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Select item 14915690391.

rs1491569039 has merged into rs555618890 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAAAAAAAAAAAA>-,AA,AAA,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAGAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 11:95868283 (GRCh38)
11:95601447 (GRCh37)
Canonical SPDI:: NC_000011.10:95868273:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA,NC_000011.10:95868273:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000011.10:95868273:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000011.10:95868273:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000011.10:95868273:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000011.10:95868273:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000011.10:95868273:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000011.10:95868273:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000011.10:95868273:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000011.10:95868273:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000011.10:95868273:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000011.10:95868273:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000011.10:95868273:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:95868273:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:95868273:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:95868273:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:95868273:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:95868273:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:95868273:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:95868273:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:95868273:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:95868273:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:95868273:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:95868273:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:95868273:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:95868273:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:95868273:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:95868273:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:95868273:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:95868273:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:95868273:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:95868273:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:95868273:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:95868273:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:95868273:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:95868273:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:95868273:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:95868273:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:95868273:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:95868273:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:95868273:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:95868273:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:95868273:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:95868273:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:95868273:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:95868273:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:95868273:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:95868273:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:95868273:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:95868273:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:95868273:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:95868273:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:95868273:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:95868273:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:95868273:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:95868273:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:95868273:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAGAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: MTMR2 (Varview)
Functional Consequence:: upstream_transcript_variant,genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAA=0./0 (ALFA)
-=0.275/11 (GENOME_DK)
HGVS:: NC_000011.10:g.95868283_95868301del, NC_000011.10:g.95868285_95868301del, NC_000011.10:g.95868286_95868301del, NC_000011.10:g.95868287_95868301del, NC_000011.10:g.95868288_95868301del, NC_000011.10:g.95868289_95868301del, NC_000011.10:g.95868290_95868301del, NC_000011.10:g.95868291_95868301del, NC_000011.10:g.95868292_95868301del, NC_000011.10:g.95868293_95868301del, NC_000011.10:g.95868294_95868301del, NC_000011.10:g.95868295_95868301del, NC_000011.10:g.95868296_95868301del, NC_000011.10:g.95868297_95868301del, NC_000011.10:g.95868298_95868301del, NC_000011.10:g.95868299_95868301del, NC_000011.10:g.95868300_95868301del, NC_000011.10:g.95868301del, NC_000011.10:g.95868301dup, NC_000011.10:g.95868300_95868301dup, NC_000011.10:g.95868299_95868301dup, NC_000011.10:g.95868298_95868301dup, NC_000011.10:g.95868297_95868301dup, NC_000011.10:g.95868296_95868301dup, NC_000011.10:g.95868295_95868301dup, NC_000011.10:g.95868294_95868301dup, NC_000011.10:g.95868293_95868301dup, NC_000011.10:g.95868292_95868301dup, NC_000011.10:g.95868291_95868301dup, NC_000011.10:g.95868290_95868301dup, NC_000011.10:g.95868289_95868301dup, NC_000011.10:g.95868288_95868301dup, NC_000011.10:g.95868287_95868301dup, NC_000011.10:g.95868286_95868301dup, NC_000011.10:g.95868285_95868301dup, NC_000011.10:g.95868283_95868301dup, NC_000011.10:g.95868282_95868301dup, NC_000011.10:g.95868281_95868301dup, NC_000011.10:g.95868279_95868301dup, NC_000011.10:g.95868278_95868301dup, NC_000011.10:g.95868277_95868301dup, NC_000011.10:g.95868276_95868301dup, NC_000011.10:g.95868275_95868301dup, NC_000011.10:g.95868274_95868301dup, NC_000011.10:g.95868301_95868302insAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000011.10:g.95868301_95868302insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000011.10:g.95868301_95868302insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000011.10:g.95868301_95868302insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000011.10:g.95868301_95868302insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000011.10:g.95868301_95868302insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000011.10:g.95868301_95868302insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000011.10:g.95868301_95868302insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000011.10:g.95868301_95868302insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000011.10:g.95868301_95868302insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000011.10:g.95868301_95868302insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000011.10:g.95868301_95868302insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000011.10:g.95868274_95868301A[31]GAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000011.9:g.95601447_95601465del, NC_000011.9:g.95601449_95601465del, NC_000011.9:g.95601450_95601465del, NC_000011.9:g.95601451_95601465del, NC_000011.9:g.95601452_95601465del, NC_000011.9:g.95601453_95601465del, NC_000011.9:g.95601454_95601465del, NC_000011.9:g.95601455_95601465del, NC_000011.9:g.95601456_95601465del, NC_000011.9:g.95601457_95601465del, NC_000011.9:g.95601458_95601465del, NC_000011.9:g.95601459_95601465del, NC_000011.9:g.95601460_95601465del, NC_000011.9:g.95601461_95601465del, NC_000011.9:g.95601462_95601465del, NC_000011.9:g.95601463_95601465del, NC_000011.9:g.95601464_95601465del, NC_000011.9:g.95601465del, NC_000011.9:g.95601465dup, NC_000011.9:g.95601464_95601465dup, NC_000011.9:g.95601463_95601465dup, NC_000011.9:g.95601462_95601465dup, NC_000011.9:g.95601461_95601465dup, NC_000011.9:g.95601460_95601465dup, NC_000011.9:g.95601459_95601465dup, NC_000011.9:g.95601458_95601465dup, NC_000011.9:g.95601457_95601465dup, NC_000011.9:g.95601456_95601465dup, NC_000011.9:g.95601455_95601465dup, NC_000011.9:g.95601454_95601465dup, NC_000011.9:g.95601453_95601465dup, NC_000011.9:g.95601452_95601465dup, NC_000011.9:g.95601451_95601465dup, NC_000011.9:g.95601450_95601465dup, NC_000011.9:g.95601449_95601465dup, NC_000011.9:g.95601447_95601465dup, NC_000011.9:g.95601446_95601465dup, NC_000011.9:g.95601445_95601465dup, NC_000011.9:g.95601443_95601465dup, NC_000011.9:g.95601442_95601465dup, NC_000011.9:g.95601441_95601465dup, NC_000011.9:g.95601440_95601465dup, NC_000011.9:g.95601439_95601465dup, NC_000011.9:g.95601438_95601465dup, NC_000011.9:g.95601465_95601466insAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000011.9:g.95601465_95601466insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000011.9:g.95601465_95601466insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000011.9:g.95601465_95601466insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000011.9:g.95601465_95601466insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000011.9:g.95601465_95601466insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000011.9:g.95601465_95601466insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000011.9:g.95601465_95601466insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000011.9:g.95601465_95601466insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000011.9:g.95601465_95601466insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000011.9:g.95601465_95601466insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000011.9:g.95601465_95601466insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000011.9:g.95601438_95601465A[31]GAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NG_008333.1:g.60916_60934del, NG_008333.1:g.60918_60934del, NG_008333.1:g.60919_60934del, NG_008333.1:g.60920_60934del, NG_008333.1:g.60921_60934del, NG_008333.1:g.60922_60934del, NG_008333.1:g.60923_60934del, NG_008333.1:g.60924_60934del, NG_008333.1:g.60925_60934del, NG_008333.1:g.60926_60934del, NG_008333.1:g.60927_60934del, NG_008333.1:g.60928_60934del, NG_008333.1:g.60929_60934del, NG_008333.1:g.60930_60934del, NG_008333.1:g.60931_60934del, NG_008333.1:g.60932_60934del, NG_008333.1:g.60933_60934del, NG_008333.1:g.60934del, NG_008333.1:g.60934dup, NG_008333.1:g.60933_60934dup, NG_008333.1:g.60932_60934dup, NG_008333.1:g.60931_60934dup, NG_008333.1:g.60930_60934dup, NG_008333.1:g.60929_60934dup, NG_008333.1:g.60928_60934dup, NG_008333.1:g.60927_60934dup, NG_008333.1:g.60926_60934dup, NG_008333.1:g.60925_60934dup, NG_008333.1:g.60924_60934dup, NG_008333.1:g.60923_60934dup, NG_008333.1:g.60922_60934dup, NG_008333.1:g.60921_60934dup, NG_008333.1:g.60920_60934dup, NG_008333.1:g.60919_60934dup, NG_008333.1:g.60918_60934dup, NG_008333.1:g.60916_60934dup, NG_008333.1:g.60915_60934dup, NG_008333.1:g.60914_60934dup, NG_008333.1:g.60912_60934dup, NG_008333.1:g.60911_60934dup, NG_008333.1:g.60910_60934dup, NG_008333.1:g.60909_60934dup, NG_008333.1:g.60908_60934dup, NG_008333.1:g.60907_60934dup, NG_008333.1:g.60934_60935insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_008333.1:g.60934_60935insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_008333.1:g.60934_60935insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_008333.1:g.60934_60935insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_008333.1:g.60934_60935insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_008333.1:g.60934_60935insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_008333.1:g.60934_60935insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_008333.1:g.60934_60935insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_008333.1:g.60934_60935insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_008333.1:g.60934_60935insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_008333.1:g.60934_60935insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_008333.1:g.60934_60935insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_008333.1:g.60907_60934T[33]CTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1]

Select item 14915677792.

rs1491567779 [Homo sapiens]

Variant type:: DEL
Alleles:: GT>- [Show Flanks]
Chromosome:: 11:95912087 (GRCh38)
11:95645251 (GRCh37)
Canonical SPDI:: NC_000011.10:95912086:GT:
Gene:: MTMR2 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
-=0.00003/1 (GnomAD)
HGVS:: NC_000011.10:g.95912087_95912088del, NC_000011.9:g.95645251_95645252del, NG_008333.1:g.17120_17121del

Select item 14915403933.

rs1491540393 [Homo sapiens]

Variant type:: DEL
Alleles:: CT>- [Show Flanks]
Chromosome:: 11:95851055 (GRCh38)
11:95584219 (GRCh37)
Canonical SPDI:: NC_000011.10:95851054:CT:
Gene:: MTMR2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
HGVS:: NC_000011.10:g.95851055_95851056del, NC_000011.9:g.95584219_95584220del, NG_008333.1:g.78152_78153del

Select item 14915205554.

rs1491520555 [Homo sapiens]

Variant type:: DEL
Alleles:: AT>- [Show Flanks]
Chromosome:: 11:95833369 (GRCh38)
11:95566533 (GRCh37)
Canonical SPDI:: NC_000011.10:95833368:AT:
Gene:: MTMR2 (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0./0 (ALFA)
-=0.000004/1 (TOPMED)
-=0.000007/1 (GnomAD)
-=0.000106/2 (TOMMO)
HGVS:: NC_000011.10:g.95833369_95833370del, NC_000011.9:g.95566533_95566534del, NG_008333.1:g.95838_95839del, NM_016156.6:c.*1920_*1921del, NM_016156.5:c.*1920_*1921del, NM_201278.3:c.*1920_*1921del, NM_201278.2:c.*1920_*1921del, NM_201281.3:c.*1920_*1921del, NM_201281.2:c.*1920_*1921del, NM_001243571.2:c.*1920_*1921del, NM_001243571.1:c.*1920_*1921del, NG_029829.1:g.47909_47910del, NR_023356.2:n.4372_4373del, NR_023354.1:n.4261_4262del, NR_023356.1:n.4211_4212del, NR_023355.1:n.4138_4139del, XM_047427807.1:c.*1920_*1921del, XM_047427806.1:c.*1920_*1921del, XM_047427808.1:c.*1920_*1921del, XM_047427805.1:c.*1920_*1921del

Select item 14914077285.

rs1491407728 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->ACT [Show Flanks]
Chromosome:: 11:95833369 (GRCh38)
11:95566534 (GRCh37)
Canonical SPDI:: NC_000011.10:95833369:T:TACT
Gene:: MTMR2 (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TACT=0./0 (ALFA)
TAC=0.000004/1 (TOPMED)
TAC=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.95833370_95833371insACT, NC_000011.9:g.95566534_95566535insACT, NG_008333.1:g.95838_95839insGTA, NM_016156.6:c.*1920_*1921insGTA, NM_016156.5:c.*1920_*1921insGTA, NM_201278.3:c.*1920_*1921insGTA, NM_201278.2:c.*1920_*1921insGTA, NM_201281.3:c.*1920_*1921insGTA, NM_201281.2:c.*1920_*1921insGTA, NM_001243571.2:c.*1920_*1921insGTA, NM_001243571.1:c.*1920_*1921insGTA, NG_029829.1:g.47910_47911insACT, NR_023356.2:n.4372_4373insGTA, NR_023354.1:n.4261_4262insGTA, NR_023356.1:n.4211_4212insGTA, NR_023355.1:n.4138_4139insGTA, XM_047427807.1:c.*1920_*1921insGTA, XM_047427806.1:c.*1920_*1921insGTA, XM_047427808.1:c.*1920_*1921insGTA, XM_047427805.1:c.*1920_*1921insGTA

Select item 14913945686.

rs1491394568 [Homo sapiens]

Variant type:: DEL
Alleles:: CT>- [Show Flanks]
Chromosome:: 11:95905327 (GRCh38)
11:95638491 (GRCh37)
Canonical SPDI:: NC_000011.10:95905326:CT:
Gene:: MTMR2 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: -=0.00067/8 (ALFA)
HGVS:: NC_000011.10:g.95905327_95905328del, NC_000011.9:g.95638491_95638492del, NG_008333.1:g.23880_23881del

Select item 14913855537.

rs1491385553 has merged into rs71040121 [Homo sapiens]

Variant type:: DELINS
Alleles:: ACACACACAC>-,AC,ACAC,ACACAC,ACACACAC,ACACACACACAC,ACACACACACACAC,ACACACACACACACAC,ACACACACACACACACAC,ACACACACACACACACACAC,ACACACACACACACACACACAC [Show Flanks]
Chromosome:: 11:95910139 (GRCh38)
11:95643303 (GRCh37)
Canonical SPDI:: NC_000011.10:95910127:CACACACACACACACACACAC:CACACACACAC,NC_000011.10:95910127:CACACACACACACACACACAC:CACACACACACAC,NC_000011.10:95910127:CACACACACACACACACACAC:CACACACACACACAC,NC_000011.10:95910127:CACACACACACACACACACAC:CACACACACACACACAC,NC_000011.10:95910127:CACACACACACACACACACAC:CACACACACACACACACAC,NC_000011.10:95910127:CACACACACACACACACACAC:CACACACACACACACACACACAC,NC_000011.10:95910127:CACACACACACACACACACAC:CACACACACACACACACACACACAC,NC_000011.10:95910127:CACACACACACACACACACAC:CACACACACACACACACACACACACAC,NC_000011.10:95910127:CACACACACACACACACACAC:CACACACACACACACACACACACACACAC,NC_000011.10:95910127:CACACACACACACACACACAC:CACACACACACACACACACACACACACACAC,NC_000011.10:95910127:CACACACACACACACACACAC:CACACACACACACACACACACACACACACACAC
Gene:: MTMR2 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: CACACACACACAC=0./0 (ALFA)
CACA=0.080494/21306 (TOPMED)
HGVS:: NC_000011.10:g.95910129AC[5], NC_000011.10:g.95910129AC[6], NC_000011.10:g.95910129AC[7], NC_000011.10:g.95910129AC[8], NC_000011.10:g.95910129AC[9], NC_000011.10:g.95910129AC[11], NC_000011.10:g.95910129AC[12], NC_000011.10:g.95910129AC[13], NC_000011.10:g.95910129AC[14], NC_000011.10:g.95910129AC[15], NC_000011.10:g.95910129AC[16], NC_000011.9:g.95643293AC[5], NC_000011.9:g.95643293AC[6], NC_000011.9:g.95643293AC[7], NC_000011.9:g.95643293AC[8], NC_000011.9:g.95643293AC[9], NC_000011.9:g.95643293AC[11], NC_000011.9:g.95643293AC[12], NC_000011.9:g.95643293AC[13], NC_000011.9:g.95643293AC[14], NC_000011.9:g.95643293AC[15], NC_000011.9:g.95643293AC[16], NG_008333.1:g.19061TG[5], NG_008333.1:g.19061TG[6], NG_008333.1:g.19061TG[7], NG_008333.1:g.19061TG[8], NG_008333.1:g.19061TG[9], NG_008333.1:g.19061TG[11], NG_008333.1:g.19061TG[12], NG_008333.1:g.19061TG[13], NG_008333.1:g.19061TG[14], NG_008333.1:g.19061TG[15], NG_008333.1:g.19061TG[16]

Select item 14913651888.

rs1491365188 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->T [Show Flanks]
Chromosome:: 11:95884873 (GRCh38)
11:95618038 (GRCh37)
Canonical SPDI:: NC_000011.10:95884873:T:TT
Gene:: MTMR2 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: TT=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000011.10:g.95884874dup, NC_000011.9:g.95618038dup, NG_008333.1:g.44334dup

Select item 14913182109.

rs1491318210 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->GCGCGCGCACGC,GCGCGCGCGCGCACGC [Show Flanks]
Chromosome:: 11:95905329 (GRCh38)
11:95638494 (GRCh37)
Canonical SPDI:: NC_000011.10:95905329:CGC:CGCGCGCGCGCACGC,NC_000011.10:95905329:CGC:CGCGCGCGCGCGCGCACGC
Gene:: MTMR2 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: CGCGCGCGCGCGCGCACGC=0.00007/1 (ALFA)
HGVS:: NC_000011.10:g.95905330_95905332CG[5]CACGC[1], NC_000011.10:g.95905330_95905332CG[7]CACGC[1], NC_000011.9:g.95638494_95638496CG[5]CACGC[1], NC_000011.9:g.95638494_95638496CG[7]CACGC[1], NG_008333.1:g.23878_23879insTGCGCGCGCGCG, NG_008333.1:g.23878_23879insTGCGCGCGCGCGCGCG

Select item 149128587010.

rs1491285870 [Homo sapiens]

Variant type:: DEL
Alleles:: TC>- [Show Flanks]
Chromosome:: 11:95912103 (GRCh38)
11:95645267 (GRCh37)
Canonical SPDI:: NC_000011.10:95912102:TC:
Gene:: MTMR2 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: -=0.00006/1 (ALFA)
HGVS:: NC_000011.10:g.95912103_95912104del, NC_000011.9:g.95645267_95645268del, NG_008333.1:g.17104_17105del

Select item 149123229811.

rs1491232298 [Homo sapiens]

Variant type:: DEL
Alleles:: TA>- [Show Flanks]
Chromosome:: 11:95868273 (GRCh38)
11:95601437 (GRCh37)
Canonical SPDI:: NC_000011.10:95868272:TA:
Gene:: MTMR2 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
HGVS:: NC_000011.10:g.95868273_95868274del, NC_000011.9:g.95601437_95601438del, NG_008333.1:g.60934_60935del

Select item 149122830312.

rs1491228303 [Homo sapiens]

Variant type:: DEL
Alleles:: CT>- [Show Flanks]
Chromosome:: 11:95881128 (GRCh38)
11:95614292 (GRCh37)
Canonical SPDI:: NC_000011.10:95881127:CT:
Gene:: MTMR2 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0./0 (ALFA)
-=0.000004/1 (TOPMED)
-=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.95881128_95881129del, NC_000011.9:g.95614292_95614293del, NG_008333.1:g.48079_48080del

Select item 149121908713.

rs1491219087 [Homo sapiens]

Variant type:: DEL
Alleles:: CT>- [Show Flanks]
Chromosome:: 11:95877332 (GRCh38)
11:95610496 (GRCh37)
Canonical SPDI:: NC_000011.10:95877331:CT:
Gene:: MTMR2 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0.00008/1 (ALFA)
-=0.00019/17 (GnomAD)
HGVS:: NC_000011.10:g.95877332_95877333del, NC_000011.9:g.95610496_95610497del, NG_008333.1:g.51875_51876del

Select item 149120659414.

rs1491206594 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->GTT [Show Flanks]
Chromosome:: 11:95877333 (GRCh38)
11:95610498 (GRCh37)
Canonical SPDI:: NC_000011.10:95877333:TT:TTGTT
Gene:: MTMR2 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency
MAF:: TTG=0.00001/1 (GnomAD)
HGVS:: NC_000011.10:g.95877335_95877336insGTT, NC_000011.9:g.95610499_95610500insGTT, NG_008333.1:g.51874_51875insCAA

Select item 149119840215.

rs1491198402 [Homo sapiens]

Variant type:: DEL
Alleles:: AT>- [Show Flanks]
Chromosome:: 11:95884873 (GRCh38)
11:95618037 (GRCh37)
Canonical SPDI:: NC_000011.10:95884872:AT:
Gene:: MTMR2 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0./0 (ALFA)
-=0.000021/3 (GnomAD)
-=0.00003/8 (TOPMED)
HGVS:: NC_000011.10:g.95884873_95884874del, NC_000011.9:g.95618037_95618038del, NG_008333.1:g.44334_44335del

Select item 149119570916.

rs1491195709 has merged into rs764782930 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTTTTTTTT>-,T,TT,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 11:95877349 (GRCh38)
11:95610513 (GRCh37)
Canonical SPDI:: NC_000011.10:95877332:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000011.10:95877332:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000011.10:95877332:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000011.10:95877332:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000011.10:95877332:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000011.10:95877332:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000011.10:95877332:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:95877332:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:95877332:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:95877332:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:95877332:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:95877332:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:95877332:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:95877332:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:95877332:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:95877332:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:95877332:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:95877332:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:95877332:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:95877332:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:95877332:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:95877332:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:95877332:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:95877332:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:95877332:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:95877332:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:95877332:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:95877332:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: MTMR2 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTTTTTTTT=0./0 (ALFA)
-=0.000004/1 (TOPMED)
HGVS:: NC_000011.10:g.95877349_95877363del, NC_000011.10:g.95877350_95877363del, NC_000011.10:g.95877351_95877363del, NC_000011.10:g.95877352_95877363del, NC_000011.10:g.95877353_95877363del, NC_000011.10:g.95877354_95877363del, NC_000011.10:g.95877355_95877363del, NC_000011.10:g.95877356_95877363del, NC_000011.10:g.95877357_95877363del, NC_000011.10:g.95877358_95877363del, NC_000011.10:g.95877359_95877363del, NC_000011.10:g.95877361_95877363del, NC_000011.10:g.95877362_95877363del, NC_000011.10:g.95877363del, NC_000011.10:g.95877363dup, NC_000011.10:g.95877362_95877363dup, NC_000011.10:g.95877361_95877363dup, NC_000011.10:g.95877360_95877363dup, NC_000011.10:g.95877359_95877363dup, NC_000011.10:g.95877358_95877363dup, NC_000011.10:g.95877357_95877363dup, NC_000011.10:g.95877356_95877363dup, NC_000011.10:g.95877355_95877363dup, NC_000011.10:g.95877351_95877363dup, NC_000011.10:g.95877347_95877363dup, NC_000011.10:g.95877363_95877364insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000011.10:g.95877363_95877364insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000011.10:g.95877363_95877364insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000011.9:g.95610513_95610527del, NC_000011.9:g.95610514_95610527del, NC_000011.9:g.95610515_95610527del, NC_000011.9:g.95610516_95610527del, NC_000011.9:g.95610517_95610527del, NC_000011.9:g.95610518_95610527del, NC_000011.9:g.95610519_95610527del, NC_000011.9:g.95610520_95610527del, NC_000011.9:g.95610521_95610527del, NC_000011.9:g.95610522_95610527del, NC_000011.9:g.95610523_95610527del, NC_000011.9:g.95610525_95610527del, NC_000011.9:g.95610526_95610527del, NC_000011.9:g.95610527del, NC_000011.9:g.95610527dup, NC_000011.9:g.95610526_95610527dup, NC_000011.9:g.95610525_95610527dup, NC_000011.9:g.95610524_95610527dup, NC_000011.9:g.95610523_95610527dup, NC_000011.9:g.95610522_95610527dup, NC_000011.9:g.95610521_95610527dup, NC_000011.9:g.95610520_95610527dup, NC_000011.9:g.95610519_95610527dup, NC_000011.9:g.95610515_95610527dup, NC_000011.9:g.95610511_95610527dup, NC_000011.9:g.95610527_95610528insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000011.9:g.95610527_95610528insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000011.9:g.95610527_95610528insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_008333.1:g.51861_51875del, NG_008333.1:g.51862_51875del, NG_008333.1:g.51863_51875del, NG_008333.1:g.51864_51875del, NG_008333.1:g.51865_51875del, NG_008333.1:g.51866_51875del, NG_008333.1:g.51867_51875del, NG_008333.1:g.51868_51875del, NG_008333.1:g.51869_51875del, NG_008333.1:g.51870_51875del, NG_008333.1:g.51871_51875del, NG_008333.1:g.51873_51875del, NG_008333.1:g.51874_51875del, NG_008333.1:g.51875del, NG_008333.1:g.51875dup, NG_008333.1:g.51874_51875dup, NG_008333.1:g.51873_51875dup, NG_008333.1:g.51872_51875dup, NG_008333.1:g.51871_51875dup, NG_008333.1:g.51870_51875dup, NG_008333.1:g.51869_51875dup, NG_008333.1:g.51868_51875dup, NG_008333.1:g.51867_51875dup, NG_008333.1:g.51863_51875dup, NG_008333.1:g.51859_51875dup, NG_008333.1:g.51875_51876insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_008333.1:g.51875_51876insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_008333.1:g.51875_51876insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

Select item 149119421817.

rs1491194218 has merged into rs55809121 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTTTTTTTTTT>-,TT,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 11:95851064 (GRCh38)
11:95584228 (GRCh37)
Canonical SPDI:: NC_000011.10:95851055:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTT,NC_000011.10:95851055:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000011.10:95851055:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000011.10:95851055:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000011.10:95851055:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000011.10:95851055:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000011.10:95851055:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000011.10:95851055:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000011.10:95851055:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000011.10:95851055:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000011.10:95851055:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000011.10:95851055:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000011.10:95851055:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000011.10:95851055:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:95851055:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:95851055:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:95851055:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:95851055:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:95851055:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:95851055:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:95851055:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:95851055:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:95851055:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:95851055:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:95851055:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:95851055:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:95851055:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:95851055:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:95851055:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: MTMR2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTT=0./0 (ALFA)
HGVS:: NC_000011.10:g.95851064_95851080del, NC_000011.10:g.95851066_95851080del, NC_000011.10:g.95851067_95851080del, NC_000011.10:g.95851068_95851080del, NC_000011.10:g.95851069_95851080del, NC_000011.10:g.95851070_95851080del, NC_000011.10:g.95851071_95851080del, NC_000011.10:g.95851072_95851080del, NC_000011.10:g.95851073_95851080del, NC_000011.10:g.95851074_95851080del, NC_000011.10:g.95851075_95851080del, NC_000011.10:g.95851076_95851080del, NC_000011.10:g.95851077_95851080del, NC_000011.10:g.95851078_95851080del, NC_000011.10:g.95851079_95851080del, NC_000011.10:g.95851080del, NC_000011.10:g.95851080dup, NC_000011.10:g.95851079_95851080dup, NC_000011.10:g.95851078_95851080dup, NC_000011.10:g.95851077_95851080dup, NC_000011.10:g.95851076_95851080dup, NC_000011.10:g.95851075_95851080dup, NC_000011.10:g.95851074_95851080dup, NC_000011.10:g.95851073_95851080dup, NC_000011.10:g.95851072_95851080dup, NC_000011.10:g.95851071_95851080dup, NC_000011.10:g.95851061_95851080dup, NC_000011.10:g.95851080_95851081insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000011.10:g.95851080_95851081insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000011.9:g.95584228_95584244del, NC_000011.9:g.95584230_95584244del, NC_000011.9:g.95584231_95584244del, NC_000011.9:g.95584232_95584244del, NC_000011.9:g.95584233_95584244del, NC_000011.9:g.95584234_95584244del, NC_000011.9:g.95584235_95584244del, NC_000011.9:g.95584236_95584244del, NC_000011.9:g.95584237_95584244del, NC_000011.9:g.95584238_95584244del, NC_000011.9:g.95584239_95584244del, NC_000011.9:g.95584240_95584244del, NC_000011.9:g.95584241_95584244del, NC_000011.9:g.95584242_95584244del, NC_000011.9:g.95584243_95584244del, NC_000011.9:g.95584244del, NC_000011.9:g.95584244dup, NC_000011.9:g.95584243_95584244dup, NC_000011.9:g.95584242_95584244dup, NC_000011.9:g.95584241_95584244dup, NC_000011.9:g.95584240_95584244dup, NC_000011.9:g.95584239_95584244dup, NC_000011.9:g.95584238_95584244dup, NC_000011.9:g.95584237_95584244dup, NC_000011.9:g.95584236_95584244dup, NC_000011.9:g.95584235_95584244dup, NC_000011.9:g.95584225_95584244dup, NC_000011.9:g.95584244_95584245insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000011.9:g.95584244_95584245insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_008333.1:g.78136_78152del, NG_008333.1:g.78138_78152del, NG_008333.1:g.78139_78152del, NG_008333.1:g.78140_78152del, NG_008333.1:g.78141_78152del, NG_008333.1:g.78142_78152del, NG_008333.1:g.78143_78152del, NG_008333.1:g.78144_78152del, NG_008333.1:g.78145_78152del, NG_008333.1:g.78146_78152del, NG_008333.1:g.78147_78152del, NG_008333.1:g.78148_78152del, NG_008333.1:g.78149_78152del, NG_008333.1:g.78150_78152del, NG_008333.1:g.78151_78152del, NG_008333.1:g.78152del, NG_008333.1:g.78152dup, NG_008333.1:g.78151_78152dup, NG_008333.1:g.78150_78152dup, NG_008333.1:g.78149_78152dup, NG_008333.1:g.78148_78152dup, NG_008333.1:g.78147_78152dup, NG_008333.1:g.78146_78152dup, NG_008333.1:g.78145_78152dup, NG_008333.1:g.78144_78152dup, NG_008333.1:g.78143_78152dup, NG_008333.1:g.78133_78152dup, NG_008333.1:g.78152_78153insAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_008333.1:g.78152_78153insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

Select item 149116789418.

rs1491167894 [Homo sapiens]

Variant type:: DEL
Alleles:: AT>- [Show Flanks]
Chromosome:: 11:95865705 (GRCh38)
11:95598869 (GRCh37)
Canonical SPDI:: NC_000011.10:95865704:AT:
Gene:: MTMR2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
-=0.000004/1 (GnomAD_exomes)
-=0.000008/1 (ExAC)
HGVS:: NC_000011.10:g.95865705_95865706del, NC_000011.9:g.95598869_95598870del, NG_008333.1:g.63502_63503del

Select item 149115870919.

rs1491158709 has merged into rs67486618 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTT>-,T,TT,TTT,TTTT,TTTTTT,TTTTTTT,TTTTTTTTTTTT [Show Flanks]
Chromosome:: 11:95912099 (GRCh38)
11:95645263 (GRCh37)
Canonical SPDI:: NC_000011.10:95912087:TTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000011.10:95912087:TTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000011.10:95912087:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000011.10:95912087:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000011.10:95912087:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000011.10:95912087:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000011.10:95912087:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000011.10:95912087:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT
Gene:: MTMR2 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTTTTTTTTT=0./0 (ALFA)
T=0.2452/1228 (1000Genomes)
HGVS:: NC_000011.10:g.95912099_95912103del, NC_000011.10:g.95912100_95912103del, NC_000011.10:g.95912101_95912103del, NC_000011.10:g.95912102_95912103del, NC_000011.10:g.95912103del, NC_000011.10:g.95912103dup, NC_000011.10:g.95912102_95912103dup, NC_000011.10:g.95912097_95912103dup, NC_000011.9:g.95645263_95645267del, NC_000011.9:g.95645264_95645267del, NC_000011.9:g.95645265_95645267del, NC_000011.9:g.95645266_95645267del, NC_000011.9:g.95645267del, NC_000011.9:g.95645267dup, NC_000011.9:g.95645266_95645267dup, NC_000011.9:g.95645261_95645267dup, NG_008333.1:g.17116_17120del, NG_008333.1:g.17117_17120del, NG_008333.1:g.17118_17120del, NG_008333.1:g.17119_17120del, NG_008333.1:g.17120del, NG_008333.1:g.17120dup, NG_008333.1:g.17119_17120dup, NG_008333.1:g.17114_17120dup

Select item 149114819420.

rs1491148194 [Homo sapiens]

Variant type:: DEL
Alleles:: TG>- [Show Flanks]
Chromosome:: 11:95905328 (GRCh38)
11:95638492 (GRCh37)
Canonical SPDI:: NC_000011.10:95905327:TG:
Gene:: MTMR2 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
HGVS:: NC_000011.10:g.95905328_95905329del, NC_000011.9:g.95638492_95638493del, NG_008333.1:g.23879_23880del

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