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 503

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5927306copy number variation1nstd209human GRCh38 chr8: 144,445,585-144,447,717 , GRCh37.p13 chr8: 145,670,968-145,673,100 ZFTRAF1
    nsv5856658copy number variation1nstd209human GRCh38 chr8: 144,445,595-144,447,594 , GRCh37.p13 chr8: 145,670,978-145,672,977 ZFTRAF1
    nsv5480943copy number variation1nstd206human GRCh38 chr8: 144,457,734-144,460,634 , GRCh37.p13 chr8: 145,683,117-145,686,017 MIR10400, ZFTRAF1
    nsv5381643copy number variation1nstd102humanUncertain significance GRCh37 chr8: 145,047,561-145,701,149 , GRCh38.p12 chr8: 143,973,393-144,475,766 ZFTRAF1, DGAT1, 40 more genes
    nsv5255340copy number variation1nstd204human GRCh38.p13 chr8: 144,464,365-144,466,564 , GRCh37.p13 chr8: 145,689,748-145,691,947 ZFTRAF1, KIFC2
    nsv5248548copy number variation1nstd204human GRCh38.p13 chr8: 143,866,301-144,531,400 , GRCh37.p13 chr8: 145,146,063-145,756,784 MIR661, EXOSC4, 51 more genes
    nsv4969174copy number variation1nstd200human GRCh37.p13 chr8|NW_003315924.1: 177,164-203,777 , GRCh38 chr8: 144,407,905-144,453,009 , GRCh37.p13 chr8: 145,633,289-145,659,901 SLC39A4, TONSL-AS1, 5 more genes
    nsv4962715copy number variation1nstd200human GRCh38 chr8: 144,465,684-144,466,512 , GRCh37.p13 chr8: 145,691,067-145,691,895 ZFTRAF1, KIFC2
    nsv4829377copy number variation1nstd200human GRCh37 chr8: 145,677,518-145,742,837 , GRCh38.p12 chr8: 144,452,135-144,517,453 MIR10400, LRRC14, 8 more genes
    nsv4813919copy number variation1nstd200human GRCh37 chr8: 145,691,067-145,691,895 , GRCh38.p12 chr8: 144,465,684-144,466,512 KIFC2, ZFTRAF1
    nsv4769373copy number variation1nstd102humanUncertain significance GRCh37 chr8: 145,033,244-146,297,937 , GRCh38.p12 chr8: 143,959,076-145,072,551 ZFTRAF1, PLEC, 68 more genes
    nsv4729603copy number variation1nstd102humanLikely pathogenic GRCh37 chr8: 144,262,042-146,295,771 , GRCh38.p12 chr8: 143,180,625-145,070,385 CYC1, EEF1D, 112 more genes
    nsv4729346copy number variation1nstd102humanUncertain significance GRCh37 chr8: 145,555,125-145,779,806 , GRCh38.p12 chr8: 144,331,462-144,554,422 FOXH1, MIR10400, 26 more genes
    nsv4675664copy number variation1nstd102humanPathogenic GRCh37 chr8: 128,877,995-146,295,771 , GRCh38.p12 chr8: 127,865,749-145,070,385 LOC105375789, LINC02990, 270 more genes
    nsv4675273copy number variation1nstd102humanPathogenic GRCh37 chr8: 121,042,467-146,295,771 , GRCh38.p12 chr8: 120,030,228-145,070,385 TOP1MT, SLA, 379 more genes
    nsv4675215copy number variation1nstd102humanUncertain significance GRCh37 chr8: 145,287,199-145,705,521 , GRCh38.p12 chr8: 144,232,296-144,480,138 BOP1, FOXH1, 25 more genes
    nsv4673042copy number variation1nstd186human GRCh37 chr8: 145,690,981-145,691,834 , GRCh38.p12 chr8: 144,465,598-144,466,451 ZFTRAF1, KIFC2
    nsv4616218copy number variation1nstd183human GRCh37 chr8: 145,690,981-145,691,834 , GRCh38.p12 chr8: 144,465,598-144,466,451 ZFTRAF1, KIFC2
    nsv4614800copy number variation1nstd183human GRCh37 chr8: 145,690,088-145,691,041 , GRCh38.p12 chr8: 144,464,705-144,465,658 ZFTRAF1, KIFC2
    nsv4612766copy number variation1nstd183human GRCh37 chr8: 145,690,416-145,692,851 , GRCh38.p12 chr8: 144,465,033-144,467,468 ZFTRAF1, KIFC2
    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