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 544

    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
    nsv7066523inversion1nstd229human GRCh38 chr17: 36,977,322-38,870,747 , GRCh37.p13 chr17: 35,372,677-37,027,000 LOC101929950, LASP1, 68 more genes
    nsv6998076copy number variation1nstd229human GRCh38 chr17: 37,021,631-37,021,825 , GRCh37.p13 chr17: 35,378,930-35,379,124 AATF
    nsv6995638copy number variation1nstd229human GRCh38 chr17: 37,052,289-37,058,043 , GRCh37.p13 chr17: 35,409,589-35,415,342 LOC105371753, AATF
    nsv6994441copy number variation1nstd229human GRCh38 chr17: 37,000,729-37,006,637 , GRCh37.p13 chr17: 35,358,028-35,363,936 AATF
    nsv6989973copy number variation1nstd229human GRCh38 chr17: 37,000,096-37,055,926 , GRCh37.p13 chr17: 35,357,395-35,413,226 MIR2909, LOC105371753, 1 more genes
    nsv6984375copy number variation1nstd229human GRCh38 chr17: 37,026,412-37,036,461 , GRCh37.p13 chr17: 35,383,709-35,393,758 MIR2909, AATF
    nsv6982316copy number variation1nstd229human GRCh38 chr17: 36,976,051-36,986,384 , GRCh37.p13 chr17: 35,333,350-35,343,683 AATF
    nsv6980247copy number variation1nstd229human GRCh38 chr17: 36,753,135-37,596,834 , GRCh37.p13 chr17: 35,168,060-35,888,667 HMGB1P24, SNORA90, 14 more genes
    nsv6980077copy number variation1nstd229human GRCh38 chr17: 36,948,522-36,960,178 , GRCh37.p13 chr17: 35,305,822-35,317,478 AATF
    nsv6979811copy number variation1nstd229human GRCh38 chr17: 37,052,564-37,119,971 , GRCh37.p13 chr17: 35,409,864-35,476,893 ACACA, AATF, 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
    nsv6635435copy number variation1nstd227human GRCh37 chr17: 35,362,972-35,694,047 , GRCh38.p12 chr17: 37,005,673-37,337,106 , GRCh38.p12 chr17|NT_187614.1: 1,242,037-1,573,112 ACACA, AATF, 6 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
    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