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 120

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7062042inversion1nstd229human GRCh38 chr15: 38,786,391-46,534,887 , GRCh37.p13 chr15: 39,078,592-46,827,085 EHD4-AS1, PLA2G4B, 219 more genes
    nsv6971514copy number variation1nstd229human GRCh38 chr15: 43,760,926-43,883,619 , GRCh37.p13 chr15: 44,053,124-44,175,817 PDIA3, SERF2-C15ORF63, 9 more genes
    nsv6970883copy number variation1nstd229human GRCh38 chr15: 43,791,001-43,792,900 , GRCh37.p13 chr15: 44,083,199-44,085,098 SERF2-C15ORF63, SERF2, 2 more genes
    nsv6513323copy number variation1nstd223human GRCh38 chr15: 43,797,493-43,916,813 , GRCh37.p13 chr15: 44,089,691-44,209,011 MFAP1, HYPK, 5 more genes
    nsv6291560copy number variation1nstd102humanUncertain significance GRCh37 chr15: 43,215,243-44,632,384 , GRCh38.p12 chr15: 42,923,045-44,340,186 PPIP5K1P1-CATSPER2, STRCP1, 44 more genes
    nsv6133147copy number variation1nstd213human GRCh37 chr15: 44,080,000-45,200,001 , GRCh38.p12 chr15: 43,787,802-44,907,803 ACTBP7, EIF3J, 24 more genes
    nsv5380758copy number variation2nstd102humanUncertain significance GRCh37 chr15: 32,964,879-91,358,519 , GRCh38.p12 chr15: 32,672,678-90,815,289 LOC105370794, HNRNPA1P45, 1173 more genes
    nsv5038422inversion1nstd200human GRCh38 chr15: 40,121,948-64,050,807 , GRCh37.p13 chr15: 40,414,149-64,343,006 , EIF4EBP2P2, 475 more genes
    nsv5005330copy number variation1nstd200human GRCh38 chr15: 43,798,223-43,813,836 , GRCh37.p13 chr15: 44,090,421-44,106,034 HYPK, MFAP1, 2 more genes
    nsv4872280inversion1nstd200human GRCh37 chr15: 40,414,149-64,343,008 , GRCh38.p12 chr15: 40,121,948-64,050,809 , DNAAF4-CCPG1, 475 more genes
    nsv4675221copy number variation1nstd102humanUncertain significance GRCh37 chr15: 43,420,601-44,198,616 , GRCh38.p12 chr15: 43,128,403-43,906,418 TGM5, CATSPER2P1, 38 more genes
    nsv4383436copy number variation1nstd173human GRCh37 chr15: 43,851,399-44,325,282 , GRCh38.p12 chr15: 43,559,201-44,033,084 PPIP5K1P1-CATSPER2, RNU6-554P, 24 more genes
    nsv4381260copy number variation1nstd173human GRCh37 chr15: 44,054,738-44,191,082 , GRCh38.p12 chr15: 43,762,540-43,898,884 SERF2-C15ORF63, SERINC4, 9 more genes
    nsv4372500copy number variation1nstd173human GRCh37 chr15: 43,992,627-44,198,616 , GRCh38.p12 chr15: 43,700,429-43,906,418 WDR76, ELL3, 13 more genes
    nsv3961571copy number variation1nstd168human GRCh38 chr15: 43,795,350-43,867,386 , GRCh37.p13 chr15: 44,087,548-44,159,584 MFAP1, SERF2, 4 more genes
    nsv3922157copy number variation1nstd102humanUncertain significance NCBI36 chr15: 29,852,369-100,338,915 , GRCh37.p13 chr15: 32,065,077-102,521,392 , GRCh38.p12 chr15: 31,772,874-101,981,189 GCHFR, SPPL2A, 1382 more genes
    nsv3919468copy number variation1nstd102humanPathogenic NCBI36 chr15: 26,996,912-100,338,915 , GRCh37.p13 chr15: 29,209,620-102,521,392 , GRCh38.p12 chr15: 28,917,417-101,981,189 RNU6-18P, GOLGA8K, 1442 more genes
    nsv3918770copy number variation1nstd102humanUncertain significance NCBI36 chr15: 20,280,728-100,338,915 , GRCh37.p13 chr15: 22,729,364-102,521,392 , GRCh38.p12 chr15: 23,319,714-101,981,189 SNRPCP18, SNORD116-30, 1622 more genes
    nsv3918644copy number variation1nstd102humanUncertain significance NCBI36 chr15: 20,313,935-100,338,915 , GRCh37.p13 chr15: 22,762,571-102,521,392 , GRCh38.p12 chr15: 23,319,714-101,981,189 SNORD116-23, UBE2Q2P6, 1622 more genes
    nsv3916249copy number variation1nstd102humanPathogenic NCBI36 chr15: 21,173,967-100,338,915 , GRCh37.p13 chr15: 23,622,526-102,521,392 , GRCh38.p12 chr15: 23,377,379-101,981,189 H3P40, EEF1B2P1, 1616 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