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 392

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148151copy number variation1nstd102humanPathogenic GRCh38 chr17: 36,486,532-37,745,203 , GRCh37.p13 chr17: 34,900,240-35,888,667 PIGW, LOC105371751, 32 more genes
    nsv7148119copy number variation1nstd102humanPathogenic GRCh37 chr17: 34,752,221-36,105,007 , GRCh38.p12 chr17|NT_187614.1: 694,163-1,984,072 , GRCh38.p12 chr17: 36,446,545-37,745,016 LOC105371756, SYNRG, 35 more genes
    nsv7137104copy number variation1nstd102humanPathogenic GRCh37 chr17: 34,842,545-36,293,050 , GRCh38.p12 chr17: 36,486,701-37,933,506 , GRCh38.p12 chr17|NT_187614.1: 721,605-2,172,115 LHX1-DT, LOC105371749, 40 more genes
    nsv7098907copy number variation1nstd102humanPathogenic GRCh38 chr17: 36,138,501-37,924,067 , GRCh37.p13 chr17: 34,900,240-35,888,667 LOC102723414, SYNRG, 51 more genes
    nsv7098735copy number variation1nstd102humanLikely pathogenic GRCh37 chr17: 34,842,542-36,104,877 , GRCh38.p12 chr17: 36,486,698-37,744,886 , GRCh38.p12 chr17|NT_187614.1: 721,602-1,983,942 ACACA, LHX1, 34 more genes
    nsv7073998inversion1nstd229human GRCh38 chr17: 32,918,710-41,148,753 , GRCh37.p13 chr17: 31,245,728-39,305,005 LOC105371750, C17orf78, 298 more genes
    nsv7064857inversion1nstd229human GRCh38 chr17: 36,496,730-36,501,385 , GRCh37.p13 chr17|NW_003315949.1: 381,480-386,135 ZNHIT3, MYO19
    nsv7063878inversion1nstd229human GRCh38 chr17: 36,492,269-36,496,831 , GRCh37.p13 chr17|NW_003315949.1: 377,019-381,581 ZNHIT3, MYO19
    nsv6996067copy number variation1nstd229human GRCh38 chr17: 36,486,601-36,491,600 , GRCh37.p13 chr17|NW_003315949.1: 371,351-376,350 RNA5SP439, LOC105371749, 1 more genes
    nsv6637369copy number variation1nstd102humanPathogenic GRCh37 chr17: 34,425,363-36,404,555 , GRCh38.p12 chr17|NT_187614.1: 332,891-2,283,620 CCL3L3, MRM1, 63 more genes
    nsv6634438copy number variation1nstd102humanPathogenic GRCh37 chr17: 34,842,544-36,104,875 , GRCh38.p12 chr17: 36,486,700-37,744,884 , GRCh38.p12 chr17|NT_187614.1: 721,604-1,983,940 HNF1B, LOC100419621, 34 more genes
    nsv6634420copy number variation1nstd102humanPathogenic GRCh37 chr17: 34,822,465-36,243,781 , GRCh38.p12 chr17|NT_187614.1: 701,523-2,122,846 , GRCh38.p12 chr17: 36,466,619-37,884,161 GGNBP2, AATF, 36 more genes
    nsv6624272copy number variation1nstd224human GRCh37 chr17: 34,815,551-36,249,430 , GRCh38.p12 chr17: 36,459,737-37,889,808 , GRCh38.p12 chr17|NT_187614.1: 694,641-2,128,495 DDX52, DUSP14, 36 more genes
    nsv6624076copy number variation1nstd224human GRCh37 chr17: 34,815,551-34,854,280 , GRCh38.p12 chr17: 36,459,737-36,498,436 , GRCh38.p12 chr17|NT_187614.1: 694,641-733,340 LOC105371749, MYO19, 2 more genes
    nsv6623850copy number variation1nstd224human GRCh37 chr17: 34,815,551-36,411,684 , GRCh38.p12 chr17|NT_187614.1: 694,641-2,290,749 LHX1, HNF1B, 44 more genes
    nsv6514989copy number variation1nstd223human GRCh38 chr17: 36,496,511-36,497,933 , GRCh37.p13 chr17|NW_003315949.1: 381,261-382,683 ZNHIT3, MYO19
    nsv6514521copy number variation1nstd223human GRCh38 chr17: 36,453,901-36,528,300 , GRCh37.p13 chr17|NW_003315949.1: 338,651-413,048 LOC105371749, ZNHIT3, 3 more genes
    nsv6513850copy number variation1nstd223human GRCh38 chr17: 36,351,001-36,630,200 , GRCh37.p13 chr17|NW_003315949.1: 235,757-429,138 MYO19, DHRS11, 14 more genes
    nsv6510440copy number variation1nstd223human GRCh38 chr17: 36,497,701-36,503,700 , GRCh37.p13 chr17|NW_003315949.1: 382,451-388,450 ZNHIT3, MYO19
    nsv6505560copy number variation1nstd223human GRCh38 chr17: 36,479,001-36,505,500 , GRCh37.p13 chr17|NW_003315949.1: 363,751-390,250 MYO19, ZNHIT3, 2 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