308_236714310dup, NC_000001.10:g.236714307_236714310dup, NC_000001.10:g.236714306_236714310dup, NC_000001.10:g.236714305_236714310dup, NC_000001.10:g.236714304_236714310dup, NC_000001.10:g.236714303_236714310dup, NC_000001.10:g.236714302_236714310dup, NC_000001.10:g.236714298_236714310dup, NC_000001.10:g.236714297_236714310dup, NM_006499.5:c.*2841_*2849del, NM_006499.5:c.*2842_*2849del, NM_006499.5:c.*2843_*2849del, NM_006499.5:c.*2848_*2849del, NM_006499.5:c.*2849del, NM_006499.5:c.*2849dup, NM_006499.5:c.*2848_*2849dup, NM_006499.5:c.*2847_*2849dup, NM_006499.5:c.*2846_*2849dup, NM_006499.5:c.*2845_*2849dup, NM_006499.5:c.*2844_*2849dup, NM_006499.5:c.*2843_*2849dup, NM_006499.5:c.*2842_*2849dup, NM_006499.5:c.*2841_*2849dup, NM_006499.5:c.*2837_*2849dup, NM_006499.5:c.*2836_*2849dup, NM_006499.4:c.*2841_*2849del, NM_006499.4:c.*2842_*2849del, NM_006499.4:c.*2843_*2849del, NM_006499.4:c.*2848_*2849del, NM_006499.4:c.*2849del, NM_006499.4:c.*2849dup, NM_006499.4:c.*2848_*2849dup, NM_006499.4:c.*2847_*2849dup, NM_006499.4:c.*2846_*2849dup, NM_006499.4:c.*2845_*2849dup, NM_006499.4:c.*2844_*2849dup, NM_006499.4:c.*2843_*2849dup, NM_006499.4:c.*2842_*2849dup, NM_006499.4:c.*2841_*2849dup, NM_006499.4:c.*2837_*2849dup, NM_006499.4:c.*2836_*2849dup, NM_201543.4:c.*2841_*2849del, NM_201543.4:c.*2842_*2849del, NM_201543.4:c.*2843_*2849del, NM_201543.4:c.*2848_*2849del, NM_201543.4:c.*2849del, NM_201543.4:c.*2849dup, NM_201543.4:c.*2848_*2849dup, NM_201543.4:c.*2847_*2849dup, NM_201543.4:c.*2846_*2849dup, NM_201543.4:c.*2845_*2849dup, NM_201543.4:c.*2844_*2849dup, NM_201543.4:c.*2843_*2849dup, NM_201543.4:c.*2842_*2849dup, NM_201543.4:c.*2841_*2849dup, NM_201543.4:c.*2837_*2849dup, NM_201543.4:c.*2836_*2849dup, NM_201543.3:c.*2841_*2849del, NM_201543.3:c.*2842_*2849del, NM_201543.3:c.*2843_*2849del, NM_201543.3:c.*2848_*2849del, NM_201543.3:c.*2849del, NM_201543.3:c.*2849dup, NM_201543.3:c.*2848_*2849dup, NM_201543.3:c.*2847_*2849dup, NM_201543.3:c.*2846_*2849dup, NM_201543.3:c.*2845_*2849dup, NM_201543.3:c.*2844_*2849dup, NM_201543.3:c.*2843_*2849dup, NM_201543.3:c.*2842_*2849dup, NM_201543.3:c.*2841_*2849dup, NM_201543.3:c.*2837_*2849dup, NM_201543.3:c.*2836_*2849dup, NM_201543.2:c.*2841_*2849del, NM_201543.2:c.*2842_*2849del, NM_201543.2:c.*2843_*2849del, NM_201543.2:c.*2848_*2849del, NM_201543.2:c.*2849del, NM_201543.2:c.*2849dup, NM_201543.2:c.*2848_*2849dup, NM_201543.2:c.*2847_*2849dup, NM_201543.2:c.*2846_*2849dup, NM_201543.2:c.*2845_*2849dup, NM_201543.2:c.*2844_*2849dup, NM_201543.2:c.*2843_*2849dup, NM_201543.2:c.*2842_*2849dup, NM_201543.2:c.*2841_*2849dup, NM_201543.2:c.*2837_*2849dup, NM_201543.2:c.*2836_*2849dup, NM_201544.4:c.*2841_*2849del, NM_201544.4:c.*2842_*2849del, NM_201544.4:c.*2843_*2849del, NM_201544.4:c.*2848_*2849del, NM_201544.4:c.*2849del, NM_201544.4:c.*2849dup, NM_201544.4:c.*2848_*2849dup, NM_201544.4:c.*2847_*2849dup, NM_201544.4:c.*2846_*2849dup, NM_201544.4:c.*2845_*2849dup, NM_201544.4:c.*2844_*2849dup, NM_201544.4:c.*2843_*2849dup, NM_201544.4:c.*2842_*2849dup, NM_201544.4:c.*2841_*2849dup, NM_201544.4:c.*2837_*2849dup, NM_201544.4:c.*2836_*2849dup, NM_201544.3:c.*2841_*2849del, NM_201544.3:c.*2842_*2849del, NM_201544.3:c.*2843_*2849del, NM_201544.3:c.*2848_*2849del, NM_201544.3:c.*2849del, NM_201544.3:c.*2849dup, NM_201544.3:c.*2848_*2849dup, NM_201544.3:c.*2847_*2849dup, NM_201544.3:c.*2846_*2849dup, NM_201544.3:c.*2845_*2849dup, NM_201544.3:c.*2844_*2849dup, NM_201544.3:c.*2843_*2849dup, NM_201544.3:c.*2842_*2849dup, NM_201544.3:c.*2841_*2849dup, NM_201544.3:c.*2837_*2849dup, NM_201544.3:c.*2836_*2849dup, NM_201544.2:c.*2841_*2849del, NM_201544.2:c.*2842_*2849del, NM_201544.2:c.*2843_*2849del, NM_201544.2:c.*2848_*2849del, NM_201544.2:c.*2849del, NM_201544.2:c.*2849dup, NM_201544.2:c.*2848_*2849dup, NM_201544.2:c.*2847_*2849dup, NM_201544.2:c.*2846_*2849dup, NM_201544.2:c.*2845_*2849dup, NM_201544.2:c.*2844_*2849dup, NM_201544.2:c.*2843_*2849dup, NM_201544.2:c.*2842_*2849dup, NM_201544.2:c.*2841_*2849dup, NM_201544.2:c.*2837_*2849dup, NM_201544.2:c.*2836_*2849dup, NM_201545.2:c.*2841_*2849del, NM_201545.2:c.*2842_*2849del, NM_201545.2:c.*2843_*2849del, NM_201545.2:c.*2848_*2849del, NM_201545.2:c.*2849del, NM_201545.2:c.*2849dup, NM_201545.2:c.*2848_*2849dup, NM_201545.2:c.*2847_*2849dup, NM_201545.2:c.*2846_*2849dup, NM_201545.2:c.*2845_*2849dup, NM_201545.2:c.*2844_*2849dup, NM_201545.2:c.*2843_*2849dup, NM_201545.2:c.*2842_*2849dup, NM_201545.2:c.*2841_*2849dup, NM_201545.2:c.*2837_*2849dup, NM_201545.2:c.*2836_*2849dup, XM_047420410.1:c.*2841_*2849del, XM_047420410.1:c.*2842_*2849del, XM_047420410.1:c.*2843_*2849del, XM_047420410.1:c.*2848_*2849del, XM_047420410.1:c.*2849del, XM_047420410.1:c.*2849dup, XM_047420410.1:c.*2848_*2849dup, XM_047420410.1:c.*2847_*2849dup, XM_047420410.1:c.*2846_*2849dup, XM_047420410.1:c.*2845_*2849dup, XM_047420410.1:c.*2844_*2849dup, XM_047420410.1:c.*2843_*2849dup, XM_047420410.1:c.*2842_*2849dup, XM_047420410.1:c.*2841_*2849dup, XM_047420410.1:c.*2837_*2849dup, XM_047420410.1:c.*2836_*2849dup, XM_047420411.1:c.*2841_*2849del, XM_047420411.1:c.*2842_*2849del, XM_047420411.1:c.*2843_*2849del, XM_047420411.1:c.*2848_*2849del, XM_047420411.1:c.*2849del, XM_047420411.1:c.*2849dup, XM_047420411.1:c.*2848_*2849dup, XM_047420411.1:c.*2847_*2849dup, XM_047420411.1:c.*2846_*2849dup, XM_047420411.1:c.*2845_*2849dup, XM_047420411.1:c.*2844_*2849dup, XM_047420411.1:c.*2843_*2849dup, XM_047420411.1:c.*2842_*2849dup, XM_047420411.1:c.*2841_*2849dup, XM_047420411.1:c.*2837_*2849dup, XM_047420411.1:c.*2836_*2849dup, XM_047420409.1:c.*2841_*2849del, XM_047420409.1:c.*2842_*2849del, XM_047420409.1:c.*2843_*2849del, XM_047420409.1:c.*2848_*2849del, XM_047420409.1:c.*2849del, XM_047420409.1:c.*2849dup, XM_047420409.1:c.*2848_*2849dup, XM_047420409.1:c.*2847_*2849dup, XM_047420409.1:c.*2846_*2849dup, XM_047420409.1:c.*2845_*2849dup, XM_047420409.1:c.*2844_*2849dup, XM_047420409.1:c.*2843_*2849dup, XM_047420409.1:c.*2842_*2849dup, XM_047420409.1:c.*2841_*2849dup, XM_047420409.1:c.*2837_*2849dup, XM_047420409.1:c.*2836_*2849dup, XM_047420416.1:c.*2841_*2849del, XM_047420416.1:c.*2842_*2849del, XM_047420416.1:c.*2843_*2849del, XM_047420416.1:c.*2848_*2849del, XM_047420416.1:c.*2849del, XM_047420416.1:c.*2849dup, XM_047420416.1:c.*2848_*2849dup, XM_047420416.1:c.*2847_*2849dup, XM_047420416.1:c.*2846_*2849dup, XM_047420416.1:c.*2845_*2849dup, XM_047420416.1:c.*2844_*2849dup, XM_047420416.1:c.*2843_*2849dup, XM_047420416.1:c.*2842_*2849dup, XM_047420416.1:c.*2841_*2849dup, XM_047420416.1:c.*2837_*2849dup, XM_047420416.1:c.*2836_*2849dup

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