U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Links from BioSystems

Items: 1 to 20 of 398214

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137808copy number variation1nstd102humanLikely pathogenic GRCh38.p12 chr19: 49,568,107-49,662,685 , GRCh37 chr19: 50,071,364-50,165,942 IRF3, PRRG2, 4 more genes
    nsv6137806copy number variation1nstd102humanUncertain significance GRCh37 chr3: 196,539,700-196,612,739 , GRCh38.p12 chr3: 196,812,829-196,885,868 SENP5, PAK2
    nsv6137796copy number variation1nstd102humanLikely benign GRCh37 chr9: 140,039,912-140,039,971 , GRCh38 chr9: 137,145,460-137,145,519 GRIN1
    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
    nsv6137755copy number variation1nstd102humanPathogenic GRCh37 chr3: 58,108,466-58,114,632 , GRCh38 chr3: 58,122,739-58,128,905 FLNB
    nsv6137750copy number variation1nstd102humanLikely pathogenic GRCh38 chr1: 1,475,764-1,518,921 , GRCh37.p13 chr1: 1,411,144-1,454,301 ATAD3A, ATAD3B
    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
    nsv6137733copy number variation1nstd102humanBenign GRCh37 chrX: 53,672,673-53,672,676 , GRCh38.p12 chrX: 53,645,721-53,645,724 HUWE1
    nsv6137731copy number variation1nstd102humanBenign GRCh37 chrX: 1,412,907-1,412,990 , GRCh38 chrX: 1,294,014-1,294,097 , GRCh38 chrY: 1,294,014-1,294,097 , GRCh37 chrY: 1,362,907-1,362,990 CSF2RA, MIR3690
    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
    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
    nsv6137706copy number variation3nstd102humanPathogenic, Uncertain significance, Likely pathogenic GRCh37 chr15: 22,770,421-23,282,799 , GRCh38.p12 chr15: 22,590,297-23,102,647 CYFIP1, NIPA2, 14 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
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Recent activity

    Clear Turn Off Turn On

    Your browsing activity is empty.

    Activity recording is turned off.

    Turn recording back on

    See more...
    You are here: NCBI > Variation > Database of Genomic Structural Variation (dbVar)
    Support Center