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Variant Placements for nstd207 (displaying 100 of 107996 variants)
Study IDVariant IDVariant Region typeVariant Call typeSampleset IDMethodAnalysis IDValidationVariant samplesSubject phenotypeClinical InterpretationAssemblyAccessionChrOuter-StartStartInner-StartInner-EndEndOuter-EndPlacement TypeRemap Score
nstd207nsv5564926copy number variationNoGRCh38 (hg38)NC_000001.111872557872659Submitted genomic
nstd207nsv5564926copy number variationNoGRCh38 (hg38)NC_000001.111872557872659Submitted genomic
nstd207nsv5565524copy number variationNoGRCh38 (hg38)NC_000001.111964575964763Submitted genomic
nstd207nsv5565524copy number variationNoGRCh38 (hg38)NC_000001.111964575964763Submitted genomic
nstd207nsv5565763copy number variationNoGRCh38 (hg38)NC_000001.111934064934875Submitted genomic
nstd207nsv5565763copy number variationNoGRCh38 (hg38)NC_000001.111934064934875Submitted genomic
nstd207nsv5566527copy number variationNoGRCh38 (hg38)NC_000001.111976737977054Submitted genomic
nstd207nsv5566527copy number variationNoGRCh38 (hg38)NC_000001.111976737977054Submitted genomic
nstd207nsv5566630copy number variationNoGRCh38 (hg38)NC_000001.111964631964705Submitted genomic
nstd207nsv5566630copy number variationNoGRCh38 (hg38)NC_000001.111964631964705Submitted genomic
nstd207nsv5567698copy number variationNoGRCh38 (hg38)NC_000001.111909006909095Submitted genomic
nstd207nsv5567698copy number variationNoGRCh38 (hg38)NC_000001.111909006909095Submitted genomic
nstd207nsv5567941copy number variationNoGRCh38 (hg38)NC_000001.111136713136833Submitted genomic
nstd207nsv5567941copy number variationNoGRCh38 (hg38)NC_000001.111136713136833Submitted genomic
nstd207nsv5568273copy number variationNoGRCh38 (hg38)NC_000001.111859110864157Submitted genomic
nstd207nsv5568273copy number variationNoGRCh38 (hg38)NC_000001.111859110864157Submitted genomic
nstd207nsv5570165copy number variationNoGRCh38 (hg38)NC_000001.111909345909525Submitted genomic
nstd207nsv5570165copy number variationNoGRCh38 (hg38)NC_000001.111909345909525Submitted genomic
nstd207nsv5570863copy number variationNoGRCh38 (hg38)NC_000001.111372568372750Submitted genomic
nstd207nsv5570863copy number variationNoGRCh38 (hg38)NC_000001.111372568372750Submitted genomic
nstd207nsv5572747copy number variationNoGRCh38 (hg38)NC_000001.111831213833731Submitted genomic
nstd207nsv5572747copy number variationNoGRCh38 (hg38)NC_000001.111831213833731Submitted genomic
nstd207nsv5572831copy number variationNoGRCh38 (hg38)NC_000001.111180551180885Submitted genomic
nstd207nsv5572831copy number variationNoGRCh38 (hg38)NC_000001.111180551180885Submitted genomic
nstd207nsv5573255copy number variationNoGRCh38 (hg38)NC_000001.111757654757796Submitted genomic
nstd207nsv5573255copy number variationNoGRCh38 (hg38)NC_000001.111757654757796Submitted genomic
nstd207nsv5573486copy number variationNoGRCh38 (hg38)NC_000001.111432630432860Submitted genomic
nstd207nsv5573486copy number variationNoGRCh38 (hg38)NC_000001.111432630432860Submitted genomic
nstd207nsv5573575copy number variationNoGRCh38 (hg38)NC_000001.111609751610513Submitted genomic
nstd207nsv5573575copy number variationNoGRCh38 (hg38)NC_000001.111609751610513Submitted genomic
nstd207nsv5573934copy number variationNoGRCh38 (hg38)NC_000001.111936234936311Submitted genomic
nstd207nsv5573934copy number variationNoGRCh38 (hg38)NC_000001.111936234936311Submitted genomic
nstd207nsv5574478copy number variationNoGRCh38 (hg38)NC_000001.111866606866703Submitted genomic
nstd207nsv5574478copy number variationNoGRCh38 (hg38)NC_000001.111866606866703Submitted genomic
nstd207nsv5574605copy number variationNoGRCh38 (hg38)NC_000001.111371856372092Submitted genomic
nstd207nsv5574605copy number variationNoGRCh38 (hg38)NC_000001.111371856372092Submitted genomic
nstd207nsv5575097copy number variationNoGRCh38 (hg38)NC_000001.111367566367683Submitted genomic
nstd207nsv5575097copy number variationNoGRCh38 (hg38)NC_000001.111367566367683Submitted genomic
nstd207nsv5575457copy number variationNoGRCh38 (hg38)NC_000001.111769238773392Submitted genomic
nstd207nsv5575457copy number variationNoGRCh38 (hg38)NC_000001.111769238773392Submitted genomic
nstd207nsv5576036copy number variationNoGRCh38 (hg38)NC_000001.111180283180506Submitted genomic
nstd207nsv5576036copy number variationNoGRCh38 (hg38)NC_000001.111180283180506Submitted genomic
nstd207nsv5576399copy number variationNoGRCh38 (hg38)NC_000001.111909419909508Submitted genomic
nstd207nsv5576399copy number variationNoGRCh38 (hg38)NC_000001.111909419909508Submitted genomic
nstd207nsv5576596copy number variationNoGRCh38 (hg38)NC_000001.111811390811810Submitted genomic
nstd207nsv5576596copy number variationNoGRCh38 (hg38)NC_000001.111811390811810Submitted genomic
nstd207nsv5576712copy number variationNoGRCh38 (hg38)NC_000001.111977224977315Submitted genomic
nstd207nsv5576712copy number variationNoGRCh38 (hg38)NC_000001.111977224977315Submitted genomic
nstd207nsv5576759copy number variationNoGRCh38 (hg38)NC_000001.111126241164870Submitted genomic
nstd207nsv5576759copy number variationNoGRCh38 (hg38)NC_000001.111126241164870Submitted genomic
nstd207nsv5577050copy number variationNoGRCh38 (hg38)NC_000001.111638156638487Submitted genomic
nstd207nsv5577050copy number variationNoGRCh38 (hg38)NC_000001.111638156638487Submitted genomic
nstd207nsv5577190copy number variationNoGRCh38 (hg38)NC_000001.111904478904575Submitted genomic
nstd207nsv5577190copy number variationNoGRCh38 (hg38)NC_000001.111904478904575Submitted genomic
nstd207nsv5577747copy number variationNoGRCh38 (hg38)NC_000001.111714324714373Submitted genomic
nstd207nsv5577747copy number variationNoGRCh38 (hg38)NC_000001.111714324714373Submitted genomic
nstd207nsv5578826copy number variationNoGRCh38 (hg38)NC_000001.111888491888571Submitted genomic
nstd207nsv5578826copy number variationNoGRCh38 (hg38)NC_000001.111888491888571Submitted genomic
nstd207nsv5579062copy number variationNoGRCh38 (hg38)NC_000001.111728521729420Submitted genomic
nstd207nsv5579062copy number variationNoGRCh38 (hg38)NC_000001.111728521729420Submitted genomic
nstd207nsv5579430copy number variationNoGRCh38 (hg38)NC_000001.111629055629536Submitted genomic
nstd207nsv5579430copy number variationNoGRCh38 (hg38)NC_000001.111629055629536Submitted genomic
nstd207nsv5579437copy number variationNoGRCh38 (hg38)NC_000001.111866675866919Submitted genomic
nstd207nsv5579437copy number variationNoGRCh38 (hg38)NC_000001.111866675866919Submitted genomic
nstd207nsv5580066copy number variationNoGRCh38 (hg38)NC_000001.111181210181448Submitted genomic
nstd207nsv5580066copy number variationNoGRCh38 (hg38)NC_000001.111181210181448Submitted genomic
nstd207nsv5580628copy number variationNoGRCh38 (hg38)NC_000001.111909169909479Submitted genomic
nstd207nsv5580628copy number variationNoGRCh38 (hg38)NC_000001.111909169909479Submitted genomic
nstd207nsv5580819copy number variationNoGRCh38 (hg38)NC_000001.111368862369143Submitted genomic
nstd207nsv5580819copy number variationNoGRCh38 (hg38)NC_000001.111368862369143Submitted genomic
nstd207nsv5580945copy number variationNoGRCh38 (hg38)NC_000001.111648810648866Submitted genomic
nstd207nsv5580945copy number variationNoGRCh38 (hg38)NC_000001.111648810648866Submitted genomic
nstd207nsv5581698copy number variationNoGRCh38 (hg38)NC_000001.111853474853571Submitted genomic
nstd207nsv5581698copy number variationNoGRCh38 (hg38)NC_000001.111853474853571Submitted genomic
nstd207nsv5581718copy number variationNoGRCh38 (hg38)NC_000001.111872669872878Submitted genomic
nstd207nsv5581718copy number variationNoGRCh38 (hg38)NC_000001.111872669872878Submitted genomic
nstd207nsv5582426copy number variationNoGRCh38 (hg38)NC_000001.111934008934315Submitted genomic
nstd207nsv5582426copy number variationNoGRCh38 (hg38)NC_000001.111934008934315Submitted genomic
nstd207nsv5584151copy number variationNoGRCh38 (hg38)NC_000001.111641159641266Submitted genomic
nstd207nsv5584151copy number variationNoGRCh38 (hg38)NC_000001.111641159641266Submitted genomic
nstd207nsv5584519copy number variationNoGRCh38 (hg38)NC_000001.111933961934100Submitted genomic
nstd207nsv5584519copy number variationNoGRCh38 (hg38)NC_000001.111933961934100Submitted genomic
nstd207nsv5604957insertionNoGRCh38 (hg38)NC_000001.111789481789481Submitted genomic
nstd207nsv5604957insertionNoGRCh38 (hg38)NC_000001.111789481789481Submitted genomic
nstd207nsv5604984insertionNoGRCh38 (hg38)NC_000001.111775241775241Submitted genomic
nstd207nsv5604984insertionNoGRCh38 (hg38)NC_000001.111775241775241Submitted genomic
nstd207nsv5605431insertionNoGRCh38 (hg38)NC_000001.1119025890258Submitted genomic
nstd207nsv5605431insertionNoGRCh38 (hg38)NC_000001.1119025890258Submitted genomic
nstd207nsv5606179insertionNoGRCh38 (hg38)NC_000001.111876014876014Submitted genomic
nstd207nsv5606179insertionNoGRCh38 (hg38)NC_000001.111876014876014Submitted genomic
nstd207nsv5606346insertionNoGRCh38 (hg38)NC_000001.111136789136789Submitted genomic
nstd207nsv5606346insertionNoGRCh38 (hg38)NC_000001.111136789136789Submitted genomic
nstd207nsv5606364insertionNoGRCh38 (hg38)NC_000001.111868470868470Submitted genomic
nstd207nsv5606364insertionNoGRCh38 (hg38)NC_000001.111868470868470Submitted genomic
nstd207nsv5606440insertionNoGRCh38 (hg38)NC_000001.111934889934889Submitted genomic
nstd207nsv5606440insertionNoGRCh38 (hg38)NC_000001.111934889934889Submitted genomic
nstd207nsv5606446insertionNoGRCh38 (hg38)NC_000001.111904636904636Submitted genomic
nstd207nsv5606446insertionNoGRCh38 (hg38)NC_000001.111904636904636Submitted genomic
nstd207nsv5606687insertionNoGRCh38 (hg38)NC_000001.111611325611325Submitted genomic
nstd207nsv5606687insertionNoGRCh38 (hg38)NC_000001.111611325611325Submitted genomic
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