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 62802

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    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
    nsv6137672copy number variation1nstd102humannot provided GRCh38 chr2: 124,348,648-129,410,245 , GRCh37.p13 chr2: 125,106,225-130,167,818 LOC105373603, MYO7B, 59 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
    nsv6131413insertion1nstd186human GRCh37 chr19: 46,022,710-46,023,020 , GRCh38.p12 chr19: 45,519,452-45,519,762 VASP, LOC107985315
    nsv6131403insertion1nstd186human GRCh37 chr20: 60,121,135-60,121,141 , GRCh38.p12 chr20: 61,546,079-61,546,085 CDH4
    nsv6131337insertion1nstd186human GRCh37 chr16: 83,133,229-83,133,229 , GRCh38.p12 chr16: 83,099,624-83,099,624 CDH13
    nsv6131307insertion1nstd186human GRCh37 chr20: 60,106,389-60,106,429 , GRCh38.p12 chr20: 61,531,333-61,531,373 CDH4
    nsv6131273insertion1nstd186human GRCh37 chr16: 61,994,268-61,994,280 , GRCh38.p12 chr16: 61,960,364-61,960,376 CDH8
    nsv6130979insertion1nstd186human GRCh37 chr18: 49,992,150-49,992,192 , GRCh38.p12 chr18: 52,465,780-52,465,822 DCC
    nsv6130941insertion1nstd186human GRCh37 chr16: 83,478,446-83,478,493 , GRCh38.p12 chr16: 83,444,841-83,444,888 CDH13
    nsv6130884insertion1nstd186human GRCh37 chr21: 10,697,897-44,966,043 , GRCh38.p12 chr21: 12,965,809-43,546,162 , APP, 533 more genes
    nsv6130653insertion1nstd186human GRCh37 chr20: 60,195,262-60,195,277 , GRCh38.p12 chr20: 61,620,206-61,620,221 CDH4
    nsv6130547insertion1nstd186human GRCh37 chr19: 36,326,966-36,326,966 , GRCh38.p12 chr19: 35,836,064-35,836,064 NPHS1
    nsv6130375insertion1nstd186human GRCh37 chr21: 41,658,660-41,658,660 , GRCh38.p12 chr21: 40,286,733-40,286,733 DSCAM
    nsv6130320mobile element insertion1nstd186human GRCh37 chr20: 60,132,832-60,132,883 , GRCh38.p12 chr20: 61,557,776-61,557,827 CDH4
    nsv6130097insertion1nstd186human GRCh37 chr21: 41,673,539-41,673,539 , GRCh38.p12 chr21: 40,301,612-40,301,612 DSCAM
    nsv6130079insertion1nstd186human GRCh37 chr18: 50,732,626-50,732,868 , GRCh38.p12 chr18: 53,206,256-53,206,498 DCC
    nsv6130017insertion1nstd186human GRCh37 chr16: 82,827,967-82,828,002 , GRCh38.p12 chr16: 82,794,362-82,794,397 CDH13, LOC101928446
    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