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 454

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6127999copy number variation1nstd186human GRCh37 chr20: 61,347,850-61,347,967 , GRCh38.p12 chr20: 62,716,498-62,716,615 , NTSR1
    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
    nsv5959193copy number variation1nstd209human GRCh38 chr20: 62,747,304-62,747,483 , GRCh37.p13 chr20: 61,378,656-61,378,835 NTSR1
    nsv5958709copy number variation1nstd209human GRCh38 chr20: 62,738,179-62,738,231 , GRCh37.p13 chr20: 61,369,531-61,369,583 NTSR1
    nsv5952059copy number variation1nstd209human GRCh38 chr20: 62,715,072-62,717,608 , GRCh37.p13 chr20: 61,346,424-61,348,960 , NTSR1
    nsv5948005copy number variation1nstd209human GRCh38 chr20: 62,741,271-62,743,418 , GRCh37.p13 chr20: 61,372,623-61,374,770 NTSR1
    nsv5885566copy number variation1nstd209human GRCh38 chr20: 62,715,033-62,717,832 , GRCh37.p13 chr20: 61,346,385-61,349,184 , NTSR1
    nsv5873183copy number variation1nstd209human GRCh38 chr20: 62,741,265-62,743,403 , GRCh37.p13 chr20: 61,372,617-61,374,755 NTSR1
    nsv5869649copy number variation2nstd209human GRCh38 chr20: 62,743,404-62,744,503 , GRCh37.p13 chr20: 61,374,756-61,375,855 NTSR1
    nsv5672380insertion1nstd207human GRCh38 chr20: 62,755,413-62,755,413 , GRCh37.p13 chr20: 61,386,765-61,386,765 NTSR1
    nsv5672098insertion1nstd207human GRCh38 chr20: 62,740,469-62,740,469 , GRCh37.p13 chr20: 61,371,821-61,371,821 NTSR1
    nsv5671084insertion1nstd207human GRCh38 chr20: 62,755,221-62,755,221 , GRCh37.p13 chr20: 61,386,573-61,386,573 NTSR1
    nsv5669788insertion1nstd207human GRCh38 chr20: 62,716,605-62,716,605 , GRCh37.p13 chr20: 61,347,957-61,347,957 , NTSR1
    nsv5669520insertion2nstd207human GRCh38 chr20: 62,755,580-62,755,580 , GRCh37.p13 chr20: 61,386,932-61,386,932 NTSR1
    nsv5668690insertion1nstd207human GRCh38 chr20: 62,755,061-62,755,061 , GRCh37.p13 chr20: 61,386,413-61,386,413 NTSR1
    nsv5667219insertion1nstd207human GRCh38 chr20: 62,738,024-62,738,024 , GRCh37.p13 chr20: 61,369,376-61,369,376 NTSR1
    nsv5665173insertion1nstd207human GRCh38 chr20: 62,755,722-62,755,722 , GRCh37.p13 chr20: 61,387,074-61,387,074 NTSR1
    nsv5595041copy number variation1nstd207human GRCh38 chr20: 62,740,309-62,740,383 , GRCh37.p13 chr20: 61,371,661-61,371,735 NTSR1
    nsv5591092copy number variation1nstd207human GRCh38 chr20: 62,747,309-62,747,491 , GRCh37.p13 chr20: 61,378,661-61,378,843 NTSR1
    nsv5585018copy number variation1nstd207human GRCh38 chr20: 62,741,271-62,743,418 , GRCh37.p13 chr20: 61,372,623-61,374,770 NTSR1
    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