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 135

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5555882sequence alteration1nstd206human GRCh38 chr19: 45,580,124-46,272,839 , GRCh37.p13 chr19: 46,083,382-46,776,096 , SYMPK, 39 more genes
    nsv5524310copy number variation1nstd206human GRCh38 chr19: 46,004,031-46,005,049 , GRCh37.p13 chr19: 46,507,289-46,508,307 CCDC61
    nsv5520230copy number variation1nstd206human GRCh38 chr19: 46,004,912-46,005,080 , GRCh37.p13 chr19: 46,508,170-46,508,338 CCDC61
    nsv5515679copy number variation1nstd206human GRCh38 chr19: 46,002,655-46,004,154 , GRCh37.p13 chr19: 46,505,913-46,507,412 CCDC61
    nsv5020738copy number variation1nstd200human GRCh38 chr19: 46,004,923-46,005,080 , GRCh37.p13 chr19: 46,508,181-46,508,338 CCDC61
    nsv5020737copy number variation1nstd200human GRCh38 chr19: 46,004,108-46,004,988 , GRCh37.p13 chr19: 46,507,366-46,508,246 CCDC61
    nsv5020736copy number variation1nstd200human GRCh38 chr19: 46,002,686-46,005,242 , GRCh37.p13 chr19: 46,505,944-46,508,500 CCDC61
    nsv5020735copy number variation1nstd200human GRCh38 chr19: 46,002,655-46,004,154 , GRCh37.p13 chr19: 46,505,913-46,507,412 CCDC61
    nsv5020734copy number variation1nstd200human GRCh38 chr19: 45,995,186-46,009,059 , GRCh37.p13 chr19: 46,498,444-46,512,317 CCDC61
    nsv4853114copy number variation1nstd200human GRCh37 chr19: 46,507,897-46,508,257 , GRCh38.p12 chr19: 46,004,639-46,004,999 CCDC61
    nsv4853113copy number variation1nstd200human GRCh37 chr19: 46,507,346-46,508,231 , GRCh38.p12 chr19: 46,004,088-46,004,973 CCDC61
    nsv4853112copy number variation1nstd200human GRCh37 chr19: 46,505,944-46,508,501 , GRCh38.p12 chr19: 46,002,686-46,005,243 CCDC61
    nsv4853111copy number variation1nstd200human GRCh37 chr19: 46,505,909-46,507,412 , GRCh38.p12 chr19: 46,002,651-46,004,154 CCDC61
    nsv4853110copy number variation1nstd200human GRCh37 chr19: 46,498,444-46,512,317 , GRCh38.p12 chr19: 45,995,186-46,009,059 CCDC61
    nsv4676357copy number variation1nstd102humanPathogenic GRCh37 chr19: 44,738,088-53,621,561 , GRCh38.p12 chr19: 44,233,935-53,118,308 MIR4324, KLK9, 485 more genes
    nsv4676350copy number variation1nstd102humanUncertain significance GRCh37 chr19: 45,531,056-48,174,177 , GRCh38.p12 chr19: 45,027,798-47,670,920 NKPD1, IGFL1, 112 more genes
    nsv4625503copy number variation1nstd183human GRCh37 chr19: 46,506,172-46,506,921 , GRCh38.p12 chr19: 46,002,914-46,003,663 CCDC61
    nsv4622765copy number variation1nstd183human GRCh37 chr19: 46,519,461-46,519,540 , GRCh38.p12 chr19: 46,016,203-46,016,282 CCDC61
    nsv4620710copy number variation1nstd183human GRCh37 chr19: 46,498,413-46,499,008 , GRCh38.p12 chr19: 45,995,155-45,995,750 CCDC61
    nsv4620709copy number variation2nstd183human GRCh37 chr19: 46,498,343-46,499,055 , GRCh38.p12 chr19: 45,995,085-45,995,797 CCDC61
    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