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 118

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5941246copy number variation1nstd209human GRCh38 chr19: 31,586,425-31,586,493 , GRCh37.p13 chr19: 32,077,331-32,077,399 LINC03103
    nsv5650983insertion1nstd207human GRCh38 chr19: 31,586,425-31,586,425 , GRCh37.p13 chr19: 32,077,331-32,077,331 LINC03103
    nsv5024519copy number variation1nstd200human GRCh38 chr19: 28,925,173-32,768,971 , GRCh37.p13 chr19: 29,416,080-33,259,877 , LOC105372355, 53 more genes
    nsv4730014copy number variation1nstd102humanUncertain significance GRCh37 chr19: 31,911,128-32,233,752 , GRCh38.p12 chr19: 31,420,222-31,742,846 LOC105372361, TSHZ3-AS1, 3 more genes
    nsv4729966copy number variation1nstd102humanUncertain significance GRCh37 chr19: 31,532,896-32,341,833 , GRCh38.p12 chr19: 31,041,990-31,850,927 RNA5SP471, LOC105372358, 10 more genes
    nsv4711580copy number variation1nstd195human GRCh37 chr19: 31,289,751-32,144,301 , GRCh38.p12 chr19: 30,798,844-31,653,395 TSHZ3, LOC105372355, 8 more genes
    nsv4707819copy number variation1nstd195human GRCh37 chr19: 30,684,501-32,144,251 , GRCh38.p12 chr19: 30,193,594-31,653,345 LOC105372356, LINC01834, 9 more genes
    nsv4656965copy number variation2nstd186human GRCh37 chr19: 32,077,331-32,077,404 , GRCh38.p12 chr19: 31,586,425-31,586,498 LINC03103
    nsv4533445copy number variation1nstd166human GRCh37.p13 chr19: 32,077,331-32,077,404 , GRCh38.p12 chr19: 31,586,425-31,586,498 LINC03103
    nsv4457781copy number variation1nstd102humanUncertain significance GRCh37 chr19: 30,741,915-32,212,809 , GRCh38.p12 chr19: 30,251,008-31,721,903 LOC105372355, LOC105372361, 11 more genes
    nsv4457372copy number variation1nstd102humanPathogenic GRCh37 chr19: 28,271,106-49,213,832 , GRCh38.p12 chr19: 27,780,198-48,710,575 ZNF461, LOC101927572, 735 more genes
    nsv4436646copy number variation1nstd102humanUncertain significance GRCh37 chr19: 31,139,482-32,198,771 , GRCh38.p12 chr19: 30,648,575-31,707,865 ZNF536, LOC105372354, 10 more genes
    nsv4264487copy number variation1nstd166human GRCh37.p13 chr19: 32,049,000-32,084,000 , GRCh38.p12 chr19: 31,558,094-31,593,094 LINC03103
    nsv3957941copy number variation1nstd168human GRCh38 chr19: 31,590,159-31,618,893 , GRCh37.p13 chr19: 32,081,065-32,109,799 LINC03103
    nsv3957493insertion1nstd168human GRCh38 chr19: 31,587,809-31,590,159 , GRCh37.p13 chr19: 32,078,715-32,081,065 LINC03103
    nsv3920776copy number variation1nstd102humanLikely pathogenic NCBI36 chr19: 34,234,635-37,150,342 , GRCh37 chr19: 29,542,795-32,458,502 , GRCh38 chr19: 29,051,888-31,967,596 CCNE1, UQCRFS1, 30 more genes
    nsv3919618copy number variation1nstd102humanUncertain significance NCBI36 chr19: 32,962,986-39,966,686 , GRCh38 chr19: 27,780,238-34,783,942 , GRCh37 chr19: 28,271,146-35,274,846 LINC00906, TDRD12, 112 more genes
    nsv3919296copy number variation1nstd102humanPathogenic NCBI36 chr19: 34,844,605-43,297,203 , GRCh37 chr19: 30,152,765-38,605,363 , GRCh38 chr19: 29,661,858-38,114,723 UBA2, ZNF529, 241 more genes
    nsv3918197copy number variation1nstd102humanPathogenic GRCh38 chr19: 31,367,353-35,417,098 , NCBI36 chr19: 36,550,099-40,599,840 , GRCh37 chr19: 31,858,259-35,908,000 LINC01531, FXYD5, 110 more genes
    nsv3916007copy number variation1nstd102humanPathogenic GRCh37 chr19: 30,162,231-38,393,630 , NCBI36 chr19: 34,854,071-43,085,470 , GRCh38 chr19: 29,671,324-37,902,990 MAG, RNU6-967P, 238 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