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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6995164copy number variation1nstd229human GRCh38 chr17: 42,111,850-42,112,357 , GRCh37.p13 chr17: 40,263,868-40,264,375 , GRCh37.p13 chr17|NW_003571052.1: 398,492-398,999 DHX58, KAT2A
    nsv6984984copy number variation1nstd229human GRCh38 chr17: 38,377,708-42,855,253 , GRCh37.p13 chr17: 36,701,616-41,007,270 ZNF385C, AOC2, 248 more genes
    nsv6982861copy number variation1nstd229human GRCh38 chr17: 38,291,672-47,498,259 , GRCh37.p13 chr17: 36,510,266-45,575,625 KRT20, PLEKHH3, 442 more genes
    nsv6197655copy number variation1nstd214human GRCh38 chr17: 42,115,235-42,115,294 , GRCh37.p13 chr17|NW_003571052.1: 401,877-401,936 , GRCh37.p13 chr17: 40,267,253-40,267,312 KAT2A
    nsv6189622copy number variation1nstd214human GRCh38 chr17: 42,115,419-42,115,479 , GRCh37.p13 chr17|NW_003571052.1: 402,061-402,121 , GRCh37.p13 chr17: 40,267,437-40,267,497 KAT2A
    nsv6133289copy number variation1nstd213human GRCh37 chr17: 40,255,333-40,670,620 , GRCh38.p12 chr17: 42,103,315-42,518,602 ATP6V0A1, KAT2A, 15 more genes
    nsv6133061copy number variation1nstd213human GRCh37 chr17: 39,870,000-40,890,001 , GRCh38.p12 chr17: 41,713,748-42,737,983 ACLY, ATP6V0A1, 51 more genes
    nsv6133060copy number variation1nstd213human GRCh37 chr17: 39,870,000-40,880,001 , GRCh38.p12 chr17: 41,713,748-42,727,983 ACLY, ATP6V0A1, 51 more genes
    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
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