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 109

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5704365mobile element insertion2nstd211human GRCh38 chr15: 49,177,060-49,177,060 , GRCh37.p13 chr15: 49,469,257-49,469,257 GALK2, RPL15P19
    nsv5420983mobile element insertion1nstd206human GRCh38 chr15: 49,177,060-49,177,103 , GRCh37.p13 chr15: 49,469,257-49,469,300 RPL15P19, GALK2
    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
    nsv5153557mobile element insertion1nstd203human GRCh38 chr15: 49,177,044-49,177,060 , GRCh37.p13 chr15: 49,469,241-49,469,257 GALK2, RPL15P19
    nsv5038422inversion1nstd200human GRCh38 chr15: 40,121,948-64,050,807 , GRCh37.p13 chr15: 40,414,149-64,343,006 , EIF4EBP2P2, 475 more genes
    nsv5005372copy number variation1nstd200human GRCh38 chr15: 49,124,333-49,268,997 , GRCh37.p13 chr15: 49,416,530-49,561,194 MIR4716, COPS2, 4 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
    nsv4863777copy number variation1nstd200human GRCh37 chr15: 49,416,530-49,561,194 , GRCh38.p12 chr15: 49,124,333-49,268,997 GALK2, MIR4716, 4 more genes
    nsv4769387copy number variation1nstd102humanPathogenic GRCh37 chr15: 48,744,917-53,851,050 , GRCh38.p12 chr15: 48,452,720-53,558,853 BCL2L10, RNA5SP394, 86 more genes
    nsv4728937copy number variation1nstd102humanUncertain significance GRCh37 chr15: 49,452,059-49,550,863 , GRCh38.p12 chr15: 49,159,862-49,258,666 RN7SL307P, GALK2, 2 more genes
    nsv4675095copy number variation1nstd102humanPathogenic GRCh37 chr15: 47,192,561-50,819,726 , GRCh38.p12 chr15: 46,900,363-50,527,529 LOC102724587, LOC645405, 51 more genes
    nsv4674873copy number variation1nstd102humanUncertain significance GRCh37 chr15: 49,142,668-49,514,861 , GRCh38.p12 chr15: 48,850,471-49,222,664 KRT8P24, EID1, 9 more genes
    nsv4540831insertion1nstd166human GRCh37.p13 chr15: 49,469,241-49,469,241 , GRCh38.p12 chr15: 49,177,044-49,177,044 GALK2, RPL15P19
    nsv4456196copy number variation1nstd102humanPathogenic GRCh37 chr15: 48,000,433-60,747,551 , GRCh38.p12 chr15: 47,708,236-60,455,352 MIR1266, AQP9, 199 more genes
    nsv4455359copy number variation1nstd102humanPathogenic GRCh37 chr15: 49,031,132-56,740,397 , GRCh38.p12 chr15: 48,738,935-56,448,199 MIR4716, RPS13P8, 112 more genes
    nsv3922320copy number variation1nstd102humanUncertain significance GRCh37 chr15: 49,356,530-50,468,980 , GRCh38 chr15: 49,064,333-50,176,783 , NCBI36 chr15: 47,143,822-48,256,272 DTWD1, GALK2, 13 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
    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