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Items: 1 to 20 of 302

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7050067inversion1nstd229human GRCh38 chr3: 14,975,618-14,986,766 , GRCh37.p13 chr3: 15,017,125-15,028,273 NR2C2
    nsv7046618inversion1nstd229human GRCh38 chr3: 15,003,519-15,003,558 , GRCh37.p13 chr3: 15,045,026-15,045,065 NR2C2
    nsv7045040inversion1nstd229human GRCh38 chr3: 15,001,366-15,001,504 , GRCh37.p13 chr3: 15,042,873-15,043,011 NR2C2
    nsv7041160inversion1nstd229human GRCh38 chr3: 15,006,447-15,006,513 , GRCh37.p13 chr3: 15,047,954-15,048,020 NR2C2
    nsv6717823copy number variation1nstd229human GRCh38 chr3: 14,971,056-14,971,848 , GRCh37.p13 chr3: 15,012,563-15,013,355 NR2C2
    nsv6716998copy number variation1nstd229human GRCh38 chr3: 15,018,201-15,075,400 , GRCh37.p13 chr3: 15,059,708-15,116,907 RBSN, NR2C2, 1 more genes
    nsv6715984copy number variation1nstd229human GRCh38 chr3: 15,044,392-15,065,048 , GRCh37.p13 chr3: 15,085,899-15,106,555 NR2C2, MRPS25
    nsv6715123copy number variation1nstd229human GRCh38 chr3: 14,989,401-14,994,406 , GRCh37.p13 chr3: 15,030,908-15,035,913 NR2C2
    nsv6714404copy number variation1nstd229human GRCh38 chr3: 14,951,614-14,956,395 , GRCh37.p13 chr3: 14,993,121-14,997,902 NR2C2
    nsv6712034copy number variation1nstd229human GRCh38 chr3: 14,670,901-15,564,100 , GRCh37.p13 chr3: 14,712,408-15,605,607 COLQ, RNU6-1024P, 22 more genes
    nsv6711601copy number variation1nstd229human GRCh38 chr3: 14,965,523-14,973,250 , GRCh37.p13 chr3: 15,007,030-15,014,757 NR2C2
    nsv6708950copy number variation1nstd229human GRCh38 chr3: 15,020,513-15,020,906 , GRCh37.p13 chr3: 15,062,020-15,062,413 NR2C2
    nsv6700878copy number variation1nstd229human GRCh38 chr3: 14,962,401-15,023,400 , GRCh37.p13 chr3: 15,003,908-15,064,907 NR2C2
    nsv6634367copy number variation1nstd102humanPathogenic GRCh37 chr3: 13,836,340-25,357,427 , GRCh38.p12 chr3: 13,794,843-25,315,936 TMEM43, SLC6A6, 132 more genes
    nsv6545132inversion1nstd223human GRCh38 chr3: 15,018,023-15,019,017 , GRCh37.p13 chr3: 15,059,530-15,060,524 NR2C2
    nsv6537825inversion1nstd223human GRCh38 chr3: 15,005,505-15,006,118 , GRCh37.p13 chr3: 15,047,012-15,047,625 NR2C2
    nsv6374923copy number variation1nstd223human GRCh38 chr3: 15,005,033-15,006,924 , GRCh37.p13 chr3: 15,046,540-15,048,431 NR2C2
    nsv6372440copy number variation1nstd223human GRCh38 chr3: 14,978,706-14,979,082 , GRCh37.p13 chr3: 15,020,213-15,020,589 NR2C2
    nsv6367471copy number variation1nstd223human GRCh38 chr3: 14,946,001-14,949,400 , GRCh37.p13 chr3: 14,987,508-14,990,907 NR2C2, FGD5-AS1
    nsv6366178copy number variation1nstd223human GRCh38 chr3: 15,032,564-15,033,092 , GRCh37.p13 chr3: 15,074,071-15,074,599 NR2C2
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