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Supporting Variant Placements for nstd164
Study IDVariant IDVariant Region typeVariant Call typeSampleset IDMethodAnalysis IDValidationVariant samplesSubject phenotypeClinical InterpretationAssemblyAccessionChrOuter-StartStartInner-StartInner-EndEndOuter-EndPlacement TypeRemap Score
nstd164nssv14814876copy number lossOligo aCGHCuratedNoP006GRCh37 (hg19)NC_000017.101758089454580901376034602860346711Submitted genomic
nstd164nssv14814876copy number lossOligo aCGHCuratedNoP006GRCh37 (hg19)NC_000017.101758089454580901376034602860346711Submitted genomic
nstd164nssv14814876copy number lossOligo aCGHCuratedNoP006GRCh38.p12NC_000017.111760012093600127766226866762269350Remapped1
nstd164nssv14814877copy number lossOligo aCGHCuratedNoP009GRCh37 (hg19)NC_000017.101758090283580906566034685760347230Submitted genomic
nstd164nssv14814877copy number lossOligo aCGHCuratedNoP009GRCh37 (hg19)NC_000017.101758090283580906566034685760347230Submitted genomic
nstd164nssv14814877copy number lossOligo aCGHCuratedNoP009GRCh38.p12NC_000017.111760012922600132956226949662269869Remapped1
nstd164nssv14814878copy number lossOligo aCGHCuratedNoP012GRCh37 (hg19)NC_000017.101758088933580894536034550860346028Submitted genomic
nstd164nssv14814878copy number lossOligo aCGHCuratedNoP012GRCh37 (hg19)NC_000017.101758088933580894536034550860346028Submitted genomic
nstd164nssv14814878copy number lossOligo aCGHCuratedNoP012GRCh38.p12NC_000017.111760011572600120926226814762268667Remapped1
nstd164nssv14814879copy number lossOligo aCGHCuratedNoP019GRCh37 (hg19)NC_000017.10175816748560174066Submitted genomic
nstd164nssv14814879copy number lossOligo aCGHCuratedNoP019GRCh37 (hg19)NC_000017.10175816748560174066Submitted genomic
nstd164nssv14814879copy number lossOligo aCGHCuratedNoP019GRCh38.p12NC_000017.11176009012462096705Remapped1
nstd164nssv14814880copy number lossOligo aCGHCuratedNoP026GRCh37 (hg19)NC_000017.101758088933580894536034550860346028Submitted genomic
nstd164nssv14814880copy number lossOligo aCGHCuratedNoP026GRCh37 (hg19)NC_000017.101758088933580894536034550860346028Submitted genomic
nstd164nssv14814880copy number lossOligo aCGHCuratedNoP026GRCh38.p12NC_000017.111760011572600120926226814762268667Remapped1
nstd164nssv14814881copy number lossOligo aCGHCuratedNoP073GRCh37 (hg19)NC_000017.101758086876580879366034345660344516Submitted genomic
nstd164nssv14814881copy number lossOligo aCGHCuratedNoP073GRCh37 (hg19)NC_000017.101758086876580879366034345660344516Submitted genomic
nstd164nssv14814881copy number lossOligo aCGHCuratedNoP073GRCh38.p12NC_000017.111760009515600105756226609562267155Remapped1
nstd164nssv14814882copy number lossOligo aCGHCuratedNoP035GRCh37 (hg19)NC_000017.101759272842592728466139299361392997Submitted genomic
nstd164nssv14814882copy number lossOligo aCGHCuratedNoP035GRCh37 (hg19)NC_000017.101759272842592728466139299361392997Submitted genomic
nstd164nssv14814882copy number lossOligo aCGHCuratedNoP035GRCh38.p12NC_000017.111761195481611954856331563263315636Remapped1
nstd164nssv14814883copy number lossOligo aCGHCuratedNoP015GRCh37 (hg19)NC_000017.101759542891595428945955150059551503Submitted genomic
nstd164nssv14814883copy number lossOligo aCGHCuratedNoP015GRCh37 (hg19)NC_000017.101759542891595428945955150059551503Submitted genomic
nstd164nssv14814883copy number lossOligo aCGHCuratedNoP015GRCh38.p12NC_000017.111761465530614655336147413961474142Remapped1
nstd164nssv14814884copy number lossOligo aCGHCuratedNoP016GRCh37 (hg19)NC_000017.101759542891595428945955150059551503Submitted genomic
nstd164nssv14814884copy number lossOligo aCGHCuratedNoP016GRCh37 (hg19)NC_000017.101759542891595428945955150059551503Submitted genomic
nstd164nssv14814884copy number lossOligo aCGHCuratedNoP016GRCh38.p12NC_000017.111761465530614655336147413961474142Remapped1
nstd164nssv14814885copy number lossOligo aCGHCuratedNoP038GRCh37 (hg19)NC_000017.101758857889588578985886832858868337Submitted genomic
nstd164nssv14814885copy number lossOligo aCGHCuratedNoP038GRCh37 (hg19)NC_000017.101758857889588578985886832858868337Submitted genomic
nstd164nssv14814885copy number lossOligo aCGHCuratedNoP038GRCh38.p12NC_000017.111760780528607805376079096760790976Remapped1
nstd164nssv14814886copy number lossSequencingCuratedNoP040GRCh37 (hg19)NC_000005.9543957152439572204613514146135209Submitted genomic
nstd164nssv14814886copy number lossSequencingCuratedNoP040GRCh37 (hg19)NC_000005.9543957152439572204613514146135209Submitted genomic
nstd164nssv14814886copy number lossSequencingCuratedNoP040GRCh38.p12NC_000005.10543957050439571184613503946135107Remapped1
nstd164nssv14814887copy number lossSequencingCuratedNoP041GRCh37 (hg19)NC_000005.9543957152439572204613514146135209Submitted genomic
nstd164nssv14814887copy number lossSequencingCuratedNoP041GRCh37 (hg19)NC_000005.9543957152439572204613514146135209Submitted genomic
nstd164nssv14814887copy number lossSequencingCuratedNoP041GRCh38.p12NC_000005.10543957050439571184613503946135107Remapped1
nstd164nssv14814888copy number lossSequencingCuratedNoP076GRCh37 (hg19)NC_000005.954298502345244787Submitted genomic
nstd164nssv14814888copy number lossSequencingCuratedNoP076GRCh37 (hg19)NC_000005.954298502345244787Submitted genomic
nstd164nssv14814888copy number lossSequencingCuratedNoP076GRCh38.p12NC_000005.1054298492145244685Remapped1
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