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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4675267copy number variation1nstd102humanUncertain significance GRCh37 chr15: 34,348,337-34,404,263 , GRCh38.p12 chr15: 34,056,136-34,112,062 EMC7, AVEN, 3 more genes
    nsv3916249copy number variation1nstd102humanPathogenic NCBI36 chr15: 21,173,967-100,338,915 , GRCh37.p13 chr15: 23,622,526-102,521,392 , GRCh38.p12 chr15: 23,377,379-101,981,189 EMC7, H3P40, 1616 more genes
    nsv3919468copy number variation1nstd102humanPathogenic NCBI36 chr15: 26,996,912-100,338,915 , GRCh37.p13 chr15: 29,209,620-102,521,392 , GRCh38.p12 chr15: 28,917,417-101,981,189 EMC7, RNU6-18P, 1442 more genes
    nsv3917652copy number variation1nstd102humanPathogenic NCBI36 chr15: 20,249,886-36,169,075 , GRCh38 chr15: 23,319,714-38,089,582 , GRCh37 chr15: 22,698,522-38,381,783 EMC7, LOC105370764, 345 more genes
    nsv4674936copy number variation1nstd102humanPathogenic GRCh37 chr15: 22,770,421-36,861,479 , GRCh38.p12 chr15: 23,319,714-36,569,278 EMC7, SNORD115-48, 330 more genes
    nsv3921026copy number variation1nstd102humanPathogenic NCBI36 chr15: 22,830,109-35,283,797 , GRCh38 chr15: 25,033,869-37,204,304 , GRCh37 chr15: 25,279,016-37,496,505 EMC7, SNORD116-17, 303 more genes
    nsv3915967copy number variation1nstd102humanPathogenic GRCh38 chr15: 32,635,803-40,233,825 , GRCh37 chr15: 32,928,004-40,526,026 , NCBI36 chr15: 30,715,296-38,313,318 EMC7, ANP32AP1, 112 more genes
    nsv3920384copy number variation1nstd102humanPathogenic NCBI36 chr15: 30,405,629-37,473,561 , GRCh38 chr15: 32,326,136-39,394,068 , GRCh37 chr15: 32,618,337-39,686,269 EMC7, PGBD4, 113 more genes
    nsv6315190copy number variation1nstd102humanPathogenic GRCh37 chr15: 33,809,650-40,027,263 , GRCh38.p12 chr15: 33,517,449-39,735,062 EMC7, RYR3, 84 more genes
    nsv4675391copy number variation1nstd102humanPathogenic GRCh37 chr15: 34,197,488-38,656,254 , GRCh38.p12 chr15: 33,905,287-38,364,053 EMC7, TPST2P1, 65 more genes
    nsv4675702copy number variation1nstd102humanPathogenic GRCh37 chr15: 31,675,452-35,689,958 , GRCh38.p12 chr15: 31,383,249-35,397,757 , GRCh38.p12 chr15|NT_187660.1: 2,721,316-5,161,414 EMC7, AVEN, 113 more genes
    nsv3900281copy number variation1nstd102humanPathogenic GRCh37 chr15: 20,016,811-102,493,540 , GRCh38.p12 chr15: 19,811,558-101,953,337 EMC7, MYZAP, 1750 more genes
    nsv3913581copy number variation1nstd102humanPathogenic NCBI36 chr15: 18,323,354-100,338,915 , GRCh37.p13 chr15: 20,063,340-102,521,392 , GRCh38.p12 chr15: 19,858,087-101,981,189 EMC7, MIR4513, 1754 more genes
    nsv3904086copy number variation1nstd102humanPathogenic GRCh37 chr15: 20,071,673-102,461,162 , GRCh38.p12 chr15: 19,866,420-101,920,959 EMC7, TMEM202, 1747 more genes
    nsv3905138copy number variation1nstd102humanPathogenic GRCh37 chr15: 20,733,395-102,511,616 , GRCh38.p12 chr15: 20,528,156-101,971,413 EMC7, FES, 1738 more genes
    nsv3892955copy number variation2nstd102humanPathogenic GRCh37 chr15: 22,770,422-102,429,112 , GRCh38.p12 chr15: 23,319,714-101,888,909 EMC7, FAM81A, 1614 more genes
    nsv3876912copy number variation1nstd102humanPathogenic GRCh37 chr15: 31,115,047-102,354,857 , GRCh38.p12 chr15: 30,822,844-101,814,654 EMC7, RNU6-953P, 1385 more genes
    nsv3912885copy number variation1nstd102humanPathogenic GRCh38 chr15: 23,319,714-38,545,325 , NCBI36 chr15: 20,316,992-36,624,818 , GRCh37 chr15: 22,765,628-38,837,526 EMC7, LOC105370773, 350 more genes
    nsv3921227copy number variation1nstd102humanPathogenic NCBI36 chr15: 30,686,791-33,279,922 , GRCh37 chr15: 32,899,499-35,492,630 , GRCh38 chr15: 32,607,298-35,200,429 EMC7, TMCO5B, 52 more genes
    nsv6634442copy number variation1nstd102humanPathogenic GRCh37 chr15: 32,915,722-34,671,601 , GRCh38.p12 chr15: 32,623,521-34,379,400 EMC7, KATNBL1, 27 more genes
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