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 114

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5360044translocation1nstd200human GRCh38 chr20: 10,057,093-10,057,093 , GRCh38 chr20: 10,761,634-10,761,634 , GRCh37.p13 chr20: 10,037,741-10,037,741 , GRCh37.p13 chr20: 10,742,282-10,742,282 ANKEF1, SNAP25-AS1
    nsv5025122copy number variation1nstd200human GRCh38 chr20: 9,705,634-10,153,660 , GRCh37.p13 chr20: 9,686,282-10,134,308 SNAP25-AS1, PAK5, 2 more genes
    nsv4676419copy number variation1nstd102humanPathogenic GRCh37 chr20: 8,571,696-22,088,650 , GRCh38.p12 chr20: 8,591,049-22,108,012 PGAM3P, EEF1A1P34, 182 more genes
    nsv4349190copy number variation1nstd102humanPathogenic GRCh37 chr20: 61,568-26,305,479 , GRCh38.p12 chr20: 80,927-26,324,843 LOC105372582, LOC101929937, 473 more genes
    nsv4336704sequence alteration1nstd166human GRCh37.p13 chr20: 8,105,854-23,795,733 , GRCh38.p12 chr20: 8,125,207-23,815,096 , BFSP1, 242 more genes
    nsv3923490copy number variation1nstd102humanPathogenic GRCh38 chr20: 80,106-13,029,401 , NCBI36 chr20: 8,747-12,958,049 , GRCh37 chr20: 60,747-13,010,049 LINC01751, RNA5SP474, 238 more genes
    nsv3922272copy number variation1nstd102humanPathogenic GRCh38 chr20: 80,106-30,227,427 , NCBI36 chr20: 8,747-28,075,764 , GRCh37 chr20: 60,747-29,462,103 ISM1-AS1, CST2, 498 more genes
    nsv3922170copy number variation1nstd102humanPathogenic NCBI36 chr20: 9,479,622-12,012,082 , GRCh38 chr20: 9,550,975-12,083,434 , GRCh37 chr20: 9,531,622-12,064,082 LOC107985384, PGAM3P, 32 more genes
    nsv3921972copy number variation1nstd102humanPathogenic NCBI36 chr20: 18,580-19,074,923 , GRCh38 chr20: 89,939-19,146,279 , GRCh37 chr20: 70,580-19,126,923 PTMAP3, LOC105372517, 331 more genes
    nsv3920218copy number variation1nstd102humanPathogenic GRCh37 chr20: 80,198-62,908,674 , GRCh38 chr20: 99,557-64,277,321 , NCBI36 chr20: 28,198-62,379,118 MIR3646, NPEPL1, 1310 more genes
    nsv3920089copy number variation1nstd102humanPathogenic GRCh38 chr20: 6,617,695-13,392,559 , NCBI36 chr20: 6,546,342-13,321,206 , GRCh37 chr20: 6,598,342-13,373,206 RN7SKP111, LOC105372517, 68 more genes
    nsv3919898copy number variation1nstd102humanPathogenic GRCh37 chr20: 61,568-26,305,479 , GRCh38 chr20: 80,927-26,324,843 , NCBI36 chr20: 9,568-26,253,479 MIR3192, CFAP61, 473 more genes
    nsv3917353copy number variation1nstd102humanUncertain significance GRCh38 chr20: 9,290,612-14,648,536 , NCBI36 chr20: 9,219,259-14,577,182 , GRCh37 chr20: 9,271,259-14,629,182 LOC107985384, LOC107985407, 63 more genes
    nsv3914413copy number variation1nstd102humanPathogenic NCBI36 chr20: 18,580-19,000,139 , GRCh38 chr20: 89,939-19,071,495 , GRCh37 chr20: 70,580-19,052,139 ZNF343, C20orf96, 331 more genes
    nsv3914070copy number variation1nstd102humanPathogenic GRCh38 chr20: 80,928-18,688,031 , NCBI36 chr20: 9,569-18,616,675 , GRCh37 chr20: 61,569-18,668,675 CDC25B, LOC105372517, 324 more genes
    nsv3913796copy number variation1nstd102humanPathogenic NCBI36 chr20: 18,580-28,133,653 , GRCh37.p13 chr20: 70,580-29,519,992 , GRCh38.p12 chr20: 89,939-30,285,316 RNY4P11, EIF4E2P1, 500 more genes
    nsv3913704copy number variation1nstd102humanPathogenic GRCh38 chr20: 89,939-25,697,564 , NCBI36 chr20: 18,580-25,626,200 , GRCh37 chr20: 70,580-25,678,200 NRSN2, LOC102724545, 459 more genes
    nsv3911315copy number variation1nstd102humanPathogenic GRCh37 chr20: 7,547,291-11,009,342 , NCBI36 chr20: 7,495,291-10,957,342 , GRCh38 chr20: 7,566,644-11,028,694 RNU105B, LOC105372522, 34 more genes
    nsv3910142copy number variation1nstd102humanPathogenic GRCh37 chr20: 9,792,081-37,945,599 , GRCh38 chr20: 9,811,433-39,316,956 , NCBI36 chr20: 9,740,081-37,379,013 DYNLRB1, LOC107985402, 555 more genes
    nsv3908959copy number variation1nstd102humanPathogenic GRCh37 chr20: 67,837-29,638,363 , GRCh38.p12 chr20: 87,196-30,403,687 ISM1-AS1, CST9LP2, 504 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