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 174

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137156copy number variation1nstd233human GRCh37.p13 chr17: 59,529,098-60,599,347 , GRCh38 chr17: 61,451,737-62,521,986 TBX4, MED13, 20 more genes
    nsv7070986inversion1nstd229human GRCh38 chr17: 59,331,393-62,738,993 , GRCh37.p13 chr17: 57,408,754-60,816,354 MIR21, LINC01476, 83 more genes
    nsv7070223inversion1nstd229human GRCh38 chr17: 61,482,736-62,369,304 , GRCh37.p13 chr17: 59,560,097-60,446,665 TBC1D3P2, TBX4, 12 more genes
    nsv6637728copy number variation1nstd102humanUncertain significance GRCh37 chr17: 60,070,415-60,450,079 , GRCh38.p12 chr17: 61,993,054-62,372,718 MED13, LOC100996361, 8 more genes
    nsv6624498copy number variation1nstd224human GRCh37 chr17: 60,199,130-60,440,732 , GRCh38.p12 chr17: 62,121,769-62,363,371 POLRMTP1, TBC1D3P2, 5 more genes
    nsv6531321copy number variation1nstd223human GRCh38 chr17: 61,981,221-62,425,637 , GRCh37.p13 chr17: 60,058,582-60,502,998 TBC1D3P2, RPL36AP47, 13 more genes
    nsv6289794copy number variation1nstd102humanLikely pathogenic GRCh37 chr17: 58,076,721-60,362,868 , GRCh38.p12 chr17: 59,999,360-62,285,507 CA4, TBX2, 49 more genes
    nsv6133316copy number variation1nstd213human GRCh37 chr17: 53,930,000-62,410,001 , GRCh38.p12 chr17: 55,852,639-64,332,641 CA4, CD79B, 208 more genes
    nsv5701265mobile element insertion1nstd211human GRCh38 chr17: 62,281,462-62,281,462 , GRCh37.p13 chr17: 60,358,823-60,358,823 USP32P4
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5141610mobile element insertion1nstd203human GRCh38 chr17: 62,281,427-62,281,462 , GRCh37.p13 chr17: 60,358,788-60,358,823 USP32P4
    nsv5013898copy number variation1nstd200human GRCh38 chr17: 62,225,835-62,280,888 , GRCh37.p13 chr17: 60,303,196-60,358,249 LOC100996361, LOC105371853, 2 more genes
    nsv5013891copy number variation1nstd200human GRCh38 chr17: 62,115,455-62,351,528 , GRCh37.p13 chr17: 60,192,816-60,428,889 RPL36AP47, POLRMTP1, 5 more genes
    nsv5013890copy number variation1nstd200human GRCh38 chr17: 61,981,265-62,425,676 , GRCh37.p13 chr17: 60,058,626-60,503,037 TBC1D3P2, LOC105371853, 13 more genes
    nsv4630335copy number variation1nstd183human GRCh37 chr17: 60,196,797-60,436,249 , GRCh38.p12 chr17: 62,119,436-62,358,888 POLRMTP1, TBC1D3P2, 5 more genes
    nsv4622524copy number variation2nstd183human GRCh37 chr17: 60,299,089-60,363,037 , GRCh38.p12 chr17: 62,221,728-62,285,676 TBC1D3P2, USP32P4, 2 more genes
    nsv4501185mobile element insertion1nstd166human GRCh37.p13 chr17: 60,358,788-60,358,788 , GRCh38.p12 chr17: 62,281,427-62,281,427 USP32P4
    nsv4457799copy number variation1nstd102humanPathogenic GRCh37 chr17: 57,869,604-67,078,443 , GRCh38.p12 chr17: 59,792,243-69,082,302 PECAM1, TBX2-AS1, 215 more genes
    nsv4429243copy number variation1nstd174human GRCh37 chr17: 60,295,590-60,365,330 , GRCh38.p12 chr17: 62,218,229-62,287,969 LOC100996361, TBC1D3P2, 2 more genes
    nsv4413737copy number variation1nstd174human GRCh37 chr17: 60,325,332-60,369,016 , GRCh38.p12 chr17: 62,247,971-62,291,655 LOC105371853, TBC1D3P2, 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