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Items: 1 to 20 of 168

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5562780sequence alteration1nstd206human GRCh38 chr17: 41,964,018-42,255,340 , GRCh37.p13 chr17|NW_003571052.1: 250,660-412,535 , GRCh37.p13 chr17: 40,116,036-40,277,911 KAT2A, STAT5B, 13 more genes
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5358869translocation1nstd200human GRCh38 chr17: 42,121,582-42,121,582 , GRCh38 chr17: 42,120,964-42,120,964 , GRCh37.p13 chr17|NW_003571052.1: 407,606-407,606 , GRCh37.p13 chr17|NW_003571052.1: 408,224-408,224 , GRCh37.p13 chr17: 40,272,982-40,272,982 , GRCh37.p13 chr17: 40,273,600-40,273,600 HSPB9, KAT2A
    nsv5326373copy number variation1nstd204human GRCh38.p13 chr17: 42,113,413-42,133,533 , GRCh37.p13 chr17: 40,265,431-40,277,918 , GRCh37.p13 chr17|NW_003571052.1: 400,055-412,542 HSPB9, RAB5C, 1 more genes
    nsv5280830copy number variation1nstd204human GRCh38.p13 chr17: 42,113,449-42,132,188 , GRCh37.p13 chr17|NW_003571052.1: 400,091-412,535 , GRCh37.p13 chr17: 40,265,467-40,277,911 RAB5C, HSPB9, 1 more genes
    nsv5013711copy number variation1nstd200human GRCh38 chr17: 42,113,421-42,133,526 , GRCh37.p13 chr17|NW_003571052.1: 400,063-412,535 , GRCh37.p13 chr17: 40,265,439-40,277,911 HSPB9, RAB5C, 1 more genes
    nsv4867021copy number variation1nstd200human GRCh37 chr17: 40,272,982-40,273,600 , GRCh38.p12 chr17: 42,120,964-42,121,582 KAT2A, HSPB9
    nsv4864656copy number variation1nstd200human GRCh37 chr17: 40,265,439-40,285,544 , GRCh38.p12 chr17: 42,113,421-42,133,526 HSPB9, KAT2A, 1 more genes
    nsv4680071copy number variation1nstd189human GRCh37.p13 chr17: 39,432,725-40,293,644 , GRCh38.p12 chr17: 41,276,473-42,141,626 ACLY, CNP, 50 more genes
    nsv4634273copy number variation1nstd183human GRCh37 chr17: 40,264,694-40,264,850 , GRCh38.p12 chr17: 42,112,676-42,112,832 DHX58, KAT2A
    nsv4631537copy number variation1nstd183human GRCh37 chr17: 40,264,193-40,264,583 , GRCh38.p12 chr17: 42,112,175-42,112,565 DHX58, KAT2A
    nsv4630258copy number variation2nstd183human GRCh37 chr17: 40,264,705-40,264,750 , GRCh38.p12 chr17: 42,112,687-42,112,732 KAT2A, DHX58
    nsv4628811copy number variation1nstd183human GRCh37 chr17: 40,264,694-40,265,198 , GRCh38.p12 chr17: 42,112,676-42,113,180 KAT2A, DHX58
    nsv4628576copy number variation1nstd183human GRCh37 chr17: 40,269,713-40,269,830 , GRCh38.p12 chr17: 42,117,695-42,117,812 KAT2A
    nsv4623642copy number variation1nstd183human GRCh37 chr17: 40,177,853-40,515,234 , GRCh38.p12 chr17: 42,025,835-42,363,216 NKIRAS2, STAT3, 12 more genes
    nsv4619927copy number variation2nstd183human GRCh37 chr17: 40,264,694-40,264,750 , GRCh38.p12 chr17: 42,112,676-42,112,732 DHX58, KAT2A
    nsv4330632inversion1nstd166human GRCh37.p13 chr17: 18,838,526-72,042,289 , GRCh38.p12 chr17: 18,935,213-74,046,150 , ACACA, 1499 more genes
    nsv3914783copy number variation1nstd102humanPathogenic NCBI36 chr17: 16,698,288-78,654,742 , GRCh37.p13 chr17: 16,757,563-81,048,189 , GRCh38.p12 chr17: 16,854,249-83,103,577 LOC105371922, GJD3, 1855 more genes
    nsv3913552copy number variation1nstd102humanPathogenic GRCh38 chr17: 36,449,220-75,053,130 , NCBI36 chr17: 54,950,518-70,560,820 , GRCh37 chr17: 57,595,736-73,049,225 RNU6-131P, ZNF652, 1075 more genes
    nsv3911811copy number variation1nstd102humanPathogenic NCBI36 chr17: 31,824,931-78,654,742 , GRCh37.p13 chr17: 34,750,818-81,048,189 , GRCh38.p12 chr17: 36,382,248-83,103,577 PRPSAP1, CACNG1, 1350 more genes
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