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nsv6313856

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: Yes
  • Region Size:237,505
  • Description:GRCh37/hg19 6p25.3(chr6:1527437-1764940) AND not specified

Genome View

Select assembly:
Overlapping variant regions from other studies: 856 SVs from 78 studies. See in: genome view    
Remapped(Score: Perfect):1,527,202-1,764,706Question Mark
Overlapping variant regions from other studies: 856 SVs from 78 studies. See in: genome view    
Submitted genomic1,527,437-1,764,940Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv6313856RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000006.12Chr61,527,2021,764,706
nsv6313856Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000006.11Chr61,527,4371,764,940

Variant Call Information

Variant Call IDTypeMethodAnalysisSubject PhenotypeClinical InterpretationSource of InterpretationClinVar ID
nssv17970074copy number gainMultipleMultiplenot specifiedUncertain significanceClinVarRCV002053546.3, VCV001527214.3

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv17970074RemappedPerfectNC_000006.12:g.(?_
1527202)_(1764706_
?)dup
GRCh38.p12First PassNC_000006.12Chr61,527,2021,764,706
nssv17970074Submitted genomicNC_000006.11:g.(?_
1527437)_(1764940_
?)dup
GRCh37 (hg19)NC_000006.11Chr61,527,4371,764,940

No validation data were submitted for this variant

Clinical Assertions

Variant Call IDHGVSTypeAllele OriginSubject PhenotypeClinical InterpretationSource of InterpretationClinVar ID
nssv17970074GRCh37: NC_000006.11:g.(?_1527437)_(1764940_?)dupcopy number gaingermlinenot specifiedUncertain significanceClinVarRCV002053546.3, VCV001527214.3

No genotype data were submitted for this variant

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