U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Links from Gene

Items: 1 to 20 of 184

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148201copy number variation1nstd102humanPathogenic GRCh38 chr3: 93,979,547-124,774,010 , GRCh37.p13 chr3: 93,698,391-124,492,857 NECTIN3, H2BP3, 418 more genes
    nsv7096929copy number variation1nstd102humanUncertain significance GRCh37 chr3: 124,449,319-124,459,066 , GRCh38.p12 chr3: 124,730,472-124,740,219 MIR544B, RPS26P22, 1 more genes
    nsv7096928copy number variation1nstd102humanUncertain significance GRCh37 chr3: 123,003,455-125,313,644 , GRCh38.p12 chr3: 123,284,608-125,594,800 MIR544B, OSBPL11, 33 more genes
    nsv7096531copy number variation1nstd102humanUncertain significance GRCh37 chr3: 121,489,192-125,313,644 , GRCh38.p12 chr3: 121,770,345-125,594,800 MEMO1P6, HACD2, 62 more genes
    nsv7053781inversion1nstd229human GRCh38 chr3: 123,490,767-125,244,776 , GRCh37.p13 chr3: 123,209,614-124,963,620 MIR6083, MYLK, 25 more genes
    nsv7051352inversion1nstd229human GRCh38 chr3: 124,728,042-124,728,517 , GRCh37.p13 chr3: 124,446,889-124,447,364 UMPS
    nsv6715925copy number variation1nstd229human GRCh38 chr3: 124,740,599-124,740,801 , GRCh37.p13 chr3: 124,459,446-124,459,648 UMPS
    nsv6705544copy number variation1nstd229human GRCh38 chr3: 124,723,301-124,808,700 , GRCh37.p13 chr3: 124,442,148-124,527,547 UMPS, RPS26P22, 3 more genes
    nsv6703931copy number variation1nstd229human GRCh38 chr3: 118,573,267-126,079,281 , GRCh37.p13 chr3: 118,292,114-125,798,124 RPS24P9, LOC105374064, 149 more genes
    nsv6702863copy number variation1nstd229human GRCh38 chr3: 124,668,834-124,796,566 , GRCh37.p13 chr3: 124,387,681-124,515,413 KALRN, MIR544B, 3 more genes
    nsv6702195copy number variation1nstd229human GRCh38 chr3: 124,734,801-124,742,100 , GRCh37.p13 chr3: 124,453,648-124,460,947 UMPS
    nsv6701572copy number variation1nstd229human GRCh38 chr3: 124,741,742-124,751,473 , GRCh37.p13 chr3: 124,460,589-124,470,320 UMPS
    nsv6699037copy number variation1nstd229human GRCh38 chr3: 124,629,401-124,952,500 , GRCh37.p13 chr3: 124,348,248-124,671,344 MUC13, ITGB5, 5 more genes
    nsv6637156copy number variation1nstd102humanPathogenic GRCh37 chr3: 116,620,308-172,042,292 , GRCh38.p12 chr3: 116,901,461-172,324,502 H1-10, AADACL2-AS1, 846 more genes
    nsv6562259inversion1nstd223human GRCh38 chr3: 123,977,549-125,974,993 , GRCh37.p13 chr3: 123,696,396-125,693,836 ROPN1B, DNAJB6P7, 46 more genes
    nsv6556022inversion1nstd223human GRCh38 chr3: 123,151,729-129,172,574 , GRCh37.p13 chr3: 122,870,576-128,891,417 UMPS, CHST13, 139 more genes
    nsv6311770copy number variation1nstd102humanPathogenic GRCh37 chr3: 120,365,818-133,465,047 , GRCh38.p12 chr3: 120,646,971-133,746,203 HNRNPA1P23, MIX23, 278 more genes
    nsv6134661copy number variation1nstd213human GRCh37 chr3: 124,430,000-125,730,001 , GRCh38.p12 chr3: 124,711,153-126,011,158 ITGB5, UMPS, 39 more genes
    nsv6134660copy number variation1nstd213human GRCh37 chr3: 124,410,000-124,610,001 , GRCh38.p12 chr3: 124,691,153-124,891,154 ITGB5, UMPS, 4 more genes
    nsv6134575copy number variation1nstd213human GRCh37 chr3: 116,870,000-132,100,001 , GRCh38.p12 chr3: 117,151,153-132,381,157 ACP3, ADCY5, 308 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