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 328

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097529copy number variation1nstd102humanUncertain significance GRCh37 chr5: 32,355,866-32,786,451 , GRCh38.p12 chr5: 32,355,760-32,786,345 TMEM183AP2, NPR3, 4 more genes
    nsv7039407inversion1nstd229human GRCh38 chr5: 32,373,124-34,861,255 , GRCh37.p13 chr5: 32,373,230-34,861,360 TTC23L, LOC105374715, 31 more genes
    nsv6777196copy number variation1nstd229human GRCh38 chr5: 32,766,301-32,769,700 , GRCh37.p13 chr5: 32,766,407-32,769,806 NPR3
    nsv6774338copy number variation1nstd229human GRCh38 chr5: 32,780,085-32,787,836 , GRCh37.p13 chr5: 32,780,191-32,787,942 NPR3
    nsv6772473copy number variation1nstd229human GRCh38 chr5: 32,699,714-33,194,983 , GRCh37.p13 chr5: 32,699,820-33,195,089 LOC105374715, RPS8P8, 2 more genes
    nsv6770578copy number variation1nstd229human GRCh38 chr5: 32,675,392-32,712,326 , GRCh37.p13 chr5: 32,675,498-32,712,432 NPR3
    nsv6770095copy number variation1nstd229human GRCh38 chr5: 32,780,559-32,780,787 , GRCh37.p13 chr5: 32,780,665-32,780,893 NPR3
    nsv6769898copy number variation1nstd229human GRCh38 chr5: 32,753,748-32,753,964 , GRCh37.p13 chr5: 32,753,854-32,754,070 NPR3
    nsv6769463copy number variation1nstd229human GRCh38 chr5: 32,683,815-32,687,106 , GRCh37.p13 chr5: 32,683,921-32,687,212 NPR3
    nsv6769164copy number variation1nstd229human GRCh38 chr5: 32,731,959-32,732,274 , GRCh37.p13 chr5: 32,732,065-32,732,380 NPR3
    nsv6766364copy number variation1nstd229human GRCh38 chr5: 32,614,001-32,722,900 , GRCh37.p13 chr5: 32,614,107-32,723,006 LINC02061, NPR3
    nsv6766340copy number variation1nstd229human GRCh38 chr5: 32,711,901-32,714,300 , GRCh37.p13 chr5: 32,712,007-32,714,406 NPR3
    nsv6765252copy number variation1nstd229human GRCh38 chr5: 32,693,101-32,700,300 , GRCh37.p13 chr5: 32,693,207-32,700,406 NPR3
    nsv6763348copy number variation1nstd229human GRCh38 chr5: 32,657,492-32,698,794 , GRCh37.p13 chr5: 32,657,598-32,698,900 NPR3
    nsv6759470copy number variation1nstd229human GRCh38 chr5: 32,698,720-32,701,300 , GRCh37.p13 chr5: 32,698,826-32,701,406 NPR3
    nsv6636973copy number variation1nstd102humanPathogenic GRCh37 chr5: 29,348,753-46,389,339 , GRCh38.p12 chr5: 29,348,646-46,389,237 SUB1, LOC105374740, 210 more genes
    nsv6630398copy number variation1nstd224human GRCh37 chr5: 32,625,480-32,722,499 , GRCh38.p12 chr5: 32,625,374-32,722,393 LINC02061, NPR3
    nsv6571646inversion1nstd223human GRCh38 chr5: 32,705,410-32,706,260 , GRCh37.p13 chr5: 32,705,516-32,706,366 NPR3
    nsv6392726copy number variation1nstd223human GRCh38 chr5: 32,779,228-32,779,241 , GRCh37.p13 chr5: 32,779,334-32,779,347 NPR3
    nsv6385921copy number variation1nstd223human GRCh38 chr5: 32,709,701-32,713,400 , GRCh37.p13 chr5: 32,709,807-32,713,506 NPR3
    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