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 172

    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
    nsv7076478inversion1nstd229human GRCh38 chr15: 79,261,836-81,280,491 , GRCh37.p13 chr15: 79,554,178-81,572,832 CFAP161, TMED3, 34 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
    nsv7063009inversion1nstd229human GRCh38 chr15: 80,220,949-81,163,179 , GRCh37.p13 chr15: 80,513,291-81,455,520 CEMIP, ARNT2, 13 more genes
    nsv6976831copy number variation1nstd229human GRCh38 chr15: 80,974,112-80,997,607 , GRCh37.p13 chr15: 81,266,453-81,289,948 MIR4514, MESD
    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
    nsv6967975copy number variation1nstd229human GRCh38 chr15: 80,950,061-80,953,852 , GRCh37.p13 chr15: 81,242,402-81,246,193 CEMIP, MESD
    nsv6965791copy number variation1nstd229human GRCh38 chr15: 80,776,401-80,977,900 , GRCh37.p13 chr15: 81,068,742-81,270,241 CEMIP, MIR549A, 1 more genes
    nsv6963242copy number variation1nstd229human GRCh38 chr15: 80,947,570-80,947,788 , GRCh37.p13 chr15: 81,239,911-81,240,129 MESD, CEMIP
    nsv6962791copy number variation1nstd229human GRCh38 chr15: 80,975,206-80,979,886 , GRCh37.p13 chr15: 81,267,547-81,272,227 MESD
    nsv6961552copy number variation1nstd229human GRCh38 chr15: 80,912,960-81,015,220 , GRCh37.p13 chr15: 81,205,301-81,307,561 TLNRD1, MESD, 2 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
    nsv6637608copy number variation1nstd102humanUncertain significance GRCh37 chr15: 79,996,626-82,097,796 , GRCh38.p12 chr15: 79,704,284-81,805,455 ARNT2, LOC105370921, 31 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
    nsv6579316inversion1nstd223human GRCh38 chr15: 80,355,809-82,694,011 , GRCh37.p13 chr15: 80,648,151-83,362,763 MIR549A, RPS17, 46 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
    nsv6514019copy number variation1nstd223human GRCh38 chr15: 80,894,502-81,778,437 , GRCh37.p13 chr15: 81,186,843-82,070,778 LOC102723985, MIR4514, 10 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