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 376

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148056copy number variation1nstd102humanPathogenic GRCh37 chr2: 186,698,504-223,918,111 , GRCh38.p12 chr2: 185,833,777-223,053,393 DNAJB1P1, MTCO2P17, 580 more genes
    nsv7056673inversion1nstd229human GRCh38 chr2: 200,789,164-201,081,461 , GRCh37.p13 chr2: 201,653,887-201,946,184 ORC2, CLK1, 17 more genes
    nsv7051353inversion1nstd229human GRCh38 chr2: 200,635,082-200,934,973 , GRCh37.p13 chr2: 201,499,805-201,799,696 NIF3L1, RNU6-312P, 15 more genes
    nsv7049459inversion1nstd229human GRCh38 chr2: 199,624,566-202,238,851 , GRCh37.p13 chr2: 200,489,289-203,103,574 LOC105373833, NDUFB3, 76 more genes
    nsv7044131inversion1nstd229human GRCh38 chr2: 200,766,186-201,065,779 , GRCh37.p13 chr2: 201,630,909-201,930,502 AOX3P-AOX2P, HYCC2, 16 more genes
    nsv6697595copy number variation1nstd229human GRCh38 chr2: 200,784,480-200,794,787 , GRCh37.p13 chr2: 201,649,203-201,659,510 AOX2P, BZW1-AS1, 1 more genes
    nsv6697182copy number variation1nstd229human GRCh38 chr2: 192,562,889-202,434,958 , GRCh37.p13 chr2: 193,427,615-203,299,681 RNU6-915P, SLC44A3P1, 150 more genes
    nsv6695023copy number variation1nstd229human GRCh38 chr2: 200,695,459-200,700,948 , GRCh37.p13 chr2: 201,560,182-201,565,671 AOX3P-AOX2P, AOX3P
    nsv6694581copy number variation1nstd229human GRCh38 chr2: 200,708,495-200,709,295 , GRCh37.p13 chr2: 201,573,218-201,574,018 AOX3P-AOX2P, AOX3P
    nsv6693516copy number variation1nstd229human GRCh38 chr2: 200,749,344-200,749,459 , GRCh37.p13 chr2: 201,614,067-201,614,182 AOX2P, AOX3P-AOX2P
    nsv6691622copy number variation1nstd229human GRCh38 chr2: 200,751,520-200,807,757 , GRCh37.p13 chr2: 201,616,243-201,672,480 AOX3P-AOX2P, RNU1-133P, 2 more genes
    nsv6687890copy number variation1nstd229human GRCh38 chr2: 200,744,178-200,751,156 , GRCh37.p13 chr2: 201,608,901-201,615,879 AOX2P, AOX3P-AOX2P
    nsv6681891copy number variation1nstd229human GRCh38 chr2: 200,782,298-200,785,334 , GRCh37.p13 chr2: 201,647,021-201,650,057 AOX2P, AOX3P-AOX2P, 1 more genes
    nsv6679982copy number variation1nstd229human GRCh38 chr2: 200,747,725-200,750,263 , GRCh37.p13 chr2: 201,612,448-201,614,986 AOX2P, AOX3P-AOX2P
    nsv6679183copy number variation1nstd229human GRCh38 chr2: 200,771,630-200,785,892 , GRCh37.p13 chr2: 201,636,353-201,650,615 BZW1-AS1, AOX2P, 2 more genes
    nsv6678516copy number variation1nstd229human GRCh38 chr2: 200,792,577-200,798,097 , GRCh37.p13 chr2: 201,657,300-201,662,820 AOX3P-AOX2P, BZW1-AS1
    nsv6637127copy number variation1nstd102humanPathogenic GRCh37 chr2: 189,909,904-209,468,383 , GRCh38.p12 chr2: 189,045,178-208,603,658 LOC100421409, LOC100507443, 310 more genes
    nsv6553867inversion1nstd223human GRCh38 chr2: 200,780,316-200,781,065 , GRCh37.p13 chr2: 201,645,039-201,645,788 AOX2P, BZW1-AS1, 1 more genes
    nsv6354004copy number variation1nstd223human GRCh38 chr2: 200,788,534-200,789,882 , GRCh37.p13 chr2: 201,653,257-201,654,605 AOX3P-AOX2P, BZW1-AS1, 1 more genes
    nsv6350550copy number variation1nstd223human GRCh38 chr2: 200,788,563-200,790,055 , GRCh37.p13 chr2: 201,653,286-201,654,778 AOX3P-AOX2P, BZW1-AS1, 1 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