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 866

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7146869insertion1nstd232human GRCh37.p13 chr2: 45,641,924-45,641,924 , GRCh38.p12 chr2: 45,414,785-45,414,785 SRBD1
    nsv7145304insertion1nstd232human GRCh37.p13 chr2: 45,814,107-45,814,107 , GRCh38.p12 chr2: 45,586,968-45,586,968 SRBD1
    nsv7096653copy number variation1nstd102humanUncertain significance GRCh37 chr2: 38,121,051-47,710,088 , GRCh38.p12 chr2: 37,893,908-47,482,949 PLEKHH2, RNU6-566P, 151 more genes
    nsv7057350inversion1nstd229human GRCh38 chr2: 45,603,869-45,603,892 , GRCh37.p13 chr2: 45,831,008-45,831,031 SRBD1
    nsv7053897inversion1nstd229human GRCh38 chr2: 45,503,709-45,689,801 , GRCh37.p13 chr2: 45,730,848-45,916,940 PRKCE-AS1, RN7SL414P, 3 more genes
    nsv7039759inversion1nstd229human GRCh38 chr2: 39,986,388-47,339,194 , GRCh37.p13 chr2: 40,213,528-47,566,333 RPL36AP14, CRIPT, 105 more genes
    nsv7038088inversion1nstd229human GRCh38 chr2: 45,443,862-45,448,581 , GRCh37.p13 chr2: 45,671,001-45,675,720 SRBD1
    nsv6677512copy number variation1nstd229human GRCh38 chr2: 45,596,135-45,635,179 , GRCh37.p13 chr2: 45,823,274-45,862,318 SRBD1
    nsv6677451copy number variation1nstd229human GRCh38 chr2: 45,495,120-45,498,756 , GRCh37.p13 chr2: 45,722,259-45,725,895 SRBD1
    nsv6674984copy number variation1nstd229human GRCh38 chr2: 45,427,301-45,431,100 , GRCh37.p13 chr2: 45,654,440-45,658,239 SRBD1
    nsv6674919copy number variation1nstd229human GRCh38 chr2: 45,587,901-45,641,700 , GRCh37.p13 chr2: 45,815,040-45,868,839 SRBD1
    nsv6674789copy number variation1nstd229human GRCh38 chr2: 45,442,939-45,700,735 , GRCh37.p13 chr2: 45,670,078-45,927,874 LOC102724965, PRKCE-AS1, 3 more genes
    nsv6674691copy number variation1nstd229human GRCh38 chr2: 45,507,700-45,513,843 , GRCh37.p13 chr2: 45,734,839-45,740,982 SRBD1
    nsv6673128copy number variation1nstd229human GRCh38 chr2: 45,524,098-45,527,483 , GRCh37.p13 chr2: 45,751,237-45,754,622 SRBD1
    nsv6671923copy number variation1nstd229human GRCh38 chr2: 45,181,670-45,749,104 , GRCh37.p13 chr2: 45,408,809-45,976,243 TRQ-TTG5-1, LINC01121, 7 more genes
    nsv6671772copy number variation1nstd229human GRCh38 chr2: 45,425,601-45,562,800 , GRCh37.p13 chr2: 45,652,740-45,789,939 SRBD1
    nsv6671719copy number variation1nstd229human GRCh38 chr2: 45,590,525-45,595,752 , GRCh37.p13 chr2: 45,817,664-45,822,891 SRBD1
    nsv6671637copy number variation1nstd229human GRCh38 chr2: 45,466,508-45,472,566 , GRCh37.p13 chr2: 45,693,647-45,699,705 SRBD1
    nsv6671367copy number variation1nstd229human GRCh38 chr2: 45,454,201-45,472,100 , GRCh37.p13 chr2: 45,681,340-45,699,239 SRBD1
    nsv6670248copy number variation1nstd229human GRCh38 chr2: 45,517,762-45,521,451 , GRCh37.p13 chr2: 45,744,901-45,748,590 SRBD1
    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