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Items: 1 to 20 of 178405

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137806copy number variation1nstd102humanUncertain significance GRCh37 chr3: 196,539,700-196,612,739 , GRCh38.p12 chr3: 196,812,829-196,885,868 SENP5, PAK2
    nsv6137788copy number variation1nstd102humanPathogenic GRCh37 chr2: 24,601,818-43,466,284 , GRCh38.p12 chr2: 24,378,949-43,239,145 GTF3C2-AS1, MAPRE3-AS1, 316 more genes
    nsv6137761copy number variation1nstd102humanLikely benign GRCh37 chrX: 53,672,687-53,672,691 , GRCh38.p12 chrX: 53,645,735-53,645,748 HUWE1
    nsv6137736copy number variation1nstd102humanPathogenic GRCh37 chrX: 153,263,517-155,260,560 , GRCh38.p12 chrX: 153,998,066-156,030,895 H2AB3, GDI1, 83 more genes
    nsv6137733copy number variation1nstd102humanBenign GRCh37 chrX: 53,672,673-53,672,676 , GRCh38.p12 chrX: 53,645,721-53,645,724 HUWE1
    nsv6137727copy number variation2nstd102humanUncertain significance GRCh38 chr3: 12,589,035-12,766,981 , GRCh37.p13 chr3: 12,630,534-12,808,480 RAF1, CRIP1P1, 1 more genes
    nsv6137724copy number variation1nstd102humanPathogenic GRCh37 chr1: 16,785,250-23,491,592 , GRCh38.p12 chr1: 16,458,755-23,165,099 PADI1, RPS15AP6, 176 more genes
    nsv6137723copy number variation1nstd102humanBenign GRCh37 chr16: 729,959-730,023 , GRCh38 chr16: 679,959-680,023 JMJD8, STUB1, 1 more genes
    nsv6137707copy number variation1nstd102humanPathogenic GRCh37 chr16: 29,565,626-30,221,925 , GRCh38.p12 chr16: 29,554,305-30,210,604 TAOK2, SLC7A5P1, 44 more genes
    nsv6137705copy number variation1nstd102humanPathogenic GRCh37 chr9: 36,419,493-40,774,118 , GRCh38.p12 chr9: 61,281,967-67,217,006 , GRCh38.p12 chr9: 36,419,496-39,445,729 ZNF658B, LOC105379814, 208 more genes
    nsv6137704copy number variation1nstd102humanPathogenic GRCh37 chr9: 36,426,622-38,787,479 , GRCh38.p12 chr9: 36,426,625-38,787,482 MELK, SLC25A51, 55 more genes
    nsv6137702copy number variation1nstd102humanPathogenic GRCh37 chr9: 35,059,633-37,660,586 , GRCh38.p12 chr9: 35,059,636-37,660,589 ARHGEF39, LOC105376026, 84 more genes
    nsv6137700copy number variation1nstd102humanPathogenic GRCh37 chr9: 36,088,563-39,092,820 , GRCh38.p12 chr9: 36,088,566-39,092,823 SNX18P3, VN1R48P, 69 more genes
    nsv6137666copy number variation1nstd102humanPathogenic GRCh37 chrX: 91,829,757-113,050,225 , GRCh38.p12 chrX: 92,574,758-113,806,943 TCEAL8, MTND5P26, 272 more genes
    nsv6131680insertion1nstd186human GRCh37 chr16: 2,102,234-2,102,266 , GRCh38.p12 chr16: 2,052,233-2,052,265 TSC2
    nsv6131658insertion1nstd186human GRCh37 chr19: 45,850,178-45,850,202 , GRCh38.p12 chr19: 45,346,920-45,346,944 KLC3
    nsv6131603insertion1nstd186human GRCh37 chr18: 60,565,268-60,565,299 , GRCh38.p12 chr18: 62,898,035-62,898,066 PHLPP1
    nsv6131519insertion1nstd186human GRCh37 chr14: 104,632,182-104,632,182 , GRCh38.p12 chr14: 104,165,845-104,165,845 KIF26A
    nsv6131506insertion1nstd186human GRCh37 chr19: 16,308,819-16,308,837 , GRCh38.p12 chr19: 16,198,008-16,198,026 AP1M1
    nsv6131472insertion1nstd186human GRCh37 chr18: 60,450,270-60,450,310 , GRCh38.p12 chr18: 62,783,037-62,783,077 PHLPP1
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