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Items: 1 to 20 of 160

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6996323copy number variation1nstd229human GRCh38 chr17: 42,645,101-42,650,700 , GRCh37.p13 chr17: 40,797,119-40,802,718 HMGB3P27, ATP5MGP7
    nsv6988610copy number variation1nstd229human GRCh38 chr17: 42,643,901-42,649,700 , GRCh37.p13 chr17: 40,795,919-40,801,718 ATP5MGP7, HMGB3P27
    nsv6987773copy number variation1nstd229human GRCh38 chr17: 42,636,990-42,646,553 , GRCh37.p13 chr17: 40,789,008-40,798,571 HMGB3P27, ATP5MGP7
    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
    nsv6982034copy number variation1nstd229human GRCh38 chr17: 42,616,577-42,649,743 , GRCh37.p13 chr17: 40,768,595-40,801,761 ATP5MGP7, HMGB3P27
    nsv6978179copy number variation1nstd229human GRCh38 chr17: 42,645,208-42,649,664 , GRCh37.p13 chr17: 40,797,226-40,801,682 ATP5MGP7, HMGB3P27
    nsv6515582copy number variation1nstd223human GRCh38 chr17: 42,644,101-42,649,700 , GRCh37.p13 chr17: 40,796,119-40,801,718 HMGB3P27, ATP5MGP7
    nsv6133246copy number variation1nstd213human GRCh37 chr17: 40,670,000-41,570,001 , GRCh38.p12 chr17: 42,517,982-43,492,633 AOC2, ARL4D, 65 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
    nsv5946554copy number variation1nstd209human GRCh38 chr17: 42,645,204-42,649,658 , GRCh37.p13 chr17: 40,797,222-40,801,676 HMGB3P27, ATP5MGP7
    nsv5931517copy number variation1nstd209human GRCh38 chr17: 42,616,574-42,649,699 , GRCh37.p13 chr17: 40,768,592-40,801,717 HMGB3P27, ATP5MGP7
    nsv5885250copy number variation2nstd209human GRCh38 chr17: 42,645,150-42,649,399 , GRCh37.p13 chr17: 40,797,168-40,801,417 ATP5MGP7, HMGB3P27
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5532414copy number variation1nstd206human GRCh38 chr17: 42,645,058-42,649,659 , GRCh37.p13 chr17: 40,797,076-40,801,677 ATP5MGP7, HMGB3P27
    nsv5524894copy number variation1nstd206human GRCh38 chr17: 42,616,574-42,649,731 , GRCh37.p13 chr17: 40,768,592-40,801,749 ATP5MGP7, HMGB3P27
    nsv5293339copy number variation1nstd204human GRCh38.p13 chr17: 42,464,901-42,659,200 , GRCh37.p13 chr17: 40,616,919-40,811,218 ATP5MGP7, PTP4A2P1, 14 more genes
    nsv5290577copy number variation1nstd204human GRCh38.p13 chr17: 42,610,501-42,660,100 , GRCh37.p13 chr17: 40,762,519-40,812,118 HMGB3P27, TUBG1, 2 more genes
    nsv5287967copy number variation1nstd204human GRCh38.p13 chr17: 42,647,750-42,648,749 , GRCh37.p13 chr17: 40,799,768-40,800,767 HMGB3P27, ATP5MGP7
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