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 121

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094147copy number variation1nstd102humanPathogenic GRCh37 chr12: 56,396,006-56,437,938 , GRCh38.p12 chr12: 56,002,222-56,044,154 SUOX, IKZF4, 2 more genes
    nsv7074641inversion1nstd229human GRCh38 chr12: 52,659,002-59,632,575 , GRCh37.p13 chr12: 53,052,786-60,026,356 , LOC105369777, 292 more genes
    nsv7071931inversion1nstd229human GRCh38 chr12: 55,156,710-64,781,897 , GRCh37.p13 chr12: 55,550,494-65,175,677 ZBTB39, MIR548Z, 236 more genes
    nsv7065167inversion1nstd229human GRCh38 chr12: 55,524,684-56,392,713 , GRCh37.p13 chr12: 55,918,468-56,786,497 TMEM198B, BLOC1S1, 57 more genes
    nsv7060060inversion1nstd229human GRCh38 chr12: 55,500,913-56,344,820 , GRCh37.p13 chr12: 55,894,697-56,738,604 MYL6B, OR6C64P, 54 more genes
    nsv6932689copy number variation1nstd229human GRCh38 chr12: 56,034,691-56,047,000 , GRCh37.p13 chr12: 56,428,475-56,440,784 RPS26, IKZF4
    nsv6924218copy number variation1nstd229human GRCh38 chr12: 55,714,201-56,819,900 , GRCh37.p13 chr12: 56,107,985-57,213,684 ESYT1, STAT2, 66 more genes
    nsv6637639copy number variation1nstd102humanUncertain significance GRCh37 chr12: 56,056,806-56,438,901 , GRCh38.p12 chr12: 55,663,022-56,045,117 DGKA, PYM1, 24 more genes
    nsv6588914inversion1nstd223human GRCh38 chr12: 55,524,684-56,392,758 , GRCh37.p13 chr12: 55,918,468-56,786,542 IL23A, RPL41, 57 more genes
    nsv6473183copy number variation1nstd223human GRCh38 chr12: 56,034,691-56,047,000 , GRCh37.p13 chr12: 56,428,475-56,440,784 IKZF4, RPS26
    nsv6315199copy number variation1nstd102humanUncertain significance GRCh38 chr12: 55,986,511-56,885,590 , GRCh37.p13 chr12: 56,380,295-57,279,374 ERBB3, APOF, 47 more genes
    nsv6313979copy number variation1nstd102humanUncertain significance GRCh37 chr12: 56,333,262-57,010,442 , GRCh38.p12 chr12: 55,939,478-56,616,658 TRS-CGA4-1, ANKRD52, 42 more genes
    nsv6309481copy number variation1nstd102humanUncertain significance GRCh37 chr12: 56,435,951-56,437,938 , GRCh38.p12 chr12: 56,042,167-56,044,154 RPS26
    nsv6143026copy number variation1nstd206human GRCh38 chr12: 48,500,915-111,724,058 , GRCh37.p13 chr12: 48,894,698-112,161,862 , LINC00592, 1206 more genes
    nsv6132699copy number variation1nstd213human GRCh37 chr12: 56,390,000-56,610,001 , GRCh38.p12 chr12: 55,996,216-56,216,217 MYL6, RPS26, 15 more genes
    nsv5278526copy number variation1nstd204human GRCh38.p13 chr12: 55,839,801-56,299,500 , GRCh37.p13 chr12: 56,233,585-56,693,284 , NABP2, 30 more genes
    nsv5183871mobile element insertion1nstd203human GRCh38 chr12: 56,041,242-56,041,253 , GRCh37.p13 chr12: 56,435,026-56,435,037 , RPS26
    nsv5040224inversion1nstd200human GRCh38 chr12: 47,213,128-71,357,206 , GRCh37.p13 chr12: 47,606,911-71,750,986 , NR4A1, 686 more genes
    nsv5036282inversion1nstd200human GRCh38 chr12: 52,338,357-95,425,642 , GRCh37.p13 chr12: 52,732,141-95,819,418 , MIR6502, 769 more genes
    nsv4883504inversion1nstd200human GRCh37 chr12: 52,732,141-95,819,418 , GRCh38.p12 chr12: 52,338,357-95,425,642 , MYL6B, 769 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