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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6995335copy number variation1nstd229human GRCh38 chr17: 41,782,883-41,783,653 , GRCh37.p13 chr17|NW_003571052.1: 69,525-70,295 , GRCh37.p13 chr17: 39,939,135-39,939,905 JUP
    nsv6993800copy number variation1nstd229human GRCh38 chr17: 41,758,872-41,762,981 , GRCh37.p13 chr17: 39,915,124-39,919,233 , GRCh37.p13 chr17|NW_003571052.1: 45,514-49,623 JUP
    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
    nsv6984219copy number variation1nstd229human GRCh38 chr17: 41,756,214-41,757,415 , GRCh37.p13 chr17|NW_003571052.1: 42,856-44,057 , GRCh37.p13 chr17: 39,912,466-39,913,667 JUP
    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
    nsv6978225copy number variation1nstd229human GRCh38 chr17: 41,771,865-41,772,817 , GRCh37.p13 chr17|NW_003571052.1: 58,507-59,459 , GRCh37.p13 chr17: 39,928,117-39,929,069 JUP
    nsv6310304copy number variation1nstd102humanUncertain significance GRCh37 chr17: 39,923,611-39,978,660 , GRCh38.p12 chr17: 41,767,359-41,822,408 P3H4, JUP, 1 more genes
    nsv6250797mobile element insertion1nstd215human GRCh38 chr17: 41,758,045-41,758,045 , GRCh37.p13 chr17|NW_003571052.1: 44,687-44,687 , GRCh37.p13 chr17: 39,914,297-39,914,297 JUP
    nsv6133357copy number variation1nstd213human GRCh37 chr17: 39,920,000-40,260,001 , GRCh38.p12 chr17: 41,763,748-42,107,983 ACLY, CNP, 12 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
    nsv6100193insertion1nstd212human GRCh38 chr17: 41,771,557-41,771,557 , GRCh37.p13 chr17: 39,927,809-39,927,809 , GRCh37.p13 chr17|NW_003571052.1: 58,199-58,199 JUP
    nsv6029622copy number variation1nstd212human GRCh38 chr17: 41,762,124-41,762,182 , GRCh37.p13 chr17|NW_003571052.1: 48,766-48,824 , GRCh37.p13 chr17: 39,918,376-39,918,434 JUP
    nsv5974171insertion1nstd209human GRCh38 chr17: 41,762,147-41,762,147 , GRCh37.p13 chr17|NW_003571052.1: 48,789-48,789 , GRCh37.p13 chr17: 39,918,399-39,918,399 JUP
    nsv5709138mobile element insertion1nstd211human GRCh38 chr17: 41,758,045-41,758,045 , GRCh37.p13 chr17: 39,914,297-39,914,297 , GRCh37.p13 chr17|NW_003571052.1: 44,687-44,687 JUP
    nsv5699545mobile element insertion1nstd211human GRCh38 chr17: 41,786,996-41,786,996 , GRCh37.p13 chr17: 39,943,248-39,943,248 , GRCh37.p13 chr17|NW_003571052.1: 73,638-73,638 JUP
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5531331copy number variation1nstd206human GRCh38 chr17: 41,780,410-41,780,739 , GRCh37.p13 chr17: 39,936,662-39,936,991 , GRCh37.p13 chr17|NW_003571052.1: 67,052-67,381 JUP
    nsv5522325copy number variation1nstd206human GRCh38 chr17: 41,755,842-41,755,929 , GRCh37.p13 chr17|NW_003571052.1: 42,484-42,571 , GRCh37.p13 chr17: 39,912,094-39,912,181 JUP
    nsv5515767copy number variation1nstd206human GRCh38 chr17: 41,771,524-41,771,590 , GRCh37.p13 chr17|NW_003571052.1: 58,166-58,232 , GRCh37.p13 chr17: 39,927,776-39,927,842 JUP
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