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 94

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148267copy number variation1nstd102humanPathogenic GRCh38 chr20: 87,153-23,635,465 , GRCh37.p13 chr20: 67,794-23,616,102 KRT18P3, RSPO4, 413 more genes
    nsv7095546copy number variation1nstd102humanPathogenic GRCh37 chr20: 17,587,682-18,168,103 , GRCh38.p12 chr20: 17,607,037-18,187,459 SNX5, PET117, 14 more genes
    nsv7073551inversion1nstd229human GRCh38 chr20: 10,362,744-19,023,342 , GRCh37.p13 chr20: 10,343,392-19,003,986 SLX4IP, RPL15P1, 122 more genes
    nsv7070199inversion1nstd229human GRCh38 chr20: 13,206,278-18,470,226 , GRCh37.p13 chr20: 13,186,925-18,450,870 LOC105372545, MACROD2, 73 more genes
    nsv7068244inversion1nstd229human GRCh38 chr20: 17,080,202-18,490,897 , GRCh37.p13 chr20: 17,060,847-18,471,541 DSTN, RNU2-56P, 42 more genes
    nsv7065399inversion1nstd229human GRCh38 chr20: 13,871,578-20,212,622 , GRCh37.p13 chr20: 13,852,224-20,193,266 SLC24A3, LOC107985418, 92 more genes
    nsv6599358inversion1nstd223human GRCh38 chr20: 10,362,749-19,023,339 , GRCh37.p13 chr20: 10,343,397-19,003,983 JAG1, BFSP1, 122 more genes
    nsv6531236copy number variation1nstd223human GRCh38 chr20: 17,697,143-17,725,637 , GRCh37.p13 chr20: 17,677,788-17,706,282 BANF2, LOC105372547
    nsv6290339copy number variation1nstd102humanUncertain significance GRCh37 chr20: 11,702,911-19,179,706 , GRCh38.p12 chr20: 11,722,263-19,199,062 LOC105372530, MACROD2-AS1, 105 more genes
    nsv6134272copy number variation1nstd213human GRCh37 chr20: 17,130,000-18,000,001 , GRCh38.p12 chr20: 17,149,355-18,019,357 BFSP1, PCSK2, 20 more genes
    nsv6134271copy number variation1nstd213human GRCh37 chr20: 15,280,000-18,930,001 , GRCh38.p12 chr20: 15,299,354-18,949,357 PTMAP3, SEC23B, 66 more genes
    nsv6134268copy number variation1nstd213human GRCh37 chr20: 13,380,000-22,450,001 , GRCh38.p12 chr20: 13,399,353-22,469,363 BFSP1, INSM1, 134 more genes
    nsv5025171copy number variation1nstd200human GRCh38 chr20: 17,697,143-17,725,644 , GRCh37.p13 chr20: 17,677,788-17,706,289 LOC105372547, BANF2
    nsv4865463copy number variation1nstd200human GRCh37 chr20: 17,677,788-17,706,289 , GRCh38.p12 chr20: 17,697,143-17,725,644 LOC105372547, BANF2
    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
    nsv4350090copy number variation1nstd102humanPathogenic GRCh37 chr20: 11,716,825-19,331,055 , GRCh38.p12 chr20: 11,736,177-19,350,411 ENSAP1, BANF2, 107 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
    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
    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
    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