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 180

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5708433mobile element insertion1nstd211human GRCh38 chr10: 38,014,063-38,014,063 , GRCh37.p13 chr10: 38,302,991-38,302,991 ZNF33A
    nsv5638214insertion1nstd207human GRCh38 chr10: 38,027,170-38,027,170 , GRCh37.p13 chr10: 38,316,098-38,316,098 ZNF33A
    nsv5635269insertion1nstd207human GRCh38 chr10: 38,063,979-38,063,979 , GRCh37.p13 chr10: 38,352,907-38,352,907 ZNF33A
    nsv5631688insertion1nstd207human GRCh38 chr10: 38,018,937-38,018,937 , GRCh37.p13 chr10: 38,307,865-38,307,865 ZNF33A
    nsv5631581insertion1nstd207human GRCh38 chr10: 38,021,423-38,021,423 , GRCh37.p13 chr10: 38,310,351-38,310,351 ZNF33A
    nsv5600146copy number variation1nstd207human GRCh38 chr10: 38,018,936-38,019,482 , GRCh37.p13 chr10: 38,307,864-38,308,410 ZNF33A
    nsv5594038copy number variation1nstd207human GRCh38 chr10: 38,043,205-38,043,679 , GRCh37.p13 chr10: 38,332,133-38,332,607 RNU6-795P, ZNF33A
    nsv5591038copy number variation1nstd207human GRCh38 chr10: 38,058,499-38,058,604 , GRCh37.p13 chr10: 38,347,427-38,347,532 ZNF33A
    nsv5585042copy number variation1nstd207human GRCh38 chr10: 38,043,670-38,043,773 , GRCh37.p13 chr10: 38,332,598-38,332,701 RNU6-795P, ZNF33A
    nsv5540983insertion1nstd206human GRCh38 chr10: 38,021,423-38,021,423 , GRCh37.p13 chr10: 38,310,351-38,310,351 ZNF33A
    nsv5135575mobile element insertion1nstd203human GRCh38 chr10: 38,021,376-38,021,423 , GRCh37.p13 chr10: 38,310,304-38,310,351 ZNF33A
    nsv5035636inversion1nstd200human GRCh38 chr10: 32,580,256-50,959,654 , GRCh37.p13 chr10: 32,869,184-52,719,414 , ZNF32-AS2, 320 more genes
    nsv5033632inversion1nstd200human GRCh38 chr10: 36,819,152-58,318,428 , GRCh37.p13 chr10: 37,108,080-60,078,188 , LOC107001062, 306 more genes
    nsv4988771copy number variation1nstd200human GRCh38 chr10: 37,648,412-38,162,310 , GRCh37.p13 chr10: 37,937,340-38,451,238 , ZNF25, 12 more genes
    nsv4986267copy number variation1nstd200human GRCh38 chr10: 38,066,309-38,066,360 , GRCh37.p13 chr10: 38,355,237-38,355,288 ZNF33A
    nsv4870857inversion1nstd200human GRCh37 chr10: 37,108,081-60,078,188 , GRCh38.p12 chr10: 36,819,153-58,318,428 , NCOA4, 306 more genes
    nsv4843698copy number variation1nstd200human GRCh37 chr10: 38,355,237-38,355,288 , GRCh38.p12 chr10: 38,066,309-38,066,360 ZNF33A
    nsv4768937insertion1nstd186human GRCh37 chr10: 38,310,352-38,310,352 , GRCh38.p12 chr10: 38,021,424-38,021,424 ZNF33A
    nsv4762460insertion1nstd199human GRCh37 chr10: 38,310,349-38,310,349 , GRCh38.p12 chr10: 38,021,421-38,021,421 ZNF33A
    nsv4685229insertion1nstd194human GRCh37 chr10: 38,310,352-38,310,352 , GRCh38.p12 chr10: 38,021,424-38,021,424 ZNF33A
    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