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Items: 1 to 20 of 540

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095440copy number variation1nstd102humanUncertain significance GRCh37 chr18: 28,647,981-29,648,347 , GRCh38.p12 chr18: 31,068,015-32,068,384 RNU6-167P, LOC390846, 22 more genes
    nsv7076177inversion1nstd229human GRCh38 chr18: 31,871,875-31,871,958 , GRCh37.p13 chr18: 29,451,838-29,451,921 TRAPPC8
    nsv7074645inversion1nstd229human GRCh38 chr18: 30,537,670-35,063,371 , GRCh37.p13 chr18: 28,117,636-32,643,335 DSC1, RN7SKP44, 46 more genes
    nsv7071971inversion1nstd229human GRCh38 chr18: 31,938,930-32,318,381 , GRCh37.p13 chr18: 29,518,893-29,898,344 TRAPPC8, RNA5SP453, 9 more genes
    nsv7071421inversion1nstd229human GRCh38 chr18: 31,321,802-32,119,916 , GRCh37.p13 chr18: 28,901,765-29,699,879 TTR, B4GALT6, 20 more genes
    nsv7070163inversion1nstd229human GRCh38 chr18: 31,760,869-32,125,867 , GRCh37.p13 chr18: 29,340,832-29,705,830 HMGN2P44, RNF138, 8 more genes
    nsv7069546inversion1nstd229human GRCh38 chr18: 31,852,982-31,853,032 , GRCh37.p13 chr18: 29,432,945-29,432,995 TRAPPC8
    nsv7064867inversion1nstd229human GRCh38 chr18: 31,692,782-32,067,362 , GRCh37.p13 chr18: 29,272,745-29,647,325 LOC100421591, LOC390846, 10 more genes
    nsv7059881inversion1nstd229human GRCh38 chr18: 31,754,105-32,126,675 , GRCh37.p13 chr18: 29,334,068-29,706,638 LOC100287539, PGDP1, 8 more genes
    nsv7058542inversion1nstd229human GRCh38 chr18: 31,933,803-31,933,858 , GRCh37.p13 chr18: 29,513,766-29,513,821 TRAPPC8
    nsv7017321copy number variation1nstd229human GRCh38 chr18: 31,918,281-31,918,735 , GRCh37.p13 chr18: 29,498,244-29,498,698 TRAPPC8
    nsv7016008copy number variation1nstd229human GRCh38 chr18: 31,925,460-31,928,552 , GRCh37.p13 chr18: 29,505,423-29,508,515 TRAPPC8
    nsv7015782copy number variation1nstd229human GRCh38 chr18: 31,911,401-31,973,100 , GRCh37.p13 chr18: 29,491,364-29,553,063 LOC100287539, PGDP1, 2 more genes
    nsv7015144copy number variation1nstd229human GRCh38 chr18: 31,754,101-31,938,900 , GRCh37.p13 chr18: 29,334,064-29,518,863 TRAPPC8, LOC100421591, 2 more genes
    nsv7015077copy number variation1nstd229human GRCh38 chr18: 31,940,584-31,940,911 , GRCh37.p13 chr18: 29,520,547-29,520,874 TRAPPC8
    nsv7009944copy number variation1nstd229human GRCh38 chr18: 31,918,119-31,927,891 , GRCh37.p13 chr18: 29,498,082-29,507,854 TRAPPC8
    nsv7006288copy number variation1nstd229human GRCh38 chr18: 31,887,560-31,889,831 , GRCh37.p13 chr18: 29,467,523-29,469,794 TRAPPC8
    nsv7005602copy number variation1nstd229human GRCh38 chr18: 31,881,743-31,882,204 , GRCh37.p13 chr18: 29,461,706-29,462,167 TRAPPC8, LOC100421591
    nsv7004076copy number variation1nstd229human GRCh38 chr18: 31,888,813-32,220,544 , GRCh37.p13 chr18: 29,468,776-29,800,507 TRAPPC8, RNU6-1050P, 9 more genes
    nsv6637941copy number variation1nstd102humanUncertain significance GRCh37 chr18: 29,152,719-29,422,344 , GRCh38.p12 chr18: 31,572,756-31,842,381 B4GALT6, LRRC37A7P, 5 more genes
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