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
    nsv5974385inversion1nstd209human GRCh38 chr2: 64,078,330-67,334,176 , GRCh37.p13 chr2: 64,305,464-67,561,308 , MEIS1, 63 more genes
    nsv5833684copy number variation1nstd209human GRCh38 chr2: 64,455,203-64,456,219 , GRCh37.p13 chr2: 64,682,337-64,683,353 LGALSL-DT, LGALSL
    nsv5554214mobile element insertion1nstd206human GRCh38 chr2: 43,826,578-177,947,868 , GRCh37.p13 chr2: 44,053,717-178,812,595 , POLR1B, 2149 more genes
    nsv5292387copy number variation1nstd204human GRCh37.p13 chr2: 64,681,729-64,682,033 , GRCh38.p13 chr2: 64,454,595-64,454,899 LGALSL-DT, LGALSL
    nsv4595714copy number variation1nstd183human GRCh37 chr2: 63,604,871-64,778,328 , GRCh38.p12 chr2: 63,377,736-64,551,194 MDH1, RPL23AP37, 22 more genes
    nsv4586337copy number variation1nstd183human GRCh37 chr2: 64,648,439-64,778,328 , GRCh38.p12 chr2: 64,421,305-64,551,194 LGALSL, AFTPH, 5 more genes
    nsv4586331copy number variation1nstd183human GRCh37 chr2: 64,083,427-64,780,137 , GRCh38.p12 chr2: 63,856,293-64,553,003 AFTPH, LOC105374773, 15 more genes
    nsv4584359copy number variation2nstd183human GRCh37 chr2: 64,245,362-64,751,413 , GRCh38.p12 chr2: 64,018,228-64,524,279 MIR4433A, LGALSL, 14 more genes
    nsv4467632mobile element insertion1nstd166human GRCh37.p13 chr2: 64,683,728-64,683,728 , GRCh38.p12 chr2: 64,456,594-64,456,594 LGALSL
    nsv4453429copy number variation1nstd102humanPathogenic GRCh37 chr2: 63,536,353-65,793,944 , GRCh38.p12 chr2: 63,309,218-65,566,810 RPS4XP5, RNU6-548P, 48 more genes
    nsv4382747copy number variation1nstd173human GRCh37 chr2: 64,595,522-64,803,172 , GRCh38.p12 chr2: 64,368,388-64,576,038 LGALSL, AFTPH, 5 more genes
    nsv4069851copy number variation1nstd166human GRCh37.p13 chr2: 64,437,744-65,187,981 , GRCh38.p12 chr2: 64,210,610-64,960,847 , SERTAD2, 26 more genes
    nsv3916821copy number variation1nstd102humanPathogenic NCBI36 chr2: 47,701,031-86,783,356 , GRCh37.p13 chr2: 47,847,527-86,929,845 , GRCh38.p12 chr2: 47,620,388-86,702,722 NAGK, NRXN1-DT, 595 more genes
    nsv3912946copy number variation1nstd102humanPathogenic NCBI36 chr2: 63,500,157-66,199,275 , GRCh37.p13 chr2: 63,646,653-66,345,771 , GRCh38.p12 chr2: 63,419,518-66,118,638 CSP1, LINC01805, 52 more genes
    nsv3910630copy number variation1nstd102humanPathogenic NCBI36 chr2: 50,739,936-242,751,149 , GRCh37.p13 chr2: 50,886,432-243,102,476 , GRCh38.p12 chr2: 50,659,294-242,160,331 DAZAP2P1, RPL36AP16, 2991 more genes
    nsv3903805copy number variation1nstd102humanBenign GRCh37 chr2: 7,635,254-88,005,418 , NCBI36 chr2: 7,552,705-87,786,533 , GRCh38 chr2: 7,495,123-87,705,899 LOC101927723, SANBR, 1246 more genes
    nsv3900298copy number variation1nstd102humanPathogenic GRCh37 chr2: 58,506,654-83,814,086 , GRCh38 chr2: 58,279,519-83,586,962 , NCBI36 chr2: 58,360,158-83,667,597 MIR1285-2, SERTAD2, 404 more genes
    nsv3897743copy number variation1nstd102humanPathogenic GRCh38 chr2: 63,311,999-67,309,291 , GRCh37 chr2: 63,539,134-67,536,423 , NCBI36 chr2: 63,392,638-67,389,927 PELI1, KRT18P33, 68 more genes
    nsv3889156copy number variation1nstd102humanBenign GRCh37 chr2: 64,098,730-64,800,452 , GRCh38.p12 chr2: 63,871,596-64,573,318 UGP2, LINC00309, 15 more genes
    nsv3885544copy number variation1nstd102humanPathogenic GRCh37 chr2: 14,238-243,048,760 , GRCh38.p12 chr2: 14,238-242,106,609 RNU6-674P, KANSL3, 3735 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