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Variant Placements for estd192 (displaying 100 of 61187 variants)
Study IDVariant IDVariant Region typeVariant Call typeSampleset IDMethodAnalysis IDValidationVariant samplesSubject phenotypeClinical InterpretationAssemblyAccessionChrOuter-StartStartInner-StartInner-EndEndOuter-EndPlacement TypeRemap Score
estd192esv3754925copy number variationNoGRCh38.p12NC_000001.1113643552364375236442263644426Remapped1
estd192esv3756016copy number variationNoGRCh38.p12NC_000001.1112544159254417925443112544331Remapped1
estd192esv3757001complex chromosomal rearrangementNoGRCh38.p12NC_000001.1112001013200103320010132001033Remapped1
estd192esv3757403complex chromosomal rearrangementNoGRCh38.p12NC_000001.1112110943211096321109432110963Remapped1
estd192esv3758436inversionNoGRCh38.p12NC_000001.11134796873727821Remapped1
estd192esv3758546inversionNoGRCh38.p12NC_000001.111972925972945972925972945Remapped1
estd192esv3758546inversionNoGRCh38.p12NC_000001.111974695974715974695974715Remapped1
estd192esv3759931complex chromosomal rearrangementNoGRCh38.p12NC_000001.11120685742068574Remapped1
estd192esv3760290complex chromosomal rearrangementNoGRCh38.p12NC_000001.111431593431613431593431613Remapped1
estd192esv3760421tandem duplicationNoGRCh38.p12NC_000001.1112211658221185822120912212291Remapped1
estd192esv3761845complex chromosomal rearrangementNoGRCh38.p12NC_000001.1112849943284996328499432849963Remapped1
estd192esv3763195inversionNoGRCh38.p12NC_000001.1111455938145595814559381455958Remapped1
estd192esv3763940copy number variationNoGRCh38.p12NC_000001.1113938227393824739854963985516Remapped1
estd192esv3764551tandem duplicationNoGRCh38.p12NC_000001.1111846702184670228498542849854Remapped1.01505
estd192esv3764636copy number variationNoGRCh38.p12NC_000001.1111098199109821911900751190095Remapped1
estd192esv3764681complex chromosomal rearrangementNoGRCh38.p12NC_000001.111861092861112861092861112Remapped1
estd192esv3766259complex chromosomal rearrangementNoGRCh38.p12NC_000001.111667139667159667139667159Remapped1
estd192esv3767474copy number variationNoGRCh38.p12NC_000001.1111499811150001115021331502333Remapped1
estd192esv3767607copy number variationNoGRCh38.p12NC_000001.1113775965377596541542574154257Remapped0.72499
estd192esv3767654copy number variationNoGRCh38.p12NC_000001.111609429609449610683610703Remapped1
estd192esv3767809copy number variationNoGRCh38.p12NC_000001.1111080608108062810930381093058Remapped1
estd192esv3767972complex chromosomal rearrangementNoGRCh38.p12NC_000001.11132709253270925Remapped1
estd192esv3768262complex chromosomal rearrangementNoGRCh38.p12NC_000001.1111096658109667810966581096678Remapped1
estd192esv3768809copy number variationNoGRCh38.p12NC_000001.1112539653253967325556502555670Remapped1
estd192esv3769575copy number variationNoGRCh38.p12NC_000001.1113549020354904035505693550589Remapped1
estd192esv3769874copy number variationNoGRCh38.p12NC_000001.1111396048139606813964001396420Remapped1
estd192esv3772451complex chromosomal rearrangementNoGRCh38.p12NC_000001.1112120409212042921204092120429Remapped1
estd192esv3772765tandem duplicationNoGRCh38.p12NC_000001.1111268228126824813685161368536Remapped1
estd192esv3773485inversionNoGRCh38.p12NC_000001.1113274033327405332740333274053Remapped1
estd192esv3773587copy number variationNoGRCh38.p12NC_000001.1111693002169302217356671735687Remapped1
estd192esv3774900tandem duplicationNoGRCh38.p12NC_000001.1112409229240924924143112414331Remapped1
estd192esv3775873complex chromosomal rearrangementNoGRCh38.p12NC_000001.1111287898128791812878981287918Remapped1
estd192esv3776372tandem duplicationNoGRCh38.p12NC_000001.11125517172551717108502419108502419Remapped0.99426
estd192esv3777390tandem duplicationNoGRCh38.p12NC_000001.1112511848251186825399192539939Remapped1
estd192esv3777541tandem duplicationNoGRCh38.p12NC_000001.1111521930152195015286811528701Remapped1
estd192esv3778915copy number variationNoGRCh38.p12NC_000001.1113643709364372936443843644404Remapped1
estd192esv3780144complex chromosomal rearrangementNoGRCh38.p12NC_000001.1111019781101980110197811019801Remapped1
estd192esv3781052tandem duplicationNoGRCh38.p12NC_000001.1113039701303972134422893442309Remapped1
estd192esv3781526inversionNoGRCh38.p12NC_000001.1111101006110102611010061101026Remapped1
estd192esv3782910complex chromosomal rearrangementNoGRCh38.p12NC_000001.111820480820480Remapped1
estd192esv3782910complex chromosomal rearrangementNoGRCh38.p12NC_000001.111820940820940Remapped1
estd192esv3783067tandem duplicationNoGRCh38.p12NC_000001.1113577987357800737680143768034Remapped1
estd192esv3783486copy number variationNoGRCh38.p12NC_000001.1113701300370132037389293738949Remapped1
estd192esv3784104copy number variationNoGRCh38.p12NC_000001.1111934926193494619355751935595Remapped1
estd192esv3784421tandem duplicationNoGRCh38.p12NC_000001.1111838467183848718548531854873Remapped1
estd192esv3785847complex chromosomal rearrangementNoGRCh38.p12NC_000001.11121936902193690Remapped1
estd192esv3786002inversionNoGRCh38.p12NC_000001.1111776544177656417765441776564Remapped1
estd192esv3786101copy number variationNoGRCh38.p12NC_000001.111279364327936432772939327729393Remapped0.98383
estd192esv3786965complex chromosomal rearrangementNoGRCh38.p12NC_000001.1113081292308131230812923081312Remapped1
estd192esv3789068copy number variationNoGRCh38.p12NC_000001.1112849583284960328513102851330Remapped1
estd192esv3789169complex chromosomal rearrangementNoGRCh38.p12NC_000001.1111538449153846915384491538469Remapped1
estd192esv3789943copy number variationNoGRCh38.p12NC_000001.1112701012270101227731862773186Remapped1.25999
estd192esv3790778copy number variationNoGRCh38.p12NC_000001.111344483552829998Remapped0.989
estd192esv3790974complex chromosomal rearrangementNoGRCh38.p12NC_000001.11129000932900093Remapped1
estd192esv3791300copy number variationNoGRCh38.p12NC_000001.1112086168208618820941662094186Remapped1
estd192esv3791315complex chromosomal rearrangementNoGRCh38.p12NC_000001.111633710633730633710633730Remapped1
estd192esv3791710complex chromosomal rearrangementNoGRCh38.p12NC_000001.1111099976109999610999761099996Remapped1
estd192esv3792033copy number variationNoGRCh38.p12NC_000001.1112502027250204725023542502374Remapped1
estd192esv3792066tandem duplicationNoGRCh38.p12NC_000001.1111199109119912912232051223225Remapped1
estd192esv3792480copy number variationNoGRCh38.p12NC_000001.1113504455350447535053143505334Remapped1
estd192esv3792482copy number variationNoGRCh38.p12NC_000001.1111934922193494219352101935230Remapped1
estd192esv3793071tandem duplicationNoGRCh38.p12NC_000001.1112772040277224027731822773382Remapped1
estd192esv3794600tandem duplicationNoGRCh38.p12NC_000001.1111696242169626217066411706661Remapped1
estd192esv3794766tandem duplicationNoGRCh38.p12NC_000001.1119864639864634604134746041347Remapped0.98837
estd192esv3795559tandem duplicationNoGRCh38.p12NC_000001.11196075796077715868851586905Remapped1
estd192esv3796106copy number variationNoGRCh38.p12NC_000001.11194377494379410683261068346Remapped1
estd192esv3796790tandem duplicationNoGRCh38.p12NC_000001.1113176053317607331762803176300Remapped1
estd192esv3796802copy number variationNoGRCh38.p12NC_000001.1111706642170666217484741748494Remapped1
estd192esv3797252complex chromosomal rearrangementNoGRCh38.p12NC_000001.1113706920370694037069203706940Remapped1
estd192esv3798115complex chromosomal rearrangementNoGRCh38.p12NC_000001.111353540353560353540353560Remapped1
estd192esv3798352tandem duplicationNoGRCh38.p12NC_000001.1111657032165703217226261722626Remapped1.00017
estd192esv3799497copy number variationNoGRCh38.p12NC_000001.1112270647227066722962132296233Remapped1
estd192esv3800929complex chromosomal rearrangementNoGRCh38.p12NC_000001.1111415941141596114159411415961Remapped1
estd192esv3801363complex chromosomal rearrangementNoGRCh38.p12NC_000001.111286890286910286890286910Remapped1
estd192esv3802940complex chromosomal rearrangementNoGRCh38.p12NC_000001.1112327812232783223278122327832Remapped1
estd192esv3803145copy number variationNoGRCh38.p12NC_000001.1112258328225834822632052263225Remapped1
estd192esv3803206tandem duplicationNoGRCh38.p12NC_000001.111789386789386224014653224014653Remapped0.99887
estd192esv3804248tandem duplicationNoGRCh38.p12NC_000001.1111333168133318813332411333261Remapped1
estd192esv3804534tandem duplicationNoGRCh38.p12NC_000001.1113176039317605931762793176299Remapped1
estd192esv3804678tandem duplicationNoGRCh38.p12NC_000001.1112292418229243823721612372181Remapped1
estd192esv3805306complex chromosomal rearrangementNoGRCh38.p12NC_000001.1113706884370690437068843706904Remapped1
estd192esv3806045complex chromosomal rearrangementNoGRCh38.p12NC_000001.111431277431297431277431297Remapped1
estd192esv3806930complex chromosomal rearrangementNoGRCh38.p12NC_000001.11116278461627846Remapped1
estd192esv3807628copy number variationNoGRCh38.p12NC_000001.111169257016925702284197322841973Remapped0.98166
estd192esv3808107tandem duplicationNoGRCh38.p12NC_000001.11195832795834713220961322116Remapped1
estd192esv3808407complex chromosomal rearrangementNoGRCh38.p12NC_000001.111829160829360829160829360Remapped1
estd192esv3808777tandem duplicationNoGRCh38.p12NC_000001.11190110090112012775481277568Remapped1
estd192esv3808806tandem duplicationNoGRCh38.p12NC_000001.1111019178101919811830731183093Remapped1
estd192esv3809154copy number variationNoGRCh38.p12NC_000001.1111810277181029718405611840581Remapped1
estd192esv3809272complex chromosomal rearrangementNoGRCh38.p12NC_000001.1111085373108539310853731085393Remapped1
estd192esv3810180complex chromosomal rearrangementNoGRCh38.p12NC_000001.11139352693935269Remapped1
estd192esv3810974complex chromosomal rearrangementNoGRCh38.p12NC_000001.1111704149170416917041491704169Remapped1
estd192esv3811285tandem duplicationNoGRCh38.p12NC_000001.1111189133118915314580621458082Remapped1
estd192esv3811359inversionNoGRCh38.p12NC_000001.1111280039128005912800391280059Remapped1
estd192esv3811865tandem duplicationNoGRCh38.p12NC_000001.1112231520223154022406312240651Remapped1
estd192esv3812199complex chromosomal rearrangementNoGRCh38.p12NC_000001.1113899411389981138994113899811Remapped1
estd192esv3812868complex chromosomal rearrangementNoGRCh38.p12NC_000001.1111942371194239119423711942391Remapped1
estd192esv3814628inversionNoGRCh38.p12NC_000001.11136849773735914Remapped1
estd192esv3814958copy number variationNoGRCh38.p12NC_000001.1111811226181124618128451812865Remapped1
estd192esv3815533copy number variationNoGRCh38.p12NC_000001.1113637797363781736689383668958Remapped1
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