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Items: 1 to 20 of 89

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6310022copy number variation1nstd102humanPathogenic GRCh37 chr16: 88,712,514-88,718,096 , GRCh38.p12 chr16: 88,646,106-88,651,688 MVD, CYBA
    nsv6310023copy number variation1nstd102humanPathogenic GRCh37 chr16: 88,713,499-88,718,353 , GRCh38.p12 chr16: 88,647,091-88,651,945 MVD, CYBA
    nsv6310102copy number variation1nstd102humanPathogenic GRCh37 chr16: 88,717,354-88,718,353 , GRCh38.p12 chr16: 88,650,946-88,651,945 MVD, CYBA
    nsv4451072copy number variation1nstd102humanUncertain significance GRCh37 chr16: 88,709,737-88,718,353 , GRCh38 chr16: 88,643,329-88,651,945 MVD, CYBA
    nsv3877297copy number variation1nstd102humanPathogenic GRCh37 chr16: 86,890,893-89,398,630 , GRCh38.p12 chr16: 86,857,287-89,332,222 MVD, LOC112268182, 68 more genes
    nsv3917970copy number variation1nstd102humanPathogenic GRCh38 chr16: 86,950,106-89,335,814 , NCBI36 chr16: 85,541,213-87,929,723 , GRCh37 chr16: 86,983,712-89,402,222 MVD, CDH15, 68 more genes
    nsv3879843copy number variation1nstd102humanPathogenic GRCh37 chr16: 87,183,661-89,520,803 , GRCh38.p12 chr16: 87,150,055-89,454,395 MVD, LOC100287036, 68 more genes
    nsv3913039copy number variation1nstd102humanPathogenic GRCh38 chr16: 87,306,529-89,269,079 , GRCh37 chr16: 87,340,135-89,335,487 , NCBI36 chr16: 85,897,636-87,862,988 MVD, ZNF778, 61 more genes
    nsv3885545copy number variation1nstd102humanPathogenic GRCh37 chr16: 87,340,135-89,335,428 , GRCh38.p12 chr16: 87,306,529-89,269,020 MVD, GALNS, 61 more genes
    nsv3899619copy number variation1nstd102humanPathogenic GRCh37 chr16: 88,116,155-89,524,926 , GRCh38.p12 chr16: 88,082,549-89,458,518 MVD, PIEZO1, 47 more genes
    nsv3920773copy number variation1nstd102humanPathogenic GRCh37 chr16: 88,193,266-89,572,450 , NCBI36 chr16: 86,750,767-88,099,951 , GRCh38 chr16: 88,159,660-89,506,042 MVD, LOC101930112, 48 more genes
    nsv6315145copy number variation1nstd102humanPathogenic GRCh37 chr16: 88,365,786-89,584,412 , GRCh38.p12 chr16: 88,332,180-89,518,004 MVD, SPG7, 46 more genes
    nsv4456065copy number variation1nstd102humanPathogenic GRCh37 chr16: 88,453,448-89,569,215 , GRCh38.p12 chr16: 88,387,040-89,502,807 MVD, LOC101927863, 45 more genes
    nsv3876943copy number variation1nstd102humanPathogenic GRCh37 chr16: 88,230,760-89,363,742 , GRCh38.p12 chr16: 88,197,154-89,297,334 MVD, LINC02138, 40 more genes
    nsv3874480copy number variation1nstd102humanPathogenic GRCh37 chr16: 88,230,961-89,363,602 , GRCh38.p12 chr16: 88,197,355-89,297,194 MVD, CDH15, 40 more genes
    nsv3877335copy number variation1nstd102humanPathogenic GRCh37 chr16: 88,556,191-89,557,911 , GRCh38.p12 chr16: 88,489,783-89,491,503 MVD, SNAI3-AS1, 42 more genes
    nsv3871782copy number variation1nstd102humanPathogenic GRCh37 chr16: 88,635,000-89,628,950 , GRCh38.p12 chr16: 88,568,592-89,562,542 MVD, LOC339059, 41 more genes
    nsv3877060copy number variation1nstd102humanPathogenic GRCh37 chr16: 88,630,607-89,607,742 , GRCh38.p12 chr16: 88,564,199-89,541,334 MVD, LOC339059, 39 more genes
    nsv3913965copy number variation1nstd102humanPathogenic GRCh37 chr16: 88,706,524-89,596,883 , GRCh38 chr16: 88,640,116-89,530,475 , NCBI36 chr16: 87,234,025-88,124,384 MVD, LOC100129697, 38 more genes
    nsv3876360copy number variation1nstd102humanPathogenic GRCh37 chr16: 88,666,177-89,472,627 , GRCh38.p12 chr16: 88,599,769-89,406,219 MVD, LINC00304, 33 more genes
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