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Items: 1 to 20 of 465

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095441copy number variation1nstd102humanUncertain significance GRCh37 chr18: 29,645,845-29,648,347 , GRCh38.p12 chr18: 32,065,882-32,068,384 RNF125
    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
    nsv7094933copy number variation1nstd102humanUncertain significance GRCh37 chr18: 29,598,827-29,648,347 , GRCh38.p12 chr18: 32,018,864-32,068,384 RNF125, HMGN2P44
    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
    nsv7070057inversion1nstd229human GRCh38 chr18: 32,031,487-32,031,567 , GRCh37.p13 chr18: 29,611,450-29,611,530 RNF125, HMGN2P44
    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
    nsv7012998copy number variation1nstd229human GRCh38 chr18: 32,051,934-32,054,249 , GRCh37.p13 chr18: 29,631,897-29,634,212 RNF125
    nsv7012011copy number variation1nstd229human GRCh38 chr18: 32,019,864-32,123,267 , GRCh37.p13 chr18: 29,599,827-29,703,230 RNF138, HMGN2P44, 2 more genes
    nsv7011745copy number variation1nstd229human GRCh38 chr18: 32,086,517-32,098,372 , GRCh37.p13 chr18: 29,666,480-29,678,335 RNF125, RNF138
    nsv7010652copy number variation1nstd229human GRCh38 chr18: 32,081,671-32,084,445 , GRCh37.p13 chr18: 29,661,634-29,664,408 RNF125
    nsv7008596copy number variation1nstd229human GRCh38 chr18: 32,031,103-32,044,372 , GRCh37.p13 chr18: 29,611,066-29,624,335 RNF125, HMGN2P44
    nsv7008256copy number variation1nstd229human GRCh38 chr18: 32,055,745-32,163,262 , GRCh37.p13 chr18: 29,635,708-29,743,225 RNF138, RPS15AP35, 1 more genes
    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
    nsv7002676copy number variation1nstd229human GRCh38 chr18: 32,056,715-32,065,962 , GRCh37.p13 chr18: 29,636,678-29,645,925 RNF125
    nsv7001888copy number variation1nstd229human GRCh38 chr18: 31,952,405-32,070,751 , GRCh37.p13 chr18: 29,532,368-29,650,714 HMGN2P44, PGDP1, 2 more genes
    nsv7000620copy number variation1nstd229human GRCh38 chr18: 32,025,585-32,029,508 , GRCh37.p13 chr18: 29,605,548-29,609,471 RNF125
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