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Variant Placements for nstd137 (displaying 100 of 32954 variants)
Study IDVariant IDVariant Region typeVariant Call typeSampleset IDMethodAnalysis IDValidationVariant samplesSubject phenotypeClinical InterpretationAssemblyAccessionChrOuter-StartStartInner-StartInner-EndEndOuter-EndPlacement TypeRemap Score
nstd137nsv2799683copy number variationNoGRCh38 (hg38)NC_000001.11110762311076498Submitted genomic
nstd137nsv2799683copy number variationNoGRCh38 (hg38)NC_000001.11110762311076498Submitted genomic
nstd137nsv2799684copy number variationNoGRCh38 (hg38)NC_000001.11110773321078471Submitted genomic
nstd137nsv2799684copy number variationNoGRCh38 (hg38)NC_000001.11110773321078471Submitted genomic
nstd137nsv2799685copy number variationNoGRCh38 (hg38)NC_000001.11110788021078861Submitted genomic
nstd137nsv2799685copy number variationNoGRCh38 (hg38)NC_000001.11110788021078861Submitted genomic
nstd137nsv2799705insertionNoGRCh38 (hg38)NC_000001.11111414361141436Submitted genomic
nstd137nsv2799705insertionNoGRCh38 (hg38)NC_000001.11111414361141436Submitted genomic
nstd137nsv2799733insertionNoGRCh38 (hg38)NC_000001.11112490381249038Submitted genomic
nstd137nsv2799733insertionNoGRCh38 (hg38)NC_000001.11112490381249038Submitted genomic
nstd137nsv2800111insertionNoGRCh38 (hg38)NC_000001.11112884671288467Submitted genomic
nstd137nsv2800111insertionNoGRCh38 (hg38)NC_000001.11112884671288467Submitted genomic
nstd137nsv2800112insertionNoGRCh38 (hg38)NC_000001.11112894341289434Submitted genomic
nstd137nsv2800112insertionNoGRCh38 (hg38)NC_000001.11112894341289434Submitted genomic
nstd137nsv2800114copy number variationNoGRCh38 (hg38)NC_000001.11113500471351046Submitted genomic
nstd137nsv2800114copy number variationNoGRCh38 (hg38)NC_000001.11113500471351046Submitted genomic
nstd137nsv2800115copy number variationNoGRCh38 (hg38)NC_000001.11113512871351446Submitted genomic
nstd137nsv2800115copy number variationNoGRCh38 (hg38)NC_000001.11113512871351446Submitted genomic
nstd137nsv2800118insertionNoGRCh38 (hg38)NC_000001.11113825881382588Submitted genomic
nstd137nsv2800118insertionNoGRCh38 (hg38)NC_000001.11113825881382588Submitted genomic
nstd137nsv2800323insertionNoGRCh38 (hg38)NC_000001.11110490511049051Submitted genomic
nstd137nsv2800323insertionNoGRCh38 (hg38)NC_000001.11110490511049051Submitted genomic
nstd137nsv2800332insertionNoGRCh38 (hg38)NC_000001.11110765361076536Submitted genomic
nstd137nsv2800332insertionNoGRCh38 (hg38)NC_000001.11110765361076536Submitted genomic
nstd137nsv2800334insertionNoGRCh38 (hg38)NC_000001.11110792851079285Submitted genomic
nstd137nsv2800334insertionNoGRCh38 (hg38)NC_000001.11110792851079285Submitted genomic
nstd137nsv2800350copy number variationNoGRCh38 (hg38)NC_000001.11111398241140189Submitted genomic
nstd137nsv2800350copy number variationNoGRCh38 (hg38)NC_000001.11111398241140189Submitted genomic
nstd137nsv2800417insertionNoGRCh38 (hg38)NC_000001.11110688251068825Submitted genomic
nstd137nsv2800417insertionNoGRCh38 (hg38)NC_000001.11110688251068825Submitted genomic
nstd137nsv2800418copy number variationNoGRCh38 (hg38)NC_000001.11110770901077151Submitted genomic
nstd137nsv2800418copy number variationNoGRCh38 (hg38)NC_000001.11110770901077151Submitted genomic
nstd137nsv2800419insertionNoGRCh38 (hg38)NC_000001.11110809171080917Submitted genomic
nstd137nsv2800419insertionNoGRCh38 (hg38)NC_000001.11110809171080917Submitted genomic
nstd137nsv2800427copy number variationNoGRCh38 (hg38)NC_000001.11111404121140472Submitted genomic
nstd137nsv2800427copy number variationNoGRCh38 (hg38)NC_000001.11111404121140472Submitted genomic
nstd137nsv2800437copy number variationNoGRCh38 (hg38)NC_000001.11111846561184871Submitted genomic
nstd137nsv2800437copy number variationNoGRCh38 (hg38)NC_000001.11111846561184871Submitted genomic
nstd137nsv2800457insertionNoGRCh38 (hg38)NC_000001.11112887111288711Submitted genomic
nstd137nsv2800457insertionNoGRCh38 (hg38)NC_000001.11112887111288711Submitted genomic
nstd137nsv2800458insertionNoGRCh38 (hg38)NC_000001.11112888761288876Submitted genomic
nstd137nsv2800458insertionNoGRCh38 (hg38)NC_000001.11112888761288876Submitted genomic
nstd137nsv2800459insertionNoGRCh38 (hg38)NC_000001.11112889791288979Submitted genomic
nstd137nsv2800459insertionNoGRCh38 (hg38)NC_000001.11112889791288979Submitted genomic
nstd137nsv2800460insertionNoGRCh38 (hg38)NC_000001.11112891881289188Submitted genomic
nstd137nsv2800460insertionNoGRCh38 (hg38)NC_000001.11112891881289188Submitted genomic
nstd137nsv2800461insertionNoGRCh38 (hg38)NC_000001.11112893141289314Submitted genomic
nstd137nsv2800461insertionNoGRCh38 (hg38)NC_000001.11112893141289314Submitted genomic
nstd137nsv2800462insertionNoGRCh38 (hg38)NC_000001.11112895401289540Submitted genomic
nstd137nsv2800462insertionNoGRCh38 (hg38)NC_000001.11112895401289540Submitted genomic
nstd137nsv2800463insertionNoGRCh38 (hg38)NC_000001.11112900821290082Submitted genomic
nstd137nsv2800463insertionNoGRCh38 (hg38)NC_000001.11112900821290082Submitted genomic
nstd137nsv2800466copy number variationNoGRCh38 (hg38)NC_000001.11113509271351166Submitted genomic
nstd137nsv2800466copy number variationNoGRCh38 (hg38)NC_000001.11113509271351166Submitted genomic
nstd137nsv2800567insertionNoGRCh38 (hg38)NC_000001.11110490861049086Submitted genomic
nstd137nsv2800567insertionNoGRCh38 (hg38)NC_000001.11110490861049086Submitted genomic
nstd137nsv2800574copy number variationNoGRCh38 (hg38)NC_000001.11110765261076765Submitted genomic
nstd137nsv2800574copy number variationNoGRCh38 (hg38)NC_000001.11110765261076765Submitted genomic
nstd137nsv2800589copy number variationNoGRCh38 (hg38)NC_000001.11111396411139701Submitted genomic
nstd137nsv2800589copy number variationNoGRCh38 (hg38)NC_000001.11111396411139701Submitted genomic
nstd137nsv2800759insertionNoGRCh38 (hg38)NC_000001.11112884281288428Submitted genomic
nstd137nsv2800759insertionNoGRCh38 (hg38)NC_000001.11112884281288428Submitted genomic
nstd137nsv2800760insertionNoGRCh38 (hg38)NC_000001.11112886731288673Submitted genomic
nstd137nsv2800760insertionNoGRCh38 (hg38)NC_000001.11112886731288673Submitted genomic
nstd137nsv2800761insertionNoGRCh38 (hg38)NC_000001.11112887941288794Submitted genomic
nstd137nsv2800761insertionNoGRCh38 (hg38)NC_000001.11112887941288794Submitted genomic
nstd137nsv2800762insertionNoGRCh38 (hg38)NC_000001.11112891441289144Submitted genomic
nstd137nsv2800762insertionNoGRCh38 (hg38)NC_000001.11112891441289144Submitted genomic
nstd137nsv2800763insertionNoGRCh38 (hg38)NC_000001.11112892201289220Submitted genomic
nstd137nsv2800763insertionNoGRCh38 (hg38)NC_000001.11112892201289220Submitted genomic
nstd137nsv2800764insertionNoGRCh38 (hg38)NC_000001.11112894011289401Submitted genomic
nstd137nsv2800764insertionNoGRCh38 (hg38)NC_000001.11112894011289401Submitted genomic
nstd137nsv2800765insertionNoGRCh38 (hg38)NC_000001.11112895161289516Submitted genomic
nstd137nsv2800765insertionNoGRCh38 (hg38)NC_000001.11112895161289516Submitted genomic
nstd137nsv2800766insertionNoGRCh38 (hg38)NC_000001.11112896431289643Submitted genomic
nstd137nsv2800766insertionNoGRCh38 (hg38)NC_000001.11112896431289643Submitted genomic
nstd137nsv2800767insertionNoGRCh38 (hg38)NC_000001.11112898381289838Submitted genomic
nstd137nsv2800767insertionNoGRCh38 (hg38)NC_000001.11112898381289838Submitted genomic
nstd137nsv2800769copy number variationNoGRCh38 (hg38)NC_000001.11113499751350654Submitted genomic
nstd137nsv2800769copy number variationNoGRCh38 (hg38)NC_000001.11113499751350654Submitted genomic
nstd137nsv2800992insertionNoGRCh38 (hg38)NC_000001.11112841661284166Submitted genomic
nstd137nsv2800992insertionNoGRCh38 (hg38)NC_000001.11112841661284166Submitted genomic
nstd137nsv2800993insertionNoGRCh38 (hg38)NC_000001.11112841721284172Submitted genomic
nstd137nsv2800993insertionNoGRCh38 (hg38)NC_000001.11112841721284172Submitted genomic
nstd137nsv2800994insertionNoGRCh38 (hg38)NC_000001.11112885201288520Submitted genomic
nstd137nsv2800994insertionNoGRCh38 (hg38)NC_000001.11112885201288520Submitted genomic
nstd137nsv2800995insertionNoGRCh38 (hg38)NC_000001.11112886281288628Submitted genomic
nstd137nsv2800995insertionNoGRCh38 (hg38)NC_000001.11112886281288628Submitted genomic
nstd137nsv2800996insertionNoGRCh38 (hg38)NC_000001.11112889131288913Submitted genomic
nstd137nsv2800996insertionNoGRCh38 (hg38)NC_000001.11112889131288913Submitted genomic
nstd137nsv2800997insertionNoGRCh38 (hg38)NC_000001.11112893581289358Submitted genomic
nstd137nsv2800997insertionNoGRCh38 (hg38)NC_000001.11112893581289358Submitted genomic
nstd137nsv2800998insertionNoGRCh38 (hg38)NC_000001.11112896121289612Submitted genomic
nstd137nsv2800998insertionNoGRCh38 (hg38)NC_000001.11112896121289612Submitted genomic
nstd137nsv2800999insertionNoGRCh38 (hg38)NC_000001.11112897171289717Submitted genomic
nstd137nsv2800999insertionNoGRCh38 (hg38)NC_000001.11112897171289717Submitted genomic
nstd137nsv2801002insertionNoGRCh38 (hg38)NC_000001.11113827491382749Submitted genomic
nstd137nsv2801002insertionNoGRCh38 (hg38)NC_000001.11113827491382749Submitted genomic
nstd137nsv2801014insertionNoGRCh38 (hg38)NC_000001.11114779411477941Submitted genomic
nstd137nsv2801014insertionNoGRCh38 (hg38)NC_000001.11114779411477941Submitted genomic
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