U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Search results

Items: 1 to 20 of 268

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv508853insertion3nstd49human GRCh38.p12 chr2: 104,791,117-104,833,091 , NCBI35 chr2: 104,866,093-104,908,067 , GRCh37.p13 chr2: 105,407,575-105,449,549 PANTR1
    nsv6691328copy number variation1nstd229human GRCh38 chr2: 104,814,601-104,822,200 , GRCh37.p13 chr2: 105,431,059-105,438,658 PANTR1
    nsv6693745copy number variation1nstd229human GRCh38 chr2: 104,799,736-104,806,340 , GRCh37.p13 chr2: 105,416,194-105,422,798 PANTR1
    nsv6696536copy number variation1nstd229human GRCh38 chr2: 104,817,450-104,820,539 , GRCh37.p13 chr2: 105,433,908-105,436,997 PANTR1
    nsv6681549copy number variation1nstd229human GRCh38 chr2: 104,847,281-104,847,311 , GRCh37.p13 chr2: 105,463,739-105,463,769 PANTR1
    nsv6339536copy number variation1nstd223human GRCh38 chr2: 104,816,524-104,818,022 , GRCh37.p13 chr2: 105,432,982-105,434,480 PANTR1
    nsv6354794copy number variation1nstd223human GRCh38 chr2: 104,856,801-104,857,500 , GRCh37.p13 chr2: 105,473,259-105,473,958 POU3F3
    nsv5442804copy number variation1nstd206human GRCh38 chr2: 104,816,469-104,818,042 , GRCh37.p13 chr2: 105,432,927-105,434,500 PANTR1
    nsv4786721copy number variation1nstd200human GRCh37 chr2: 105,432,952-105,434,460 , GRCh38.p12 chr2: 104,816,494-104,818,002 PANTR1
    nsv4052931copy number variation1nstd166human GRCh37.p13 chr2: 105,422,546-105,422,598 , GRCh38.p12 chr2: 104,806,088-104,806,140 PANTR1
    nsv3203352copy number variation1nstd152human GRCh38 chr2: 104,855,582-104,855,840 , GRCh37.p13 chr2: 105,472,040-105,472,298 POU3F3
    esv3825416copy number variation1estd219human GRCh37 chr2: 105,432,982-105,434,385 , GRCh38.p12 chr2: 104,816,524-104,817,927 PANTR1
    esv3591820copy number variation1estd214human GRCh37 chr2: 105,432,982-105,434,385 , GRCh38.p12 chr2: 104,816,524-104,817,927 PANTR1
    nsv1072960copy number variation1nstd99human GRCh37 chr2: 105,471,299-105,472,800 , GRCh38.p12 chr2: 104,854,841-104,856,342 POU3F3
    nsv1136303copy number variation1nstd106human GRCh37 chr2: 105,471,600-105,475,100 , GRCh38.p12 chr2: 104,855,142-104,858,642 POU3F3
    nsv1126557copy number variation1nstd106human GRCh37 chr2: 105,471,600-105,472,700 , GRCh38.p12 chr2: 104,855,142-104,856,242 POU3F3
    nsv1123364copy number variation1nstd106human GRCh37 chr2: 105,447,233-105,447,309 , GRCh38.p12 chr2: 104,830,775-104,830,851 PANTR1
    nsv1116777copy number variation1nstd106human GRCh37 chr2: 105,446,868-105,446,919 , GRCh38.p12 chr2: 104,830,410-104,830,461 PANTR1
    esv3016599copy number variation1estd209human GRCh37 chr2: 105,441,055-105,441,058 , GRCh38.p12 chr2: 104,824,597-104,824,600 PANTR1
    esv3016601copy number variation1estd209human GRCh37 chr2: 105,463,148-105,463,149 , GRCh38.p12 chr2: 104,846,690-104,846,691 PANTR1
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Search details

    See more...

    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