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Items: 1 to 20 of 227

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148155copy number variation1nstd102humanPathogenic GRCh37 chr17: 72,718,277-74,142,256 , GRCh38.p12 chr17: 74,722,138-76,146,175 TRIM65, TEN1, 74 more genes
    nsv7098900copy number variation1nstd102humanUncertain significance GRCh37 chr17: 72,864,876-73,328,878 , GRCh38.p12 chr17: 74,868,753-75,332,797 CDR2L, OTOP2, 28 more genes
    nsv6997214copy number variation1nstd229human GRCh38 chr17: 75,106,036-75,110,289 , GRCh37.p13 chr17: 73,102,131-73,106,384 ARMC7, SLC16A5
    nsv6997005copy number variation1nstd229human GRCh38 chr17: 75,096,783-75,099,728 , GRCh37.p13 chr17: 73,092,878-73,095,823 SLC16A5
    nsv6996972copy number variation1nstd229human GRCh38 chr17: 75,095,694-75,096,633 , GRCh37.p13 chr17: 73,091,789-73,092,728 SLC16A5
    nsv6994090copy number variation1nstd229human GRCh38 chr17: 75,053,032-75,108,705 , GRCh37.p13 chr17: 73,049,127-73,104,800 SLC16A5, TRIM80P, 2 more genes
    nsv6988813copy number variation1nstd229human GRCh38 chr17: 75,095,602-75,096,327 , GRCh37.p13 chr17: 73,091,697-73,092,422 SLC16A5
    nsv6986215copy number variation1nstd229human GRCh38 chr17: 75,085,951-75,090,498 , GRCh37.p13 chr17: 73,082,046-73,086,593 SLC16A5
    nsv6984264copy number variation1nstd229human GRCh38 chr17: 74,239,313-78,611,254 , GRCh37.p13 chr17: 72,235,452-76,607,336 SNORD1C, PRCD, 178 more genes
    nsv6978465copy number variation1nstd229human GRCh38 chr17: 75,083,586-75,093,202 , GRCh37.p13 chr17: 73,079,681-73,089,297 SLC16A5
    nsv6624308copy number variation1nstd224human GRCh37 chr17: 72,877,346-73,127,348 , GRCh38.p12 chr17: 74,881,216-75,131,253 SLC16A5, KCTD2, 18 more genes
    nsv6580372inversion1nstd223human GRCh38 chr17: 72,236,607-79,483,477 , GRCh37.p13 chr17: 70,232,748-77,412,076 TNRC6C, PTMAP13, 217 more genes
    nsv6532507copy number variation1nstd223human GRCh38 chr17: 75,103,364-75,104,452 , GRCh37.p13 chr17: 73,099,459-73,100,547 SLC16A5
    nsv6526236copy number variation1nstd223human GRCh38 chr17: 75,095,795-75,096,664 , GRCh37.p13 chr17: 73,091,890-73,092,759 SLC16A5
    nsv6519331copy number variation1nstd223human GRCh38 chr17: 75,096,653-75,099,511 , GRCh37.p13 chr17: 73,092,748-73,095,606 SLC16A5
    nsv6314018copy number variation1nstd102humanUncertain significance GRCh37 chr17: 73,049,227-73,533,226 , GRCh38.p12 chr17: 75,053,132-75,537,145 MIF4GD-DT, TSEN54, 21 more genes
    nsv6291659copy number variation1nstd102humanUncertain significance GRCh37 chr17: 73,045,938-73,310,951 , GRCh38.p12 chr17: 75,049,843-75,314,870 SLC25A19, NUP85, 12 more genes
    nsv6145962copy number variation1nstd206human GRCh38 chr17: 75,095,796-75,096,624 , GRCh37.p13 chr17: 73,091,891-73,092,719 SLC16A5
    nsv6133070copy number variation1nstd213human GRCh37 chr17: 62,460,000-73,800,001 , GRCh38.p12 chr17: 64,464,645-75,803,920 APOH, CACNG1, 225 more genes
    nsv5944378copy number variation1nstd209human GRCh38 chr17: 75,095,749-75,096,619 , GRCh37.p13 chr17: 73,091,844-73,092,714 SLC16A5
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