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 236

    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
    nsv6667108copy number variation1nstd229human GRCh38 chr2: 46,596,979-46,622,620 , GRCh37.p13 chr2: 46,824,118-46,849,759 PIGF, CRIPT
    nsv6666857copy number variation1nstd229human GRCh38 chr2: 46,604,801-46,611,400 , GRCh37.p13 chr2: 46,831,940-46,838,539 PIGF
    nsv6666729copy number variation1nstd229human GRCh38 chr2: 46,584,901-46,591,000 , GRCh37.p13 chr2: 46,812,040-46,818,139 RHOQ, PIGF
    nsv6665632copy number variation1nstd229human GRCh38 chr2: 46,611,003-46,666,172 , GRCh37.p13 chr2: 46,838,142-46,893,311 LOC105374584, CRIPT, 1 more genes
    nsv6664781copy number variation1nstd229human GRCh38 chr2: 46,615,401-46,628,800 , GRCh37.p13 chr2: 46,842,540-46,855,939 PIGF, CRIPT
    nsv6658586copy number variation1nstd229human GRCh38 chr2: 46,614,677-46,614,998 , GRCh37.p13 chr2: 46,841,816-46,842,137 PIGF
    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
    nsv6540920inversion1nstd223human GRCh38 chr2: 46,594,632-46,595,927 , GRCh37.p13 chr2: 46,821,771-46,823,066 PIGF
    nsv6537703inversion1nstd223human GRCh38 chr2: 46,610,548-46,611,429 , GRCh37.p13 chr2: 46,837,687-46,838,568 PIGF
    nsv6351322copy number variation1nstd223human GRCh38 chr2: 46,589,601-46,590,500 , GRCh37.p13 chr2: 46,816,740-46,817,639 PIGF
    nsv6346023copy number variation1nstd223human GRCh38 chr2: 46,612,600-46,618,149 , GRCh37.p13 chr2: 46,839,739-46,845,288 CRIPT, PIGF
    nsv6339220copy number variation1nstd223human GRCh38 chr2: 46,582,001-46,584,700 , GRCh37.p13 chr2: 46,809,140-46,811,839 PIGF, RHOQ
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 more genes
    nsv6315248copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 46,844,310-46,845,911 , GRCh38.p12 chr2: 46,617,171-46,618,772 PIGF, CRIPT
    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
    nsv6134459copy number variation1nstd213human GRCh37 chr2: 40,080,000-50,820,001 , GRCh38.p12 chr2: 39,852,860-50,592,863 , BCYRN1, 149 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