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 192

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112778copy number variation1nstd102humanPathogenic GRCh37 chr20: 51,799,648-62,916,626 , GRCh38.p12 chr20: 53,183,109-64,285,273 LINC01742, MTCO2P1, 253 more genes
    nsv5673183copy number variation1nstd102humanLikely pathogenic GRCh37 chr20: 62,292,641-62,327,221 , GRCh38.p12 chr20: 63,661,288-63,695,868 TNFRSF6B, RTEL1, 1 more genes
    nsv5562694sequence alteration1nstd206human GRCh38 chr20: 63,525,502-63,937,515 , GRCh37.p13 chr20: 62,156,855-62,568,868 , STMN3, 26 more genes
    nsv5559866sequence alteration1nstd206human GRCh38 chr20: 62,865,770-63,725,218 , GRCh37.p13 chr20: 61,497,122-62,356,570 , PTK6, 46 more genes
    nsv5381223copy number variation2nstd102humanUncertain significance GRCh37 chr20: 60,831,241-62,664,346 , GRCh38.p12 chr20: 62,256,185-64,032,993 KCNQ2-AS1, HAR1B, 100 more genes
    nsv5293467copy number variation1nstd204human GRCh38.p13 chr20: 62,966,101-64,149,200 , GRCh37.p13 chr20: 61,597,453-62,780,553 , ZGPAT, 72 more genes
    nsv4729740copy number variation1nstd102humanPathogenic GRCh37 chr20: 61,975,605-62,915,555 , GRCh38.p12 chr20: 63,344,253-64,284,202 STMN3, KCNQ2-AS1, 53 more genes
    nsv4681029copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chr20: 61,977,556-62,562,941 , GRCh38.p12 chr20: 63,346,204-63,931,588 RNU1-134P, MIR941-5, 35 more genes
    nsv4676208copy number variation1nstd102humanPathogenic GRCh37 chr20: 61,152,321-62,915,555 , GRCh38.p12 chr20: 62,555,114-64,284,202 GMEB2, LOC105372727, 94 more genes
    nsv4676181copy number variation1nstd102humanPathogenic GRCh37 chr20: 56,788,101-62,762,405 , GRCh38.p12 chr20: 58,213,045-64,131,052 LOC105372697, MIR647, 174 more genes
    nsv4422849copy number variation1nstd174human GRCh37 chr20: 62,281,501-62,463,200 , GRCh38.p12 chr20: 63,650,148-63,831,847 , RTEL1, 9 more genes
    nsv3970619copy number variation1nstd168human GRCh38 chr20: 63,676,282-63,706,377 , GRCh37.p13 chr20: 62,307,635-62,337,729 ARFRP1, ZGPAT, 3 more genes
    nsv3969506insertion1nstd168human GRCh38 chr20: 63,663,060-63,723,741 , GRCh37.p13 chr20: 62,294,413-62,355,093 TNFRSF6B, ARFRP1, 3 more genes
    nsv3963570complex substitution1nstd168human GRCh37.p13 chr20: 62,297,863-62,338,203 , GRCh38 chr20: 63,666,510-63,706,851 TNFRSF6B, ARFRP1, 3 more genes
    nsv3924353copy number variation1nstd102humanPathogenic NCBI36 chr20: 59,335,000-62,379,123 , GRCh38 chr20: 61,326,549-64,277,326 , GRCh37 chr20: 59,901,605-62,908,679 PPDPF, CRMA, 126 more genes
    nsv3922908copy number variation1nstd102humanPathogenic NCBI36 chr20: 61,010,752-62,435,964 , GRCh37.p13 chr20: 61,540,307-62,965,520 , GRCh38.p12 chr20: 62,908,955-64,334,167 NPBWR2, ZBTB46, 78 more genes
    nsv3922590copy number variation1nstd102humanPathogenic NCBI36 chr20: 60,553,022-62,343,283 , GRCh38 chr20: 62,545,370-64,241,486 , GRCh37 chr20: 61,142,577-62,872,839 RPL7P3, BHLHE23, 95 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
    nsv3916789copy number variation1nstd102humanPathogenic GRCh37 chr20: 57,617,021-62,908,674 , GRCh38 chr20: 59,041,966-64,277,321 , NCBI36 chr20: 57,050,416-62,379,118 RNU7-141P, UCKL1, 153 more genes
    nsv3916713copy number variation2nstd102humanPathogenic, Likely pathogenic NCBI36 chr20: 61,300,817-62,379,118 , GRCh37 chr20: 61,830,372-62,908,674 , GRCh38 chr20: 63,199,020-64,277,321 CHRNA4, EEF1A2, 62 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