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 197

    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
    nsv7094636copy number variation1nstd102humanUncertain significance GRCh37 chr15: 78,857,986-81,282,132 , GRCh38.p12 chr15: 78,565,644-80,989,791 LOC646934, RNU6-415P, 51 more genes
    nsv7064472inversion1nstd229human GRCh38 chr15: 73,034,378-79,475,825 , GRCh37.p13 chr15: 73,326,719-79,768,167 ANP32BP1, PSTPIP1, 169 more genes
    nsv7063463inversion1nstd229human GRCh38 chr15: 75,234,241-81,337,543 , GRCh37.p13 chr15: 75,526,582-81,629,884 RN7SL327P, LOC105370910, 138 more genes
    nsv7062055inversion1nstd229human GRCh38 chr15: 72,671,162-80,404,440 , GRCh37.p13 chr15: 72,963,503-80,696,782 MIR184, TRK-CTT16-1, 194 more genes
    nsv6974707copy number variation1nstd229human GRCh38 chr15: 78,934,699-79,044,905 , GRCh37.p13 chr15: 79,227,041-79,337,247 RASGRF1, CTSH, 2 more genes
    nsv6971702copy number variation1nstd229human GRCh38 chr15: 78,917,108-78,920,779 , GRCh37.p13 chr15: 79,209,450-79,213,121 CTSH
    nsv6969044copy number variation1nstd229human GRCh38 chr15: 77,623,918-81,694,021 , GRCh37.p13 chr15: 77,916,260-81,986,362 ST20-MTHFS, CSPG4P13, 87 more genes
    nsv6966368copy number variation1nstd229human GRCh38 chr15: 78,944,738-79,000,373 , GRCh37.p13 chr15: 79,237,080-79,292,715 RASGRF1, CTSH, 2 more genes
    nsv6962124copy number variation1nstd229human GRCh38 chr15: 78,654,299-78,984,293 , GRCh37.p13 chr15: 78,946,641-79,276,635 TRK-CTT1-2, CTSH, 14 more genes
    nsv6959921copy number variation1nstd229human GRCh38 chr15: 78,924,232-78,926,403 , GRCh37.p13 chr15: 79,216,574-79,218,745 CTSH
    nsv6958660copy number variation1nstd229human GRCh38 chr15: 78,925,837-78,928,441 , GRCh37.p13 chr15: 79,218,179-79,220,783 CTSH
    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
    nsv6579530inversion1nstd223human GRCh38 chr15: 77,618,605-83,035,894 , GRCh37.p13 chr15: 77,910,947-83,704,646 CIB2, TFDP1P3, 127 more genes
    nsv6579525inversion1nstd223human GRCh38 chr15: 77,618,608-83,164,280 , GRCh37.p13 chr15: 77,910,950-83,833,032 STARD5, RPL9P8, 131 more genes
    nsv6578911inversion1nstd223human GRCh38 chr15: 77,618,608-84,708,062 , GRCh37.p13 chr15: 77,910,950-85,251,293 TMC3-AS1, LOC642677, 177 more genes
    nsv6506983copy number variation1nstd223human GRCh38 chr15: 78,932,131-78,933,405 , GRCh37.p13 chr15: 79,224,473-79,225,747 CTSH
    nsv6206146copy number variation1nstd214human GRCh38 chr15: 78,945,497-78,945,686 , GRCh37.p13 chr15: 79,237,839-79,238,028 CTSH
    nsv6189033copy number variation1nstd214human GRCh38 chr15: 78,945,497-78,945,718 , GRCh37.p13 chr15: 79,237,839-79,238,060 CTSH
    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