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 170

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148092copy number variation1nstd102humanPathogenic GRCh37 chr15: 75,165,490-102,520,892 , GRCh38.p12 chr15: 74,873,149-101,980,689 RPL9P8, COMMD4P1, 547 more genes
    nsv7098897copy number variation1nstd102humanPathogenic GRCh37 chr15: 67,358,491-91,644,328 , GRCh38.p12 chr15: 67,066,153-91,101,098 LINC00933, DNM1P9, 540 more genes
    nsv7098892copy number variation1nstd102humanPathogenic GRCh37 chr15: 84,228,005-102,264,590 , GRCh38.p12 chr15: 83,559,253-101,724,387 CIB1, RPS12P26, 326 more genes
    nsv7094312copy number variation2nstd102humanUncertain significance GRCh37 chr15: 89,379,429-91,565,479 , GRCh38.p12 chr15: 88,836,198-91,022,249 IQGAP1, WDR93, 77 more genes
    nsv7093404copy number variation1nstd102humannot provided GRCh37 chr15: 91,422,650-91,497,515 , GRCh38.p12 chr15: 90,879,420-90,954,285 FURIN, RCCD1, 4 more genes
    nsv7069337inversion1nstd229human GRCh38 chr15: 90,802,705-90,945,658 , GRCh37.p13 chr15: 91,345,935-91,488,888 BLM, LOC105370969, 6 more genes
    nsv7065612inversion1nstd229human GRCh38 chr15: 89,041,442-91,616,740 , GRCh37.p13 chr15: 89,584,673-92,159,970 ZNF774, CRAT37, 77 more genes
    nsv7061932inversion1nstd229human GRCh38 chr15: 90,790,050-90,927,117 , GRCh37.p13 chr15: 91,333,280-91,470,347 FURIN, RN7SL363P, 4 more genes
    nsv6976510copy number variation1nstd229human GRCh38 chr15: 86,730,503-91,149,191 , GRCh37.p13 chr15: 87,273,734-91,692,421 , IQGAP1, 105 more genes
    nsv6976150copy number variation1nstd229human GRCh38 chr15: 90,790,101-90,986,300 , GRCh37.p13 chr15: 91,333,331-91,529,530 UNC45A, MAN2A2, 9 more genes
    nsv6971390copy number variation1nstd229human GRCh38 chr15: 90,916,990-90,931,603 , GRCh37.p13 chr15: 91,460,220-91,474,833 MAN2A2, UNC45A, 1 more genes
    nsv6962202copy number variation1nstd229human GRCh38 chr15: 90,873,702-90,968,294 , GRCh37.p13 chr15: 91,416,932-91,511,524 UNC45A, MAN2A2, 6 more genes
    nsv6962030copy number variation1nstd229human GRCh38 chr15: 90,808,301-90,945,700 , GRCh37.p13 chr15: 91,351,531-91,488,930 HDDC3, LOC105370969, 6 more genes
    nsv6637683copy number variation1nstd102humanPathogenic GRCh37 chr15: 77,512,817-102,035,027 , GRCh38.p12 chr15: 77,220,475-101,494,824 LINC02253, LOC107984790, 463 more genes
    nsv6509838copy number variation1nstd223human GRCh38 chr15: 90,900,091-90,900,880 , GRCh37.p13 chr15: 91,443,321-91,444,110 MAN2A2
    nsv6500515copy number variation1nstd223human GRCh38 chr15: 90,920,799-90,922,753 , GRCh37.p13 chr15: 91,464,029-91,465,983 MAN2A2
    nsv6291795copy number variation1nstd102humanPathogenic GRCh37 chr15: 89,520,451-93,926,491 , GRCh38.p12 chr15: 88,977,220-93,383,262 LINC00930, TRY-GTA12-1, 106 more genes
    nsv6290316copy number variation1nstd102humanPathogenic GRCh37 chr15: 88,465,861-94,411,846 , GRCh38.p12 chr15: 87,922,630-93,868,617 LOC105370964, MRPL46, 130 more genes
    nsv6133155copy number variation1nstd213human GRCh37 chr15: 72,730,000-102,440,001 , GRCh38.p12 chr15: 72,437,659-101,899,798 , BLM, 609 more genes
    nsv6132917copy number variation1nstd213human GRCh37 chr15: 90,230,000-95,470,001 , GRCh38.p12 chr15: 89,686,769-94,926,772 BLM, ST8SIA2, 101 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