SNP Links for Nucleotide (Select 929981612) - SNP

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Select item 14915852651.

rs1491585265 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->GT [Show Flanks]
Chromosome:: 16:14585365 (GRCh38)
16:14679223 (GRCh37)
Canonical SPDI:: NC_000016.10:14585365:T:TGT
Gene:: PARN (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: TGT=0./0 (ALFA)
HGVS:: NC_000016.10:g.14585366_14585367insGT, NC_000016.9:g.14679223_14679224insGT, NG_042871.1:g.49906_49907insCA, NT_187607.1:g.158223_158224insGT

Select item 14915800102.

rs1491580010 [Homo sapiens]

Variant type:: DEL
Alleles:: TA>- [Show Flanks]
Chromosome:: 16:14553111 (GRCh38)
16:14646968 (GRCh37)
Canonical SPDI:: NC_000016.10:14553110:TA:
Gene:: PARN (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
-=0.000007/1 (GnomAD)
HGVS:: NC_000016.10:g.14553111_14553112del, NC_000016.9:g.14646968_14646969del, NG_042871.1:g.82160_82161del, NT_187607.1:g.125968_125969del

Select item 14915625283.

rs1491562528 has merged into rs36030259 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTTTT>-,TT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 16:14585374 (GRCh38)
16:14679231 (GRCh37)
Canonical SPDI:: NC_000016.10:14585364:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTT,NC_000016.10:14585364:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000016.10:14585364:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000016.10:14585364:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000016.10:14585364:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000016.10:14585364:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000016.10:14585364:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000016.10:14585364:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000016.10:14585364:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000016.10:14585364:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000016.10:14585364:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000016.10:14585364:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000016.10:14585364:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000016.10:14585364:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000016.10:14585364:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000016.10:14585364:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000016.10:14585364:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: PARN (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTT=0./0 (ALFA)
T=0.3099/1552 (1000Genomes)
HGVS:: NC_000016.10:g.14585374_14585384del, NC_000016.10:g.14585376_14585384del, NC_000016.10:g.14585378_14585384del, NC_000016.10:g.14585379_14585384del, NC_000016.10:g.14585380_14585384del, NC_000016.10:g.14585381_14585384del, NC_000016.10:g.14585382_14585384del, NC_000016.10:g.14585383_14585384del, NC_000016.10:g.14585384del, NC_000016.10:g.14585384dup, NC_000016.10:g.14585383_14585384dup, NC_000016.10:g.14585382_14585384dup, NC_000016.10:g.14585381_14585384dup, NC_000016.10:g.14585380_14585384dup, NC_000016.10:g.14585377_14585384dup, NC_000016.10:g.14585374_14585384dup, NC_000016.10:g.14585372_14585384dup, NC_000016.9:g.14679231_14679241del, NC_000016.9:g.14679233_14679241del, NC_000016.9:g.14679235_14679241del, NC_000016.9:g.14679236_14679241del, NC_000016.9:g.14679237_14679241del, NC_000016.9:g.14679238_14679241del, NC_000016.9:g.14679239_14679241del, NC_000016.9:g.14679240_14679241del, NC_000016.9:g.14679241del, NC_000016.9:g.14679241dup, NC_000016.9:g.14679240_14679241dup, NC_000016.9:g.14679239_14679241dup, NC_000016.9:g.14679238_14679241dup, NC_000016.9:g.14679237_14679241dup, NC_000016.9:g.14679234_14679241dup, NC_000016.9:g.14679231_14679241dup, NC_000016.9:g.14679229_14679241dup, NG_042871.1:g.49897_49907del, NG_042871.1:g.49899_49907del, NG_042871.1:g.49901_49907del, NG_042871.1:g.49902_49907del, NG_042871.1:g.49903_49907del, NG_042871.1:g.49904_49907del, NG_042871.1:g.49905_49907del, NG_042871.1:g.49906_49907del, NG_042871.1:g.49907del, NG_042871.1:g.49907dup, NG_042871.1:g.49906_49907dup, NG_042871.1:g.49905_49907dup, NG_042871.1:g.49904_49907dup, NG_042871.1:g.49903_49907dup, NG_042871.1:g.49900_49907dup, NG_042871.1:g.49897_49907dup, NG_042871.1:g.49895_49907dup, NT_187607.1:g.158231_158241del, NT_187607.1:g.158233_158241del, NT_187607.1:g.158235_158241del, NT_187607.1:g.158236_158241del, NT_187607.1:g.158237_158241del, NT_187607.1:g.158238_158241del, NT_187607.1:g.158239_158241del, NT_187607.1:g.158240_158241del, NT_187607.1:g.158241del, NT_187607.1:g.158241dup, NT_187607.1:g.158240_158241dup, NT_187607.1:g.158239_158241dup, NT_187607.1:g.158238_158241dup, NT_187607.1:g.158237_158241dup, NT_187607.1:g.158234_158241dup, NT_187607.1:g.158231_158241dup, NT_187607.1:g.158229_158241dup

Select item 14915277024.

rs1491527702 [Homo sapiens]

Variant type:: DEL
Alleles:: TA>- [Show Flanks]
Chromosome:: 16:14532194 (GRCh38)
16:14626051 (GRCh37)
Canonical SPDI:: NC_000016.10:14532193:TA:
Gene:: PARN (Varview), LOC107984865 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0./0 (ALFA)
-=0.000173/24 (GnomAD)
HGVS:: NC_000016.10:g.14532194_14532195del, NC_000016.9:g.14626051_14626052del, NG_042871.1:g.103077_103078del, NT_187607.1:g.105051_105052del, XR_001752089.3:n.18834_18835del, XR_001756351.3:n.18834_18835del

Select item 14915264525.

rs1491526452 has merged into rs869041563 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAAAAAAAAAA>-,AAA,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAATAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAATAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAATAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAATAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAATAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAACAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAATAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 16:14451876 (GRCh38)
16:14545733 (GRCh37)
Canonical SPDI:: NC_000016.10:14451869:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAA,NC_000016.10:14451869:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA,NC_000016.10:14451869:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA,NC_000016.10:14451869:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000016.10:14451869:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000016.10:14451869:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000016.10:14451869:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000016.10:14451869:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000016.10:14451869:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000016.10:14451869:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000016.10:14451869:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000016.10:14451869:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000016.10:14451869:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000016.10:14451869:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000016.10:14451869:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000016.10:14451869:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000016.10:14451869:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000016.10:14451869:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000016.10:14451869:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000016.10:14451869:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000016.10:14451869:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000016.10:14451869:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000016.10:14451869:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000016.10:14451869:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000016.10:14451869:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000016.10:14451869:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000016.10:14451869:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000016.10:14451869:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000016.10:14451869:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000016.10:14451869:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000016.10:14451869:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000016.10:14451869:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000016.10:14451869:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000016.10:14451869:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000016.10:14451869:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000016.10:14451869:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000016.10:14451869:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000016.10:14451869:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000016.10:14451869:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000016.10:14451869:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000016.10:14451869:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000016.10:14451869:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000016.10:14451869:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000016.10:14451869:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000016.10:14451869:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000016.10:14451869:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000016.10:14451869:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000016.10:14451869:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000016.10:14451869:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000016.10:14451869:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000016.10:14451869:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAATAAAAAAAAAAAAAAAAAAAAAAA,NC_000016.10:14451869:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAATAAAAAAAAAAAAAAAAAAAAAAAA,NC_000016.10:14451869:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAATAAAAAAAAAAAAAAAAAAAAAAAA,NC_000016.10:14451869:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAATAAAAAAAAAAAAAAAAAAAAAAA,NC_000016.10:14451869:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAATAAAAAAAAAAAAAAAAAAAAAAAA,NC_000016.10:14451869:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAACAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000016.10:14451869:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAATAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: PARN (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAA=0./0 (ALFA)
HGVS:: NC_000016.10:g.14451876_14451892del, NC_000016.10:g.14451879_14451892del, NC_000016.10:g.14451880_14451892del, NC_000016.10:g.14451881_14451892del, NC_000016.10:g.14451882_14451892del, NC_000016.10:g.14451883_14451892del, NC_000016.10:g.14451884_14451892del, NC_000016.10:g.14451885_14451892del, NC_000016.10:g.14451886_14451892del, NC_000016.10:g.14451887_14451892del, NC_000016.10:g.14451888_14451892del, NC_000016.10:g.14451889_14451892del, NC_000016.10:g.14451890_14451892del, NC_000016.10:g.14451891_14451892del, NC_000016.10:g.14451892del, NC_000016.10:g.14451892dup, NC_000016.10:g.14451891_14451892dup, NC_000016.10:g.14451890_14451892dup, NC_000016.10:g.14451889_14451892dup, NC_000016.10:g.14451888_14451892dup, NC_000016.10:g.14451887_14451892dup, NC_000016.10:g.14451886_14451892dup, NC_000016.10:g.14451885_14451892dup, NC_000016.10:g.14451884_14451892dup, NC_000016.10:g.14451883_14451892dup, NC_000016.10:g.14451882_14451892dup, NC_000016.10:g.14451881_14451892dup, NC_000016.10:g.14451880_14451892dup, NC_000016.10:g.14451879_14451892dup, NC_000016.10:g.14451878_14451892dup, NC_000016.10:g.14451877_14451892dup, NC_000016.10:g.14451876_14451892dup, NC_000016.10:g.14451875_14451892dup, NC_000016.10:g.14451874_14451892dup, NC_000016.10:g.14451873_14451892dup, NC_000016.10:g.14451872_14451892dup, NC_000016.10:g.14451871_14451892dup, NC_000016.10:g.14451870_14451892dup, NC_000016.10:g.14451892_14451893insAAAAAAAAAAAAAAAAAAAAAAAA, NC_000016.10:g.14451892_14451893insAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000016.10:g.14451892_14451893insAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000016.10:g.14451892_14451893insAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000016.10:g.14451892_14451893insAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000016.10:g.14451892_14451893insAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000016.10:g.14451892_14451893insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000016.10:g.14451892_14451893insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000016.10:g.14451892_14451893insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000016.10:g.14451892_14451893insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000016.10:g.14451892_14451893insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000016.10:g.14451892_14451893insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000016.10:g.14451870_14451892A[32]TAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000016.10:g.14451870_14451892A[32]TAAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000016.10:g.14451870_14451892A[31]TAAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000016.10:g.14451870_14451892A[30]TAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000016.10:g.14451870_14451892A[25]TAAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000016.10:g.14451870_14451892A[24]CAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000016.10:g.14451870_14451892A[24]TAAAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000016.9:g.14545733_14545749del, NC_000016.9:g.14545736_14545749del, NC_000016.9:g.14545737_14545749del, NC_000016.9:g.14545738_14545749del, NC_000016.9:g.14545739_14545749del, NC_000016.9:g.14545740_14545749del, NC_000016.9:g.14545741_14545749del, NC_000016.9:g.14545742_14545749del, NC_000016.9:g.14545743_14545749del, NC_000016.9:g.14545744_14545749del, NC_000016.9:g.14545745_14545749del, NC_000016.9:g.14545746_14545749del, NC_000016.9:g.14545747_14545749del, NC_000016.9:g.14545748_14545749del, NC_000016.9:g.14545749del, NC_000016.9:g.14545749dup, NC_000016.9:g.14545748_14545749dup, NC_000016.9:g.14545747_14545749dup, NC_000016.9:g.14545746_14545749dup, NC_000016.9:g.14545745_14545749dup, NC_000016.9:g.14545744_14545749dup, NC_000016.9:g.14545743_14545749dup, NC_000016.9:g.14545742_14545749dup, NC_000016.9:g.14545741_14545749dup, NC_000016.9:g.14545740_14545749dup, NC_000016.9:g.14545739_14545749dup, NC_000016.9:g.14545738_14545749dup, NC_000016.9:g.14545737_14545749dup, NC_000016.9:g.14545736_14545749dup, NC_000016.9:g.14545735_14545749dup, NC_000016.9:g.14545734_14545749dup, NC_000016.9:g.14545733_14545749dup, NC_000016.9:g.14545732_14545749dup, NC_000016.9:g.14545731_14545749dup, NC_000016.9:g.14545730_14545749dup, NC_000016.9:g.14545729_14545749dup, NC_000016.9:g.14545728_14545749dup, NC_000016.9:g.14545727_14545749dup, NC_000016.9:g.14545749_14545750insAAAAAAAAAAAAAAAAAAAAAAAA, NC_000016.9:g.14545749_14545750insAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000016.9:g.14545749_14545750insAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000016.9:g.14545749_14545750insAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000016.9:g.14545749_14545750insAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000016.9:g.14545749_14545750insAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000016.9:g.14545749_14545750insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000016.9:g.14545749_14545750insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000016.9:g.14545749_14545750insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000016.9:g.14545749_14545750insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000016.9:g.14545749_14545750insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000016.9:g.14545749_14545750insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000016.9:g.14545727_14545749A[32]TAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000016.9:g.14545727_14545749A[32]TAAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000016.9:g.14545727_14545749A[31]TAAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000016.9:g.14545727_14545749A[30]TAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000016.9:g.14545727_14545749A[25]TAAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000016.9:g.14545727_14545749A[24]CAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000016.9:g.14545727_14545749A[24]TAAAAAAAAAAAAAAAAAAAAAAAAA[1], NG_042871.1:g.183386_183402del, NG_042871.1:g.183389_183402del, NG_042871.1:g.183390_183402del, NG_042871.1:g.183391_183402del, NG_042871.1:g.183392_183402del, NG_042871.1:g.183393_183402del, NG_042871.1:g.183394_183402del, NG_042871.1:g.183395_183402del, NG_042871.1:g.183396_183402del, NG_042871.1:g.183397_183402del, NG_042871.1:g.183398_183402del, NG_042871.1:g.183399_183402del, NG_042871.1:g.183400_183402del, NG_042871.1:g.183401_183402del, NG_042871.1:g.183402del, NG_042871.1:g.183402dup, NG_042871.1:g.183401_183402dup, NG_042871.1:g.183400_183402dup, NG_042871.1:g.183399_183402dup, NG_042871.1:g.183398_183402dup, NG_042871.1:g.183397_183402dup, NG_042871.1:g.183396_183402dup, NG_042871.1:g.183395_183402dup, NG_042871.1:g.183394_183402dup, NG_042871.1:g.183393_183402dup, NG_042871.1:g.183392_183402dup, NG_042871.1:g.183391_183402dup, NG_042871.1:g.183390_183402dup, NG_042871.1:g.183389_183402dup, NG_042871.1:g.183388_183402dup, NG_042871.1:g.183387_183402dup, NG_042871.1:g.183386_183402dup, NG_042871.1:g.183385_183402dup, NG_042871.1:g.183384_183402dup, NG_042871.1:g.183383_183402dup, NG_042871.1:g.183382_183402dup, NG_042871.1:g.183381_183402dup, NG_042871.1:g.183380_183402dup, NG_042871.1:g.183402_183403insTTTTTTTTTTTTTTTTTTTTTTTT, NG_042871.1:g.183402_183403insTTTTTTTTTTTTTTTTTTTTTTTTT, NG_042871.1:g.183402_183403insTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_042871.1:g.183402_183403insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_042871.1:g.183402_183403insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_042871.1:g.183402_183403insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_042871.1:g.183402_183403insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_042871.1:g.183402_183403insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_042871.1:g.183402_183403insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_042871.1:g.183402_183403insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_042871.1:g.183402_183403insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_042871.1:g.183402_183403insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_042871.1:g.183380_183402T[23]ATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NG_042871.1:g.183380_183402T[24]ATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NG_042871.1:g.183380_183402T[24]ATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NG_042871.1:g.183380_183402T[23]ATTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NG_042871.1:g.183380_183402T[24]ATTTTTTTTTTTTTTTTTTTTTTTTT[1], NG_042871.1:g.183380_183402T[35]GTTTTTTTTTTTTTTTTTTTTTTTT[1], NG_042871.1:g.183380_183402T[25]ATTTTTTTTTTTTTTTTTTTTTTTT[1], NT_187607.1:g.24733_24749del, NT_187607.1:g.24736_24749del, NT_187607.1:g.24737_24749del, NT_187607.1:g.24738_24749del, NT_187607.1:g.24739_24749del, NT_187607.1:g.24740_24749del, NT_187607.1:g.24741_24749del, NT_187607.1:g.24742_24749del, NT_187607.1:g.24743_24749del, NT_187607.1:g.24744_24749del, NT_187607.1:g.24745_24749del, NT_187607.1:g.24746_24749del, NT_187607.1:g.24747_24749del, NT_187607.1:g.24748_24749del, NT_187607.1:g.24749del, NT_187607.1:g.24749dup, NT_187607.1:g.24748_24749dup, NT_187607.1:g.24747_24749dup, NT_187607.1:g.24746_24749dup, NT_187607.1:g.24745_24749dup, NT_187607.1:g.24744_24749dup, NT_187607.1:g.24743_24749dup, NT_187607.1:g.24742_24749dup, NT_187607.1:g.24741_24749dup, NT_187607.1:g.24740_24749dup, NT_187607.1:g.24739_24749dup, NT_187607.1:g.24738_24749dup, NT_187607.1:g.24737_24749dup, NT_187607.1:g.24736_24749dup, NT_187607.1:g.24735_24749dup, NT_187607.1:g.24734_24749dup, NT_187607.1:g.24733_24749dup, NT_187607.1:g.24732_24749dup, NT_187607.1:g.24731_24749dup, NT_187607.1:g.24730_24749dup, NT_187607.1:g.24729_24749dup, NT_187607.1:g.24728_24749dup, NT_187607.1:g.24727_24749dup, NT_187607.1:g.24749_24750insAAAAAAAAAAAAAAAAAAAAAAAA, NT_187607.1:g.24749_24750insAAAAAAAAAAAAAAAAAAAAAAAAA, NT_187607.1:g.24749_24750insAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_187607.1:g.24749_24750insAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_187607.1:g.24749_24750insAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_187607.1:g.24749_24750insAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_187607.1:g.24749_24750insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_187607.1:g.24749_24750insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_187607.1:g.24749_24750insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_187607.1:g.24749_24750insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_187607.1:g.24749_24750insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_187607.1:g.24749_24750insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_187607.1:g.24727_24749A[32]TAAAAAAAAAAAAAAAAAAAAAAA[1], NT_187607.1:g.24727_24749A[32]TAAAAAAAAAAAAAAAAAAAAAAAA[1], NT_187607.1:g.24727_24749A[31]TAAAAAAAAAAAAAAAAAAAAAAAA[1], NT_187607.1:g.24727_24749A[30]TAAAAAAAAAAAAAAAAAAAAAAA[1], NT_187607.1:g.24727_24749A[25]TAAAAAAAAAAAAAAAAAAAAAAAA[1], NT_187607.1:g.24727_24749A[24]CAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NT_187607.1:g.24727_24749A[24]TAAAAAAAAAAAAAAAAAAAAAAAAA[1], XR_007064883.1:n.11676_11692del, XR_007064883.1:n.11679_11692del, XR_007064883.1:n.11680_11692del, XR_007064883.1:n.11681_11692del, XR_007064883.1:n.11682_11692del, XR_007064883.1:n.11683_11692del, XR_007064883.1:n.11684_11692del, XR_007064883.1:n.11685_11692del, XR_007064883.1:n.11686_11692del, XR_007064883.1:n.11687_11692del, XR_007064883.1:n.11688_11692del, XR_007064883.1:n.11689_11692del, XR_007064883.1:n.11690_11692del, XR_007064883.1:n.11691_11692del, XR_007064883.1:n.11692del, XR_007064883.1:n.11692dup, XR_007064883.1:n.11691_11692dup, XR_007064883.1:n.11690_11692dup, XR_007064883.1:n.11689_11692dup, XR_007064883.1:n.11688_11692dup, XR_007064883.1:n.11687_11692dup, XR_007064883.1:n.11686_11692dup, XR_007064883.1:n.11685_11692dup, XR_007064883.1:n.11684_11692dup, XR_007064883.1:n.11683_11692dup, XR_007064883.1:n.11682_11692dup, XR_007064883.1:n.11681_11692dup, XR_007064883.1:n.11680_11692dup, XR_007064883.1:n.11679_11692dup, XR_007064883.1:n.11678_11692dup, XR_007064883.1:n.11677_11692dup, XR_007064883.1:n.11676_11692dup, XR_007064883.1:n.11675_11692dup, XR_007064883.1:n.11674_11692dup, XR_007064883.1:n.11673_11692dup, XR_007064883.1:n.11672_11692dup, XR_007064883.1:n.11671_11692dup, XR_007064883.1:n.11670_11692dup, XR_007064883.1:n.11692_11693insTTTTTTTTTTTTTTTTTTTTTTTT, XR_007064883.1:n.11692_11693insTTTTTTTTTTTTTTTTTTTTTTTTT, XR_007064883.1:n.11692_11693insTTTTTTTTTTTTTTTTTTTTTTTTTT, XR_007064883.1:n.11692_11693insTTTTTTTTTTTTTTTTTTTTTTTTTTT, XR_007064883.1:n.11692_11693insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XR_007064883.1:n.11692_11693insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XR_007064883.1:n.11692_11693insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XR_007064883.1:n.11692_11693insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XR_007064883.1:n.11692_11693insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XR_007064883.1:n.11692_11693insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XR_007064883.1:n.11692_11693insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XR_007064883.1:n.11692_11693insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XR_007064883.1:n.11670_11692T[23]ATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], XR_007064883.1:n.11670_11692T[24]ATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], XR_007064883.1:n.11670_11692T[24]ATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], XR_007064883.1:n.11670_11692T[23]ATTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], XR_007064883.1:n.11670_11692T[24]ATTTTTTTTTTTTTTTTTTTTTTTTT[1], XR_007064883.1:n.11670_11692T[35]GTTTTTTTTTTTTTTTTTTTTTTTT[1], XR_007064883.1:n.11670_11692T[25]ATTTTTTTTTTTTTTTTTTTTTTTT[1], XR_007064882.1:n.11190_11206del, XR_007064882.1:n.11193_11206del, XR_007064882.1:n.11194_11206del, XR_007064882.1:n.11195_11206del, XR_007064882.1:n.11196_11206del, XR_007064882.1:n.11197_11206del, XR_007064882.1:n.11198_11206del, XR_007064882.1:n.11199_11206del, XR_007064882.1:n.11200_11206del, XR_007064882.1:n.11201_11206del, XR_007064882.1:n.11202_11206del, XR_007064882.1:n.11203_11206del, XR_007064882.1:n.11204_11206del, XR_007064882.1:n.11205_11206del, XR_007064882.1:n.11206del, XR_007064882.1:n.11206dup, XR_007064882.1:n.11205_11206dup, XR_007064882.1:n.11204_11206dup, XR_007064882.1:n.11203_11206dup, XR_007064882.1:n.11202_11206dup, XR_007064882.1:n.11201_11206dup, XR_007064882.1:n.11200_11206dup, XR_007064882.1:n.11199_11206dup, XR_007064882.1:n.11198_11206dup, XR_007064882.1:n.11197_11206dup, XR_007064882.1:n.11196_11206dup, XR_007064882.1:n.11195_11206dup, XR_007064882.1:n.11194_11206dup, XR_007064882.1:n.11193_11206dup, XR_007064882.1:n.11192_11206dup, XR_007064882.1:n.11191_11206dup, XR_007064882.1:n.11190_11206dup, XR_007064882.1:n.11189_11206dup, XR_007064882.1:n.11188_11206dup, XR_007064882.1:n.11187_11206dup, XR_007064882.1:n.11186_11206dup, XR_007064882.1:n.11185_11206dup, XR_007064882.1:n.11184_11206dup, XR_007064882.1:n.11206_11207insTTTTTTTTTTTTTTTTTTTTTTTT, XR_007064882.1:n.11206_11207insTTTTTTTTTTTTTTTTTTTTTTTTT, XR_007064882.1:n.11206_11207insTTTTTTTTTTTTTTTTTTTTTTTTTT, XR_007064882.1:n.11206_11207insTTTTTTTTTTTTTTTTTTTTTTTTTTT, XR_007064882.1:n.11206_11207insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XR_007064882.1:n.11206_11207insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XR_007064882.1:n.11206_11207insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XR_007064882.1:n.11206_11207insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XR_007064882.1:n.11206_11207insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XR_007064882.1:n.11206_11207insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XR_007064882.1:n.11206_11207insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XR_007064882.1:n.11206_11207insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XR_007064882.1:n.11184_11206T[23]ATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], XR_007064882.1:n.11184_11206T[24]ATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], XR_007064882.1:n.11184_11206T[24]ATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], XR_007064882.1:n.11184_11206T[23]ATTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], XR_007064882.1:n.11184_11206T[24]ATTTTTTTTTTTTTTTTTTTTTTTTT[1], XR_007064882.1:n.11184_11206T[35]GTTTTTTTTTTTTTTTTTTTTTTTT[1], XR_007064882.1:n.11184_11206T[25]ATTTTTTTTTTTTTTTTTTTTTTTT[1], XR_007064881.1:n.11754_11770del, XR_007064881.1:n.11757_11770del, XR_007064881.1:n.11758_11770del, XR_007064881.1:n.11759_11770del, XR_007064881.1:n.11760_11770del, XR_007064881.1:n.11761_11770del, XR_007064881.1:n.11762_11770del, XR_007064881.1:n.11763_11770del, XR_007064881.1:n.11764_11770del, XR_007064881.1:n.11765_11770del, XR_007064881.1:n.11766_11770del, XR_007064881.1:n.11767_11770del, XR_007064881.1:n.11768_11770del, XR_007064881.1:n.11769_11770del, XR_007064881.1:n.11770del, XR_007064881.1:n.11770dup, XR_007064881.1:n.11769_11770dup, XR_007064881.1:n.11768_11770dup, XR_007064881.1:n.11767_11770dup, XR_007064881.1:n.11766_11770dup, XR_007064881.1:n.11765_11770dup, XR_007064881.1:n.11764_11770dup, XR_007064881.1:n.11763_11770dup, XR_007064881.1:n.11762_11770dup, XR_007064881.1:n.11761_11770dup, XR_007064881.1:n.11760_11770dup, XR_007064881.1:n.11759_11770dup, XR_007064881.1:n.11758_11770dup, XR_007064881.1:n.11757_11770dup, XR_007064881.1:n.11756_11770dup, XR_007064881.1:n.11755_11770dup, XR_007064881.1:n.11754_11770dup, XR_007064881.1:n.11753_11770dup, XR_007064881.1:n.11752_11770dup, XR_007064881.1:n.11751_11770dup, XR_007064881.1:n.11750_11770dup, XR_007064881.1:n.11749_11770dup, XR_007064881.1:n.11748_11770dup, XR_007064881.1:n.11770_11771insTTTTTTTTTTTTTTTTTTTTTTTT, XR_007064881.1:n.11770_11771insTTTTTTTTTTTTTTTTTTTTTTTTT, XR_007064881.1:n.11770_11771insTTTTTTTTTTTTTTTTTTTTTTTTTT, XR_007064881.1:n.11770_11771insTTTTTTTTTTTTTTTTTTTTTTTTTTT, XR_007064881.1:n.11770_11771insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XR_007064881.1:n.11770_11771insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XR_007064881.1:n.11770_11771insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XR_007064881.1:n.11770_11771insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XR_007064881.1:n.11770_11771insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XR_007064881.1:n.11770_11771insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XR_007064881.1:n.11770_11771insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XR_007064881.1:n.11770_11771insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XR_007064881.1:n.11748_11770T[23]ATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], XR_007064881.1:n.11748_11770T[24]ATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], XR_007064881.1:n.11748_11770T[24]ATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], XR_007064881.1:n.11748_11770T[23]ATTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], XR_007064881.1:n.11748_11770T[24]ATTTTTTTTTTTTTTTTTTTTTTTTT[1], XR_007064881.1:n.11748_11770T[35]GTTTTTTTTTTTTTTTTTTTTTTTT[1], XR_007064881.1:n.11748_11770T[25]ATTTTTTTTTTTTTTTTTTTTTTTT[1], XR_007064884.1:n.11671_11687del, XR_007064884.1:n.11674_11687del, XR_007064884.1:n.11675_11687del, XR_007064884.1:n.11676_11687del, XR_007064884.1:n.11677_11687del, XR_007064884.1:n.11678_11687del, XR_007064884.1:n.11679_11687del, XR_007064884.1:n.11680_11687del, XR_007064884.1:n.11681_11687del, XR_007064884.1:n.11682_11687del, XR_007064884.1:n.11683_11687del, XR_007064884.1:n.11684_11687del, XR_007064884.1:n.11685_11687del, XR_007064884.1:n.11686_11687del, XR_007064884.1:n.11687del, XR_007064884.1:n.11687dup, XR_007064884.1:n.11686_11687dup, XR_007064884.1:n.11685_11687dup, XR_007064884.1:n.11684_11687dup, XR_007064884.1:n.11683_11687dup, XR_007064884.1:n.11682_11687dup, XR_007064884.1:n.11681_11687dup, XR_007064884.1:n.11680_11687dup, XR_007064884.1:n.11679_11687dup, XR_007064884.1:n.11678_11687dup, XR_007064884.1:n.11677_11687dup, XR_007064884.1:n.11676_11687dup, XR_007064884.1:n.11675_11687dup, XR_007064884.1:n.11674_11687dup, XR_007064884.1:n.11673_11687dup, XR_007064884.1:n.11672_11687dup, XR_007064884.1:n.11671_11687dup, XR_007064884.1:n.11670_11687dup, XR_007064884.1:n.11669_11687dup, XR_007064884.1:n.11668_11687dup, XR_007064884.1:n.11667_11687dup, XR_007064884.1:n.11666_11687dup, XR_007064884.1:n.11665_11687dup, XR_007064884.1:n.11687_11688insTTTTTTTTTTTTTTTTTTTTTTTT, XR_007064884.1:n.11687_11688insTTTTTTTTTTTTTTTTTTTTTTTTT, XR_007064884.1:n.11687_11688insTTTTTTTTTTTTTTTTTTTTTTTTTT, XR_007064884.1:n.11687_11688insTTTTTTTTTTTTTTTTTTTTTTTTTTT, XR_007064884.1:n.11687_11688insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XR_007064884.1:n.11687_11688insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XR_007064884.1:n.11687_11688insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XR_007064884.1:n.11687_11688insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XR_007064884.1:n.11687_11688insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XR_007064884.1:n.11687_11688insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XR_007064884.1:n.11687_11688insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XR_007064884.1:n.11687_11688insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XR_007064884.1:n.11665_11687T[23]ATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], XR_007064884.1:n.11665_11687T[24]ATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], XR_007064884.1:n.11665_11687T[24]ATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], XR_007064884.1:n.11665_11687T[23]ATTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], XR_007064884.1:n.11665_11687T[24]ATTTTTTTTTTTTTTTTTTTTTTTTT[1], XR_007064884.1:n.11665_11687T[35]GTTTTTTTTTTTTTTTTTTTTTTTT[1], XR_007064884.1:n.11665_11687T[25]ATTTTTTTTTTTTTTTTTTTTTTTT[1]

Select item 14915231976.

rs1491523197 has merged into rs373143309 [Homo sapiens]

Variant type:: DELINS
Alleles:: A>-,AA [Show Flanks]
Chromosome:: 16:14532195 (GRCh38)
16:14626052 (GRCh37)
Canonical SPDI:: NC_000016.10:14532194:AA:A,NC_000016.10:14532194:AA:AAA
Gene:: PARN (Varview), LOC107984865 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AA=0.01497/235 (ALFA)
-=0.00004/1 (TOMMO)
-=0.01234/79 (1000Genomes)
-=0.06061/36 (NorthernSweden)
-=0.1/4 (GENOME_DK)
HGVS:: NC_000016.10:g.14532196del, NC_000016.10:g.14532196dup, NC_000016.9:g.14626053del, NC_000016.9:g.14626053dup, NG_042871.1:g.103077del, NG_042871.1:g.103077dup, NT_187607.1:g.105053del, NT_187607.1:g.105053dup, XR_001752089.3:n.18834del, XR_001752089.3:n.18834dup, XR_001756351.3:n.18834del, XR_001756351.3:n.18834dup

Select item 14915181177.

rs1491518117 [Homo sapiens]

Variant type:: INS
Alleles:: ->AT,C [Show Flanks]
Chromosome:: 16:14435278 (GRCh38)
16:14529136 (GRCh37)
Canonical SPDI:: NC_000016.10:14435278::AT,NC_000016.10:14435278::C
Gene:: PARN (Varview)
Functional Consequence:: 500B_downstream_variant,downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
AT=0.00209/35 (TOMMO)
HGVS:: NC_000016.10:g.14435278_14435279insAT, NC_000016.10:g.14435278_14435279insC, NC_000016.9:g.14529135_14529136insAT, NC_000016.9:g.14529135_14529136insC, NG_042871.1:g.199993_199994insAT, NG_042871.1:g.199993_199994insG, NT_187607.1:g.8135_8136insAT, NT_187607.1:g.8135_8136insC

Select item 14915043828.

rs1491504382 [Homo sapiens]

Variant type:: DEL
Alleles:: TC>- [Show Flanks]
Chromosome:: 16:14435896 (GRCh38)
16:14529753 (GRCh37)
Canonical SPDI:: NC_000016.10:14435895:TC:
Gene:: PARN (Varview)
Functional Consequence:: 3_prime_UTR_variant,genic_downstream_transcript_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0.00059/7 (ALFA)
-=0.00376/374 (GnomAD)
HGVS:: NC_000016.10:g.14435896_14435897del, NC_000016.9:g.14529753_14529754del, NG_042871.1:g.199375_199376del, NM_002582.4:c.*820_*821del, NM_002582.3:c.*820_*821del, NM_001134477.3:c.*820_*821del, NM_001134477.2:c.*820_*821del, NM_001242992.2:c.*820_*821del, NM_001242992.1:c.*820_*821del, NT_187607.1:g.8753_8754del, XR_007064883.1:n.17550_17551del, XR_007064882.1:n.17064_17065del, XR_007064881.1:n.17628_17629del, XR_007064884.1:n.17545_17546del

Select item 14914862699.

rs1491486269 [Homo sapiens]

Variant type:: INS
Alleles:: ->C [Show Flanks]
Chromosome:: 16:14621354 (GRCh38)
16:14715212 (GRCh37)
Canonical SPDI:: NC_000016.10:14621354::C
Gene:: PARN (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
C=0.000008/2 (TOPMED)
HGVS:: NC_000016.10:g.14621354_14621355insC, NC_000016.9:g.14715211_14715212insC, NG_042871.1:g.13917_13918insG, NT_187607.1:g.194210_194211insC

Select item 149146588010.

rs1491465880 has merged into rs543071760 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTT>-,T,TT,TTT,TTTTT,TTTTTT,TTTTTTT [Show Flanks]
Chromosome:: 16:14568227 (GRCh38)
16:14662084 (GRCh37)
Canonical SPDI:: NC_000016.10:14568214:TTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000016.10:14568214:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000016.10:14568214:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000016.10:14568214:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000016.10:14568214:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000016.10:14568214:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000016.10:14568214:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT
Gene:: PARN (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTTTTT=0./0 (ALFA)
-=0.14816/742 (1000Genomes)
-=0.325/13 (GENOME_DK)
HGVS:: NC_000016.10:g.14568227_14568230del, NC_000016.10:g.14568228_14568230del, NC_000016.10:g.14568229_14568230del, NC_000016.10:g.14568230del, NC_000016.10:g.14568230dup, NC_000016.10:g.14568229_14568230dup, NC_000016.10:g.14568228_14568230dup, NC_000016.9:g.14662084_14662087del, NC_000016.9:g.14662085_14662087del, NC_000016.9:g.14662086_14662087del, NC_000016.9:g.14662087del, NC_000016.9:g.14662087dup, NC_000016.9:g.14662086_14662087dup, NC_000016.9:g.14662085_14662087dup, NG_042871.1:g.67054_67057del, NG_042871.1:g.67055_67057del, NG_042871.1:g.67056_67057del, NG_042871.1:g.67057del, NG_042871.1:g.67057dup, NG_042871.1:g.67056_67057dup, NG_042871.1:g.67055_67057dup, NT_187607.1:g.141084_141087del, NT_187607.1:g.141085_141087del, NT_187607.1:g.141086_141087del, NT_187607.1:g.141087del, NT_187607.1:g.141087dup, NT_187607.1:g.141086_141087dup, NT_187607.1:g.141085_141087dup

Select item 149142931011.

rs1491429310 [Homo sapiens]

Variant type:: DEL
Alleles:: CT>- [Show Flanks]
Chromosome:: 16:14568214 (GRCh38)
16:14662071 (GRCh37)
Canonical SPDI:: NC_000016.10:14568213:CT:
Gene:: PARN (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: -=0.000071/1 (ALFA)
-=0.000007/1 (GnomAD)
HGVS:: NC_000016.10:g.14568214_14568215del, NC_000016.9:g.14662071_14662072del, NG_042871.1:g.67057_67058del, NT_187607.1:g.141071_141072del

Select item 149141414212.

rs1491414142 [Homo sapiens]

Variant type:: DEL
Alleles:: TA>- [Show Flanks]
Chromosome:: 16:14593492 (GRCh38)
16:14687349 (GRCh37)
Canonical SPDI:: NC_000016.10:14593491:TA:
Gene:: PARN (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0.00894/106 (ALFA)
-=0.0436/1031 (GnomAD)
HGVS:: NC_000016.10:g.14593492_14593493del, NC_000016.9:g.14687349_14687350del, NG_042871.1:g.41779_41780del, NT_187607.1:g.166349_166350del

Select item 149140690013.

rs1491406900 has merged into rs145797278 [Homo sapiens]

Variant type:: DELINS
Alleles:: GGG>-,G,GG,GGGG,GGGGG,GGGGGG [Show Flanks]
Chromosome:: 16:14463848 (GRCh38)
16:14557705 (GRCh37)
Canonical SPDI:: NC_000016.10:14463838:GGGGGGGGGGGG:GGGGGGGGG,NC_000016.10:14463838:GGGGGGGGGGGG:GGGGGGGGGG,NC_000016.10:14463838:GGGGGGGGGGGG:GGGGGGGGGGG,NC_000016.10:14463838:GGGGGGGGGGGG:GGGGGGGGGGGGG,NC_000016.10:14463838:GGGGGGGGGGGG:GGGGGGGGGGGGGG,NC_000016.10:14463838:GGGGGGGGGGGG:GGGGGGGGGGGGGGG
Gene:: PARN (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: GGGGGGGGGGG=0./0 (ALFA)
-=0.1174/588 (1000Genomes)
G=0.2/8 (GENOME_DK)
HGVS:: NC_000016.10:g.14463848_14463850del, NC_000016.10:g.14463849_14463850del, NC_000016.10:g.14463850del, NC_000016.10:g.14463850dup, NC_000016.10:g.14463849_14463850dup, NC_000016.10:g.14463848_14463850dup, NC_000016.9:g.14557705_14557707del, NC_000016.9:g.14557706_14557707del, NC_000016.9:g.14557707del, NC_000016.9:g.14557707dup, NC_000016.9:g.14557706_14557707dup, NC_000016.9:g.14557705_14557707dup, NG_042871.1:g.171431_171433del, NG_042871.1:g.171432_171433del, NG_042871.1:g.171433del, NG_042871.1:g.171433dup, NG_042871.1:g.171432_171433dup, NG_042871.1:g.171431_171433dup, NT_187607.1:g.36705_36707del, NT_187607.1:g.36706_36707del, NT_187607.1:g.36707del, NT_187607.1:g.36707dup, NT_187607.1:g.36706_36707dup, NT_187607.1:g.36705_36707dup

Select item 149139789814.

rs1491397898 has merged into rs35330393 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAA>-,A,AA,AAAA,AAAAA [Show Flanks]
Chromosome:: 16:14531914 (GRCh38)
16:14625771 (GRCh37)
Canonical SPDI:: NC_000016.10:14531899:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000016.10:14531899:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000016.10:14531899:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000016.10:14531899:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000016.10:14531899:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA
Gene:: PARN (Varview), LOC107984865 (Varview)
Functional Consequence:: non_coding_transcript_variant,genic_downstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAAAAAA=0./0 (ALFA)
-=0.02574/14 (NorthernSweden)
-=0.175/7 (GENOME_DK)
HGVS:: NC_000016.10:g.14531914_14531916del, NC_000016.10:g.14531915_14531916del, NC_000016.10:g.14531916del, NC_000016.10:g.14531916dup, NC_000016.10:g.14531915_14531916dup, NC_000016.9:g.14625771_14625773del, NC_000016.9:g.14625772_14625773del, NC_000016.9:g.14625773del, NC_000016.9:g.14625773dup, NC_000016.9:g.14625772_14625773dup, NG_042871.1:g.103370_103372del, NG_042871.1:g.103371_103372del, NG_042871.1:g.103372del, NG_042871.1:g.103372dup, NG_042871.1:g.103371_103372dup, NT_187607.1:g.104771_104773del, NT_187607.1:g.104772_104773del, NT_187607.1:g.104773del, NT_187607.1:g.104773dup, NT_187607.1:g.104772_104773dup, XR_001752089.3:n.19127_19129del, XR_001752089.3:n.19128_19129del, XR_001752089.3:n.19129del, XR_001752089.3:n.19129dup, XR_001752089.3:n.19128_19129dup, XR_001752089.2:n.3_4insTTTTTTTTTTTTTT, XR_001752089.2:n.3_4insTTTTTTTTTTT, XR_001752089.2:n.3_4insTTTTTTTTTTTT, XR_001752089.2:n.3_4insTTTTTTTTTTTTT, XR_001752089.2:n.3_4insTTTTTTTTTTTTTTT, XR_001752089.2:n.3_4insTTTTTTTTTTTTTTTT, XR_001752089.1:n.3_4insTTTTTTTTTTTTTT, XR_001752089.1:n.3_4insTTTTTTTTTTT, XR_001752089.1:n.3_4insTTTTTTTTTTTT, XR_001752089.1:n.3_4insTTTTTTTTTTTTT, XR_001752089.1:n.3_4insTTTTTTTTTTTTTTT, XR_001752089.1:n.3_4insTTTTTTTTTTTTTTTT, XR_001756351.3:n.19127_19129del, XR_001756351.3:n.19128_19129del, XR_001756351.3:n.19129del, XR_001756351.3:n.19129dup, XR_001756351.3:n.19128_19129dup, XR_001756351.2:n.3_4insTTTTTTTTTTTTTT, XR_001756351.2:n.3_4insTTTTTTTTTTT, XR_001756351.2:n.3_4insTTTTTTTTTTTT, XR_001756351.2:n.3_4insTTTTTTTTTTTTT, XR_001756351.2:n.3_4insTTTTTTTTTTTTTTT, XR_001756351.2:n.3_4insTTTTTTTTTTTTTTTT, XR_001756351.1:n.3_4insTTTTTTTTTTTTTT, XR_001756351.1:n.3_4insTTTTTTTTTTT, XR_001756351.1:n.3_4insTTTTTTTTTTTT, XR_001756351.1:n.3_4insTTTTTTTTTTTTT, XR_001756351.1:n.3_4insTTTTTTTTTTTTTTT, XR_001756351.1:n.3_4insTTTTTTTTTTTTTTTT

Select item 149138144215.

rs1491381442 [Homo sapiens]

Variant type:: DEL
Alleles:: CA>- [Show Flanks]
Chromosome:: 16:14489437 (GRCh38)
16:14583294 (GRCh37)
Canonical SPDI:: NC_000016.10:14489436:CA:
Gene:: PARN (Varview), LOC105371094 (Varview)
Functional Consequence:: downstream_transcript_variant,500B_downstream_variant,genic_downstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0.00008/1 (ALFA)
HGVS:: NC_000016.10:g.14489437_14489438del, NC_000016.9:g.14583294_14583295del, NG_042871.1:g.145834_145835del, NT_187607.1:g.62294_62295del

Select item 149136979716.

rs1491369797 [Homo sapiens]

Variant type:: INS
Alleles:: ->G [Show Flanks]
Chromosome:: 16:14463829 (GRCh38)
16:14557687 (GRCh37)
Canonical SPDI:: NC_000016.10:14463829::G
Gene:: PARN (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000084/1 (ALFA)
G=0.000127/13 (GnomAD)
HGVS:: NC_000016.10:g.14463829_14463830insG, NC_000016.9:g.14557686_14557687insG, NG_042871.1:g.171442_171443insC, NT_187607.1:g.36686_36687insG

Select item 149136518917.

rs1491365189 has merged into rs534284469 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAA>-,A,AA,AAAA,AAAAA,AAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 16:14579995 (GRCh38)
16:14673852 (GRCh37)
Canonical SPDI:: NC_000016.10:14579982:AAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000016.10:14579982:AAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000016.10:14579982:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000016.10:14579982:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000016.10:14579982:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000016.10:14579982:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: PARN (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAAAAA=0./0 (ALFA)
-=0.1747/875 (1000Genomes)
-=0.2595/1000 (ALSPAC)
-=0.2627/974 (TWINSUK)
HGVS:: NC_000016.10:g.14579995_14579997del, NC_000016.10:g.14579996_14579997del, NC_000016.10:g.14579997del, NC_000016.10:g.14579997dup, NC_000016.10:g.14579996_14579997dup, NC_000016.10:g.14579987_14579997dup, NC_000016.9:g.14673852_14673854del, NC_000016.9:g.14673853_14673854del, NC_000016.9:g.14673854del, NC_000016.9:g.14673854dup, NC_000016.9:g.14673853_14673854dup, NC_000016.9:g.14673844_14673854dup, NG_042871.1:g.55287_55289del, NG_042871.1:g.55288_55289del, NG_042871.1:g.55289del, NG_042871.1:g.55289dup, NG_042871.1:g.55288_55289dup, NG_042871.1:g.55279_55289dup, NT_187607.1:g.152852_152854del, NT_187607.1:g.152853_152854del, NT_187607.1:g.152854del, NT_187607.1:g.152854dup, NT_187607.1:g.152853_152854dup, NT_187607.1:g.152844_152854dup

Select item 149136303918.

rs1491363039 has merged into rs35170336 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAAAAAAAAAAAAAAAA>-,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 16:14457803 (GRCh38)
16:14551660 (GRCh37)
Canonical SPDI:: NC_000016.10:14457797:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAA,NC_000016.10:14457797:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000016.10:14457797:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000016.10:14457797:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000016.10:14457797:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000016.10:14457797:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000016.10:14457797:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000016.10:14457797:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000016.10:14457797:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000016.10:14457797:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000016.10:14457797:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000016.10:14457797:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000016.10:14457797:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000016.10:14457797:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000016.10:14457797:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000016.10:14457797:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000016.10:14457797:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000016.10:14457797:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000016.10:14457797:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000016.10:14457797:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000016.10:14457797:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000016.10:14457797:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000016.10:14457797:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000016.10:14457797:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000016.10:14457797:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000016.10:14457797:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000016.10:14457797:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: PARN (Varview)
Functional Consequence:: non_coding_transcript_variant,genic_downstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAA=0./0 (ALFA)
AAAAAAAAAAAAAAAAA=0./0 (GENOME_DK)
-=0.000004/1 (TOPMED)
HGVS:: NC_000016.10:g.14457803_14457825del, NC_000016.10:g.14457809_14457825del, NC_000016.10:g.14457810_14457825del, NC_000016.10:g.14457811_14457825del, NC_000016.10:g.14457812_14457825del, NC_000016.10:g.14457813_14457825del, NC_000016.10:g.14457814_14457825del, NC_000016.10:g.14457815_14457825del, NC_000016.10:g.14457816_14457825del, NC_000016.10:g.14457817_14457825del, NC_000016.10:g.14457818_14457825del, NC_000016.10:g.14457819_14457825del, NC_000016.10:g.14457820_14457825del, NC_000016.10:g.14457821_14457825del, NC_000016.10:g.14457822_14457825del, NC_000016.10:g.14457823_14457825del, NC_000016.10:g.14457824_14457825del, NC_000016.10:g.14457825del, NC_000016.10:g.14457825dup, NC_000016.10:g.14457824_14457825dup, NC_000016.10:g.14457823_14457825dup, NC_000016.10:g.14457822_14457825dup, NC_000016.10:g.14457821_14457825dup, NC_000016.10:g.14457820_14457825dup, NC_000016.10:g.14457819_14457825dup, NC_000016.10:g.14457817_14457825dup, NC_000016.10:g.14457812_14457825dup, NC_000016.9:g.14551660_14551682del, NC_000016.9:g.14551666_14551682del, NC_000016.9:g.14551667_14551682del, NC_000016.9:g.14551668_14551682del, NC_000016.9:g.14551669_14551682del, NC_000016.9:g.14551670_14551682del, NC_000016.9:g.14551671_14551682del, NC_000016.9:g.14551672_14551682del, NC_000016.9:g.14551673_14551682del, NC_000016.9:g.14551674_14551682del, NC_000016.9:g.14551675_14551682del, NC_000016.9:g.14551676_14551682del, NC_000016.9:g.14551677_14551682del, NC_000016.9:g.14551678_14551682del, NC_000016.9:g.14551679_14551682del, NC_000016.9:g.14551680_14551682del, NC_000016.9:g.14551681_14551682del, NC_000016.9:g.14551682del, NC_000016.9:g.14551682dup, NC_000016.9:g.14551681_14551682dup, NC_000016.9:g.14551680_14551682dup, NC_000016.9:g.14551679_14551682dup, NC_000016.9:g.14551678_14551682dup, NC_000016.9:g.14551677_14551682dup, NC_000016.9:g.14551676_14551682dup, NC_000016.9:g.14551674_14551682dup, NC_000016.9:g.14551669_14551682dup, NG_042871.1:g.177452_177474del, NG_042871.1:g.177458_177474del, NG_042871.1:g.177459_177474del, NG_042871.1:g.177460_177474del, NG_042871.1:g.177461_177474del, NG_042871.1:g.177462_177474del, NG_042871.1:g.177463_177474del, NG_042871.1:g.177464_177474del, NG_042871.1:g.177465_177474del, NG_042871.1:g.177466_177474del, NG_042871.1:g.177467_177474del, NG_042871.1:g.177468_177474del, NG_042871.1:g.177469_177474del, NG_042871.1:g.177470_177474del, NG_042871.1:g.177471_177474del, NG_042871.1:g.177472_177474del, NG_042871.1:g.177473_177474del, NG_042871.1:g.177474del, NG_042871.1:g.177474dup, NG_042871.1:g.177473_177474dup, NG_042871.1:g.177472_177474dup, NG_042871.1:g.177471_177474dup, NG_042871.1:g.177470_177474dup, NG_042871.1:g.177469_177474dup, NG_042871.1:g.177468_177474dup, NG_042871.1:g.177466_177474dup, NG_042871.1:g.177461_177474dup, NT_187607.1:g.30660_30682del, NT_187607.1:g.30666_30682del, NT_187607.1:g.30667_30682del, NT_187607.1:g.30668_30682del, NT_187607.1:g.30669_30682del, NT_187607.1:g.30670_30682del, NT_187607.1:g.30671_30682del, NT_187607.1:g.30672_30682del, NT_187607.1:g.30673_30682del, NT_187607.1:g.30674_30682del, NT_187607.1:g.30675_30682del, NT_187607.1:g.30676_30682del, NT_187607.1:g.30677_30682del, NT_187607.1:g.30678_30682del, NT_187607.1:g.30679_30682del, NT_187607.1:g.30680_30682del, NT_187607.1:g.30681_30682del, NT_187607.1:g.30682del, NT_187607.1:g.30682dup, NT_187607.1:g.30681_30682dup, NT_187607.1:g.30680_30682dup, NT_187607.1:g.30679_30682dup, NT_187607.1:g.30678_30682dup, NT_187607.1:g.30677_30682dup, NT_187607.1:g.30676_30682dup, NT_187607.1:g.30674_30682dup, NT_187607.1:g.30669_30682dup, XR_007064883.1:n.5742_5764del, XR_007064883.1:n.5748_5764del, XR_007064883.1:n.5749_5764del, XR_007064883.1:n.5750_5764del, XR_007064883.1:n.5751_5764del, XR_007064883.1:n.5752_5764del, XR_007064883.1:n.5753_5764del, XR_007064883.1:n.5754_5764del, XR_007064883.1:n.5755_5764del, XR_007064883.1:n.5756_5764del, XR_007064883.1:n.5757_5764del, XR_007064883.1:n.5758_5764del, XR_007064883.1:n.5759_5764del, XR_007064883.1:n.5760_5764del, XR_007064883.1:n.5761_5764del, XR_007064883.1:n.5762_5764del, XR_007064883.1:n.5763_5764del, XR_007064883.1:n.5764del, XR_007064883.1:n.5764dup, XR_007064883.1:n.5763_5764dup, XR_007064883.1:n.5762_5764dup, XR_007064883.1:n.5761_5764dup, XR_007064883.1:n.5760_5764dup, XR_007064883.1:n.5759_5764dup, XR_007064883.1:n.5758_5764dup, XR_007064883.1:n.5756_5764dup, XR_007064883.1:n.5751_5764dup, XR_007064882.1:n.5256_5278del, XR_007064882.1:n.5262_5278del, XR_007064882.1:n.5263_5278del, XR_007064882.1:n.5264_5278del, XR_007064882.1:n.5265_5278del, XR_007064882.1:n.5266_5278del, XR_007064882.1:n.5267_5278del, XR_007064882.1:n.5268_5278del, XR_007064882.1:n.5269_5278del, XR_007064882.1:n.5270_5278del, XR_007064882.1:n.5271_5278del, XR_007064882.1:n.5272_5278del, XR_007064882.1:n.5273_5278del, XR_007064882.1:n.5274_5278del, XR_007064882.1:n.5275_5278del, XR_007064882.1:n.5276_5278del, XR_007064882.1:n.5277_5278del, XR_007064882.1:n.5278del, XR_007064882.1:n.5278dup, XR_007064882.1:n.5277_5278dup, XR_007064882.1:n.5276_5278dup, XR_007064882.1:n.5275_5278dup, XR_007064882.1:n.5274_5278dup, XR_007064882.1:n.5273_5278dup, XR_007064882.1:n.5272_5278dup, XR_007064882.1:n.5270_5278dup, XR_007064882.1:n.5265_5278dup, XR_007064881.1:n.5820_5842del, XR_007064881.1:n.5826_5842del, XR_007064881.1:n.5827_5842del, XR_007064881.1:n.5828_5842del, XR_007064881.1:n.5829_5842del, XR_007064881.1:n.5830_5842del, XR_007064881.1:n.5831_5842del, XR_007064881.1:n.5832_5842del, XR_007064881.1:n.5833_5842del, XR_007064881.1:n.5834_5842del, XR_007064881.1:n.5835_5842del, XR_007064881.1:n.5836_5842del, XR_007064881.1:n.5837_5842del, XR_007064881.1:n.5838_5842del, XR_007064881.1:n.5839_5842del, XR_007064881.1:n.5840_5842del, XR_007064881.1:n.5841_5842del, XR_007064881.1:n.5842del, XR_007064881.1:n.5842dup, XR_007064881.1:n.5841_5842dup, XR_007064881.1:n.5840_5842dup, XR_007064881.1:n.5839_5842dup, XR_007064881.1:n.5838_5842dup, XR_007064881.1:n.5837_5842dup, XR_007064881.1:n.5836_5842dup, XR_007064881.1:n.5834_5842dup, XR_007064881.1:n.5829_5842dup, XR_007064884.1:n.5737_5759del, XR_007064884.1:n.5743_5759del, XR_007064884.1:n.5744_5759del, XR_007064884.1:n.5745_5759del, XR_007064884.1:n.5746_5759del, XR_007064884.1:n.5747_5759del, XR_007064884.1:n.5748_5759del, XR_007064884.1:n.5749_5759del, XR_007064884.1:n.5750_5759del, XR_007064884.1:n.5751_5759del, XR_007064884.1:n.5752_5759del, XR_007064884.1:n.5753_5759del, XR_007064884.1:n.5754_5759del, XR_007064884.1:n.5755_5759del, XR_007064884.1:n.5756_5759del, XR_007064884.1:n.5757_5759del, XR_007064884.1:n.5758_5759del, XR_007064884.1:n.5759del, XR_007064884.1:n.5759dup, XR_007064884.1:n.5758_5759dup, XR_007064884.1:n.5757_5759dup, XR_007064884.1:n.5756_5759dup, XR_007064884.1:n.5755_5759dup, XR_007064884.1:n.5754_5759dup, XR_007064884.1:n.5753_5759dup, XR_007064884.1:n.5751_5759dup, XR_007064884.1:n.5746_5759dup

Select item 149133687219.

rs1491336872 has merged into rs909541843 [Homo sapiens]

Variant type:: DELINS
Alleles:: GAGAGA>-,GA,GAGA,GAGAGAGA,GAGAGAGAGA [Show Flanks]
Chromosome:: 16:14457954 (GRCh38)
16:14551811 (GRCh37)
Canonical SPDI:: NC_000016.10:14457947:GAGAGAGAGAGA:GAGAGA,NC_000016.10:14457947:GAGAGAGAGAGA:GAGAGAGA,NC_000016.10:14457947:GAGAGAGAGAGA:GAGAGAGAGA,NC_000016.10:14457947:GAGAGAGAGAGA:GAGAGAGAGAGAGA,NC_000016.10:14457947:GAGAGAGAGAGA:GAGAGAGAGAGAGAGA
Gene:: PARN (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: GAGAGAGAGA=0./0 (ALFA)
-=0.000227/60 (TOPMED)
HGVS:: NC_000016.10:g.14457948GA[3], NC_000016.10:g.14457948GA[4], NC_000016.10:g.14457948GA[5], NC_000016.10:g.14457948GA[7], NC_000016.10:g.14457948GA[8], NC_000016.9:g.14551805GA[3], NC_000016.9:g.14551805GA[4], NC_000016.9:g.14551805GA[5], NC_000016.9:g.14551805GA[7], NC_000016.9:g.14551805GA[8], NG_042871.1:g.177313TC[3], NG_042871.1:g.177313TC[4], NG_042871.1:g.177313TC[5], NG_042871.1:g.177313TC[7], NG_042871.1:g.177313TC[8], NT_187607.1:g.30805GA[3], NT_187607.1:g.30805GA[4], NT_187607.1:g.30805GA[5], NT_187607.1:g.30805GA[7], NT_187607.1:g.30805GA[8], XR_007064883.1:n.5603TC[3], XR_007064883.1:n.5603TC[4], XR_007064883.1:n.5603TC[5], XR_007064883.1:n.5603TC[7], XR_007064883.1:n.5603TC[8], XR_007064882.1:n.5117TC[3], XR_007064882.1:n.5117TC[4], XR_007064882.1:n.5117TC[5], XR_007064882.1:n.5117TC[7], XR_007064882.1:n.5117TC[8], XR_007064881.1:n.5681TC[3], XR_007064881.1:n.5681TC[4], XR_007064881.1:n.5681TC[5], XR_007064881.1:n.5681TC[7], XR_007064881.1:n.5681TC[8], XR_007064884.1:n.5598TC[3], XR_007064884.1:n.5598TC[4], XR_007064884.1:n.5598TC[5], XR_007064884.1:n.5598TC[7], XR_007064884.1:n.5598TC[8]

Select item 149131785220.

rs1491317852 has merged into rs35250440 [Homo sapiens]

Variant type:: DELINS
Alleles:: CACACACACACACACACACACA>-,CACACA,CACACACA,CACACACACA,CACACACACACA,CACACACACACACA,CACACACACACACACA,CACACACACACACACACA,CACACACACACACACACACA,CACACACACACACACACACACACA,CACACACACACACACACACACACACA,CACACACACACACACACACACACACACA,CACACACACACACACACACACACACACACA,CACACACACACACACACACACACACACACACA,CACACACACACACACACACACACACACACACACA [Show Flanks]
Chromosome:: 16:14523236 (GRCh38)
16:14617093 (GRCh37)
Canonical SPDI:: NC_000016.10:14523224:ACACACACACACACACACACACACACACACACA:ACACACACACA,NC_000016.10:14523224:ACACACACACACACACACACACACACACACACA:ACACACACACACACACA,NC_000016.10:14523224:ACACACACACACACACACACACACACACACACA:ACACACACACACACACACA,NC_000016.10:14523224:ACACACACACACACACACACACACACACACACA:ACACACACACACACACACACA,NC_000016.10:14523224:ACACACACACACACACACACACACACACACACA:ACACACACACACACACACACACA,NC_000016.10:14523224:ACACACACACACACACACACACACACACACACA:ACACACACACACACACACACACACA,NC_000016.10:14523224:ACACACACACACACACACACACACACACACACA:ACACACACACACACACACACACACACA,NC_000016.10:14523224:ACACACACACACACACACACACACACACACACA:ACACACACACACACACACACACACACACA,NC_000016.10:14523224:ACACACACACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACA,NC_000016.10:14523224:ACACACACACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACACA,NC_000016.10:14523224:ACACACACACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACACACA,NC_000016.10:14523224:ACACACACACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACACACACA,NC_000016.10:14523224:ACACACACACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACACACACACA,NC_000016.10:14523224:ACACACACACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACACACACACACA,NC_000016.10:14523224:ACACACACACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACACACACACACACA
Gene:: PARN (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: ACACACACACACACACA=0./0 (ALFA)
-=0.000004/1 (TOPMED)
HGVS:: NC_000016.10:g.14523226CA[5], NC_000016.10:g.14523226CA[8], NC_000016.10:g.14523226CA[9], NC_000016.10:g.14523226CA[10], NC_000016.10:g.14523226CA[11], NC_000016.10:g.14523226CA[12], NC_000016.10:g.14523226CA[13], NC_000016.10:g.14523226CA[14], NC_000016.10:g.14523226CA[15], NC_000016.10:g.14523226CA[17], NC_000016.10:g.14523226CA[18], NC_000016.10:g.14523226CA[19], NC_000016.10:g.14523226CA[20], NC_000016.10:g.14523226CA[21], NC_000016.10:g.14523226CA[22], NC_000016.9:g.14617083CA[5], NC_000016.9:g.14617083CA[8], NC_000016.9:g.14617083CA[9], NC_000016.9:g.14617083CA[10], NC_000016.9:g.14617083CA[11], NC_000016.9:g.14617083CA[12], NC_000016.9:g.14617083CA[13], NC_000016.9:g.14617083CA[14], NC_000016.9:g.14617083CA[15], NC_000016.9:g.14617083CA[17], NC_000016.9:g.14617083CA[18], NC_000016.9:g.14617083CA[19], NC_000016.9:g.14617083CA[20], NC_000016.9:g.14617083CA[21], NC_000016.9:g.14617083CA[22], NG_042871.1:g.112016GT[5], NG_042871.1:g.112016GT[8], NG_042871.1:g.112016GT[9], NG_042871.1:g.112016GT[10], NG_042871.1:g.112016GT[11], NG_042871.1:g.112016GT[12], NG_042871.1:g.112016GT[13], NG_042871.1:g.112016GT[14], NG_042871.1:g.112016GT[15], NG_042871.1:g.112016GT[17], NG_042871.1:g.112016GT[18], NG_042871.1:g.112016GT[19], NG_042871.1:g.112016GT[20], NG_042871.1:g.112016GT[21], NG_042871.1:g.112016GT[22], NT_187607.1:g.96083CA[5], NT_187607.1:g.96083CA[8], NT_187607.1:g.96083CA[9], NT_187607.1:g.96083CA[10], NT_187607.1:g.96083CA[11], NT_187607.1:g.96083CA[12], NT_187607.1:g.96083CA[13], NT_187607.1:g.96083CA[14], NT_187607.1:g.96083CA[15], NT_187607.1:g.96083CA[17], NT_187607.1:g.96083CA[18], NT_187607.1:g.96083CA[19], NT_187607.1:g.96083CA[20], NT_187607.1:g.96083CA[21], NT_187607.1:g.96083CA[22]

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