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Items: 1 to 20 of 67747

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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
    nsv6137755copy number variation1nstd102humanPathogenic GRCh37 chr3: 58,108,466-58,114,632 , GRCh38 chr3: 58,122,739-58,128,905 FLNB
    nsv6137751copy number variation1nstd102humanBenign GRCh37 chr21: 47,543,092-47,543,170 , GRCh38 chr21: 46,123,178-46,123,256 COL6A2
    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
    nsv6137735copy number variation1nstd102humanPathogenic GRCh37 chrX: 153,194,251-153,623,000 , GRCh38.p12 chrX: 153,928,798-154,394,658 EMD, MIR3202-1, 20 more genes
    nsv6137728copy number variation1nstd102humanPathogenic GRCh37 chr3: 58,086,558-58,092,989 , GRCh38 chr3: 58,100,831-58,107,262 FLNB
    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
    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
    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
    nsv6137701copy number variation1nstd102humanLikely pathogenic GRCh37 chr13: 28,669,064-31,367,407 , GRCh38.p12 chr13: 28,094,927-30,793,270 ALOX5AP, FLT1, 41 more genes
    nsv6137692copy number variation1nstd102humanLikely benign GRCh37 chr13: 111,145,433-111,145,496 , GRCh38 chr13: 110,493,086-110,493,149 COL4A2
    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
    nsv6137654copy number variation1nstd102humanLikely benign GRCh37 chr21: 47,402,822-47,402,823 , GRCh38 chr21: 45,982,908-45,982,909 COL6A1
    nsv6131435insertion1nstd186human GRCh37 chr21: 47,410,378-47,410,380 , GRCh38.p12 chr21: 45,990,464-45,990,466 COL6A1
    nsv6131413insertion1nstd186human GRCh37 chr19: 46,022,710-46,023,020 , GRCh38.p12 chr19: 45,519,452-45,519,762 VASP, LOC107985315
    nsv6131390insertion1nstd186human GRCh37 chr17: 48,140,446-48,140,448 , GRCh38.p12 chr17: 50,063,082-50,063,084 ITGA3
    nsv6131271insertion1nstd186human GRCh37 chr20: 9,746,880-9,746,895 , GRCh38.p12 chr20: 9,766,232-9,766,247 PAK5
    nsv6131202insertion1nstd186human GRCh37 chr19: 54,402,184-54,402,187 , GRCh38.p12 chr19: 53,898,930-53,898,933 PRKCG
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