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 245

    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
    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
    nsv6696708copy number variation1nstd229human GRCh38 chr2: 200,916,982-200,927,347 , GRCh37.p13 chr2: 201,781,705-201,792,070 ORC2
    nsv6695401copy number variation1nstd229human GRCh38 chr2: 200,904,997-200,954,368 , GRCh37.p13 chr2: 201,769,720-201,819,091 ORC2
    nsv6689158copy number variation1nstd229human GRCh38 chr2: 200,899,054-200,907,170 , GRCh37.p13 chr2: 201,763,777-201,771,893 ORC2, NIF3L1, 1 more genes
    nsv6688532copy number variation1nstd229human GRCh38 chr2: 200,911,117-200,915,433 , GRCh37.p13 chr2: 201,775,840-201,780,156 ORC2
    nsv6685548copy number variation1nstd229human GRCh38 chr2: 200,905,199-200,909,363 , GRCh37.p13 chr2: 201,769,922-201,774,086 ORC2
    nsv6680543copy number variation1nstd229human GRCh38 chr2: 200,925,502-200,929,776 , GRCh37.p13 chr2: 201,790,225-201,794,499 ORC2
    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
    nsv6551017inversion1nstd223human GRCh38 chr2: 200,948,558-200,949,262 , GRCh37.p13 chr2: 201,813,281-201,813,985 ORC2
    nsv6546318inversion1nstd223human GRCh38 chr2: 200,927,396-200,928,059 , GRCh37.p13 chr2: 201,792,119-201,792,782 ORC2
    nsv6539543inversion1nstd223human GRCh38 chr2: 200,923,536-200,924,077 , GRCh37.p13 chr2: 201,788,259-201,788,800 ORC2
    nsv6315398copy number variation1nstd102humanPathogenic GRCh37 chr2: 185,697,659-213,002,074 , GRCh38.p12 chr2: 184,832,932-212,137,349 LOC107985785, MYO1B, 381 more genes
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 more genes
    nsv6313730copy number variation1nstd102humanPathogenic GRCh37 chr2: 200,851,079-209,054,267 , GRCh38.p12 chr2: 199,986,356-208,189,543 RN7SKP200, PIMREGP1, 179 more genes
    nsv6134530copy number variation1nstd213human GRCh37 chr2: 201,780,000-202,780,001 , GRCh38.p12 chr2: 200,915,277-201,915,278 CASP8, CASP10, 37 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