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Items: 1 to 20 of 181

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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
    nsv6985303copy number variation1nstd229human GRCh38 chr17: 75,042,760-75,046,636 , GRCh37.p13 chr17: 73,038,855-73,042,731 KCTD2, ATP5PD
    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
    nsv6982661copy number variation1nstd229human GRCh38 chr17: 75,044,187-75,044,504 , GRCh37.p13 chr17: 73,040,282-73,040,599 KCTD2, ATP5PD
    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
    nsv6525954copy number variation1nstd223human GRCh38 chr17: 75,046,301-75,048,100 , GRCh37.p13 chr17: 73,042,396-73,044,195 ATP5PD, KCTD2
    nsv6519372copy number variation1nstd223human GRCh38 chr17: 75,044,187-75,044,504 , GRCh37.p13 chr17: 73,040,282-73,040,599 KCTD2, ATP5PD
    nsv6515680copy number variation1nstd223human GRCh38 chr17: 75,035,605-75,037,074 , GRCh37.p13 chr17: 73,031,700-73,033,169 TRR-TCG3-1, KCTD2, 1 more genes
    nsv6272514copy number variation1nstd214human GRCh38 chr17: 75,044,354-75,044,487 , GRCh37.p13 chr17: 73,040,449-73,040,582 ATP5PD, KCTD2
    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
    nsv6127234copy number variation1nstd186human GRCh37 chr17: 73,040,299-73,040,599 , GRCh38.p12 chr17: 75,044,204-75,044,504 KCTD2, ATP5PD
    nsv6036439copy number variation1nstd212human GRCh38 chr17: 75,044,372-75,044,509 , GRCh37.p13 chr17: 73,040,467-73,040,604 ATP5PD, KCTD2
    nsv6025107copy number variation1nstd212human GRCh38 chr17: 75,044,187-75,044,504 , GRCh37.p13 chr17: 73,040,282-73,040,599 ATP5PD, KCTD2
    nsv5971172insertion1nstd209human GRCh38 chr17: 75,044,503-75,044,503 , GRCh37.p13 chr17: 73,040,598-73,040,598 KCTD2, ATP5PD
    nsv5940984copy number variation1nstd209human GRCh38 chr17: 75,044,187-75,044,503 , GRCh37.p13 chr17: 73,040,282-73,040,598 ATP5PD, KCTD2
    nsv5931204copy number variation1nstd209human GRCh38 chr17: 75,042,897-75,043,235 , GRCh37.p13 chr17: 73,038,992-73,039,330 ATP5PD, KCTD2
    nsv5596959copy number variation1nstd207human GRCh38 chr17: 75,044,187-75,044,503 , GRCh37.p13 chr17: 73,040,282-73,040,598 KCTD2, ATP5PD
    nsv5519944copy number variation1nstd206human GRCh38 chr17: 75,044,204-75,044,504 , GRCh37.p13 chr17: 73,040,299-73,040,599 ATP5PD, KCTD2
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