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Select item 14915696081.

rs1491569608 [Homo sapiens]

Variant type:: DEL
Alleles:: CA>- [Show Flanks]
Chromosome:: 10:62077530 (GRCh38)
10:63837289 (GRCh37)
Canonical SPDI:: NC_000010.11:62077529:CA:
Gene:: ARID5B (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0./0 (ALFA)
-=0.000008/1 (GnomAD)
-=0.000008/2 (TOPMED)
-=0.000035/1 (TOMMO)
HGVS:: NC_000010.11:g.62077530_62077531del, NC_000010.10:g.63837289_63837290del, NG_030027.1:g.181277_181278del

Select item 14915458552.

rs1491545855 has merged into rs1318859700 [Homo sapiens]

Variant type:: DELINS
Alleles:: TCTC>-,TC,TCTCTC [Show Flanks]
Chromosome:: 10:62083067 (GRCh38)
10:63842826 (GRCh37)
Canonical SPDI:: NC_000010.11:62083063:CTCTCTC:CTC,NC_000010.11:62083063:CTCTCTC:CTCTC,NC_000010.11:62083063:CTCTCTC:CTCTCTCTC
Gene:: ARID5B (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: CTCTC=0./0 (ALFA)
CT=0.000011/3 (TOPMED)
HGVS:: NC_000010.11:g.62083065TC[1], NC_000010.11:g.62083065TC[2], NC_000010.11:g.62083065TC[4], NC_000010.10:g.63842824TC[1], NC_000010.10:g.63842824TC[2], NC_000010.10:g.63842824TC[4], NG_030027.1:g.186812TC[1], NG_030027.1:g.186812TC[2], NG_030027.1:g.186812TC[4]

Select item 14915443843.

rs1491544384 has merged into rs71299289 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAA>-,A,AA,AAA,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 10:62087310 (GRCh38)
10:63847069 (GRCh37)
Canonical SPDI:: NC_000010.11:62087298:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000010.11:62087298:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000010.11:62087298:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000010.11:62087298:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000010.11:62087298:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000010.11:62087298:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000010.11:62087298:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000010.11:62087298:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000010.11:62087298:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000010.11:62087298:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000010.11:62087298:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:62087298:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:62087298:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:62087298:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:62087298:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:62087298:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:62087298:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:62087298:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:62087298:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:62087298:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:62087298:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:62087298:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:62087298:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:62087298:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:62087298:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:62087298:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:62087298:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:62087298:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:62087298:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:62087298:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:62087298:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:62087298:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:62087298:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: ARID5B (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAAA=0./0 (ALFA)
HGVS:: NC_000010.11:g.62087310_62087318del, NC_000010.11:g.62087311_62087318del, NC_000010.11:g.62087312_62087318del, NC_000010.11:g.62087313_62087318del, NC_000010.11:g.62087314_62087318del, NC_000010.11:g.62087315_62087318del, NC_000010.11:g.62087316_62087318del, NC_000010.11:g.62087317_62087318del, NC_000010.11:g.62087318del, NC_000010.11:g.62087318dup, NC_000010.11:g.62087317_62087318dup, NC_000010.11:g.62087316_62087318dup, NC_000010.11:g.62087315_62087318dup, NC_000010.11:g.62087314_62087318dup, NC_000010.11:g.62087313_62087318dup, NC_000010.11:g.62087312_62087318dup, NC_000010.11:g.62087311_62087318dup, NC_000010.11:g.62087310_62087318dup, NC_000010.11:g.62087309_62087318dup, NC_000010.11:g.62087308_62087318dup, NC_000010.11:g.62087307_62087318dup, NC_000010.11:g.62087306_62087318dup, NC_000010.11:g.62087305_62087318dup, NC_000010.11:g.62087304_62087318dup, NC_000010.11:g.62087303_62087318dup, NC_000010.11:g.62087302_62087318dup, NC_000010.11:g.62087301_62087318dup, NC_000010.11:g.62087300_62087318dup, NC_000010.11:g.62087299_62087318dup, NC_000010.11:g.62087318_62087319insAAAAAAAAAAAAAAAAAAAAAA, NC_000010.11:g.62087318_62087319insAAAAAAAAAAAAAAAAAAAAAAA, NC_000010.11:g.62087318_62087319insAAAAAAAAAAAAAAAAAAAAAAAA, NC_000010.11:g.62087318_62087319insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000010.10:g.63847069_63847077del, NC_000010.10:g.63847070_63847077del, NC_000010.10:g.63847071_63847077del, NC_000010.10:g.63847072_63847077del, NC_000010.10:g.63847073_63847077del, NC_000010.10:g.63847074_63847077del, NC_000010.10:g.63847075_63847077del, NC_000010.10:g.63847076_63847077del, NC_000010.10:g.63847077del, NC_000010.10:g.63847077dup, NC_000010.10:g.63847076_63847077dup, NC_000010.10:g.63847075_63847077dup, NC_000010.10:g.63847074_63847077dup, NC_000010.10:g.63847073_63847077dup, NC_000010.10:g.63847072_63847077dup, NC_000010.10:g.63847071_63847077dup, NC_000010.10:g.63847070_63847077dup, NC_000010.10:g.63847069_63847077dup, NC_000010.10:g.63847068_63847077dup, NC_000010.10:g.63847067_63847077dup, NC_000010.10:g.63847066_63847077dup, NC_000010.10:g.63847065_63847077dup, NC_000010.10:g.63847064_63847077dup, NC_000010.10:g.63847063_63847077dup, NC_000010.10:g.63847062_63847077dup, NC_000010.10:g.63847061_63847077dup, NC_000010.10:g.63847060_63847077dup, NC_000010.10:g.63847059_63847077dup, NC_000010.10:g.63847058_63847077dup, NC_000010.10:g.63847077_63847078insAAAAAAAAAAAAAAAAAAAAAA, NC_000010.10:g.63847077_63847078insAAAAAAAAAAAAAAAAAAAAAAA, NC_000010.10:g.63847077_63847078insAAAAAAAAAAAAAAAAAAAAAAAA, NC_000010.10:g.63847077_63847078insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_030027.1:g.191057_191065del, NG_030027.1:g.191058_191065del, NG_030027.1:g.191059_191065del, NG_030027.1:g.191060_191065del, NG_030027.1:g.191061_191065del, NG_030027.1:g.191062_191065del, NG_030027.1:g.191063_191065del, NG_030027.1:g.191064_191065del, NG_030027.1:g.191065del, NG_030027.1:g.191065dup, NG_030027.1:g.191064_191065dup, NG_030027.1:g.191063_191065dup, NG_030027.1:g.191062_191065dup, NG_030027.1:g.191061_191065dup, NG_030027.1:g.191060_191065dup, NG_030027.1:g.191059_191065dup, NG_030027.1:g.191058_191065dup, NG_030027.1:g.191057_191065dup, NG_030027.1:g.191056_191065dup, NG_030027.1:g.191055_191065dup, NG_030027.1:g.191054_191065dup, NG_030027.1:g.191053_191065dup, NG_030027.1:g.191052_191065dup, NG_030027.1:g.191051_191065dup, NG_030027.1:g.191050_191065dup, NG_030027.1:g.191049_191065dup, NG_030027.1:g.191048_191065dup, NG_030027.1:g.191047_191065dup, NG_030027.1:g.191046_191065dup, NG_030027.1:g.191065_191066insAAAAAAAAAAAAAAAAAAAAAA, NG_030027.1:g.191065_191066insAAAAAAAAAAAAAAAAAAAAAAA, NG_030027.1:g.191065_191066insAAAAAAAAAAAAAAAAAAAAAAAA, NG_030027.1:g.191065_191066insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

Select item 14915088244.

rs1491508824 has merged into rs199587188 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTTTTTTTTTTT>-,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 10:61947269 (GRCh38)
10:63707028 (GRCh37)
Canonical SPDI:: NC_000010.11:61947261:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTT,NC_000010.11:61947261:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000010.11:61947261:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000010.11:61947261:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000010.11:61947261:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000010.11:61947261:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000010.11:61947261:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000010.11:61947261:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000010.11:61947261:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000010.11:61947261:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000010.11:61947261:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000010.11:61947261:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000010.11:61947261:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000010.11:61947261:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:61947261:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:61947261:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:61947261:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:61947261:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:61947261:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:61947261:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:61947261:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:61947261:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:61947261:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:61947261:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:61947261:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:61947261:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:61947261:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:61947261:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:61947261:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:61947261:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:61947261:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:61947261:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:61947261:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:61947261:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:61947261:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:61947261:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:61947261:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:61947261:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:61947261:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:61947261:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:61947261:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:61947261:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:61947261:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:61947261:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:61947261:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:61947261:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:61947261:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:61947261:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:61947261:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:61947261:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:61947261:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:61947261:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:61947261:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:61947261:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:61947261:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:61947261:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:61947261:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:61947261:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: ARID5B (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTT=0./0 (ALFA)
TTTTTTTTTTTTTT=0./0 (GENOME_DK)
TTTTTTTTTTTTTT=0.0064/32 (1000Genomes)
HGVS:: NC_000010.11:g.61947269_61947286del, NC_000010.11:g.61947272_61947286del, NC_000010.11:g.61947273_61947286del, NC_000010.11:g.61947274_61947286del, NC_000010.11:g.61947275_61947286del, NC_000010.11:g.61947276_61947286del, NC_000010.11:g.61947277_61947286del, NC_000010.11:g.61947278_61947286del, NC_000010.11:g.61947279_61947286del, NC_000010.11:g.61947280_61947286del, NC_000010.11:g.61947281_61947286del, NC_000010.11:g.61947282_61947286del, NC_000010.11:g.61947283_61947286del, NC_000010.11:g.61947284_61947286del, NC_000010.11:g.61947285_61947286del, NC_000010.11:g.61947286del, NC_000010.11:g.61947286dup, NC_000010.11:g.61947285_61947286dup, NC_000010.11:g.61947284_61947286dup, NC_000010.11:g.61947283_61947286dup, NC_000010.11:g.61947282_61947286dup, NC_000010.11:g.61947281_61947286dup, NC_000010.11:g.61947280_61947286dup, NC_000010.11:g.61947279_61947286dup, NC_000010.11:g.61947278_61947286dup, NC_000010.11:g.61947277_61947286dup, NC_000010.11:g.61947276_61947286dup, NC_000010.11:g.61947275_61947286dup, NC_000010.11:g.61947274_61947286dup, NC_000010.11:g.61947273_61947286dup, NC_000010.11:g.61947272_61947286dup, NC_000010.11:g.61947271_61947286dup, NC_000010.11:g.61947270_61947286dup, NC_000010.11:g.61947269_61947286dup, NC_000010.11:g.61947268_61947286dup, NC_000010.11:g.61947267_61947286dup, NC_000010.11:g.61947266_61947286dup, NC_000010.11:g.61947265_61947286dup, NC_000010.11:g.61947264_61947286dup, NC_000010.11:g.61947263_61947286dup, NC_000010.11:g.61947262_61947286dup, NC_000010.11:g.61947286_61947287insTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000010.11:g.61947286_61947287insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000010.11:g.61947286_61947287insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000010.11:g.61947286_61947287insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000010.11:g.61947286_61947287insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000010.11:g.61947286_61947287insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000010.11:g.61947286_61947287insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000010.11:g.61947286_61947287insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000010.11:g.61947286_61947287insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000010.11:g.61947286_61947287insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000010.11:g.61947286_61947287insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000010.11:g.61947286_61947287insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000010.11:g.61947286_61947287insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000010.11:g.61947286_61947287insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000010.11:g.61947286_61947287insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000010.11:g.61947286_61947287insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000010.11:g.61947286_61947287insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000010.10:g.63707028_63707045del, NC_000010.10:g.63707031_63707045del, NC_000010.10:g.63707032_63707045del, NC_000010.10:g.63707033_63707045del, NC_000010.10:g.63707034_63707045del, NC_000010.10:g.63707035_63707045del, NC_000010.10:g.63707036_63707045del, NC_000010.10:g.63707037_63707045del, NC_000010.10:g.63707038_63707045del, NC_000010.10:g.63707039_63707045del, NC_000010.10:g.63707040_63707045del, NC_000010.10:g.63707041_63707045del, NC_000010.10:g.63707042_63707045del, NC_000010.10:g.63707043_63707045del, NC_000010.10:g.63707044_63707045del, NC_000010.10:g.63707045del, NC_000010.10:g.63707045dup, NC_000010.10:g.63707044_63707045dup, NC_000010.10:g.63707043_63707045dup, NC_000010.10:g.63707042_63707045dup, NC_000010.10:g.63707041_63707045dup, NC_000010.10:g.63707040_63707045dup, NC_000010.10:g.63707039_63707045dup, NC_000010.10:g.63707038_63707045dup, NC_000010.10:g.63707037_63707045dup, NC_000010.10:g.63707036_63707045dup, NC_000010.10:g.63707035_63707045dup, NC_000010.10:g.63707034_63707045dup, NC_000010.10:g.63707033_63707045dup, NC_000010.10:g.63707032_63707045dup, NC_000010.10:g.63707031_63707045dup, NC_000010.10:g.63707030_63707045dup, NC_000010.10:g.63707029_63707045dup, NC_000010.10:g.63707028_63707045dup, NC_000010.10:g.63707027_63707045dup, NC_000010.10:g.63707026_63707045dup, NC_000010.10:g.63707025_63707045dup, NC_000010.10:g.63707024_63707045dup, NC_000010.10:g.63707023_63707045dup, NC_000010.10:g.63707022_63707045dup, NC_000010.10:g.63707021_63707045dup, NC_000010.10:g.63707045_63707046insTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000010.10:g.63707045_63707046insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000010.10:g.63707045_63707046insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000010.10:g.63707045_63707046insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000010.10:g.63707045_63707046insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000010.10:g.63707045_63707046insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000010.10:g.63707045_63707046insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000010.10:g.63707045_63707046insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000010.10:g.63707045_63707046insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000010.10:g.63707045_63707046insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000010.10:g.63707045_63707046insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000010.10:g.63707045_63707046insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000010.10:g.63707045_63707046insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000010.10:g.63707045_63707046insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000010.10:g.63707045_63707046insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000010.10:g.63707045_63707046insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000010.10:g.63707045_63707046insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_030027.1:g.51016_51033del, NG_030027.1:g.51019_51033del, NG_030027.1:g.51020_51033del, NG_030027.1:g.51021_51033del, NG_030027.1:g.51022_51033del, NG_030027.1:g.51023_51033del, NG_030027.1:g.51024_51033del, NG_030027.1:g.51025_51033del, NG_030027.1:g.51026_51033del, NG_030027.1:g.51027_51033del, NG_030027.1:g.51028_51033del, NG_030027.1:g.51029_51033del, NG_030027.1:g.51030_51033del, NG_030027.1:g.51031_51033del, NG_030027.1:g.51032_51033del, NG_030027.1:g.51033del, NG_030027.1:g.51033dup, NG_030027.1:g.51032_51033dup, NG_030027.1:g.51031_51033dup, NG_030027.1:g.51030_51033dup, NG_030027.1:g.51029_51033dup, NG_030027.1:g.51028_51033dup, NG_030027.1:g.51027_51033dup, NG_030027.1:g.51026_51033dup, NG_030027.1:g.51025_51033dup, NG_030027.1:g.51024_51033dup, NG_030027.1:g.51023_51033dup, NG_030027.1:g.51022_51033dup, NG_030027.1:g.51021_51033dup, NG_030027.1:g.51020_51033dup, NG_030027.1:g.51019_51033dup, NG_030027.1:g.51018_51033dup, NG_030027.1:g.51017_51033dup, NG_030027.1:g.51016_51033dup, NG_030027.1:g.51015_51033dup, NG_030027.1:g.51014_51033dup, NG_030027.1:g.51013_51033dup, NG_030027.1:g.51012_51033dup, NG_030027.1:g.51011_51033dup, NG_030027.1:g.51010_51033dup, NG_030027.1:g.51009_51033dup, NG_030027.1:g.51033_51034insTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_030027.1:g.51033_51034insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_030027.1:g.51033_51034insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_030027.1:g.51033_51034insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_030027.1:g.51033_51034insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_030027.1:g.51033_51034insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_030027.1:g.51033_51034insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_030027.1:g.51033_51034insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_030027.1:g.51033_51034insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_030027.1:g.51033_51034insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_030027.1:g.51033_51034insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_030027.1:g.51033_51034insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_030027.1:g.51033_51034insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_030027.1:g.51033_51034insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_030027.1:g.51033_51034insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_030027.1:g.51033_51034insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_030027.1:g.51033_51034insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Select item 14914887275.

rs1491488727 [Homo sapiens]

Variant type:: DEL
Alleles:: CA>- [Show Flanks]
Chromosome:: 10:62042914 (GRCh38)
10:63802673 (GRCh37)
Canonical SPDI:: NC_000010.11:62042913:CA:
Gene:: ARID5B (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0./0 (ALFA)
-=0.00031/9 (GnomAD)
HGVS:: NC_000010.11:g.62042914_62042915del, NC_000010.10:g.63802673_63802674del, NG_030027.1:g.146661_146662del

Select item 14914881916.

rs1491488191 [Homo sapiens]

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

Select item 14914728917.

rs1491472891 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->T [Show Flanks]
Chromosome:: 10:61903528 (GRCh38)
10:63663288 (GRCh37)
Canonical SPDI:: NC_000010.11:61903528:T:TT
Gene:: ARID5B (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: TT=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000010.11:g.61903529dup, NC_000010.10:g.63663288dup, NG_030027.1:g.7276dup

Select item 14914682408.

rs1491468240 [Homo sapiens]

Variant type:: DELINS
Alleles:: A>-,AA,AAA [Show Flanks]
Chromosome:: 10:61919053 (GRCh38)
10:63678812 (GRCh37)
Canonical SPDI:: NC_000010.11:61919052:AAAAAAA:AAAAAA,NC_000010.11:61919052:AAAAAAA:AAAAAAAA,NC_000010.11:61919052:AAAAAAA:AAAAAAAAA
Gene:: ARID5B (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAA=0./0 (ALFA)
-=0.000004/1 (TOPMED)
HGVS:: NC_000010.11:g.61919059del, NC_000010.11:g.61919059dup, NC_000010.11:g.61919058_61919059dup, NC_000010.10:g.63678818del, NC_000010.10:g.63678818dup, NC_000010.10:g.63678817_63678818dup, NG_030027.1:g.22806del, NG_030027.1:g.22806dup, NG_030027.1:g.22805_22806dup

Select item 14914644079.

rs1491464407 has merged into rs1554841204 [Homo sapiens]

Variant type:: DELINS
Alleles:: AA>-,AAA [Show Flanks]
Chromosome:: 10:61968215 (GRCh38)
10:63727974 (GRCh37)
Canonical SPDI:: NC_000010.11:61968213:AAA:A,NC_000010.11:61968213:AAA:AAAA
Gene:: ARID5B (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.007672/91 (ALFA)
-=0.008986/45 (1000Genomes)
-=0.008988/1231 (GnomAD)
HGVS:: NC_000010.11:g.61968215_61968216del, NC_000010.11:g.61968216dup, NC_000010.10:g.63727974_63727975del, NC_000010.10:g.63727975dup, NG_030027.1:g.71962_71963del, NG_030027.1:g.71963dup

Select item 149145655910.

rs1491456559 has merged into rs59459790 [Homo sapiens]

Variant type:: DELINS
Alleles:: GTGTGTGTGTGTGT>-,GT,GTGT,GTGTGT,GTGTGTGT,GTGTGTGTGT,GTGTGTGTGTGT,GTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT [Show Flanks]
Chromosome:: 10:61902689 (GRCh38)
10:63662448 (GRCh37)
Canonical SPDI:: NC_000010.11:61902673:TGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGT,NC_000010.11:61902673:TGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGT,NC_000010.11:61902673:TGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGT,NC_000010.11:61902673:TGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGT,NC_000010.11:61902673:TGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGT,NC_000010.11:61902673:TGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGT,NC_000010.11:61902673:TGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000010.11:61902673:TGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000010.11:61902673:TGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000010.11:61902673:TGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000010.11:61902673:TGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000010.11:61902673:TGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000010.11:61902673:TGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000010.11:61902673:TGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT
Gene:: ARID5B (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TGTGTGTGTGTGTGTGT=0./0 (ALFA)
-=0.3466/1736 (1000Genomes)
HGVS:: NC_000010.11:g.61902675GT[7], NC_000010.11:g.61902675GT[8], NC_000010.11:g.61902675GT[9], NC_000010.11:g.61902675GT[10], NC_000010.11:g.61902675GT[11], NC_000010.11:g.61902675GT[12], NC_000010.11:g.61902675GT[13], NC_000010.11:g.61902675GT[15], NC_000010.11:g.61902675GT[16], NC_000010.11:g.61902675GT[17], NC_000010.11:g.61902675GT[18], NC_000010.11:g.61902675GT[20], NC_000010.11:g.61902675GT[21], NC_000010.11:g.61902675GT[22], NC_000010.10:g.63662434GT[7], NC_000010.10:g.63662434GT[8], NC_000010.10:g.63662434GT[9], NC_000010.10:g.63662434GT[10], NC_000010.10:g.63662434GT[11], NC_000010.10:g.63662434GT[12], NC_000010.10:g.63662434GT[13], NC_000010.10:g.63662434GT[15], NC_000010.10:g.63662434GT[16], NC_000010.10:g.63662434GT[17], NC_000010.10:g.63662434GT[18], NC_000010.10:g.63662434GT[20], NC_000010.10:g.63662434GT[21], NC_000010.10:g.63662434GT[22], NG_030027.1:g.6422GT[7], NG_030027.1:g.6422GT[8], NG_030027.1:g.6422GT[9], NG_030027.1:g.6422GT[10], NG_030027.1:g.6422GT[11], NG_030027.1:g.6422GT[12], NG_030027.1:g.6422GT[13], NG_030027.1:g.6422GT[15], NG_030027.1:g.6422GT[16], NG_030027.1:g.6422GT[17], NG_030027.1:g.6422GT[18], NG_030027.1:g.6422GT[20], NG_030027.1:g.6422GT[21], NG_030027.1:g.6422GT[22]

Select item 149144535311.

rs1491445353 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->CTTTT [Show Flanks]
Chromosome:: 10:61932414 (GRCh38)
10:63692174 (GRCh37)
Canonical SPDI:: NC_000010.11:61932414:TTTT:TTTTCTTTT
Gene:: ARID5B (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: TTTTCTTTT=0./0 (ALFA)
TTTTC=0.000026/3 (GnomAD)
HGVS:: NC_000010.11:g.61932415_61932418T[4]CTTTT[1], NC_000010.10:g.63692174_63692177T[4]CTTTT[1], NG_030027.1:g.36162_36165T[4]CTTTT[1]

Select item 149144523412.

rs1491445234 has merged into rs11363274 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAA>-,A,AA,AAAA,AAAAA,AAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 10:62076572 (GRCh38)
10:63836331 (GRCh37)
Canonical SPDI:: NC_000010.11:62076561:AAAAAAAAAAAAAAAAA:AAAAAAAAAA,NC_000010.11:62076561:AAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000010.11:62076561:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000010.11:62076561:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000010.11:62076561:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000010.11:62076561:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000010.11:62076561:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000010.11:62076561:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000010.11:62076561:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000010.11:62076561:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000010.11:62076561:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:62076561:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:62076561:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:62076561:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:62076561:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:62076561:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:62076561:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:62076561:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:62076561:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:62076561:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:62076561:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:62076561:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:62076561:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:62076561:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:62076561:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: ARID5B (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAA=0./0 (ALFA)
-=0.3381/1693 (1000Genomes)
HGVS:: NC_000010.11:g.62076572_62076578del, NC_000010.11:g.62076573_62076578del, NC_000010.11:g.62076574_62076578del, NC_000010.11:g.62076576_62076578del, NC_000010.11:g.62076577_62076578del, NC_000010.11:g.62076578del, NC_000010.11:g.62076578dup, NC_000010.11:g.62076577_62076578dup, NC_000010.11:g.62076576_62076578dup, NC_000010.11:g.62076575_62076578dup, NC_000010.11:g.62076574_62076578dup, NC_000010.11:g.62076573_62076578dup, NC_000010.11:g.62076572_62076578dup, NC_000010.11:g.62076571_62076578dup, NC_000010.11:g.62076570_62076578dup, NC_000010.11:g.62076569_62076578dup, NC_000010.11:g.62076568_62076578dup, NC_000010.11:g.62076567_62076578dup, NC_000010.11:g.62076566_62076578dup, NC_000010.11:g.62076565_62076578dup, NC_000010.11:g.62076564_62076578dup, NC_000010.11:g.62076563_62076578dup, NC_000010.11:g.62076562_62076578dup, NC_000010.11:g.62076578_62076579insAAAAAAAAAAAAAAAAAA, NC_000010.11:g.62076578_62076579insAAAAAAAAAAAAAAAAAAA, NC_000010.10:g.63836331_63836337del, NC_000010.10:g.63836332_63836337del, NC_000010.10:g.63836333_63836337del, NC_000010.10:g.63836335_63836337del, NC_000010.10:g.63836336_63836337del, NC_000010.10:g.63836337del, NC_000010.10:g.63836337dup, NC_000010.10:g.63836336_63836337dup, NC_000010.10:g.63836335_63836337dup, NC_000010.10:g.63836334_63836337dup, NC_000010.10:g.63836333_63836337dup, NC_000010.10:g.63836332_63836337dup, NC_000010.10:g.63836331_63836337dup, NC_000010.10:g.63836330_63836337dup, NC_000010.10:g.63836329_63836337dup, NC_000010.10:g.63836328_63836337dup, NC_000010.10:g.63836327_63836337dup, NC_000010.10:g.63836326_63836337dup, NC_000010.10:g.63836325_63836337dup, NC_000010.10:g.63836324_63836337dup, NC_000010.10:g.63836323_63836337dup, NC_000010.10:g.63836322_63836337dup, NC_000010.10:g.63836321_63836337dup, NC_000010.10:g.63836337_63836338insAAAAAAAAAAAAAAAAAA, NC_000010.10:g.63836337_63836338insAAAAAAAAAAAAAAAAAAA, NG_030027.1:g.180319_180325del, NG_030027.1:g.180320_180325del, NG_030027.1:g.180321_180325del, NG_030027.1:g.180323_180325del, NG_030027.1:g.180324_180325del, NG_030027.1:g.180325del, NG_030027.1:g.180325dup, NG_030027.1:g.180324_180325dup, NG_030027.1:g.180323_180325dup, NG_030027.1:g.180322_180325dup, NG_030027.1:g.180321_180325dup, NG_030027.1:g.180320_180325dup, NG_030027.1:g.180319_180325dup, NG_030027.1:g.180318_180325dup, NG_030027.1:g.180317_180325dup, NG_030027.1:g.180316_180325dup, NG_030027.1:g.180315_180325dup, NG_030027.1:g.180314_180325dup, NG_030027.1:g.180313_180325dup, NG_030027.1:g.180312_180325dup, NG_030027.1:g.180311_180325dup, NG_030027.1:g.180310_180325dup, NG_030027.1:g.180309_180325dup, NG_030027.1:g.180325_180326insAAAAAAAAAAAAAAAAAA, NG_030027.1:g.180325_180326insAAAAAAAAAAAAAAAAAAA

Select item 149144488513.

rs1491444885 has merged into rs747189859 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAA>-,AA,AAA,AAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 10:62086704 (GRCh38)
10:63846463 (GRCh37)
Canonical SPDI:: NC_000010.11:62086690:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000010.11:62086690:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000010.11:62086690:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000010.11:62086690:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000010.11:62086690:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000010.11:62086690:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000010.11:62086690:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000010.11:62086690:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:62086690:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:62086690:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:62086690:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:62086690:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:62086690:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:62086690:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:62086690:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: ARID5B (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAAAAAA=0./0 (ALFA)
HGVS:: NC_000010.11:g.62086704_62086712del, NC_000010.11:g.62086706_62086712del, NC_000010.11:g.62086707_62086712del, NC_000010.11:g.62086708_62086712del, NC_000010.11:g.62086710_62086712del, NC_000010.11:g.62086711_62086712del, NC_000010.11:g.62086712del, NC_000010.11:g.62086712dup, NC_000010.11:g.62086711_62086712dup, NC_000010.11:g.62086710_62086712dup, NC_000010.11:g.62086709_62086712dup, NC_000010.11:g.62086708_62086712dup, NC_000010.11:g.62086707_62086712dup, NC_000010.11:g.62086705_62086712dup, NC_000010.11:g.62086701_62086712dup, NC_000010.10:g.63846463_63846471del, NC_000010.10:g.63846465_63846471del, NC_000010.10:g.63846466_63846471del, NC_000010.10:g.63846467_63846471del, NC_000010.10:g.63846469_63846471del, NC_000010.10:g.63846470_63846471del, NC_000010.10:g.63846471del, NC_000010.10:g.63846471dup, NC_000010.10:g.63846470_63846471dup, NC_000010.10:g.63846469_63846471dup, NC_000010.10:g.63846468_63846471dup, NC_000010.10:g.63846467_63846471dup, NC_000010.10:g.63846466_63846471dup, NC_000010.10:g.63846464_63846471dup, NC_000010.10:g.63846460_63846471dup, NG_030027.1:g.190451_190459del, NG_030027.1:g.190453_190459del, NG_030027.1:g.190454_190459del, NG_030027.1:g.190455_190459del, NG_030027.1:g.190457_190459del, NG_030027.1:g.190458_190459del, NG_030027.1:g.190459del, NG_030027.1:g.190459dup, NG_030027.1:g.190458_190459dup, NG_030027.1:g.190457_190459dup, NG_030027.1:g.190456_190459dup, NG_030027.1:g.190455_190459dup, NG_030027.1:g.190454_190459dup, NG_030027.1:g.190452_190459dup, NG_030027.1:g.190448_190459dup

Select item 149144001214.

rs1491440012 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->ATGT [Show Flanks]
Chromosome:: 10:61938965 (GRCh38)
10:63698725 (GRCh37)
Canonical SPDI:: NC_000010.11:61938965:TGT:TGTATGT
Gene:: ARID5B (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: TGTATGT=0.00008/1 (ALFA)
HGVS:: NC_000010.11:g.61938968_61938969insATGT, NC_000010.10:g.63698727_63698728insATGT, NG_030027.1:g.42715_42716insATGT

Select item 149143592815.

rs1491435928 [Homo sapiens]

Variant type:: DEL
Alleles:: CA>- [Show Flanks]
Chromosome:: 10:61919052 (GRCh38)
10:63678811 (GRCh37)
Canonical SPDI:: NC_000010.11:61919051:CA:
Gene:: ARID5B (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0.00017/2 (ALFA)
-=0.0001/7 (GnomAD)
HGVS:: NC_000010.11:g.61919052_61919053del, NC_000010.10:g.63678811_63678812del, NG_030027.1:g.22799_22800del

Select item 149142043716.

rs1491420437 [Homo sapiens]

Variant type:: DEL
Alleles:: TG>- [Show Flanks]
Chromosome:: 10:62083312 (GRCh38)
10:63843071 (GRCh37)
Canonical SPDI:: NC_000010.11:62083311:TG:
Gene:: ARID5B (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: -=0.00013/2 (ALFA)
-=0.00005/5 (GnomAD)
HGVS:: NC_000010.11:g.62083312_62083313del, NC_000010.10:g.63843071_63843072del, NG_030027.1:g.187059_187060del

Select item 149139680517.

rs1491396805 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->CAAAAAA [Show Flanks]
Chromosome:: 10:62087299 (GRCh38)
10:63847059 (GRCh37)
Canonical SPDI:: NC_000010.11:62087299:AAAAAA:AAAAAACAAAAAA
Gene:: ARID5B (Varview)
Functional Consequence:: intron_variant
Validated:: by cluster
HGVS:: NC_000010.11:g.62087300_62087305A[6]CAAAAAA[1], NC_000010.10:g.63847059_63847064A[6]CAAAAAA[1], NG_030027.1:g.191047_191052A[6]CAAAAAA[1]

Select item 149138797118.

rs1491387971 has merged into rs55969343 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAAAAAAAA>-,A,AAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 10:62062790 (GRCh38)
10:63822549 (GRCh37)
Canonical SPDI:: NC_000010.11:62062779:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA,NC_000010.11:62062779:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000010.11:62062779:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000010.11:62062779:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000010.11:62062779:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000010.11:62062779:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000010.11:62062779:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000010.11:62062779:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000010.11:62062779:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000010.11:62062779:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000010.11:62062779:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:62062779:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:62062779:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:62062779:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:62062779:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:62062779:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:62062779:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:62062779:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:62062779:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: ARID5B (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAA=0./0 (ALFA)
HGVS:: NC_000010.11:g.62062790_62062804del, NC_000010.11:g.62062791_62062804del, NC_000010.11:g.62062793_62062804del, NC_000010.11:g.62062795_62062804del, NC_000010.11:g.62062796_62062804del, NC_000010.11:g.62062797_62062804del, NC_000010.11:g.62062798_62062804del, NC_000010.11:g.62062799_62062804del, NC_000010.11:g.62062800_62062804del, NC_000010.11:g.62062801_62062804del, NC_000010.11:g.62062802_62062804del, NC_000010.11:g.62062803_62062804del, NC_000010.11:g.62062804del, NC_000010.11:g.62062804dup, NC_000010.11:g.62062803_62062804dup, NC_000010.11:g.62062802_62062804dup, NC_000010.11:g.62062801_62062804dup, NC_000010.11:g.62062800_62062804dup, NC_000010.11:g.62062798_62062804dup, NC_000010.10:g.63822549_63822563del, NC_000010.10:g.63822550_63822563del, NC_000010.10:g.63822552_63822563del, NC_000010.10:g.63822554_63822563del, NC_000010.10:g.63822555_63822563del, NC_000010.10:g.63822556_63822563del, NC_000010.10:g.63822557_63822563del, NC_000010.10:g.63822558_63822563del, NC_000010.10:g.63822559_63822563del, NC_000010.10:g.63822560_63822563del, NC_000010.10:g.63822561_63822563del, NC_000010.10:g.63822562_63822563del, NC_000010.10:g.63822563del, NC_000010.10:g.63822563dup, NC_000010.10:g.63822562_63822563dup, NC_000010.10:g.63822561_63822563dup, NC_000010.10:g.63822560_63822563dup, NC_000010.10:g.63822559_63822563dup, NC_000010.10:g.63822557_63822563dup, NG_030027.1:g.166537_166551del, NG_030027.1:g.166538_166551del, NG_030027.1:g.166540_166551del, NG_030027.1:g.166542_166551del, NG_030027.1:g.166543_166551del, NG_030027.1:g.166544_166551del, NG_030027.1:g.166545_166551del, NG_030027.1:g.166546_166551del, NG_030027.1:g.166547_166551del, NG_030027.1:g.166548_166551del, NG_030027.1:g.166549_166551del, NG_030027.1:g.166550_166551del, NG_030027.1:g.166551del, NG_030027.1:g.166551dup, NG_030027.1:g.166550_166551dup, NG_030027.1:g.166549_166551dup, NG_030027.1:g.166548_166551dup, NG_030027.1:g.166547_166551dup, NG_030027.1:g.166545_166551dup

Select item 149138046319.

rs1491380463 has merged into rs1164342402 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTTTTTTTTTTT>-,T,TT,TTT,TTTT,TTTTT,TTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 10:61983881 (GRCh38)
10:63743640 (GRCh37)
Canonical SPDI:: NC_000010.11:61983867:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000010.11:61983867:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000010.11:61983867:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000010.11:61983867:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000010.11:61983867:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000010.11:61983867:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000010.11:61983867:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000010.11:61983867:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000010.11:61983867:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:61983867:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:61983867:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:61983867:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:61983867:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:61983867:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:61983867:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:61983867:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:61983867:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:61983867:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:61983867:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:61983867:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:61983867:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:61983867:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:61983867:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:61983867:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:61983867:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:61983867:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:61983867:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:61983867:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:61983867:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:61983867:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:61983867:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:61983867:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:61983867:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:61983867:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:61983867:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:61983867:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:61983867:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:61983867:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:61983867:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:61983867:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:61983867:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:61983867:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: ARID5B (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTTTT=0./0 (ALFA)
HGVS:: NC_000010.11:g.61983881_61983898del, NC_000010.11:g.61983882_61983898del, NC_000010.11:g.61983883_61983898del, NC_000010.11:g.61983884_61983898del, NC_000010.11:g.61983885_61983898del, NC_000010.11:g.61983886_61983898del, NC_000010.11:g.61983887_61983898del, NC_000010.11:g.61983889_61983898del, NC_000010.11:g.61983890_61983898del, NC_000010.11:g.61983892_61983898del, NC_000010.11:g.61983893_61983898del, NC_000010.11:g.61983894_61983898del, NC_000010.11:g.61983895_61983898del, NC_000010.11:g.61983896_61983898del, NC_000010.11:g.61983897_61983898del, NC_000010.11:g.61983898del, NC_000010.11:g.61983898dup, NC_000010.11:g.61983897_61983898dup, NC_000010.11:g.61983896_61983898dup, NC_000010.11:g.61983895_61983898dup, NC_000010.11:g.61983894_61983898dup, NC_000010.11:g.61983893_61983898dup, NC_000010.11:g.61983892_61983898dup, NC_000010.11:g.61983891_61983898dup, NC_000010.11:g.61983890_61983898dup, NC_000010.11:g.61983889_61983898dup, NC_000010.11:g.61983888_61983898dup, NC_000010.11:g.61983887_61983898dup, NC_000010.11:g.61983886_61983898dup, NC_000010.11:g.61983885_61983898dup, NC_000010.11:g.61983884_61983898dup, NC_000010.11:g.61983883_61983898dup, NC_000010.11:g.61983882_61983898dup, NC_000010.11:g.61983881_61983898dup, NC_000010.11:g.61983880_61983898dup, NC_000010.11:g.61983879_61983898dup, NC_000010.11:g.61983878_61983898dup, NC_000010.11:g.61983877_61983898dup, NC_000010.11:g.61983876_61983898dup, NC_000010.11:g.61983874_61983898dup, NC_000010.11:g.61983872_61983898dup, NC_000010.11:g.61983871_61983898dup, NC_000010.10:g.63743640_63743657del, NC_000010.10:g.63743641_63743657del, NC_000010.10:g.63743642_63743657del, NC_000010.10:g.63743643_63743657del, NC_000010.10:g.63743644_63743657del, NC_000010.10:g.63743645_63743657del, NC_000010.10:g.63743646_63743657del, NC_000010.10:g.63743648_63743657del, NC_000010.10:g.63743649_63743657del, NC_000010.10:g.63743651_63743657del, NC_000010.10:g.63743652_63743657del, NC_000010.10:g.63743653_63743657del, NC_000010.10:g.63743654_63743657del, NC_000010.10:g.63743655_63743657del, NC_000010.10:g.63743656_63743657del, NC_000010.10:g.63743657del, NC_000010.10:g.63743657dup, NC_000010.10:g.63743656_63743657dup, NC_000010.10:g.63743655_63743657dup, NC_000010.10:g.63743654_63743657dup, NC_000010.10:g.63743653_63743657dup, NC_000010.10:g.63743652_63743657dup, NC_000010.10:g.63743651_63743657dup, NC_000010.10:g.63743650_63743657dup, NC_000010.10:g.63743649_63743657dup, NC_000010.10:g.63743648_63743657dup, NC_000010.10:g.63743647_63743657dup, NC_000010.10:g.63743646_63743657dup, NC_000010.10:g.63743645_63743657dup, NC_000010.10:g.63743644_63743657dup, NC_000010.10:g.63743643_63743657dup, NC_000010.10:g.63743642_63743657dup, NC_000010.10:g.63743641_63743657dup, NC_000010.10:g.63743640_63743657dup, NC_000010.10:g.63743639_63743657dup, NC_000010.10:g.63743638_63743657dup, NC_000010.10:g.63743637_63743657dup, NC_000010.10:g.63743636_63743657dup, NC_000010.10:g.63743635_63743657dup, NC_000010.10:g.63743633_63743657dup, NC_000010.10:g.63743631_63743657dup, NC_000010.10:g.63743630_63743657dup, NG_030027.1:g.87628_87645del, NG_030027.1:g.87629_87645del, NG_030027.1:g.87630_87645del, NG_030027.1:g.87631_87645del, NG_030027.1:g.87632_87645del, NG_030027.1:g.87633_87645del, NG_030027.1:g.87634_87645del, NG_030027.1:g.87636_87645del, NG_030027.1:g.87637_87645del, NG_030027.1:g.87639_87645del, NG_030027.1:g.87640_87645del, NG_030027.1:g.87641_87645del, NG_030027.1:g.87642_87645del, NG_030027.1:g.87643_87645del, NG_030027.1:g.87644_87645del, NG_030027.1:g.87645del, NG_030027.1:g.87645dup, NG_030027.1:g.87644_87645dup, NG_030027.1:g.87643_87645dup, NG_030027.1:g.87642_87645dup, NG_030027.1:g.87641_87645dup, NG_030027.1:g.87640_87645dup, NG_030027.1:g.87639_87645dup, NG_030027.1:g.87638_87645dup, NG_030027.1:g.87637_87645dup, NG_030027.1:g.87636_87645dup, NG_030027.1:g.87635_87645dup, NG_030027.1:g.87634_87645dup, NG_030027.1:g.87633_87645dup, NG_030027.1:g.87632_87645dup, NG_030027.1:g.87631_87645dup, NG_030027.1:g.87630_87645dup, NG_030027.1:g.87629_87645dup, NG_030027.1:g.87628_87645dup, NG_030027.1:g.87627_87645dup, NG_030027.1:g.87626_87645dup, NG_030027.1:g.87625_87645dup, NG_030027.1:g.87624_87645dup, NG_030027.1:g.87623_87645dup, NG_030027.1:g.87621_87645dup, NG_030027.1:g.87619_87645dup, NG_030027.1:g.87618_87645dup

Select item 149136392020.

rs1491363920 [Homo sapiens]

Variant type:: DELINS
Alleles:: CT>- [Show Flanks]
Chromosome:: 10:62047028 (GRCh38)
10:63806787 (GRCh37)
Canonical SPDI:: NC_000010.11:62047026:TCT:T
Gene:: ARID5B (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
-=0.000007/1 (GnomAD)
-=0.000008/2 (TOPMED)
-=0.000071/2 (TOMMO)
-=0.069019/266 (ALSPAC)
-=0.090615/336 (TWINSUK)
HGVS:: NC_000010.11:g.62047028_62047029del, NC_000010.10:g.63806787_63806788del, NG_030027.1:g.150775_150776del

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