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 226

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7093376copy number variation1nstd102humanLikely pathogenic GRCh37 chr5: 156,786,013-162,945,369 , GRCh38.p12 chr5: 157,359,005-163,518,363 ADRA1B, CCNG1, 81 more genes
    nsv7052590inversion1nstd229human GRCh38 chr5: 154,695,187-159,271,728 , GRCh37.p13 chr5: 154,074,747-158,698,736 MRPL22, LOC105377673, 58 more genes
    nsv6795768copy number variation1nstd229human GRCh38 chr5: 157,548,967-157,551,177 , GRCh37.p13 chr5: 156,975,975-156,978,185 ADAM19
    nsv6794139copy number variation1nstd229human GRCh38 chr5: 157,532,100-157,532,197 , GRCh37.p13 chr5: 156,959,108-156,959,205 ADAM19
    nsv6792941copy number variation1nstd229human GRCh38 chr5: 157,544,328-157,544,924 , GRCh37.p13 chr5: 156,971,336-156,971,932 ADAM19
    nsv6788992copy number variation1nstd229human GRCh38 chr5: 157,541,064-157,548,010 , GRCh37.p13 chr5: 156,968,072-156,975,018 ADAM19
    nsv6785097copy number variation1nstd229human GRCh38 chr5: 157,527,701-157,530,700 , GRCh37.p13 chr5: 156,954,709-156,957,708 ADAM19
    nsv6784867copy number variation1nstd229human GRCh38 chr5: 157,548,718-157,549,265 , GRCh37.p13 chr5: 156,975,726-156,976,273 ADAM19
    nsv6783588copy number variation1nstd229human GRCh38 chr5: 157,490,401-157,494,300 , GRCh37.p13 chr5: 156,917,409-156,921,308 ADAM19
    nsv6782254copy number variation1nstd229human GRCh38 chr5: 157,503,504-157,504,109 , GRCh37.p13 chr5: 156,930,512-156,931,117 ADAM19
    nsv6781396copy number variation1nstd229human GRCh38 chr5: 157,557,283-157,559,109 , GRCh37.p13 chr5: 156,984,291-156,986,117 ADAM19
    nsv6636891copy number variation1nstd102humanPathogenic GRCh37 chr5: 150,535,183-172,906,793 , GRCh38.p12 chr5: 151,155,622-173,479,790 EFCAB9, LOC112267936, 287 more genes
    nsv6636540copy number variation1nstd102humanUncertain significance GRCh37 chr5: 156,486,127-156,930,814 , GRCh38.p12 chr5: 157,059,116-157,503,806 ADAM19, HAVCR1, 9 more genes
    nsv6567810inversion1nstd223human GRCh38 chr5: 157,567,601-157,568,240 , GRCh37.p13 chr5: 156,994,609-156,995,248 ADAM19
    nsv6315448copy number variation1nstd102humanPathogenic GRCh37 chr5: 149,010,383-180,719,789 , GRCh38.p12 chr5: 149,630,820-181,292,788 GRM6, MIR1229, 554 more genes
    nsv6308643mobile element insertion1nstd186human GRCh37 chr5: 156,925,824-156,925,875 , GRCh38.p12 chr5: 157,498,816-157,498,867 ADAM19
    nsv6298015copy number variation1nstd186human GRCh37 chr5: 156,990,146-156,990,213 , GRCh38.p12 chr5: 157,563,138-157,563,205 ADAM19
    nsv6290966copy number variation1nstd102humannot provided GRCh37 chr5: 155,970,607-162,450,579 , GRCh38.p12 chr5: 156,543,597-163,023,573 C1QTNF2, MED7, 86 more genes
    nsv6256332mobile element insertion1nstd215human GRCh38 chr5: 157,490,513-157,490,513 , GRCh37.p13 chr5: 156,917,521-156,917,521 ADAM19
    nsv6135388copy number variation1nstd213human GRCh37 chr5: 153,010,000-160,030,001 , GRCh38.p12 chr5: 153,630,440-160,602,994 ADRA1B, EBF1, 107 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