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Items: 1 to 20 of 577

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096465copy number variation1nstd102humanUncertain significance GRCh37 chr3: 38,495,814-38,991,853 , GRCh38.p12 chr3: 38,454,323-38,950,362 ACVR2B, LOC107986042, 8 more genes
    nsv7051268inversion1nstd229human GRCh38 chr3: 37,000,362-39,352,689 , GRCh37.p13 chr3: 37,041,853-39,394,180 PLCD1, RNU6-1227P, 59 more genes
    nsv7048850inversion1nstd229human GRCh38 chr3: 37,408,411-39,634,596 , GRCh37.p13 chr3: 37,449,902-39,676,087 OXSR1, ITGA9, 55 more genes
    nsv7046287inversion1nstd229human GRCh38 chr3: 38,983,543-38,990,449 , GRCh37.p13 chr3: 39,025,034-39,031,940 SCN11A
    nsv7039010inversion1nstd229human GRCh38 chr3: 37,851,228-39,078,678 , GRCh37.p13 chr3: 37,892,719-39,120,169 CDC42P7, LOC105377033, 28 more genes
    nsv6717285copy number variation1nstd229human GRCh38 chr3: 39,021,601-39,026,300 , GRCh37.p13 chr3: 39,063,092-39,067,791 SCN11A, RNU6-1227P
    nsv6716405copy number variation1nstd229human GRCh38 chr3: 38,900,901-38,907,400 , GRCh37.p13 chr3: 38,942,392-38,948,891 SCN11A
    nsv6716296copy number variation1nstd229human GRCh38 chr3: 38,943,828-39,042,223 , GRCh37.p13 chr3: 38,985,319-39,083,714 RNU6-1227P, SCN11A
    nsv6716114copy number variation1nstd229human GRCh38 chr3: 38,916,708-38,916,964 , GRCh37.p13 chr3: 38,958,199-38,958,455 SCN11A
    nsv6714566copy number variation1nstd229human GRCh38 chr3: 38,987,705-38,997,931 , GRCh37.p13 chr3: 39,029,196-39,039,422 SCN11A
    nsv6712579copy number variation1nstd229human GRCh38 chr3: 38,963,372-38,968,650 , GRCh37.p13 chr3: 39,004,863-39,010,141 SCN11A
    nsv6712386copy number variation1nstd229human GRCh38 chr3: 38,951,224-38,951,264 , GRCh37.p13 chr3: 38,992,715-38,992,755 SCN11A
    nsv6711902copy number variation1nstd229human GRCh38 chr3: 38,527,947-43,061,183 , GRCh37.p13 chr3: 38,569,438-43,102,675 ZBTB47, VIPR1-AS1, 90 more genes
    nsv6711682copy number variation1nstd229human GRCh38 chr3: 38,969,864-38,975,093 , GRCh37.p13 chr3: 39,011,355-39,016,584 SCN11A
    nsv6711482copy number variation1nstd229human GRCh38 chr3: 39,038,630-39,045,002 , GRCh37.p13 chr3: 39,080,121-39,086,493 SCN11A
    nsv6710673copy number variation1nstd229human GRCh38 chr3: 39,034,358-39,037,264 , GRCh37.p13 chr3: 39,075,849-39,078,755 SCN11A
    nsv6710651copy number variation1nstd229human GRCh38 chr3: 38,925,862-38,926,175 , GRCh37.p13 chr3: 38,967,353-38,967,666 SCN11A
    nsv6709409copy number variation1nstd229human GRCh38 chr3: 38,984,894-38,986,383 , GRCh37.p13 chr3: 39,026,385-39,027,874 SCN11A
    nsv6709266copy number variation1nstd229human GRCh38 chr3: 38,970,003-38,970,041 , GRCh37.p13 chr3: 39,011,494-39,011,532 SCN11A
    nsv6708355copy number variation1nstd229human GRCh38 chr3: 39,012,178-39,027,262 , GRCh37.p13 chr3: 39,053,669-39,068,753 RNU6-1227P, SCN11A
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