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 258

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7144215insertion1nstd232human GRCh37.p13 chr5: 138,658,658-138,658,658 , GRCh38.p12 chr5: 139,322,969-139,322,969 MATR3
    nsv7097125copy number variation1nstd102humanUncertain significance GRCh37 chr5: 138,643,105-138,665,084 , GRCh38.p12 chr5: 139,307,416-139,329,395 MATR3
    nsv7097024copy number variation1nstd102humanUncertain significance GRCh37 chr5: 138,266,142-138,861,289 , GRCh38.p12 chr5: 138,930,453-139,481,704 SLC23A1, RNU5B-4P, 20 more genes
    nsv7097022copy number variation1nstd102humanUncertain significance GRCh37 chr5: 136,957,787-138,861,289 , GRCh38.p12 chr5: 137,622,098-139,481,704 CDC25C, SLC23A1, 55 more genes
    nsv7096751copy number variation1nstd102humanUncertain significance GRCh37 chr5: 136,957,787-140,078,137 , GRCh38.p12 chr5: 137,622,098-140,698,552 CDC25C, LOC100128966, 94 more genes
    nsv7057082inversion1nstd229human GRCh38 chr5: 139,208,712-142,493,851 , GRCh37.p13 chr5: 138,544,401-141,873,416 SPRY4-AS1, SPRY4, 151 more genes
    nsv6796944copy number variation1nstd229human GRCh38 chr5: 139,310,340-139,400,844 , GRCh37.p13 chr5: 138,646,029-138,736,533 PROB1, PAIP2, 5 more genes
    nsv6796795copy number variation1nstd229human GRCh38 chr5: 139,309,901-139,373,300 , GRCh37.p13 chr5: 138,645,590-138,708,989 RN7SKP64, PAIP2, 2 more genes
    nsv6796360copy number variation1nstd229human GRCh38 chr5: 139,298,314-139,314,456 , GRCh37.p13 chr5: 138,634,003-138,650,145 RNA5SP195, MATR3
    nsv6794064copy number variation1nstd229human GRCh38 chr5: 139,260,658-139,274,282 , GRCh37.p13 chr5: 138,596,347-138,609,971 SNORA74D, MATR3, 1 more genes
    nsv6780567copy number variation1nstd229human GRCh38 chr5: 139,264,264-139,309,626 , GRCh37.p13 chr5: 138,599,953-138,645,315 MATR3, SNHG4, 3 more genes
    nsv6780059copy number variation1nstd229human GRCh38 chr5: 139,280,225-139,291,083 , GRCh37.p13 chr5: 138,615,914-138,626,772 SNHG4, MATR3
    nsv6779115copy number variation1nstd229human GRCh38 chr5: 139,309,190-139,312,296 , GRCh37.p13 chr5: 138,644,879-138,647,985 MATR3
    nsv6778440copy number variation1nstd229human GRCh38 chr5: 139,104,141-139,300,722 , GRCh37.p13 chr5: 138,439,830-138,636,411 SNHG4, SNORA74A, 5 more genes
    nsv6636861copy number variation1nstd102humanUncertain significance GRCh37 chr5: 137,893,096-138,868,605 , GRCh38.p12 chr5: 138,557,407-139,489,020 HSPA9, ECSCR, 27 more genes
    nsv6630305copy number variation1nstd224human GRCh37 chr5: 138,652,744-138,764,329 , GRCh38.p12 chr5: 139,317,055-139,428,640 MATR3, SLC23A1, 6 more genes
    nsv6575425inversion1nstd223human GRCh38 chr5: 139,321,319-139,321,628 , GRCh37.p13 chr5: 138,657,008-138,657,317 MATR3
    nsv6569641inversion1nstd223human GRCh38 chr5: 139,327,889-139,328,719 , GRCh37.p13 chr5: 138,663,578-138,664,408 MATR3
    nsv6565204inversion1nstd223human GRCh38 chr5: 139,320,309-139,320,915 , GRCh37.p13 chr5: 138,655,998-138,656,604 MATR3
    nsv6562146inversion1nstd223human GRCh38 chr5: 139,300,095-139,300,825 , GRCh37.p13 chr5: 138,635,784-138,636,514 MATR3, RNA5SP195
    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