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 253

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096876copy number variation1nstd102humanUncertain significance GRCh37 chr2: 46,525,051-46,851,366 , GRCh38.p12 chr2: 46,297,912-46,624,227 TMEM247, CRIPT, 8 more genes
    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
    nsv7039759inversion1nstd229human GRCh38 chr2: 39,986,388-47,339,194 , GRCh37.p13 chr2: 40,213,528-47,566,333 RPL36AP14, CRIPT, 105 more genes
    nsv6671921copy number variation1nstd229human GRCh38 chr2: 46,310,701-46,704,700 , GRCh37.p13 chr2: 46,537,840-46,931,839 SOCS5, LINC02583, 10 more genes
    nsv6671656copy number variation1nstd229human GRCh38 chr2: 46,527,522-46,527,621 , GRCh37.p13 chr2: 46,754,661-46,754,760 ATP6V1E2
    nsv6669812copy number variation1nstd229human GRCh38 chr2: 46,511,187-46,514,342 , GRCh37.p13 chr2: 46,738,326-46,741,481 ATP6V1E2
    nsv6667147copy number variation1nstd229human GRCh38 chr2: 46,497,685-46,520,733 , GRCh37.p13 chr2: 46,724,824-46,747,872 ATP6V1E2
    nsv6662809copy number variation1nstd229human GRCh38 chr2: 46,464,801-46,510,600 , GRCh37.p13 chr2: 46,691,940-46,737,739 TMEM247, ATP6V1E2
    nsv6634330copy number variation1nstd102humanPathogenic GRCh37 chr2: 11,504,318-111,365,996 , GRCh38.p12 chr2: 11,364,192-110,608,419 CYP1B1-AS1, LOC107985771, 1649 more genes
    nsv6343741copy number variation1nstd223human GRCh38 chr2: 46,511,497-46,517,266 , GRCh37.p13 chr2: 46,738,636-46,744,405 ATP6V1E2
    nsv6337353copy number variation1nstd223human GRCh38 chr2: 46,534,858-46,542,789 , GRCh37.p13 chr2: 46,761,997-46,769,928 RHOQ, ATP6V1E2
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 more genes
    nsv6314726copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 40,607,042-146,902,764 , GRCh38.p12 chr2: 40,379,902-146,145,196 ACTG2, ACYP2, 1713 more genes
    nsv6298136copy number variation1nstd186human GRCh37 chr2: 46,769,727-46,769,916 , GRCh38.p12 chr2: 46,542,588-46,542,777 ATP6V1E2, RHOQ
    nsv6161295copy number variation1nstd214human GRCh38 chr2: 46,524,061-46,524,171 , GRCh37.p13 chr2: 46,751,200-46,751,310 ATP6V1E2
    nsv6134459copy number variation1nstd213human GRCh37 chr2: 40,080,000-50,820,001 , GRCh38.p12 chr2: 39,852,860-50,592,863 , BCYRN1, 149 more genes
    nsv6134458copy number variation2nstd213human GRCh37 chr2: 38,440,000-47,670,001 , GRCh38.p12 chr2: 38,212,858-47,442,862 ASS1P2, BCYRN1, 144 more genes
    nsv6134457copy number variation1nstd213human GRCh37 chr2: 38,410,000-75,540,001 , GRCh38.p12 chr2: 38,182,858-75,312,875 , ACTG2, 598 more genes
    nsv5885855copy number variation1nstd209human GRCh38 chr2: 46,524,048-46,524,169 , GRCh37.p13 chr2: 46,751,187-46,751,308 ATP6V1E2
    nsv5691976mobile element insertion1nstd211human GRCh38 chr2: 46,510,082-46,510,082 , GRCh37.p13 chr2: 46,737,221-46,737,221 ATP6V1E2
    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