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 409

    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
    nsv7145412insertion1nstd232human GRCh37.p13 chr3: 123,272,981-123,272,981 , GRCh38.p12 chr3: 123,554,134-123,554,134 HACD2
    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
    nsv7096927copy number variation1nstd102humanPathogenic GRCh37 chr3: 123,003,455-123,512,688 , GRCh38.p12 chr3: 123,284,608-123,793,841 ADCY5, MYLK, 4 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
    nsv7055712inversion1nstd229human GRCh38 chr3: 123,546,341-123,996,479 , GRCh37.p13 chr3: 123,265,188-123,715,326 MYLK, HACD2, 5 more genes
    nsv7055351inversion1nstd229human GRCh38 chr3: 123,504,170-123,504,243 , GRCh37.p13 chr3: 123,223,017-123,223,090 HACD2
    nsv7053781inversion1nstd229human GRCh38 chr3: 123,490,767-125,244,776 , GRCh37.p13 chr3: 123,209,614-124,963,620 MIR6083, MYLK, 25 more genes
    nsv7047463inversion1nstd229human GRCh38 chr3: 123,221,334-123,949,495 , GRCh37.p13 chr3: 122,940,181-123,668,342 ADCY5, MYLK, 6 more genes
    nsv6717290copy number variation1nstd229human GRCh38 chr3: 123,541,249-123,544,523 , GRCh37.p13 chr3: 123,260,096-123,263,370 HACD2
    nsv6713177copy number variation1nstd229human GRCh38 chr3: 123,517,910-123,518,214 , GRCh37.p13 chr3: 123,236,757-123,237,061 HACD2
    nsv6712885copy number variation1nstd229human GRCh38 chr3: 123,529,101-123,546,000 , GRCh37.p13 chr3: 123,247,948-123,264,847 HACD2
    nsv6707779copy number variation1nstd229human GRCh38 chr3: 123,480,629-123,490,865 , GRCh37.p13 chr3: 123,199,476-123,209,712 HACD2
    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
    nsv6701109copy number variation1nstd229human GRCh38 chr3: 123,395,851-123,612,823 , GRCh37.p13 chr3: 123,114,698-123,331,670 MYLK-AS1, MYLK, 2 more genes
    nsv6700267copy number variation1nstd229human GRCh38 chr3: 123,505,382-123,519,836 , GRCh37.p13 chr3: 123,224,229-123,238,683 HACD2
    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
    nsv6570009inversion1nstd223human GRCh38 chr3: 123,514,064-123,515,849 , GRCh37.p13 chr3: 123,232,911-123,234,696 HACD2
    nsv6569906inversion1nstd223human GRCh38 chr3: 123,580,509-123,581,136 , GRCh37.p13 chr3: 123,299,356-123,299,983 HACD2
    nsv6567001inversion1nstd223human GRCh38 chr3: 123,545,270-123,545,747 , GRCh37.p13 chr3: 123,264,117-123,264,594 HACD2
    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