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 560

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7147560insertion1nstd232human GRCh37.p13 chr21: 16,403,226-16,403,226 , GRCh38.p12 chr21: 15,030,905-15,030,905 NRIP1
    nsv7139741copy number variation1nstd232human GRCh37.p13 chr21: 16,403,374-16,403,423 , GRCh38.p12 chr21: 15,031,053-15,031,102 NRIP1
    nsv7096276copy number variation1nstd102humanUncertain significance GRCh37 chr21: 15,554,059-16,340,513 , GRCh38.p12 chr21: 14,181,738-14,968,192 RBM11, LIPI, 11 more genes
    nsv7076188inversion1nstd229human GRCh38 chr21: 14,984,870-16,542,052 , GRCh37.p13 chr21: 16,357,191-17,914,372 SNORD74B, LOC105369292, 15 more genes
    nsv7073485inversion1nstd229human GRCh38 chr21: 14,904,480-15,065,549 , GRCh37.p13 chr21: 16,276,801-16,437,870 NRIP1, ASMER1
    nsv7072035inversion1nstd229human GRCh38 chr21: 14,943,219-15,864,162 , GRCh37.p13 chr21: 16,315,540-17,236,481 CYCSP42, LOC105369292, 8 more genes
    nsv7072003inversion1nstd229human GRCh38 chr21: 15,042,882-16,498,344 , GRCh37.p13 chr21: 16,415,203-17,870,664 MIR99AHG, SNORD74B, 13 more genes
    nsv7070632inversion1nstd229human GRCh38 chr21: 15,065,686-15,109,219 , GRCh37.p13 chr21: 16,438,007-16,481,540 NRIP1, LOC107985483
    nsv7069212inversion1nstd229human GRCh38 chr21: 14,923,958-16,588,073 , GRCh37.p13 chr21: 16,296,279-17,960,393 CYCSP42, RPS26P5, 15 more genes
    nsv7068994inversion1nstd229human GRCh38 chr21: 15,028,133-16,586,715 , GRCh37.p13 chr21: 16,400,454-17,959,035 MIRLET7C, RNU6-426P, 15 more genes
    nsv7064004inversion1nstd229human GRCh38 chr21: 14,912,129-14,973,079 , GRCh37.p13 chr21: 16,284,450-16,345,400 NRIP1, ASMER1
    nsv7063563inversion1nstd229human GRCh38 chr21: 15,011,848-16,566,835 , GRCh37.p13 chr21: 16,384,169-17,939,155 LOC107985483, RBPMSLP, 15 more genes
    nsv7063499inversion1nstd229human GRCh38 chr21: 15,027,866-16,585,199 , GRCh37.p13 chr21: 16,400,187-17,957,519 VDAC2P1, LOC107985483, 15 more genes
    nsv7062471inversion1nstd229human GRCh38 chr21: 14,989,337-16,214,615 , GRCh37.p13 chr21: 16,361,658-17,586,935 NRIP1, LOC107985483, 12 more genes
    nsv7035537copy number variation1nstd229human GRCh38 chr21: 14,969,399-14,974,606 , GRCh37.p13 chr21: 16,341,720-16,346,927 NRIP1
    nsv7034506copy number variation1nstd229human GRCh38 chr21: 15,065,641-15,066,088 , GRCh37.p13 chr21: 16,437,962-16,438,409 NRIP1
    nsv7032019copy number variation1nstd229human GRCh38 chr21: 15,023,769-15,026,843 , GRCh37.p13 chr21: 16,396,090-16,399,164 NRIP1
    nsv7031722copy number variation1nstd229human GRCh38 chr21: 14,997,067-14,997,428 , GRCh37.p13 chr21: 16,369,388-16,369,749 NRIP1
    nsv7029378copy number variation1nstd229human GRCh38 chr21: 14,980,266-14,980,613 , GRCh37.p13 chr21: 16,352,587-16,352,934 NRIP1
    nsv7027840copy number variation1nstd229human GRCh38 chr21: 14,377,890-22,678,900 , GRCh37.p13 chr21: 15,750,211-24,051,220 C1QBPP1, VDAC2P1, 74 more genes
    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