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Variant Placements for nstd168 (displaying 100 of 16424 variants)
Study IDVariant IDVariant Region typeVariant Call typeSampleset IDMethodAnalysis IDValidationVariant samplesSubject phenotypeClinical InterpretationAssemblyAccessionChrOuter-StartStartInner-StartInner-EndEndOuter-EndPlacement TypeRemap Score
nstd168nsv3955285insertionNoGRCh38 (hg38)NC_000001.11169301076948190Submitted genomic
nstd168nsv3955285insertionNoGRCh38 (hg38)NC_000001.11169301076948190Submitted genomic
nstd168nsv3955311insertionNoGRCh38 (hg38)NC_000001.11132289793235352Submitted genomic
nstd168nsv3955311insertionNoGRCh38 (hg38)NC_000001.11132289793235352Submitted genomic
nstd168nsv3955320insertionNoGRCh38 (hg38)NC_000001.11153260495337701Submitted genomic
nstd168nsv3955320insertionNoGRCh38 (hg38)NC_000001.11153260495337701Submitted genomic
nstd168nsv3955329insertionNoGRCh38 (hg38)NC_000001.11111330511155846Submitted genomic
nstd168nsv3955329insertionNoGRCh38 (hg38)NC_000001.11111330511155846Submitted genomic
nstd168nsv3955488insertionNoGRCh38 (hg38)NC_000001.111838324948235Submitted genomic
nstd168nsv3955488insertionNoGRCh38 (hg38)NC_000001.111838324948235Submitted genomic
nstd168nsv3955496insertionNoGRCh38 (hg38)NC_000001.11149764534998270Submitted genomic
nstd168nsv3955496insertionNoGRCh38 (hg38)NC_000001.11149764534998270Submitted genomic
nstd168nsv3955597insertionNoGRCh38 (hg38)NC_000001.1118818594058Submitted genomic
nstd168nsv3955597insertionNoGRCh38 (hg38)NC_000001.1118818594058Submitted genomic
nstd168nsv3955605insertionNoGRCh38 (hg38)NC_000001.111151191205354Submitted genomic
nstd168nsv3955605insertionNoGRCh38 (hg38)NC_000001.111151191205354Submitted genomic
nstd168nsv3955619copy number variationNoGRCh38 (hg38)NC_000001.11150395925051848Submitted genomic
nstd168nsv3955619copy number variationNoGRCh38 (hg38)NC_000001.11150395925051848Submitted genomic
nstd168nsv3955707insertionNoGRCh38 (hg38)NC_000001.11139985374020377Submitted genomic
nstd168nsv3955707insertionNoGRCh38 (hg38)NC_000001.11139985374020377Submitted genomic
nstd168nsv3955895insertionNoGRCh38 (hg38)NC_000001.11157987165853024Submitted genomic
nstd168nsv3955895insertionNoGRCh38 (hg38)NC_000001.11157987165853024Submitted genomic
nstd168nsv3955913copy number variationNoGRCh38 (hg38)NC_000001.11141389214228724Submitted genomic
nstd168nsv3955913copy number variationNoGRCh38 (hg38)NC_000001.11141389214228724Submitted genomic
nstd168nsv3955991insertionNoGRCh38 (hg38)NC_000001.1119762871003082Submitted genomic
nstd168nsv3955991insertionNoGRCh38 (hg38)NC_000001.1119762871003082Submitted genomic
nstd168nsv3956279copy number variationNoGRCh38 (hg38)NC_000001.11152981755341377Submitted genomic
nstd168nsv3956279copy number variationNoGRCh38 (hg38)NC_000001.11152981755341377Submitted genomic
nstd168nsv3956620copy number variationNoGRCh38 (hg38)NC_000001.111176686276083Submitted genomic
nstd168nsv3956620copy number variationNoGRCh38 (hg38)NC_000001.111176686276083Submitted genomic
nstd168nsv3956836insertionNoGRCh38 (hg38)NC_000001.111756001802867Submitted genomic
nstd168nsv3956836insertionNoGRCh38 (hg38)NC_000001.111756001802867Submitted genomic
nstd168nsv3957277copy number variationNoGRCh38 (hg38)NC_000001.11132175913232164Submitted genomic
nstd168nsv3957277copy number variationNoGRCh38 (hg38)NC_000001.11132175913232164Submitted genomic
nstd168nsv3957654insertionNoGRCh38 (hg38)NC_000001.11174181827427133Submitted genomic
nstd168nsv3957654insertionNoGRCh38 (hg38)NC_000001.11174181827427133Submitted genomic
nstd168nsv3957739insertionNoGRCh38 (hg38)NC_000001.11110509471121299Submitted genomic
nstd168nsv3957739insertionNoGRCh38 (hg38)NC_000001.11110509471121299Submitted genomic
nstd168nsv3957879copy number variationNoGRCh38 (hg38)NC_000001.11158262235899239Submitted genomic
nstd168nsv3957879copy number variationNoGRCh38 (hg38)NC_000001.11158262235899239Submitted genomic
nstd168nsv3958032copy number variationNoGRCh38 (hg38)NC_000001.11174857907524562Submitted genomic
nstd168nsv3958032copy number variationNoGRCh38 (hg38)NC_000001.11174857907524562Submitted genomic
nstd168nsv3958192complex substitutionNoGRCh38 (hg38)NC_000001.11117348031738376Submitted genomic
nstd168nsv3958192complex substitutionNoGRCh38 (hg38)NC_000001.11117348031738376Submitted genomic
nstd168nsv3958870copy number variationNoGRCh38 (hg38)NC_000001.11140318934084946Submitted genomic
nstd168nsv3958870copy number variationNoGRCh38 (hg38)NC_000001.11140318934084946Submitted genomic
nstd168nsv3958922copy number variationNoGRCh38 (hg38)NC_000001.11125088832539190Submitted genomic
nstd168nsv3958922copy number variationNoGRCh38 (hg38)NC_000001.11125088832539190Submitted genomic
nstd168nsv3958954copy number variationNoGRCh38 (hg38)NC_000001.111409389443686Submitted genomic
nstd168nsv3958954copy number variationNoGRCh38 (hg38)NC_000001.111409389443686Submitted genomic
nstd168nsv3958966copy number variationNoGRCh38 (hg38)NC_000001.111743208856315Submitted genomic
nstd168nsv3958966copy number variationNoGRCh38 (hg38)NC_000001.111743208856315Submitted genomic
nstd168nsv3959140insertionNoGRCh38 (hg38)NC_000001.11125919502792876Submitted genomic
nstd168nsv3959140insertionNoGRCh38 (hg38)NC_000001.11125919502792876Submitted genomic
nstd168nsv3959511complex substitutionNoGRCh38 (hg38)NC_000001.11126708312690685Submitted genomic
nstd168nsv3959511complex substitutionNoGRCh38 (hg38)NC_000001.11126708312690685Submitted genomic
nstd168nsv3959527copy number variationNoGRCh38 (hg38)NC_000001.11126662152869509Submitted genomic
nstd168nsv3959527copy number variationNoGRCh38 (hg38)NC_000001.11126662152869509Submitted genomic
nstd168nsv3959685insertionNoGRCh38 (hg38)NC_000001.11116308661650905Submitted genomic
nstd168nsv3959685insertionNoGRCh38 (hg38)NC_000001.11116308661650905Submitted genomic
nstd168nsv3959767insertionNoGRCh38 (hg38)NC_000001.11135483203633973Submitted genomic
nstd168nsv3959767insertionNoGRCh38 (hg38)NC_000001.11135483203633973Submitted genomic
nstd168nsv3960034insertionNoGRCh38 (hg38)NC_000001.11167033606757146Submitted genomic
nstd168nsv3960034insertionNoGRCh38 (hg38)NC_000001.11167033606757146Submitted genomic
nstd168nsv3960236insertionNoGRCh38 (hg38)NC_000001.11112224751303361Submitted genomic
nstd168nsv3960236insertionNoGRCh38 (hg38)NC_000001.11112224751303361Submitted genomic
nstd168nsv3960568complex substitutionNoGRCh38 (hg38)NC_000001.11126421882664469Submitted genomic
nstd168nsv3960568complex substitutionNoGRCh38 (hg38)NC_000001.11126421882664469Submitted genomic
nstd168nsv3960650insertionNoGRCh38 (hg38)NC_000001.11136787383712388Submitted genomic
nstd168nsv3960650insertionNoGRCh38 (hg38)NC_000001.11136787383712388Submitted genomic
nstd168nsv3960756copy number variationNoGRCh38 (hg38)NC_000001.1113809294058Submitted genomic
nstd168nsv3960756copy number variationNoGRCh38 (hg38)NC_000001.1113809294058Submitted genomic
nstd168nsv3960928insertionNoGRCh38 (hg38)NC_000001.11143162664385562Submitted genomic
nstd168nsv3960928insertionNoGRCh38 (hg38)NC_000001.11143162664385562Submitted genomic
nstd168nsv3961108copy number variationNoGRCh38 (hg38)NC_000001.11152162175243410Submitted genomic
nstd168nsv3961108copy number variationNoGRCh38 (hg38)NC_000001.11152162175243410Submitted genomic
nstd168nsv3961212insertionNoGRCh38 (hg38)NC_000001.11134325183520529Submitted genomic
nstd168nsv3961212insertionNoGRCh38 (hg38)NC_000001.11134325183520529Submitted genomic
nstd168nsv3961494insertionNoGRCh38 (hg38)NC_000001.11159399806016367Submitted genomic
nstd168nsv3961494insertionNoGRCh38 (hg38)NC_000001.11159399806016367Submitted genomic
nstd168nsv3961888copy number variationNoGRCh38 (hg38)NC_000001.11176328037641266Submitted genomic
nstd168nsv3961888copy number variationNoGRCh38 (hg38)NC_000001.11176328037641266Submitted genomic
nstd168nsv3962620insertionNoGRCh38 (hg38)NC_000001.11140549004167215Submitted genomic
nstd168nsv3962620insertionNoGRCh38 (hg38)NC_000001.11140549004167215Submitted genomic
nstd168nsv3962723insertionNoGRCh38 (hg38)NC_000001.11129618312987037Submitted genomic
nstd168nsv3962723insertionNoGRCh38 (hg38)NC_000001.11129618312987037Submitted genomic
nstd168nsv3962739copy number variationNoGRCh38 (hg38)NC_000001.11132889493295983Submitted genomic
nstd168nsv3962739copy number variationNoGRCh38 (hg38)NC_000001.11132889493295983Submitted genomic
nstd168nsv3962962complex substitutionNoGRCh38 (hg38)NC_000001.111178811190265Submitted genomic
nstd168nsv3962962complex substitutionNoGRCh38 (hg38)NC_000001.111178811190265Submitted genomic
nstd168nsv3963330copy number variationNoGRCh38 (hg38)NC_000001.11130147943124342Submitted genomic
nstd168nsv3963330copy number variationNoGRCh38 (hg38)NC_000001.11130147943124342Submitted genomic
nstd168nsv3963685insertionNoGRCh38 (hg38)NC_000001.11153509705356473Submitted genomic
nstd168nsv3963685insertionNoGRCh38 (hg38)NC_000001.11153509705356473Submitted genomic
nstd168nsv3963691insertionNoGRCh38 (hg38)NC_000001.11119205391941477Submitted genomic
nstd168nsv3963691insertionNoGRCh38 (hg38)NC_000001.11119205391941477Submitted genomic
nstd168nsv3963743insertionNoGRCh38 (hg38)NC_000001.111468241509789Submitted genomic
nstd168nsv3963743insertionNoGRCh38 (hg38)NC_000001.111468241509789Submitted genomic
nstd168nsv3963847complex substitutionNoGRCh38 (hg38)NC_000001.111865008940927Submitted genomic
nstd168nsv3963847complex substitutionNoGRCh38 (hg38)NC_000001.111865008940927Submitted genomic
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