U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Links from Gene

Items: 1 to 20 of 178

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095335copy number variation1nstd102humanUncertain significance GRCh37 chr17: 40,688,291-40,729,741 , GRCh38.p12 chr17: 42,536,273-42,577,723 HSD17B1-AS1, HSD17B1, 6 more genes
    nsv7094973copy number variation1nstd102humanPathogenic GRCh37 chr17: 40,689,396-40,690,793 , GRCh38.p12 chr17: 42,537,378-42,538,775 NAGLU
    nsv6986626copy number variation1nstd229human GRCh38 chr17: 42,422,850-42,633,538 , GRCh37.p13 chr17: 40,574,868-40,785,556 HSD17B1P1, TUBG1, 14 more genes
    nsv6985221copy number variation1nstd229human GRCh38 chr17: 42,419,782-42,607,109 , GRCh37.p13 chr17: 40,571,800-40,759,127 COASY, LOC102725238, 13 more genes
    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
    nsv6624236copy number variation1nstd224human GRCh37 chr17: 40,695,904-40,706,906 , GRCh38.p12 chr17: 42,543,886-42,554,888 NAGLU, HSD17B1P1, 2 more genes
    nsv6503236copy number variation1nstd223human GRCh38 chr17: 42,540,093-42,540,674 , GRCh37.p13 chr17: 40,692,111-40,692,692 NAGLU
    nsv6502989copy number variation1nstd223human GRCh38 chr17: 42,526,903-42,532,866 , GRCh37.p13 chr17: 40,678,921-40,684,884 NAGLU, PTP4A2P1
    nsv6499817copy number variation1nstd223human GRCh38 chr17: 42,537,722-42,538,866 , GRCh37.p13 chr17: 40,689,740-40,690,884 NAGLU
    nsv6310382copy number variation2nstd102humanPathogenic, Likely pathogenic GRCh37 chr17: 40,690,337-40,690,793 , GRCh38.p12 chr17: 42,538,319-42,538,775 NAGLU
    nsv6310171copy number variation1nstd102humanUncertain significance GRCh37 chr17: 40,688,291-40,690,793 , GRCh38.p12 chr17: 42,536,273-42,538,775 NAGLU
    nsv6310170copy number variation1nstd102humanPathogenic GRCh37 chr17: 40,688,281-40,693,234 , GRCh38.p12 chr17: 42,536,263-42,541,216 NAGLU
    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
    nsv5942250copy number variation1nstd209human GRCh38 chr17: 42,542,025-42,542,186 , GRCh37.p13 chr17: 40,694,043-40,694,204 NAGLU
    nsv5931439copy number variation1nstd209human GRCh38 chr17: 42,532,540-42,532,850 , GRCh37.p13 chr17: 40,684,558-40,684,868 PTP4A2P1, NAGLU
    nsv5673037copy number variation1nstd102humanPathogenic GRCh37 chr17: 40,690,347-40,690,783 , GRCh38.p12 chr17: 42,538,329-42,538,765 NAGLU
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Recent activity

    Clear Turn Off Turn On

    Your browsing activity is empty.

    Activity recording is turned off.

    Turn recording back on

    See more...
    You are here: NCBI > Variation > Database of Genomic Structural Variation (dbVar)
    Support Center