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Results: 1 to 20 of 25

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Number of Variants: 20

Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
nsv958885translocation2nstd83humanPathogenic 0
nsv958884copy number variation1nstd83humanUncertain significance GRCh38 chr15: 40,016,281-42,128,509 , GRCh37 (hg19) chr15: 40,308,482-42,420,707 SRP14-AS1, ANKRD63, 57 more genes
nsv958883copy number variation1nstd83humanUncertain significance GRCh38 chr12: 91,884,413-92,144,292 , GRCh37 (hg19) chr12: 92,278,189-92,538,068 C12orf79, BTG1
nsv958882translocation2nstd83humanPathogenic 0
nsv958881copy number variation1nstd83humanUncertain significance GRCh38 chr12: 91,886,561-92,144,295 , GRCh37 (hg19) chr12: 92,280,337-92,538,071 C12orf79, BTG1
nsv958880translocation2nstd83humanPathogenic 0
nsv958879translocation2nstd83humanPathogenic 0
nsv958878translocation2nstd83humanPathogenic 0
nsv958877translocation2nstd83humanPathogenic 0
nsv958876translocation2nstd83humanPathogenic 0
nsv958875translocation2nstd83humanPathogenic 0
nsv958874copy number variation1nstd83humanUncertain significance GRCh38 chr9: 36,929,046-37,026,571 , GRCh37 (hg19) chr9: 36,929,043-37,026,568 PAX5
nsv958873copy number variation1nstd83humanUncertain significance GRCh38 chr22: 22,215,242-22,245,535 , GRCh37 (hg19) chr22: 22,569,632-22,599,947 IGLV10-54, IGL, 1 more genes
nsv958872copy number variation1nstd83humanUncertain significance GRCh38 chr9: 36,929,057-37,025,649 , GRCh37 (hg19) chr9: 36,929,054-37,025,646 PAX5
nsv958871copy number variation1nstd83humanUncertain significance GRCh38 chr9: 37,010,369-37,030,701 , GRCh37 (hg19) chr9: 37,010,366-37,030,698 PAX5
nsv958870copy number variation1nstd83humanUncertain significance GRCh38 chr22: 22,031,469-22,245,246 , GRCh37 (hg19) chr22: 22,385,867-22,599,658 IGLV11-55, IGLV10-54, 7 more genes
nsv958869copy number variation1nstd83humanUncertain significance GRCh38 chr9: 36,929,057-37,121,227 , GRCh37 (hg19) chr9: 36,929,054-37,121,224 EBLN3, PAX5, 1 more genes
nsv958868copy number variation1nstd83humanUncertain significance GRCh38 chr9: 36,929,054-37,030,701 , GRCh37 (hg19) chr9: 36,929,051-37,030,698 PAX5
nsv958867copy number variation1nstd83humanUncertain significance GRCh38 chr9: 36,929,048-37,030,704 , GRCh37 (hg19) chr9: 36,929,045-37,030,701 PAX5
nsv958866copy number variation1nstd83humanUncertain significance GRCh38 chr9: 36,929,057-37,121,224 , GRCh37 (hg19) chr9: 36,929,054-37,121,221 EBLN3, PAX5, 1 more genes

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