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 74

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5906989copy number variation1nstd209human GRCh38 chr5: 151,752,338-151,752,619 , GRCh37.p13 chr5: 151,131,899-151,132,180 ATOX1, ATOX1-AS1
    nsv5457956copy number variation1nstd206human GRCh38 chr5: 151,752,338-151,752,650 , GRCh37.p13 chr5: 151,131,899-151,132,211 ATOX1, ATOX1-AS1
    nsv5362548translocation1nstd200human GRCh38 chr5: 151,752,338-151,752,338 , GRCh38 chr5: 151,752,650-151,752,650 , GRCh37.p13 chr5: 151,131,899-151,131,899 , GRCh37.p13 chr5: 151,132,211-151,132,211 ATOX1-AS1, ATOX1
    nsv5335485translocation1nstd200human GRCh37 chr5: 151,131,899-151,131,899 , GRCh37 chr5: 151,132,211-151,132,211 , GRCh38.p12 chr5: 151,752,338-151,752,338 , GRCh38.p12 chr5: 151,752,650-151,752,650 ATOX1, ATOX1-AS1
    nsv5318247copy number variation1nstd204human GRCh37.p13 chr5: 151,131,889-151,132,219 , GRCh38.p13 chr5: 151,752,328-151,752,658 ATOX1, ATOX1-AS1
    nsv5036421inversion1nstd200human GRCh38 chr5: 85,193,812-162,906,830 , GRCh37.p13 chr5: 84,489,630-162,333,836 , PRR16, 1116 more genes
    nsv4947215copy number variation1nstd200human GRCh38 chr5: 93,957,557-155,223,076 , GRCh37.p13 chr5: 93,293,262-154,602,636 , TGFBI, 937 more genes
    nsv4939220copy number variation1nstd200human GRCh38 chr5: 151,758,776-151,764,927 , GRCh37.p13 chr5: 151,138,337-151,144,488 ATOX1, RPLP1P6
    nsv4885569inversion1nstd200human GRCh37 chr5: 84,489,636-162,333,841 , GRCh38.p12 chr5: 85,193,818-162,906,835 , UBE2B, 1116 more genes
    nsv4649346copy number variation1nstd186human GRCh37 chr5: 151,131,899-151,132,484 , GRCh38.p12 chr5: 151,752,338-151,752,923 ATOX1, ATOX1-AS1
    nsv4563567mobile element insertion1nstd166human GRCh37.p13 chr5: 151,121,644-151,121,644 , GRCh38.p12 chr5: 151,742,083-151,742,083 ATOX1
    nsv4127803copy number variation1nstd166human GRCh37.p13 chr5: 151,131,899-151,132,484 , GRCh38.p12 chr5: 151,752,338-151,752,923 ATOX1, ATOX1-AS1
    nsv3923414copy number variation1nstd102humanPathogenic GRCh37 chr5: 130,196,621-154,701,371 , NCBI36 chr5: 130,224,520-154,681,564 , GRCh38 chr5: 130,860,928-155,321,811 HNRNPA3P7, RNU6-456P, 514 more genes
    nsv3921182copy number variation1nstd102humanPathogenic GRCh37 chr5: 149,094,155-180,699,152 , GRCh38 chr5: 149,714,592-181,272,151 , NCBI36 chr5: 149,074,348-180,631,758 RN7SKP148, TCOF1, 553 more genes
    nsv3914878copy number variation1nstd102humanPathogenic NCBI36 chr5: 146,520,648-163,194,778 , GRCh37.p13 chr5: 146,540,455-163,262,200 , GRCh38.p12 chr5: 147,160,892-163,835,194 LOC105378231, RN7SKP232, 247 more genes
    nsv3914009copy number variation1nstd102humanPathogenic NCBI36 chr5: 129,211,386-152,713,299 , GRCh38 chr5: 129,847,794-153,353,546 , GRCh37 chr5: 129,183,487-152,733,106 UQCRQ, SNHG4, 489 more genes
    nsv3912937copy number variation1nstd102humanPathogenic GRCh37 chr5: 105,955,289-155,551,397 , NCBI36 chr5: 105,983,188-155,483,975 , GRCh38 chr5: 106,619,588-156,124,387 LINC01023, CTB-99A3.1, 783 more genes
    nsv3912593copy number variation1nstd102humanUncertain significance NCBI36 chr5: 332,389-180,837,866 , GRCh37.p13 chr5: 279,389-180,905,260 , GRCh38.p12 chr5: 279,274-181,478,259 LOC105378993, LOC107986375, 2492 more genes
    nsv3889848copy number variation1nstd102humanPathogenic GRCh37 chr5: 17,628,741-176,575,720 , GRCh38.p12 chr5: 17,628,632-177,148,719 MEGF10, LOC100128407, 2080 more genes
    nsv3886374copy number variation1nstd102humanPathogenic GRCh37 chr5: 13,648-180,905,029 , GRCh38.p12 chr5: 13,648-181,478,028 LOC105374618, HARS1, 2499 more genes
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Recent activity

    You are here: NCBI > Variation > Database of Genomic Structural Variation (dbVar)
    Support Center