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Select item 14915792401.

rs1491579240 has merged into rs71196510 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTT>-,T,TT,TTT,TTTT,TTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 13:33190599 (GRCh38)
13:33764736 (GRCh37)
Canonical SPDI:: NC_000013.11:33190588:TTTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000013.11:33190588:TTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000013.11:33190588:TTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000013.11:33190588:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000013.11:33190588:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000013.11:33190588:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000013.11:33190588:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000013.11:33190588:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000013.11:33190588:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000013.11:33190588:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000013.11:33190588:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33190588:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33190588:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33190588:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33190588:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: STARD13 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTT=0./0 (ALFA)
-=0.10702/64 (NorthernSweden)
-=0.25/10 (GENOME_DK)
-=0.32728/1639 (1000Genomes)
HGVS:: NC_000013.11:g.33190599_33190604del, NC_000013.11:g.33190600_33190604del, NC_000013.11:g.33190601_33190604del, NC_000013.11:g.33190602_33190604del, NC_000013.11:g.33190603_33190604del, NC_000013.11:g.33190604del, NC_000013.11:g.33190604dup, NC_000013.11:g.33190603_33190604dup, NC_000013.11:g.33190602_33190604dup, NC_000013.11:g.33190601_33190604dup, NC_000013.11:g.33190600_33190604dup, NC_000013.11:g.33190599_33190604dup, NC_000013.11:g.33190597_33190604dup, NC_000013.11:g.33190596_33190604dup, NC_000013.11:g.33190595_33190604dup, NC_000013.10:g.33764736_33764741del, NC_000013.10:g.33764737_33764741del, NC_000013.10:g.33764738_33764741del, NC_000013.10:g.33764739_33764741del, NC_000013.10:g.33764740_33764741del, NC_000013.10:g.33764741del, NC_000013.10:g.33764741dup, NC_000013.10:g.33764740_33764741dup, NC_000013.10:g.33764739_33764741dup, NC_000013.10:g.33764738_33764741dup, NC_000013.10:g.33764737_33764741dup, NC_000013.10:g.33764736_33764741dup, NC_000013.10:g.33764734_33764741dup, NC_000013.10:g.33764733_33764741dup, NC_000013.10:g.33764732_33764741dup, NG_029752.2:g.491242_491247del, NG_029752.2:g.491243_491247del, NG_029752.2:g.491244_491247del, NG_029752.2:g.491245_491247del, NG_029752.2:g.491246_491247del, NG_029752.2:g.491247del, NG_029752.2:g.491247dup, NG_029752.2:g.491246_491247dup, NG_029752.2:g.491245_491247dup, NG_029752.2:g.491244_491247dup, NG_029752.2:g.491243_491247dup, NG_029752.2:g.491242_491247dup, NG_029752.2:g.491240_491247dup, NG_029752.2:g.491239_491247dup, NG_029752.2:g.491238_491247dup

Select item 14915650222.

rs1491565022 has merged into rs1435378518 [Homo sapiens]

Variant type:: DELINS
Alleles:: GGA>-,GGAGGAGGA [Show Flanks]
Chromosome:: 13:33189438 (GRCh38)
13:33763575 (GRCh37)
Canonical SPDI:: NC_000013.11:33189434:GGAGGA:GGA,NC_000013.11:33189434:GGAGGA:GGAGGAGGAGGA
Gene:: STARD13 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: GGAGGAGGAGGA=0.00025/3 (ALFA)
HGVS:: NC_000013.11:g.33189435GGA[1], NC_000013.11:g.33189435GGA[4], NC_000013.10:g.33763572GGA[1], NC_000013.10:g.33763572GGA[4], NG_029752.2:g.492396TCC[1], NG_029752.2:g.492396TCC[4]

Select item 14915646403.

rs1491564640 has merged into rs1221844260 [Homo sapiens]

Variant type:: DELINS
Alleles:: TT>-,T,TTT [Show Flanks]
Chromosome:: 13:33625719 (GRCh38)
13:34199856 (GRCh37)
Canonical SPDI:: NC_000013.11:33625710:TTTTTTTTTT:TTTTTTTT,NC_000013.11:33625710:TTTTTTTTTT:TTTTTTTTT,NC_000013.11:33625710:TTTTTTTTTT:TTTTTTTTTTT
Gene:: STARD13 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTT=0./0 (ALFA)
-=0.000106/2 (TOMMO)
T=0.000404/107 (TOPMED)
T=0.001845/8 (Estonian)
HGVS:: NC_000013.11:g.33625719_33625720del, NC_000013.11:g.33625720del, NC_000013.11:g.33625720dup, NC_000013.10:g.34199856_34199857del, NC_000013.10:g.34199857del, NC_000013.10:g.34199857dup, NG_029752.2:g.56124_56125del, NG_029752.2:g.56125del, NG_029752.2:g.56125dup

Select item 14915633574.

rs1491563357 [Homo sapiens]

Variant type:: DELINS
Alleles:: CT>- [Show Flanks]
Chromosome:: 13:33499573 (GRCh38)
13:34073710 (GRCh37)
Canonical SPDI:: NC_000013.11:33499571:TCT:T
Gene:: STARD13 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.00008/1 (ALFA)
-=0.00028/4 (TOMMO)
HGVS:: NC_000013.11:g.33499573_33499574del, NC_000013.10:g.34073710_34073711del, NG_029752.2:g.182263_182264del

Select item 14915556525.

rs1491555652 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->CTTTT [Show Flanks]
Chromosome:: 13:33659221 (GRCh38)
13:34233359 (GRCh37)
Canonical SPDI:: NC_000013.11:33659221:TTTT:TTTTCTTTT
Gene:: STARD13 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: TTTTCTTTT=0.00025/3 (ALFA)
HGVS:: NC_000013.11:g.33659222_33659225T[4]CTTTT[1], NC_000013.10:g.34233359_34233362T[4]CTTTT[1], NG_029752.2:g.22611_22614A[4]GAAAA[1]

Select item 14915537006.

rs1491553700 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->CTTC [Show Flanks]
Chromosome:: 13:33519237 (GRCh38)
13:34093375 (GRCh37)
Canonical SPDI:: NC_000013.11:33519237:TTC:TTCCTTC
Gene:: STARD13 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTCCTTC=0./0 (ALFA)
TTCC=0.000072/10 (GnomAD)
TTCC=0.000086/2 (TOMMO)
HGVS:: NC_000013.11:g.33519240_33519241insCTTC, NC_000013.10:g.34093377_34093378insCTTC, NG_029752.2:g.162598_162599insGGAA

Select item 14915499897.

rs1491549989 has merged into rs61502466 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTTTTTTTTTTTT>-,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 13:33648790 (GRCh38)
13:34222927 (GRCh37)
Canonical SPDI:: NC_000013.11:33648783:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTT,NC_000013.11:33648783:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTT,NC_000013.11:33648783:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000013.11:33648783:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000013.11:33648783:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000013.11:33648783:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000013.11:33648783:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000013.11:33648783:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000013.11:33648783:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000013.11:33648783:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000013.11:33648783:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000013.11:33648783:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000013.11:33648783:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000013.11:33648783:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33648783:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33648783:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33648783:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33648783:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33648783:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33648783:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33648783:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33648783:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33648783:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33648783:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33648783:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33648783:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33648783:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33648783:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33648783:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33648783:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33648783:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33648783:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33648783:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33648783:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33648783:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33648783:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33648783:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33648783:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33648783:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33648783:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33648783:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33648783:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33648783:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33648783:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33648783:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33648783:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33648783:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33648783:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: STARD13 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTT=0./0 (ALFA)
HGVS:: NC_000013.11:g.33648790_33648808del, NC_000013.11:g.33648793_33648808del, NC_000013.11:g.33648794_33648808del, NC_000013.11:g.33648795_33648808del, NC_000013.11:g.33648796_33648808del, NC_000013.11:g.33648797_33648808del, NC_000013.11:g.33648798_33648808del, NC_000013.11:g.33648799_33648808del, NC_000013.11:g.33648800_33648808del, NC_000013.11:g.33648801_33648808del, NC_000013.11:g.33648802_33648808del, NC_000013.11:g.33648803_33648808del, NC_000013.11:g.33648804_33648808del, NC_000013.11:g.33648805_33648808del, NC_000013.11:g.33648806_33648808del, NC_000013.11:g.33648807_33648808del, NC_000013.11:g.33648808del, NC_000013.11:g.33648808dup, NC_000013.11:g.33648807_33648808dup, NC_000013.11:g.33648806_33648808dup, NC_000013.11:g.33648784_33648808T[28]CTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000013.11:g.33648805_33648808dup, NC_000013.11:g.33648784_33648808T[29]CTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000013.11:g.33648804_33648808dup, NC_000013.11:g.33648803_33648808dup, NC_000013.11:g.33648802_33648808dup, NC_000013.11:g.33648801_33648808dup, NC_000013.11:g.33648800_33648808dup, NC_000013.11:g.33648799_33648808dup, NC_000013.11:g.33648798_33648808dup, NC_000013.11:g.33648797_33648808dup, NC_000013.11:g.33648796_33648808dup, NC_000013.11:g.33648795_33648808dup, NC_000013.11:g.33648794_33648808dup, NC_000013.11:g.33648793_33648808dup, NC_000013.11:g.33648791_33648808dup, NC_000013.11:g.33648790_33648808dup, NC_000013.11:g.33648789_33648808dup, NC_000013.11:g.33648788_33648808dup, NC_000013.11:g.33648787_33648808dup, NC_000013.11:g.33648786_33648808dup, NC_000013.11:g.33648785_33648808dup, NC_000013.11:g.33648784_33648808dup, NC_000013.11:g.33648808_33648809insTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000013.11:g.33648808_33648809insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000013.11:g.33648808_33648809insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000013.11:g.33648808_33648809insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000013.11:g.33648808_33648809insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000013.10:g.34222927_34222945del, NC_000013.10:g.34222930_34222945del, NC_000013.10:g.34222931_34222945del, NC_000013.10:g.34222932_34222945del, NC_000013.10:g.34222933_34222945del, NC_000013.10:g.34222934_34222945del, NC_000013.10:g.34222935_34222945del, NC_000013.10:g.34222936_34222945del, NC_000013.10:g.34222937_34222945del, NC_000013.10:g.34222938_34222945del, NC_000013.10:g.34222939_34222945del, NC_000013.10:g.34222940_34222945del, NC_000013.10:g.34222941_34222945del, NC_000013.10:g.34222942_34222945del, NC_000013.10:g.34222943_34222945del, NC_000013.10:g.34222944_34222945del, NC_000013.10:g.34222945del, NC_000013.10:g.34222945dup, NC_000013.10:g.34222944_34222945dup, NC_000013.10:g.34222943_34222945dup, NC_000013.10:g.34222921_34222945T[28]CTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000013.10:g.34222942_34222945dup, NC_000013.10:g.34222921_34222945T[29]CTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000013.10:g.34222941_34222945dup, NC_000013.10:g.34222940_34222945dup, NC_000013.10:g.34222939_34222945dup, NC_000013.10:g.34222938_34222945dup, NC_000013.10:g.34222937_34222945dup, NC_000013.10:g.34222936_34222945dup, NC_000013.10:g.34222935_34222945dup, NC_000013.10:g.34222934_34222945dup, NC_000013.10:g.34222933_34222945dup, NC_000013.10:g.34222932_34222945dup, NC_000013.10:g.34222931_34222945dup, NC_000013.10:g.34222930_34222945dup, NC_000013.10:g.34222928_34222945dup, NC_000013.10:g.34222927_34222945dup, NC_000013.10:g.34222926_34222945dup, NC_000013.10:g.34222925_34222945dup, NC_000013.10:g.34222924_34222945dup, NC_000013.10:g.34222923_34222945dup, NC_000013.10:g.34222922_34222945dup, NC_000013.10:g.34222921_34222945dup, NC_000013.10:g.34222945_34222946insTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000013.10:g.34222945_34222946insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000013.10:g.34222945_34222946insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000013.10:g.34222945_34222946insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000013.10:g.34222945_34222946insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_029752.2:g.33034_33052del, NG_029752.2:g.33037_33052del, NG_029752.2:g.33038_33052del, NG_029752.2:g.33039_33052del, NG_029752.2:g.33040_33052del, NG_029752.2:g.33041_33052del, NG_029752.2:g.33042_33052del, NG_029752.2:g.33043_33052del, NG_029752.2:g.33044_33052del, NG_029752.2:g.33045_33052del, NG_029752.2:g.33046_33052del, NG_029752.2:g.33047_33052del, NG_029752.2:g.33048_33052del, NG_029752.2:g.33049_33052del, NG_029752.2:g.33050_33052del, NG_029752.2:g.33051_33052del, NG_029752.2:g.33052del, NG_029752.2:g.33052dup, NG_029752.2:g.33051_33052dup, NG_029752.2:g.33050_33052dup, NG_029752.2:g.33028_33052A[29]GAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NG_029752.2:g.33049_33052dup, NG_029752.2:g.33028_33052A[31]GAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NG_029752.2:g.33048_33052dup, NG_029752.2:g.33047_33052dup, NG_029752.2:g.33046_33052dup, NG_029752.2:g.33045_33052dup, NG_029752.2:g.33044_33052dup, NG_029752.2:g.33043_33052dup, NG_029752.2:g.33042_33052dup, NG_029752.2:g.33041_33052dup, NG_029752.2:g.33040_33052dup, NG_029752.2:g.33039_33052dup, NG_029752.2:g.33038_33052dup, NG_029752.2:g.33037_33052dup, NG_029752.2:g.33035_33052dup, NG_029752.2:g.33034_33052dup, NG_029752.2:g.33033_33052dup, NG_029752.2:g.33032_33052dup, NG_029752.2:g.33031_33052dup, NG_029752.2:g.33030_33052dup, NG_029752.2:g.33029_33052dup, NG_029752.2:g.33028_33052dup, NG_029752.2:g.33052_33053insAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_029752.2:g.33052_33053insAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_029752.2:g.33052_33053insAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_029752.2:g.33052_33053insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_029752.2:g.33052_33053insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

Select item 14915404578.

rs1491540457 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->AT [Show Flanks]
Chromosome:: 13:33499762 (GRCh38)
13:34073900 (GRCh37)
Canonical SPDI:: NC_000013.11:33499762:T:TAT
Gene:: STARD13 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: TAT=0./0 (ALFA)
TA=0.00281/115 (GnomAD)
HGVS:: NC_000013.11:g.33499763_33499764insAT, NC_000013.10:g.34073900_34073901insAT, NG_029752.2:g.182073_182074insTA

Select item 14915341239.

rs1491534123 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->TC [Show Flanks]
Chromosome:: 13:33261157 (GRCh38)
13:33835295 (GRCh37)
Canonical SPDI:: NC_000013.11:33261157:TCTC:TCTCTC
Gene:: STARD13 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: TCTCTC=0./0 (ALFA)
TC=0.000004/1 (TOPMED)
HGVS:: NC_000013.11:g.33261158TC[3], NC_000013.10:g.33835295TC[3], NG_029752.2:g.420675GA[3]

Select item 149152738010.

rs1491527380 [Homo sapiens]

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

Select item 149152595211.

rs1491525952 [Homo sapiens]

Variant type:: DEL
Alleles:: AT>- [Show Flanks]
Chromosome:: 13:33528212 (GRCh38)
13:34102349 (GRCh37)
Canonical SPDI:: NC_000013.11:33528211:AT:
Gene:: STARD13 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0.001164/19 (ALFA)
-=0.000671/3 (Estonian)
-=0.001661/3 (Korea1K)
-=0.001973/204 (GnomAD)
-=0.002301/39 (TOMMO)
HGVS:: NC_000013.11:g.33528212_33528213del, NC_000013.10:g.34102349_34102350del, NG_029752.2:g.153623_153624del

Select item 149149786412.

rs1491497864 [Homo sapiens]

Variant type:: DELINS
Alleles:: CT>- [Show Flanks]
Chromosome:: 13:33499634 (GRCh38)
13:34073771 (GRCh37)
Canonical SPDI:: NC_000013.11:33499632:TCT:T
Gene:: STARD13 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: T=0.00084/10 (ALFA)
HGVS:: NC_000013.11:g.33499634_33499635del, NC_000013.10:g.34073771_34073772del, NG_029752.2:g.182202_182203del

Select item 149149629513.

rs1491496295 [Homo sapiens]

Variant type:: DELINS
Alleles:: TT>-,T,TTT [Show Flanks]
Chromosome:: 13:33519238 (GRCh38)
13:34093375 (GRCh37)
Canonical SPDI:: NC_000013.11:33519236:TTT:T,NC_000013.11:33519236:TTT:TT,NC_000013.11:33519236:TTT:TTTT
Gene:: STARD13 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
-=0.000072/10 (GnomAD)
HGVS:: NC_000013.11:g.33519238_33519239del, NC_000013.11:g.33519239del, NC_000013.11:g.33519239dup, NC_000013.10:g.34093375_34093376del, NC_000013.10:g.34093376del, NC_000013.10:g.34093376dup, NG_029752.2:g.162598_162599del, NG_029752.2:g.162599del, NG_029752.2:g.162599dup

Select item 149148896814.

rs1491488968 has merged into rs57311502 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT>-,T,TT,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 13:33650177 (GRCh38)
13:34224314 (GRCh37)
Canonical SPDI:: NC_000013.11:33650164:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000013.11:33650164:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000013.11:33650164:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000013.11:33650164:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000013.11:33650164:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000013.11:33650164:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000013.11:33650164:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000013.11:33650164:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000013.11:33650164:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000013.11:33650164:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33650164:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33650164:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33650164:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33650164:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33650164:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33650164:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33650164:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33650164:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33650164:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33650164:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33650164:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33650164:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33650164:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33650164:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33650164:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33650164:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33650164:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33650164:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33650164:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33650164:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33650164:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33650164:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33650164:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33650164:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33650164:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33650164:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33650164:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33650164:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33650164:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33650164:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33650164:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33650164:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33650164:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33650164:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33650164:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33650164:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33650164:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33650164:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: STARD13 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTTT=0./0 (ALFA)
TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0071/4 (NorthernSweden)
-=0.2778/10 (GENOME_DK)
HGVS:: NC_000013.11:g.33650177_33650208del, NC_000013.11:g.33650178_33650208del, NC_000013.11:g.33650179_33650208del, NC_000013.11:g.33650180_33650208del, NC_000013.11:g.33650181_33650208del, NC_000013.11:g.33650182_33650208del, NC_000013.11:g.33650183_33650208del, NC_000013.11:g.33650184_33650208del, NC_000013.11:g.33650185_33650208del, NC_000013.11:g.33650186_33650208del, NC_000013.11:g.33650187_33650208del, NC_000013.11:g.33650188_33650208del, NC_000013.11:g.33650189_33650208del, NC_000013.11:g.33650190_33650208del, NC_000013.11:g.33650191_33650208del, NC_000013.11:g.33650192_33650208del, NC_000013.11:g.33650193_33650208del, NC_000013.11:g.33650194_33650208del, NC_000013.11:g.33650195_33650208del, NC_000013.11:g.33650196_33650208del, NC_000013.11:g.33650197_33650208del, NC_000013.11:g.33650198_33650208del, NC_000013.11:g.33650199_33650208del, NC_000013.11:g.33650200_33650208del, NC_000013.11:g.33650201_33650208del, NC_000013.11:g.33650202_33650208del, NC_000013.11:g.33650203_33650208del, NC_000013.11:g.33650204_33650208del, NC_000013.11:g.33650205_33650208del, NC_000013.11:g.33650206_33650208del, NC_000013.11:g.33650207_33650208del, NC_000013.11:g.33650208del, NC_000013.11:g.33650208dup, NC_000013.11:g.33650207_33650208dup, NC_000013.11:g.33650206_33650208dup, NC_000013.11:g.33650205_33650208dup, NC_000013.11:g.33650204_33650208dup, NC_000013.11:g.33650203_33650208dup, NC_000013.11:g.33650202_33650208dup, NC_000013.11:g.33650201_33650208dup, NC_000013.11:g.33650200_33650208dup, NC_000013.11:g.33650199_33650208dup, NC_000013.11:g.33650198_33650208dup, NC_000013.11:g.33650197_33650208dup, NC_000013.11:g.33650196_33650208dup, NC_000013.11:g.33650193_33650208dup, NC_000013.11:g.33650187_33650208dup, NC_000013.11:g.33650171_33650208dup, NC_000013.10:g.34224314_34224345del, NC_000013.10:g.34224315_34224345del, NC_000013.10:g.34224316_34224345del, NC_000013.10:g.34224317_34224345del, NC_000013.10:g.34224318_34224345del, NC_000013.10:g.34224319_34224345del, NC_000013.10:g.34224320_34224345del, NC_000013.10:g.34224321_34224345del, NC_000013.10:g.34224322_34224345del, NC_000013.10:g.34224323_34224345del, NC_000013.10:g.34224324_34224345del, NC_000013.10:g.34224325_34224345del, NC_000013.10:g.34224326_34224345del, NC_000013.10:g.34224327_34224345del, NC_000013.10:g.34224328_34224345del, NC_000013.10:g.34224329_34224345del, NC_000013.10:g.34224330_34224345del, NC_000013.10:g.34224331_34224345del, NC_000013.10:g.34224332_34224345del, NC_000013.10:g.34224333_34224345del, NC_000013.10:g.34224334_34224345del, NC_000013.10:g.34224335_34224345del, NC_000013.10:g.34224336_34224345del, NC_000013.10:g.34224337_34224345del, NC_000013.10:g.34224338_34224345del, NC_000013.10:g.34224339_34224345del, NC_000013.10:g.34224340_34224345del, NC_000013.10:g.34224341_34224345del, NC_000013.10:g.34224342_34224345del, NC_000013.10:g.34224343_34224345del, NC_000013.10:g.34224344_34224345del, NC_000013.10:g.34224345del, NC_000013.10:g.34224345dup, NC_000013.10:g.34224344_34224345dup, NC_000013.10:g.34224343_34224345dup, NC_000013.10:g.34224342_34224345dup, NC_000013.10:g.34224341_34224345dup, NC_000013.10:g.34224340_34224345dup, NC_000013.10:g.34224339_34224345dup, NC_000013.10:g.34224338_34224345dup, NC_000013.10:g.34224337_34224345dup, NC_000013.10:g.34224336_34224345dup, NC_000013.10:g.34224335_34224345dup, NC_000013.10:g.34224334_34224345dup, NC_000013.10:g.34224333_34224345dup, NC_000013.10:g.34224330_34224345dup, NC_000013.10:g.34224324_34224345dup, NC_000013.10:g.34224308_34224345dup, NG_029752.2:g.31640_31671del, NG_029752.2:g.31641_31671del, NG_029752.2:g.31642_31671del, NG_029752.2:g.31643_31671del, NG_029752.2:g.31644_31671del, NG_029752.2:g.31645_31671del, NG_029752.2:g.31646_31671del, NG_029752.2:g.31647_31671del, NG_029752.2:g.31648_31671del, NG_029752.2:g.31649_31671del, NG_029752.2:g.31650_31671del, NG_029752.2:g.31651_31671del, NG_029752.2:g.31652_31671del, NG_029752.2:g.31653_31671del, NG_029752.2:g.31654_31671del, NG_029752.2:g.31655_31671del, NG_029752.2:g.31656_31671del, NG_029752.2:g.31657_31671del, NG_029752.2:g.31658_31671del, NG_029752.2:g.31659_31671del, NG_029752.2:g.31660_31671del, NG_029752.2:g.31661_31671del, NG_029752.2:g.31662_31671del, NG_029752.2:g.31663_31671del, NG_029752.2:g.31664_31671del, NG_029752.2:g.31665_31671del, NG_029752.2:g.31666_31671del, NG_029752.2:g.31667_31671del, NG_029752.2:g.31668_31671del, NG_029752.2:g.31669_31671del, NG_029752.2:g.31670_31671del, NG_029752.2:g.31671del, NG_029752.2:g.31671dup, NG_029752.2:g.31670_31671dup, NG_029752.2:g.31669_31671dup, NG_029752.2:g.31668_31671dup, NG_029752.2:g.31667_31671dup, NG_029752.2:g.31666_31671dup, NG_029752.2:g.31665_31671dup, NG_029752.2:g.31664_31671dup, NG_029752.2:g.31663_31671dup, NG_029752.2:g.31662_31671dup, NG_029752.2:g.31661_31671dup, NG_029752.2:g.31660_31671dup, NG_029752.2:g.31659_31671dup, NG_029752.2:g.31656_31671dup, NG_029752.2:g.31650_31671dup, NG_029752.2:g.31634_31671dup

Select item 149148825915.

rs1491488259 [Homo sapiens]

Variant type:: DEL
Alleles:: CA>- [Show Flanks]
Chromosome:: 13:33338884 (GRCh38)
13:33913021 (GRCh37)
Canonical SPDI:: NC_000013.11:33338883:CA:
Gene:: STARD13 (Varview), LOC124903152 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
HGVS:: NC_000013.11:g.33338884_33338885del, NC_000013.10:g.33913021_33913022del, NG_029752.2:g.342951_342952del

Select item 149148478516.

rs1491484785 [Homo sapiens]

Variant type:: DEL
Alleles:: TG>- [Show Flanks]
Chromosome:: 13:33429927 (GRCh38)
13:34004064 (GRCh37)
Canonical SPDI:: NC_000013.11:33429926:TG:
Gene:: STARD13 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0.002023/24 (ALFA)
-=0.000035/1 (TOMMO)
-=0.00344/438 (GnomAD)
HGVS:: NC_000013.11:g.33429927_33429928del, NC_000013.10:g.34004064_34004065del, NG_029752.2:g.251908_251909del

Select item 149147583917.

rs1491475839 [Homo sapiens]

Variant type:: DEL
Alleles:: CA>- [Show Flanks]
Chromosome:: 13:33564206 (GRCh38)
13:34138343 (GRCh37)
Canonical SPDI:: NC_000013.11:33564205:CA:
Gene:: STARD13 (Varview), LOC102723406 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
HGVS:: NC_000013.11:g.33564206_33564207del, NC_000013.10:g.34138343_34138344del, NG_029752.2:g.117629_117630del

Select item 149147122018.

rs1491471220 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->CTT [Show Flanks]
Chromosome:: 13:33370620 (GRCh38)
13:33944758 (GRCh37)
Canonical SPDI:: NC_000013.11:33370620:TT:TTCTT
Gene:: STARD13 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: TTCTT=0./0 (ALFA)
HGVS:: NC_000013.11:g.33370622_33370623insCTT, NC_000013.10:g.33944759_33944760insCTT, NG_029752.2:g.311215_311216insGAA

Select item 149146831519.

rs1491468315 has merged into rs552526416 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTTTTTT>-,TT,TTT,TTTT,TTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTATTTTTTTTTTTTTTTTTCCTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTATTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTCTTTCTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTCTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTCTTTTTTTTTTTTTTTTTTCTTTCTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTCTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTCTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCCTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 13:33308528 (GRCh38)
13:33882665 (GRCh37)
Canonical SPDI:: NC_000013.11:33308520:TTTTTTTTTTTTTTTTTTTT:TTTTTTT,NC_000013.11:33308520:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTT,NC_000013.11:33308520:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000013.11:33308520:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000013.11:33308520:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000013.11:33308520:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000013.11:33308520:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000013.11:33308520:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000013.11:33308520:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000013.11:33308520:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000013.11:33308520:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33308520:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTATTTTTTTTTTTTTTTTTCCTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33308520:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33308520:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33308520:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33308520:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33308520:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33308520:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33308520:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33308520:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33308520:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33308520:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33308520:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33308520:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33308520:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33308520:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33308520:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33308520:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33308520:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33308520:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33308520:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTATTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33308520:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33308520:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33308520:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33308520:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33308520:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33308520:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33308520:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33308520:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33308520:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTCTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33308520:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33308520:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTCTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33308520:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33308520:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTCTTTTTTTTTTTTTTTTTTCTTTCTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33308520:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33308520:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33308520:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33308520:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTCTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33308520:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33308520:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33308520:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33308520:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTCTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33308520:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33308520:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCCTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33308520:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33308520:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33308520:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33308520:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33308520:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33308520:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33308520:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33308520:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33308520:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33308520:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33308520:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33308520:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33308520:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33308520:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33308520:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33308520:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33308520:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33308520:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33308520:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33308520:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33308520:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33308520:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33308520:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33308520:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33308520:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33308520:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33308520:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:33308520:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: STARD13 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTT=0./0 (ALFA)
-=0.000026/7 (TOPMED)
T=0.445887/2233 (1000Genomes)
HGVS:: NC_000013.11:g.33308528_33308540del, NC_000013.11:g.33308530_33308540del, NC_000013.11:g.33308531_33308540del, NC_000013.11:g.33308532_33308540del, NC_000013.11:g.33308534_33308540del, NC_000013.11:g.33308536_33308540del, NC_000013.11:g.33308537_33308540del, NC_000013.11:g.33308538_33308540del, NC_000013.11:g.33308539_33308540del, NC_000013.11:g.33308540del, NC_000013.11:g.33308540dup, NC_000013.11:g.33308521_33308540T[21]ATTTTTTTTTTTTTTTTTCCTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000013.11:g.33308539_33308540dup, NC_000013.11:g.33308521_33308540T[22]CTTTTTTTTTTTTTTTTTTTTT[1], NC_000013.11:g.33308521_33308540T[22]GTTTTTTTTTTTTTTTTTTTTT[1], NC_000013.11:g.33308538_33308540dup, NC_000013.11:g.33308521_33308540T[23]CTTTTTTTTTTTTTTTTTTTTT[1], NC_000013.11:g.33308521_33308540T[23]CTTTTTTTTTTTTTTTTTTTTTT[1], NC_000013.11:g.33308521_33308540T[23]GTTTTTTTTTTTTTTTTTTTT[1], NC_000013.11:g.33308521_33308540T[23]GTTTTTTTTTTTTTTTTTTTTT[1], NC_000013.11:g.33308521_33308540T[23]GTTTTTTTTTTTTTTTTTTTTTT[1], NC_000013.11:g.33308537_33308540dup, NC_000013.11:g.33308521_33308540T[24]GTTTTTTTTTTTTTTTTTTTTT[1], NC_000013.11:g.33308536_33308540dup, NC_000013.11:g.33308535_33308540dup, NC_000013.11:g.33308521_33308540T[26]CTTTTTTTTTTTTTTTTTTTTT[1], NC_000013.11:g.33308534_33308540dup, NC_000013.11:g.33308533_33308540dup, NC_000013.11:g.33308521_33308540T[28]CTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000013.11:g.33308532_33308540dup, NC_000013.11:g.33308521_33308540T[29]ATTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTT[1], NC_000013.11:g.33308521_33308540T[29]GTTTTTTTTTTTTTTTTTTTTT[1], NC_000013.11:g.33308521_33308540T[29]GTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000013.11:g.33308531_33308540dup, NC_000013.11:g.33308521_33308540T[30]CTTTTTTTT[2]T[14]CTTTTTTTTTTTTTTTTTTTTT[1], NC_000013.11:g.33308521_33308540T[30]GTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000013.11:g.33308530_33308540dup, NC_000013.11:g.33308529_33308540dup, NC_000013.11:g.33308528_33308540dup, NC_000013.11:g.33308521_33308540T[33]CTTT[2]T[18], NC_000013.11:g.33308527_33308540dup, NC_000013.11:g.33308521_33308540T[34]CTTTTTTTTTTTTT[3]T[19], NC_000013.11:g.33308526_33308540dup, NC_000013.11:g.33308521_33308540T[35]CTTTCTTTTTTTTTTTTTTTTTT[2]TTT[1], NC_000013.11:g.33308521_33308540T[35]CTTTTTTTTTTTTTTTTTTTTT[1], NC_000013.11:g.33308521_33308540T[35]CTTTTTTTTTTTTTTTTTTTTTT[1], NC_000013.11:g.33308525_33308540dup, NC_000013.11:g.33308521_33308540T[36]CTTTTTTTTTTTTCTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000013.11:g.33308521_33308540T[36]CTTTTTTTTTTTTTTTTTTTTT[1], NC_000013.11:g.33308521_33308540T[36]CTTTTTTTTTTTTTTTTTTTTTT[1], NC_000013.11:g.33308524_33308540dup, NC_000013.11:g.33308521_33308540T[37]CTTTTT[2]T[19], NC_000013.11:g.33308523_33308540dup, NC_000013.11:g.33308521_33308540T[38]CCTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000013.11:g.33308522_33308540dup, NC_000013.11:g.33308521_33308540dup, NC_000013.11:g.33308540_33308541insTTTTTTTTTTTTTTTTTTTTT, NC_000013.11:g.33308540_33308541insTTTTTTTTTTTTTTTTTTTTTT, NC_000013.11:g.33308540_33308541insTTTTTTTTTTTTTTTTTTTTTTT, NC_000013.11:g.33308540_33308541insTTTTTTTTTTTTTTTTTTTTTTTT, NC_000013.11:g.33308521_33308540T[44]CTTTTTTTTTTTTTTTTTTTTTT[1], NC_000013.11:g.33308540_33308541insTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000013.11:g.33308521_33308540T[45]CTTTTTTTTTTTTTTTTTTTTTT[1], NC_000013.11:g.33308540_33308541insTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000013.11:g.33308540_33308541insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000013.11:g.33308540_33308541insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000013.11:g.33308540_33308541insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000013.11:g.33308540_33308541insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000013.11:g.33308540_33308541insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000013.11:g.33308540_33308541insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000013.11:g.33308540_33308541insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000013.11:g.33308540_33308541insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000013.11:g.33308540_33308541insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000013.11:g.33308540_33308541insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000013.11:g.33308540_33308541insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000013.11:g.33308540_33308541insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000013.11:g.33308540_33308541insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000013.11:g.33308540_33308541insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000013.11:g.33308540_33308541insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000013.11:g.33308540_33308541insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000013.11:g.33308540_33308541insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000013.11:g.33308540_33308541insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000013.10:g.33882665_33882677del, NC_000013.10:g.33882667_33882677del, NC_000013.10:g.33882668_33882677del, NC_000013.10:g.33882669_33882677del, NC_000013.10:g.33882671_33882677del, NC_000013.10:g.33882673_33882677del, NC_000013.10:g.33882674_33882677del, NC_000013.10:g.33882675_33882677del, NC_000013.10:g.33882676_33882677del, NC_000013.10:g.33882677del, NC_000013.10:g.33882677dup, NC_000013.10:g.33882658_33882677T[21]ATTTTTTTTTTTTTTTTTCCTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000013.10:g.33882676_33882677dup, NC_000013.10:g.33882658_33882677T[22]CTTTTTTTTTTTTTTTTTTTTT[1], NC_000013.10:g.33882658_33882677T[22]GTTTTTTTTTTTTTTTTTTTTT[1], NC_000013.10:g.33882675_33882677dup, NC_000013.10:g.33882658_33882677T[23]CTTTTTTTTTTTTTTTTTTTTT[1], NC_000013.10:g.33882658_33882677T[23]CTTTTTTTTTTTTTTTTTTTTTT[1], NC_000013.10:g.33882658_33882677T[23]GTTTTTTTTTTTTTTTTTTTT[1], NC_000013.10:g.33882658_33882677T[23]GTTTTTTTTTTTTTTTTTTTTT[1], NC_000013.10:g.33882658_33882677T[23]GTTTTTTTTTTTTTTTTTTTTTT[1], NC_000013.10:g.33882674_33882677dup, NC_000013.10:g.33882658_33882677T[24]GTTTTTTTTTTTTTTTTTTTTT[1], NC_000013.10:g.33882673_33882677dup, NC_000013.10:g.33882672_33882677dup, NC_000013.10:g.33882658_33882677T[26]CTTTTTTTTTTTTTTTTTTTTT[1], NC_000013.10:g.33882671_33882677dup, NC_000013.10:g.33882670_33882677dup, NC_000013.10:g.33882658_33882677T[28]CTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000013.10:g.33882669_33882677dup, NC_000013.10:g.33882658_33882677T[29]ATTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTT[1], NC_000013.10:g.33882658_33882677T[29]GTTTTTTTTTTTTTTTTTTTTT[1], NC_000013.10:g.33882658_33882677T[29]GTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000013.10:g.33882668_33882677dup, NC_000013.10:g.33882658_33882677T[30]CTTTTTTTT[2]T[14]CTTTTTTTTTTTTTTTTTTTTT[1], NC_000013.10:g.33882658_33882677T[30]GTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000013.10:g.33882667_33882677dup, NC_000013.10:g.33882666_33882677dup, NC_000013.10:g.33882665_33882677dup, NC_000013.10:g.33882658_33882677T[33]CTTT[2]T[18], NC_000013.10:g.33882664_33882677dup, NC_000013.10:g.33882658_33882677T[34]CTTTTTTTTTTTTT[3]T[19], NC_000013.10:g.33882663_33882677dup, NC_000013.10:g.33882658_33882677T[35]CTTTCTTTTTTTTTTTTTTTTTT[2]TTT[1], NC_000013.10:g.33882658_33882677T[35]CTTTTTTTTTTTTTTTTTTTTT[1], NC_000013.10:g.33882658_33882677T[35]CTTTTTTTTTTTTTTTTTTTTTT[1], NC_000013.10:g.33882662_33882677dup, NC_000013.10:g.33882658_33882677T[36]CTTTTTTTTTTTTCTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000013.10:g.33882658_33882677T[36]CTTTTTTTTTTTTTTTTTTTTT[1], NC_000013.10:g.33882658_33882677T[36]CTTTTTTTTTTTTTTTTTTTTTT[1], NC_000013.10:g.33882661_33882677dup, NC_000013.10:g.33882658_33882677T[37]CTTTTT[2]T[19], NC_000013.10:g.33882660_33882677dup, NC_000013.10:g.33882658_33882677T[38]CCTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000013.10:g.33882659_33882677dup, NC_000013.10:g.33882658_33882677dup, NC_000013.10:g.33882677_33882678insTTTTTTTTTTTTTTTTTTTTT, NC_000013.10:g.33882677_33882678insTTTTTTTTTTTTTTTTTTTTTT, NC_000013.10:g.33882677_33882678insTTTTTTTTTTTTTTTTTTTTTTT, NC_000013.10:g.33882677_33882678insTTTTTTTTTTTTTTTTTTTTTTTT, NC_000013.10:g.33882658_33882677T[44]CTTTTTTTTTTTTTTTTTTTTTT[1], NC_000013.10:g.33882677_33882678insTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000013.10:g.33882658_33882677T[45]CTTTTTTTTTTTTTTTTTTTTTT[1], NC_000013.10:g.33882677_33882678insTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000013.10:g.33882677_33882678insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000013.10:g.33882677_33882678insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000013.10:g.33882677_33882678insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000013.10:g.33882677_33882678insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000013.10:g.33882677_33882678insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000013.10:g.33882677_33882678insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000013.10:g.33882677_33882678insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000013.10:g.33882677_33882678insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000013.10:g.33882677_33882678insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000013.10:g.33882677_33882678insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000013.10:g.33882677_33882678insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000013.10:g.33882677_33882678insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000013.10:g.33882677_33882678insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000013.10:g.33882677_33882678insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000013.10:g.33882677_33882678insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000013.10:g.33882677_33882678insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000013.10:g.33882677_33882678insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000013.10:g.33882677_33882678insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_029752.2:g.373303_373315del, NG_029752.2:g.373305_373315del, NG_029752.2:g.373306_373315del, NG_029752.2:g.373307_373315del, NG_029752.2:g.373309_373315del, NG_029752.2:g.373311_373315del, NG_029752.2:g.373312_373315del, NG_029752.2:g.373313_373315del, NG_029752.2:g.373314_373315del, NG_029752.2:g.373315del, NG_029752.2:g.373315dup, NG_029752.2:g.373296_373315A[25]GGAAAAAAAAAAAAAAAAATAAAAAAAAAAAAAAAAAAAAA[1], NG_029752.2:g.373314_373315dup, NG_029752.2:g.373296_373315A[21]GAAAAAAAAAAAAAAAAAAAAAA[1], NG_029752.2:g.373296_373315A[21]CAAAAAAAAAAAAAAAAAAAAAA[1], NG_029752.2:g.373313_373315dup, NG_029752.2:g.373296_373315A[21]GAAAAAAAAAAAAAAAAAAAAAAA[1], NG_029752.2:g.373296_373315A[22]GAAAAAAAAAAAAAAAAAAAAAAA[1], NG_029752.2:g.373296_373315A[20]CAAAAAAAAAAAAAAAAAAAAAAA[1], NG_029752.2:g.373296_373315A[21]CAAAAAAAAAAAAAAAAAAAAAAA[1], NG_029752.2:g.373296_373315A[22]CAAAAAAAAAAAAAAAAAAAAAAA[1], NG_029752.2:g.373312_373315dup, NG_029752.2:g.373296_373315A[21]CAAAAAAAAAAAAAAAAAAAAAAAA[1], NG_029752.2:g.373311_373315dup, NG_029752.2:g.373310_373315dup, NG_029752.2:g.373296_373315A[21]GAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NG_029752.2:g.373309_373315dup, NG_029752.2:g.373308_373315dup, NG_029752.2:g.373296_373315A[44]GAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NG_029752.2:g.373307_373315dup, NG_029752.2:g.373296_373315AAAAAAAAAAAAAAAAAAAAAAG[2]A[18]TAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NG_029752.2:g.373296_373315A[21]CAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NG_029752.2:g.373296_373315A[25]CAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NG_029752.2:g.373306_373315dup, NG_029752.2:g.373296_373315AAAAAAAAAAAAAAAAAAAAAGA[2]A[7]GAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NG_029752.2:g.373296_373315A[23]CAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NG_029752.2:g.373305_373315dup, NG_029752.2:g.373304_373315dup, NG_029752.2:g.373303_373315dup, NG_029752.2:g.373296_373315A[21]GAAA[2]A[30], NG_029752.2:g.373302_373315dup, NG_029752.2:g.373296_373315A[32]GAAAAAAAAAAAAA[3]A[21], NG_029752.2:g.373301_373315dup, NG_029752.2:g.373296_373315A[21]GAAAGAAAAAAAAAAAAAAAAAA[2]A[17], NG_029752.2:g.373296_373315A[21]GAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NG_029752.2:g.373296_373315A[22]GAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NG_029752.2:g.373300_373315dup, NG_029752.2:g.373296_373315A[23]GAAAAAAAAA[2]AAAGAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NG_029752.2:g.373296_373315A[21]GAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NG_029752.2:g.373296_373315A[22]GAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NG_029752.2:g.373299_373315dup, NG_029752.2:g.373296_373315A[24]GAAAAA[2]A[32], NG_029752.2:g.373298_373315dup, NG_029752.2:g.373296_373315A[45]GGAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NG_029752.2:g.373297_373315dup, NG_029752.2:g.373296_373315dup, NG_029752.2:g.373315_373316insAAAAAAAAAAAAAAAAAAAAA, NG_029752.2:g.373315_373316insAAAAAAAAAAAAAAAAAAAAAA, NG_029752.2:g.373315_373316insAAAAAAAAAAAAAAAAAAAAAAA, NG_029752.2:g.373315_373316insAAAAAAAAAAAAAAAAAAAAAAAA, NG_029752.2:g.373296_373315A[22]GAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NG_029752.2:g.373315_373316insAAAAAAAAAAAAAAAAAAAAAAAAA, NG_029752.2:g.373296_373315A[22]GAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NG_029752.2:g.373315_373316insAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_029752.2:g.373315_373316insAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_029752.2:g.373315_373316insAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_029752.2:g.373315_373316insAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_029752.2:g.373315_373316insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_029752.2:g.373315_373316insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_029752.2:g.373315_373316insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_029752.2:g.373315_373316insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_029752.2:g.373315_373316insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_029752.2:g.373315_373316insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_029752.2:g.373315_373316insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_029752.2:g.373315_373316insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_029752.2:g.373315_373316insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_029752.2:g.373315_373316insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_029752.2:g.373315_373316insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_029752.2:g.373315_373316insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_029752.2:g.373315_373316insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_029752.2:g.373315_373316insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_029752.2:g.373315_373316insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

Select item 149145785020.

rs1491457850 [Homo sapiens]

Variant type:: DEL
Alleles:: AT>- [Show Flanks]
Chromosome:: 13:33167998 (GRCh38)
13:33742135 (GRCh37)
Canonical SPDI:: NC_000013.11:33167997:AT:
Gene:: STARD13 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0./0 (ALFA)
-=0.000156/1 (1000Genomes)
-=0.000196/25 (GnomAD)
HGVS:: NC_000013.11:g.33167998_33167999del, NC_000013.10:g.33742135_33742136del, NG_029752.2:g.513837_513838del

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