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 84

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6937414copy number variation1nstd229human GRCh38 chr12: 48,567,333-48,570,118 , GRCh37.p13 chr12: 48,961,116-48,963,901 LALBA
    nsv6921781copy number variation1nstd229human GRCh38 chr12: 48,558,291-48,565,891 , GRCh37.p13 chr12: 48,952,074-48,959,674 OR5BS1P, LALBA
    nsv6592913inversion1nstd223human GRCh38 chr12: 48,570,723-48,571,480 , GRCh37.p13 chr12: 48,964,506-48,965,263 LALBA
    nsv6143026copy number variation1nstd206human GRCh38 chr12: 48,500,915-111,724,058 , GRCh37.p13 chr12: 48,894,698-112,161,862 , LINC00592, 1206 more genes
    nsv6132248copy number variation1nstd213human GRCh37 chr12: 45,960,000-49,240,001 , GRCh38.p12 chr12: 45,566,217-48,846,218 LALBA, VDR, 83 more genes
    nsv5564512copy number variation1nstd102humanLikely pathogenic GRCh37 chr12: 37,873,948-49,578,619 , GRCh38.p12 chr12: 37,480,146-49,184,836 ADCY6, ABCD2, 187 more genes
    nsv5495323copy number variation1nstd206human GRCh38 chr12: 48,572,101-48,572,173 , GRCh37.p13 chr12: 48,965,884-48,965,956 LALBA
    nsv5040224inversion1nstd200human GRCh38 chr12: 47,213,128-71,357,206 , GRCh37.p13 chr12: 47,606,911-71,750,986 , NR4A1, 686 more genes
    nsv4837889copy number variation1nstd200human GRCh37 chr12: 48,958,653-48,959,542 , GRCh38.p12 chr12: 48,564,870-48,565,759 LALBA
    nsv4763701insertion1nstd199human GRCh37 chr12: 48,965,889-48,965,889 , GRCh38.p12 chr12: 48,572,106-48,572,106 LALBA
    nsv4755205inversion1nstd199human GRCh37 chr12: 25,956,127-125,801,151 , GRCh38.p12 chr12: 25,803,193-125,316,605 , ACACB, 1787 more genes
    nsv4736781copy number variation1nstd199human GRCh37 chr12: 25,957,322-125,801,148 , GRCh38.p12 chr12: 25,804,388-125,316,602 , RNA5SP368, 1787 more genes
    nsv4457182copy number variation1nstd102humanUncertain significance GRCh37 chr12: 48,944,713-49,265,377 , GRCh38.p12 chr12: 48,550,930-48,871,594 SNORA2A, LALBA, 17 more genes
    nsv4324772inversion1nstd166human GRCh37.p13 chr12: 27,368,635-91,765,744 , GRCh38.p12 chr12: 27,215,702-91,371,967 , ATP2B1, 1101 more genes
    nsv4195722copy number variation1nstd166human GRCh37.p13 chr12: 48,958,660-48,966,892 , GRCh38.p12 chr12: 48,564,877-48,573,109 LALBA
    nsv4193997copy number variation1nstd166human GRCh37.p13 chr12: 48,961,116-48,963,897 , GRCh38.p12 chr12: 48,567,333-48,570,114 LALBA
    nsv3920847inversion1nstd102humanUncertain significance GRCh38.p12 chr12: 26,217,318-53,967,754 , GRCh37 chr12: 26,370,251-54,361,538 , ASIC1, 491 more genes
    nsv3914194copy number variation1nstd102humanPathogenic NCBI36 chr12: 100,698-132,283,466 , GRCh37 chr12: 282,465-133,773,393 , GRCh38 chr12: 121,271-133,196,807 , BTG1P1, 2451 more genes
    nsv3907271copy number variation1nstd102humanUncertain significance GRCh37 chr12: 48,961,450-49,255,821 , GRCh38.p12 chr12: 48,567,667-48,862,038 ADCY6, DDX23, 16 more genes
    nsv3905447copy number variation2nstd102humanPathogenic GRCh37 chr12: 173,787-133,777,902 , GRCh38.p12 chr12: 64,621-133,201,316 , LOH12CR2, 2452 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