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 136

    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
    nsv7047003inversion1nstd229human GRCh38 chr3: 105,966,506-108,938,496 , GRCh37.p13 chr3: 105,685,353-108,657,343 MTND4P16, CD47, 41 more genes
    nsv7042841inversion1nstd229human GRCh38 chr3: 104,903,601-112,515,639 , GRCh37.p13 chr3: 104,622,445-112,234,486 MTND4P16, CD47, 94 more genes
    nsv6709378copy number variation1nstd229human GRCh38 chr3: 107,392,201-108,950,478 , GRCh37.p13 chr3: 107,111,048-108,669,325 RPL13P8, RETNLB, 17 more genes
    nsv6700179copy number variation1nstd229human GRCh38 chr3: 108,133,676-108,141,884 , GRCh37.p13 chr3: 107,852,523-107,860,731 LINC01215
    nsv6699632copy number variation1nstd229human GRCh38 chr3: 108,066,673-108,685,956 , GRCh37.p13 chr3: 107,785,520-108,404,803 LOC105374031, RPL13P8, 8 more genes
    nsv6698338copy number variation1nstd229human GRCh38 chr3: 108,068,211-108,497,947 , GRCh37.p13 chr3: 107,787,058-108,216,794 LOC105374031, HNRNPA1P17, 5 more genes
    nsv6636830copy number variation1nstd102humanPathogenic GRCh37 chr3: 107,059,705-115,005,256 , GRCh38.p12 chr3: 107,340,858-115,286,409 ATP6V1A, DRD3, 117 more genes
    nsv6628254copy number variation1nstd224human GRCh37 chr3: 106,647,916-112,127,787 , GRCh38.p12 chr3: 106,929,069-112,408,940 CD47, CD96, 71 more genes
    nsv6369147copy number variation1nstd223human GRCh38 chr3: 108,129,356-108,143,484 , GRCh37.p13 chr3: 107,848,203-107,862,331 LINC01215
    nsv6364708copy number variation1nstd223human GRCh38 chr3: 108,129,185-108,129,909 , GRCh37.p13 chr3: 107,848,032-107,848,756 LINC01215
    nsv6362220copy number variation1nstd223human GRCh38 chr3: 108,133,269-108,134,118 , GRCh37.p13 chr3: 107,852,116-107,852,965 LINC01215
    nsv6361583copy number variation1nstd223human GRCh38 chr3: 108,138,906-108,143,479 , GRCh37.p13 chr3: 107,857,753-107,862,326 LINC01215
    nsv6315408copy number variation1nstd102humanPathogenic GRCh37 chr3: 106,598,767-115,704,696 , GRCh38.p12 chr3: 106,879,920-115,985,849 DZIP3, MIR9900, 138 more genes
    nsv6134776copy number variation1nstd213human GRCh37 chr3: 105,120,000-116,510,001 , GRCh38.p12 chr3: 105,401,156-116,791,154 , ALCAM, 156 more genes
    nsv6134387copy number variation1nstd213human GRCh37 chr3: 107,560,000-107,890,001 , GRCh38.p12 chr3: 107,841,153-108,171,154 CD47, IFT57, 4 more genes
    nsv5440090copy number variation1nstd206human GRCh38 chr3: 107,968,309-108,404,736 , GRCh37.p13 chr3: 107,687,156-108,123,583 CD47, HHLA2, 5 more genes
    nsv5436500copy number variation1nstd206human GRCh38 chr3: 108,126,929-108,127,048 , GRCh37.p13 chr3: 107,845,776-107,845,895 LINC01215
    nsv5036857inversion1nstd200human GRCh38 chr3: 97,392,267-146,717,859 , GRCh37.p13 chr3: 97,111,111-146,435,646 , FBRSL1P1, 801 more genes
    nsv4919419copy number variation1nstd200human GRCh38 chr3: 108,138,917-108,143,519 , GRCh37.p13 chr3: 107,857,764-107,862,366 LINC01215
    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