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Select item 14915436451.

rs1491543645 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->CA,CACA,CACACA,CACACACA,CACACACACA,CACACACACACA,CACACACACACACA,CATACA,CATACACA,CATACACACA,CATACACACACA,CATACACACACACA [Show Flanks]
Chromosome:: 10:121524099 (GRCh38)
10:123283614 (GRCh37)
Canonical SPDI:: NC_000010.11:121524099:A:ACA,NC_000010.11:121524099:A:ACACA,NC_000010.11:121524099:A:ACACACA,NC_000010.11:121524099:A:ACACACACA,NC_000010.11:121524099:A:ACACACACACA,NC_000010.11:121524099:A:ACACACACACACA,NC_000010.11:121524099:A:ACACACACACACACA,NC_000010.11:121524099:A:ACATACA,NC_000010.11:121524099:A:ACATACACA,NC_000010.11:121524099:A:ACATACACACA,NC_000010.11:121524099:A:ACATACACACACA,NC_000010.11:121524099:A:ACATACACACACACA
Gene:: FGFR2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: ACACA=0./0 (ALFA)
HGVS:: NC_000010.11:g.121524100_121524101insCA, NC_000010.11:g.121524100_121524101insCACA, NC_000010.11:g.121524101CA[3], NC_000010.11:g.121524101CA[4], NC_000010.11:g.121524101CA[5], NC_000010.11:g.121524101CA[6], NC_000010.11:g.121524101CA[7], NC_000010.11:g.121524100_121524101insCATACA, NC_000010.11:g.121524100_121524101insCATACACA, NC_000010.11:g.121524100_121524101insCATACACACA, NC_000010.11:g.121524100_121524101insCATACACACACA, NC_000010.11:g.121524100_121524101insCATACACACACACA, NC_000010.10:g.123283614_123283615insCA, NC_000010.10:g.123283614_123283615insCACA, NC_000010.10:g.123283615CA[3], NC_000010.10:g.123283615CA[4], NC_000010.10:g.123283615CA[5], NC_000010.10:g.123283615CA[6], NC_000010.10:g.123283615CA[7], NC_000010.10:g.123283614_123283615insCATACA, NC_000010.10:g.123283614_123283615insCATACACA, NC_000010.10:g.123283614_123283615insCATACACACA, NC_000010.10:g.123283614_123283615insCATACACACACA, NC_000010.10:g.123283614_123283615insCATACACACACACA, NG_012449.2:g.79359_79360insGT, NG_012449.2:g.79359_79360insGTGT, NG_012449.2:g.79360GT[3], NG_012449.2:g.79360GT[4], NG_012449.2:g.79360GT[5], NG_012449.2:g.79360GT[6], NG_012449.2:g.79360GT[7], NG_012449.2:g.79359_79360insGTATGT, NG_012449.2:g.79359TG[2]TATGT[1], NG_012449.2:g.79359TG[3]TATGT[1], NG_012449.2:g.79359TG[4]TATGT[1], NG_012449.2:g.79359TG[5]TATGT[1]

Select item 14915334282.

rs1491533428 [Homo sapiens]

Variant type:: DEL
Alleles:: AT>- [Show Flanks]
Chromosome:: 10:121527592 (GRCh38)
10:123287106 (GRCh37)
Canonical SPDI:: NC_000010.11:121527591:AT:
Gene:: FGFR2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0./0 (ALFA)
-=0.000035/1 (TOMMO)
-=0.000053/14 (TOPMED)
-=0.001032/9 (GnomAD)
HGVS:: NC_000010.11:g.121527592_121527593del, NC_000010.10:g.123287106_123287107del, NG_012449.2:g.75866_75867del

Select item 14915130173.

rs1491513017 [Homo sapiens]

Variant type:: DEL
Alleles:: TG>- [Show Flanks]
Chromosome:: 10:121556434 (GRCh38)
10:123315948 (GRCh37)
Canonical SPDI:: NC_000010.11:121556433:TG:
Gene:: FGFR2 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0./0 (ALFA)
-=0.00908/35 (ALSPAC)
-=0.01753/65 (TWINSUK)
HGVS:: NC_000010.11:g.121556434_121556435del, NC_000010.10:g.123315948_123315949del, NG_012449.2:g.47024_47025del

Select item 14914826314.

rs1491482631 [Homo sapiens]

Variant type:: INS
Alleles:: ->TC,TCTCTCTCTC,TCTCTCTCTCTCTCTCTCTCTCTCTCTC [Show Flanks]
Chromosome:: 10:121556395 (GRCh38)
10:123315910 (GRCh37)
Canonical SPDI:: NC_000010.11:121556395::TC,NC_000010.11:121556395::TCTCTCTCTC,NC_000010.11:121556395::TCTCTCTCTCTCTCTCTCTCTCTCTCTC
Gene:: FGFR2 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: TC=0./0 (ALFA)
TCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.00001/1 (GnomAD)
HGVS:: NC_000010.11:g.121556395_121556396insTC, NC_000010.11:g.121556395_121556396insTCTCTCTCTC, NC_000010.11:g.121556395_121556396insTCTCTCTCTCTCTCTCTCTCTCTCTCTC, NC_000010.10:g.123315909_123315910insTC, NC_000010.10:g.123315909_123315910insTCTCTCTCTC, NC_000010.10:g.123315909_123315910insTCTCTCTCTCTCTCTCTCTCTCTCTCTC, NG_012449.2:g.47063_47064insGA, NG_012449.2:g.47063_47064insGAGAGAGAGA, NG_012449.2:g.47063_47064insGAGAGAGAGAGAGAGAGAGAGAGAGAGA

Select item 14914615005.

rs1491461500 [Homo sapiens]

Variant type:: DEL
Alleles:: TA>- [Show Flanks]
Chromosome:: 10:121556395 (GRCh38)
10:123315909 (GRCh37)
Canonical SPDI:: NC_000010.11:121556394:TA:
Gene:: FGFR2 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
HGVS:: NC_000010.11:g.121556395_121556396del, NC_000010.10:g.123315909_123315910del, NG_012449.2:g.47063_47064del

Select item 14913864206.

rs1491386420 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->CCTC [Show Flanks]
Chromosome:: 10:121556396 (GRCh38)
10:123315911 (GRCh37)
Canonical SPDI:: NC_000010.11:121556396:CTC:CTCCCTC
Gene:: FGFR2 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: CTCCCTC=0.000169/2 (ALFA)
CTCC=0.000026/3 (GnomAD)
HGVS:: NC_000010.11:g.121556399_121556400insCCTC, NC_000010.10:g.123315913_123315914insCCTC, NG_012449.2:g.47062_47063insGGAG

Select item 14913731377.

rs1491373137 [Homo sapiens]

Variant type:: DELINS
Alleles:: GG>- [Show Flanks]
Chromosome:: 10:121480124 (GRCh38)
10:123239638 (GRCh37)
Canonical SPDI:: NC_000010.11:121480122:GGG:G
Gene:: FGFR2 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: G=0.0001/1 (ALFA)
HGVS:: NC_000010.11:g.121480124_121480125del, NC_000010.10:g.123239638_123239639del, NG_012449.2:g.123335_123336del

Select item 14913641018.

rs1491364101 [Homo sapiens]

Variant type:: DEL
Alleles:: CA>- [Show Flanks]
Chromosome:: 10:121488540 (GRCh38)
10:123248054 (GRCh37)
Canonical SPDI:: NC_000010.11:121488539:CA:
Gene:: FGFR2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: -=0.00177/21 (ALFA)
HGVS:: NC_000010.11:g.121488540_121488541del, NC_000010.10:g.123248054_123248055del, NG_012449.2:g.114918_114919del

Select item 14913434699.

rs1491343469 has merged into rs60596436 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAAA>-,AA,AAA,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 10:121488550 (GRCh38)
10:123248064 (GRCh37)
Canonical SPDI:: NC_000010.11:121488540:AAAAAAAAAAAAAAAAAAA:AAAAAAAAA,NC_000010.11:121488540:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000010.11:121488540:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000010.11:121488540:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000010.11:121488540:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000010.11:121488540:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000010.11:121488540:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000010.11:121488540:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000010.11:121488540:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000010.11:121488540:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000010.11:121488540:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000010.11:121488540:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:121488540:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:121488540:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:121488540:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: FGFR2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAAA=0./0 (ALFA)
HGVS:: NC_000010.11:g.121488550_121488559del, NC_000010.11:g.121488552_121488559del, NC_000010.11:g.121488553_121488559del, NC_000010.11:g.121488554_121488559del, NC_000010.11:g.121488555_121488559del, NC_000010.11:g.121488556_121488559del, NC_000010.11:g.121488557_121488559del, NC_000010.11:g.121488558_121488559del, NC_000010.11:g.121488559del, NC_000010.11:g.121488559dup, NC_000010.11:g.121488558_121488559dup, NC_000010.11:g.121488557_121488559dup, NC_000010.11:g.121488555_121488559dup, NC_000010.11:g.121488552_121488559dup, NC_000010.11:g.121488549_121488559dup, NC_000010.10:g.123248064_123248073del, NC_000010.10:g.123248066_123248073del, NC_000010.10:g.123248067_123248073del, NC_000010.10:g.123248068_123248073del, NC_000010.10:g.123248069_123248073del, NC_000010.10:g.123248070_123248073del, NC_000010.10:g.123248071_123248073del, NC_000010.10:g.123248072_123248073del, NC_000010.10:g.123248073del, NC_000010.10:g.123248073dup, NC_000010.10:g.123248072_123248073dup, NC_000010.10:g.123248071_123248073dup, NC_000010.10:g.123248069_123248073dup, NC_000010.10:g.123248066_123248073dup, NC_000010.10:g.123248063_123248073dup, NG_012449.2:g.114909_114918del, NG_012449.2:g.114911_114918del, NG_012449.2:g.114912_114918del, NG_012449.2:g.114913_114918del, NG_012449.2:g.114914_114918del, NG_012449.2:g.114915_114918del, NG_012449.2:g.114916_114918del, NG_012449.2:g.114917_114918del, NG_012449.2:g.114918del, NG_012449.2:g.114918dup, NG_012449.2:g.114917_114918dup, NG_012449.2:g.114916_114918dup, NG_012449.2:g.114914_114918dup, NG_012449.2:g.114911_114918dup, NG_012449.2:g.114908_114918dup

Select item 149130393310.

rs1491303933 has merged into rs34753296 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAAAAAAAAAA>-,A,AA,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,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 10:121560625 (GRCh38)
10:123320139 (GRCh37)
Canonical SPDI:: NC_000010.11:121560615:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA,NC_000010.11:121560615:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA,NC_000010.11:121560615:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000010.11:121560615:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000010.11:121560615:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000010.11:121560615:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000010.11:121560615:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000010.11:121560615:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000010.11:121560615:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000010.11:121560615:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000010.11:121560615:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000010.11:121560615:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000010.11:121560615:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000010.11:121560615:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:121560615:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:121560615:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:121560615:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:121560615:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:121560615:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:121560615:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:121560615:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:121560615:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:121560615:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:121560615:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:121560615:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:121560615:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:121560615:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:121560615:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:121560615:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: FGFR2 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAA=0./0 (ALFA)
AAAAAAAA=0.0074/4 (NorthernSweden)
-=0.4/16 (GENOME_DK)
HGVS:: NC_000010.11:g.121560625_121560641del, NC_000010.11:g.121560626_121560641del, NC_000010.11:g.121560627_121560641del, NC_000010.11:g.121560628_121560641del, NC_000010.11:g.121560629_121560641del, NC_000010.11:g.121560630_121560641del, NC_000010.11:g.121560631_121560641del, NC_000010.11:g.121560632_121560641del, NC_000010.11:g.121560633_121560641del, NC_000010.11:g.121560634_121560641del, NC_000010.11:g.121560635_121560641del, NC_000010.11:g.121560636_121560641del, NC_000010.11:g.121560637_121560641del, NC_000010.11:g.121560638_121560641del, NC_000010.11:g.121560639_121560641del, NC_000010.11:g.121560640_121560641del, NC_000010.11:g.121560641del, NC_000010.11:g.121560641dup, NC_000010.11:g.121560640_121560641dup, NC_000010.11:g.121560639_121560641dup, NC_000010.11:g.121560638_121560641dup, NC_000010.11:g.121560637_121560641dup, NC_000010.11:g.121560636_121560641dup, NC_000010.11:g.121560635_121560641dup, NC_000010.11:g.121560634_121560641dup, NC_000010.11:g.121560633_121560641dup, NC_000010.11:g.121560632_121560641dup, NC_000010.11:g.121560631_121560641dup, NC_000010.11:g.121560629_121560641dup, NC_000010.10:g.123320139_123320155del, NC_000010.10:g.123320140_123320155del, NC_000010.10:g.123320141_123320155del, NC_000010.10:g.123320142_123320155del, NC_000010.10:g.123320143_123320155del, NC_000010.10:g.123320144_123320155del, NC_000010.10:g.123320145_123320155del, NC_000010.10:g.123320146_123320155del, NC_000010.10:g.123320147_123320155del, NC_000010.10:g.123320148_123320155del, NC_000010.10:g.123320149_123320155del, NC_000010.10:g.123320150_123320155del, NC_000010.10:g.123320151_123320155del, NC_000010.10:g.123320152_123320155del, NC_000010.10:g.123320153_123320155del, NC_000010.10:g.123320154_123320155del, NC_000010.10:g.123320155del, NC_000010.10:g.123320155dup, NC_000010.10:g.123320154_123320155dup, NC_000010.10:g.123320153_123320155dup, NC_000010.10:g.123320152_123320155dup, NC_000010.10:g.123320151_123320155dup, NC_000010.10:g.123320150_123320155dup, NC_000010.10:g.123320149_123320155dup, NC_000010.10:g.123320148_123320155dup, NC_000010.10:g.123320147_123320155dup, NC_000010.10:g.123320146_123320155dup, NC_000010.10:g.123320145_123320155dup, NC_000010.10:g.123320143_123320155dup, NG_012449.2:g.42827_42843del, NG_012449.2:g.42828_42843del, NG_012449.2:g.42829_42843del, NG_012449.2:g.42830_42843del, NG_012449.2:g.42831_42843del, NG_012449.2:g.42832_42843del, NG_012449.2:g.42833_42843del, NG_012449.2:g.42834_42843del, NG_012449.2:g.42835_42843del, NG_012449.2:g.42836_42843del, NG_012449.2:g.42837_42843del, NG_012449.2:g.42838_42843del, NG_012449.2:g.42839_42843del, NG_012449.2:g.42840_42843del, NG_012449.2:g.42841_42843del, NG_012449.2:g.42842_42843del, NG_012449.2:g.42843del, NG_012449.2:g.42843dup, NG_012449.2:g.42842_42843dup, NG_012449.2:g.42841_42843dup, NG_012449.2:g.42840_42843dup, NG_012449.2:g.42839_42843dup, NG_012449.2:g.42838_42843dup, NG_012449.2:g.42837_42843dup, NG_012449.2:g.42836_42843dup, NG_012449.2:g.42835_42843dup, NG_012449.2:g.42834_42843dup, NG_012449.2:g.42833_42843dup, NG_012449.2:g.42831_42843dup

Select item 149127756511.

rs1491277565 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->CAA [Show Flanks]
Chromosome:: 10:121552024 (GRCh38)
10:123311539 (GRCh37)
Canonical SPDI:: NC_000010.11:121552024:AA:AACAA
Gene:: FGFR2 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AACAA=0.00017/2 (ALFA)
AAC=0.00007/1 (TOMMO)
HGVS:: NC_000010.11:g.121552026_121552027insCAA, NC_000010.10:g.123311540_123311541insCAA, NG_012449.2:g.51434_51435insGTT

Select item 149122521412.

rs1491225214 has merged into rs35537265 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAAAAAA>-,AA,AAA,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 10:121497137 (GRCh38)
10:123256651 (GRCh37)
Canonical SPDI:: NC_000010.11:121497130:AAAAAAAAAAAAAAAAAAA:AAAAAA,NC_000010.11:121497130:AAAAAAAAAAAAAAAAAAA:AAAAAAAA,NC_000010.11:121497130:AAAAAAAAAAAAAAAAAAA:AAAAAAAAA,NC_000010.11:121497130:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAA,NC_000010.11:121497130:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000010.11:121497130:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000010.11:121497130:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000010.11:121497130:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000010.11:121497130:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000010.11:121497130:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000010.11:121497130:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000010.11:121497130:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000010.11:121497130:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000010.11:121497130:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000010.11:121497130:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:121497130:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:121497130:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:121497130:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:121497130:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: FGFR2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAA=0./0 (ALFA)
HGVS:: NC_000010.11:g.121497137_121497149del, NC_000010.11:g.121497139_121497149del, NC_000010.11:g.121497140_121497149del, NC_000010.11:g.121497141_121497149del, NC_000010.11:g.121497142_121497149del, NC_000010.11:g.121497143_121497149del, NC_000010.11:g.121497144_121497149del, NC_000010.11:g.121497145_121497149del, NC_000010.11:g.121497146_121497149del, NC_000010.11:g.121497147_121497149del, NC_000010.11:g.121497148_121497149del, NC_000010.11:g.121497149del, NC_000010.11:g.121497149dup, NC_000010.11:g.121497148_121497149dup, NC_000010.11:g.121497147_121497149dup, NC_000010.11:g.121497146_121497149dup, NC_000010.11:g.121497145_121497149dup, NC_000010.11:g.121497144_121497149dup, NC_000010.11:g.121497131_121497149dup, NC_000010.10:g.123256651_123256663del, NC_000010.10:g.123256653_123256663del, NC_000010.10:g.123256654_123256663del, NC_000010.10:g.123256655_123256663del, NC_000010.10:g.123256656_123256663del, NC_000010.10:g.123256657_123256663del, NC_000010.10:g.123256658_123256663del, NC_000010.10:g.123256659_123256663del, NC_000010.10:g.123256660_123256663del, NC_000010.10:g.123256661_123256663del, NC_000010.10:g.123256662_123256663del, NC_000010.10:g.123256663del, NC_000010.10:g.123256663dup, NC_000010.10:g.123256662_123256663dup, NC_000010.10:g.123256661_123256663dup, NC_000010.10:g.123256660_123256663dup, NC_000010.10:g.123256659_123256663dup, NC_000010.10:g.123256658_123256663dup, NC_000010.10:g.123256645_123256663dup, NG_012449.2:g.106316_106328del, NG_012449.2:g.106318_106328del, NG_012449.2:g.106319_106328del, NG_012449.2:g.106320_106328del, NG_012449.2:g.106321_106328del, NG_012449.2:g.106322_106328del, NG_012449.2:g.106323_106328del, NG_012449.2:g.106324_106328del, NG_012449.2:g.106325_106328del, NG_012449.2:g.106326_106328del, NG_012449.2:g.106327_106328del, NG_012449.2:g.106328del, NG_012449.2:g.106328dup, NG_012449.2:g.106327_106328dup, NG_012449.2:g.106326_106328dup, NG_012449.2:g.106325_106328dup, NG_012449.2:g.106324_106328dup, NG_012449.2:g.106323_106328dup, NG_012449.2:g.106310_106328dup

Select item 149122214613.

rs1491222146 [Homo sapiens]

Variant type:: INS
Alleles:: ->G [Show Flanks]
Chromosome:: 10:121497131 (GRCh38)
10:123256646 (GRCh37)
Canonical SPDI:: NC_000010.11:121497131::G
Gene:: FGFR2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
HGVS:: NC_000010.11:g.121497131_121497132insG, NC_000010.10:g.123256645_123256646insG, NG_012449.2:g.106327_106328insC

Select item 149120270314.

rs1491202703 [Homo sapiens]

Variant type:: INS
Alleles:: ->TTCTT [Show Flanks]
Chromosome:: 10:121480123 (GRCh38)
10:123239638 (GRCh37)
Canonical SPDI:: NC_000010.11:121480123::TTCTT
Gene:: FGFR2 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant
HGVS:: NC_000010.11:g.121480123_121480124insTTCTT, NC_000010.10:g.123239637_123239638insTTCTT, NG_012449.2:g.123335_123336insAAGAA

Select item 149115906415.

rs1491159064 [Homo sapiens]

Variant type:: DEL
Alleles:: AA>- [Show Flanks]
Chromosome:: 10:121527591 (GRCh38)
10:123287105 (GRCh37)
Canonical SPDI:: NC_000010.11:121527590:AA:
Gene:: FGFR2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
-=0.000014/2 (GnomAD)
HGVS:: NC_000010.11:g.121527591_121527592del, NC_000010.10:g.123287105_123287106del, NG_012449.2:g.75867_75868del

Select item 149113085116.

rs1491130851 has merged into rs1169688456 [Homo sapiens]

Variant type:: DELINS
Alleles:: GAGAGAGAGAGAGA>-,GA,GAGA,GAGAGA,GAGAGAGA,GAGAGAGAGA,GAGAGAGAGAGA,GAGAGAGAGAGAGAGA,GAGAGAGAGAGAGAGAGA,GAGAGAGAGAGAGAGAGAGA,GAGAGAGAGAGAGAGAGAGAGA,GAGAGAGAGAGAGAGAGAGAGAGA,GAGAGAGAGAGAGAGAGAGAGAGAGA,GAGAGAGAGAGAGAGAGAGAGAGAGAGA,GAGAGAGAGAGAGAGAGAGAGAGAGAGAGA,GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA,GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA,GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA,GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA,GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA,GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA,GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA,GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA [Show Flanks]
Chromosome:: 10:121577194 (GRCh38)
10:123336708 (GRCh37)
Canonical SPDI:: NC_000010.11:121577178:AGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGA,NC_000010.11:121577178:AGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGA,NC_000010.11:121577178:AGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGA,NC_000010.11:121577178:AGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGA,NC_000010.11:121577178:AGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGA,NC_000010.11:121577178:AGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGA,NC_000010.11:121577178:AGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGA,NC_000010.11:121577178:AGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA,NC_000010.11:121577178:AGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA,NC_000010.11:121577178:AGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA,NC_000010.11:121577178:AGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA,NC_000010.11:121577178:AGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA,NC_000010.11:121577178:AGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA,NC_000010.11:121577178:AGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA,NC_000010.11:121577178:AGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA,NC_000010.11:121577178:AGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA,NC_000010.11:121577178:AGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA,NC_000010.11:121577178:AGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA,NC_000010.11:121577178:AGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA,NC_000010.11:121577178:AGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA,NC_000010.11:121577178:AGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA,NC_000010.11:121577178:AGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA,NC_000010.11:121577178:AGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA
Gene:: FGFR2 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AGAGAGAGAGAGAGAGA=0./0 (ALFA)
HGVS:: NC_000010.11:g.121577180GA[7], NC_000010.11:g.121577180GA[8], NC_000010.11:g.121577180GA[9], NC_000010.11:g.121577180GA[10], NC_000010.11:g.121577180GA[11], NC_000010.11:g.121577180GA[12], NC_000010.11:g.121577180GA[13], NC_000010.11:g.121577180GA[15], NC_000010.11:g.121577180GA[16], NC_000010.11:g.121577180GA[17], NC_000010.11:g.121577180GA[18], NC_000010.11:g.121577180GA[19], NC_000010.11:g.121577180GA[20], NC_000010.11:g.121577180GA[21], NC_000010.11:g.121577180GA[22], NC_000010.11:g.121577180GA[23], NC_000010.11:g.121577180GA[24], NC_000010.11:g.121577180GA[25], NC_000010.11:g.121577180GA[26], NC_000010.11:g.121577180GA[27], NC_000010.11:g.121577180GA[28], NC_000010.11:g.121577180GA[29], NC_000010.11:g.121577180GA[30], NC_000010.10:g.123336694GA[7], NC_000010.10:g.123336694GA[8], NC_000010.10:g.123336694GA[9], NC_000010.10:g.123336694GA[10], NC_000010.10:g.123336694GA[11], NC_000010.10:g.123336694GA[12], NC_000010.10:g.123336694GA[13], NC_000010.10:g.123336694GA[15], NC_000010.10:g.123336694GA[16], NC_000010.10:g.123336694GA[17], NC_000010.10:g.123336694GA[18], NC_000010.10:g.123336694GA[19], NC_000010.10:g.123336694GA[20], NC_000010.10:g.123336694GA[21], NC_000010.10:g.123336694GA[22], NC_000010.10:g.123336694GA[23], NC_000010.10:g.123336694GA[24], NC_000010.10:g.123336694GA[25], NC_000010.10:g.123336694GA[26], NC_000010.10:g.123336694GA[27], NC_000010.10:g.123336694GA[28], NC_000010.10:g.123336694GA[29], NC_000010.10:g.123336694GA[30], NG_012449.2:g.26253CT[7], NG_012449.2:g.26253CT[8], NG_012449.2:g.26253CT[9], NG_012449.2:g.26253CT[10], NG_012449.2:g.26253CT[11], NG_012449.2:g.26253CT[12], NG_012449.2:g.26253CT[13], NG_012449.2:g.26253CT[15], NG_012449.2:g.26253CT[16], NG_012449.2:g.26253CT[17], NG_012449.2:g.26253CT[18], NG_012449.2:g.26253CT[19], NG_012449.2:g.26253CT[20], NG_012449.2:g.26253CT[21], NG_012449.2:g.26253CT[22], NG_012449.2:g.26253CT[23], NG_012449.2:g.26253CT[24], NG_012449.2:g.26253CT[25], NG_012449.2:g.26253CT[26], NG_012449.2:g.26253CT[27], NG_012449.2:g.26253CT[28], NG_012449.2:g.26253CT[29], NG_012449.2:g.26253CT[30]

Select item 149112469417.

rs1491124694 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->TACACA [Show Flanks]
Chromosome:: 10:121524101 (GRCh38)
10:123283616 (GRCh37)
Canonical SPDI:: NC_000010.11:121524101:ACA:ACATACACA
Gene:: FGFR2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: ACATACACA=0./0 (ALFA)
ACATAC=0.00005/4 (GnomAD)
HGVS:: NC_000010.11:g.121524104_121524105insTACACA, NC_000010.10:g.123283618_123283619insTACACA, NG_012449.2:g.79355_79357TG[2]TATGT[1]

Select item 149109409718.

rs1491094097 [Homo sapiens]

Variant type:: DELINS
Alleles:: CA>- [Show Flanks]
Chromosome:: 10:121565176 (GRCh38)
10:123324690 (GRCh37)
Canonical SPDI:: NC_000010.11:121565174:ACA:A
Gene:: FGFR2 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by cluster
MAF:: -=0.0054/20 (TWINSUK)
-=0.0062/24 (ALSPAC)
HGVS:: NC_000010.11:g.121565176_121565177del, NC_000010.10:g.123324690_123324691del, NG_012449.2:g.38283_38284del

Select item 149109294619.

rs1491092946 [Homo sapiens]

Variant type:: INS
Alleles:: ->T [Show Flanks]
Chromosome:: 10:121527591 (GRCh38)
10:123287106 (GRCh37)
Canonical SPDI:: NC_000010.11:121527591::T
Gene:: FGFR2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.00057/5 (GnomAD)
HGVS:: NC_000010.11:g.121527591_121527592insT, NC_000010.10:g.123287105_123287106insT, NG_012449.2:g.75867_75868insA

Select item 149108374120.

rs1491083741 has merged into rs10678814 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAAA>-,AA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 10:121506367 (GRCh38)
10:123265881 (GRCh37)
Canonical SPDI:: NC_000010.11:121506357:AAAAAAAAAAAAAAAAAAA:AAAAAAAAA,NC_000010.11:121506357:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000010.11:121506357:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000010.11:121506357:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000010.11:121506357:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000010.11:121506357:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000010.11:121506357:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000010.11:121506357:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000010.11:121506357:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000010.11:121506357:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:121506357:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:121506357:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:121506357:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:121506357:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:121506357:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:121506357:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:121506357:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:121506357:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:121506357:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:121506357:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:121506357:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:121506357:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:121506357:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:121506357:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:121506357:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: FGFR2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAA=0./0 (ALFA)
HGVS:: NC_000010.11:g.121506367_121506376del, NC_000010.11:g.121506369_121506376del, NC_000010.11:g.121506372_121506376del, NC_000010.11:g.121506373_121506376del, NC_000010.11:g.121506374_121506376del, NC_000010.11:g.121506375_121506376del, NC_000010.11:g.121506376del, NC_000010.11:g.121506376dup, NC_000010.11:g.121506375_121506376dup, NC_000010.11:g.121506374_121506376dup, NC_000010.11:g.121506373_121506376dup, NC_000010.11:g.121506372_121506376dup, NC_000010.11:g.121506371_121506376dup, NC_000010.11:g.121506370_121506376dup, NC_000010.11:g.121506369_121506376dup, NC_000010.11:g.121506367_121506376dup, NC_000010.11:g.121506366_121506376dup, NC_000010.11:g.121506365_121506376dup, NC_000010.11:g.121506364_121506376dup, NC_000010.11:g.121506363_121506376dup, NC_000010.11:g.121506362_121506376dup, NC_000010.11:g.121506361_121506376dup, NC_000010.11:g.121506360_121506376dup, NC_000010.11:g.121506359_121506376dup, NC_000010.11:g.121506376_121506377insAAAAAAAAAAAAAAAAAAAAAA, NC_000010.10:g.123265881_123265890del, NC_000010.10:g.123265883_123265890del, NC_000010.10:g.123265886_123265890del, NC_000010.10:g.123265887_123265890del, NC_000010.10:g.123265888_123265890del, NC_000010.10:g.123265889_123265890del, NC_000010.10:g.123265890del, NC_000010.10:g.123265890dup, NC_000010.10:g.123265889_123265890dup, NC_000010.10:g.123265888_123265890dup, NC_000010.10:g.123265887_123265890dup, NC_000010.10:g.123265886_123265890dup, NC_000010.10:g.123265885_123265890dup, NC_000010.10:g.123265884_123265890dup, NC_000010.10:g.123265883_123265890dup, NC_000010.10:g.123265881_123265890dup, NC_000010.10:g.123265880_123265890dup, NC_000010.10:g.123265879_123265890dup, NC_000010.10:g.123265878_123265890dup, NC_000010.10:g.123265877_123265890dup, NC_000010.10:g.123265876_123265890dup, NC_000010.10:g.123265875_123265890dup, NC_000010.10:g.123265874_123265890dup, NC_000010.10:g.123265873_123265890dup, NC_000010.10:g.123265890_123265891insAAAAAAAAAAAAAAAAAAAAAA, NG_012449.2:g.97092_97101del, NG_012449.2:g.97094_97101del, NG_012449.2:g.97097_97101del, NG_012449.2:g.97098_97101del, NG_012449.2:g.97099_97101del, NG_012449.2:g.97100_97101del, NG_012449.2:g.97101del, NG_012449.2:g.97101dup, NG_012449.2:g.97100_97101dup, NG_012449.2:g.97099_97101dup, NG_012449.2:g.97098_97101dup, NG_012449.2:g.97097_97101dup, NG_012449.2:g.97096_97101dup, NG_012449.2:g.97095_97101dup, NG_012449.2:g.97094_97101dup, NG_012449.2:g.97092_97101dup, NG_012449.2:g.97091_97101dup, NG_012449.2:g.97090_97101dup, NG_012449.2:g.97089_97101dup, NG_012449.2:g.97088_97101dup, NG_012449.2:g.97087_97101dup, NG_012449.2:g.97086_97101dup, NG_012449.2:g.97085_97101dup, NG_012449.2:g.97084_97101dup, NG_012449.2:g.97101_97102insTTTTTTTTTTTTTTTTTTTTTT

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