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 159

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv6797266copy number variation1nstd229human GRCh38 chr5: 139,391,884-139,393,777 , GRCh37.p13 chr5: 138,727,573-138,729,466 SPATA24, PROB1
    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
    nsv6794526copy number variation1nstd229human GRCh38 chr5: 139,400,923-139,411,448 , GRCh37.p13 chr5: 138,736,612-138,747,137 DNAJC18, SPATA24
    nsv6792356copy number variation1nstd229human GRCh38 chr5: 139,398,761-139,399,055 , GRCh37.p13 chr5: 138,734,450-138,734,744 SPATA24
    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
    nsv6414173copy number variation1nstd223human GRCh38 chr5: 139,398,728-139,399,490 , GRCh37.p13 chr5: 138,734,417-138,735,179 SPATA24
    nsv6405600copy number variation1nstd223human GRCh38 chr5: 137,606,101-142,582,700 , GRCh37.p13 chr5: 136,941,790-141,962,265 TMCO6, PCDHB17P, 191 more genes
    nsv6404646copy number variation1nstd223human GRCh38 chr5: 139,397,726-139,400,479 , GRCh37.p13 chr5: 138,733,415-138,736,168 SPATA24
    nsv6401789copy number variation1nstd223human GRCh38 chr5: 139,398,901-139,401,100 , GRCh37.p13 chr5: 138,734,590-138,736,789 SPATA24
    nsv6399113copy number variation1nstd223human GRCh38 chr5: 139,400,918-139,411,449 , GRCh37.p13 chr5: 138,736,607-138,747,138 DNAJC18, SPATA24
    nsv6291250copy number variation1nstd102humanUncertain significance GRCh37 chr5: 138,386,858-138,935,115 , GRCh38.p12 chr5: 139,051,169-139,555,530 STING1, SPATA24, 18 more genes
    nsv6291016copy number variation1nstd102humanUncertain significance GRCh37 chr5: 138,675,227-139,314,012 , GRCh38.p12 chr5: 139,339,538-139,934,427 PROB1, H3P25, 19 more genes
    nsv6140934copy number variation1nstd206human GRCh38 chr5: 139,398,741-139,399,075 , GRCh37.p13 chr5: 138,734,430-138,734,764 SPATA24
    nsv6140372copy number variation1nstd206human GRCh38 chr5: 139,398,968-139,399,256 , GRCh37.p13 chr5: 138,734,657-138,734,945 SPATA24
    nsv6135653copy number variation1nstd213human GRCh37 chr5: 138,340,000-143,460,001 , GRCh38.p12 chr5: 139,004,311-144,080,436 CD14, DIAPH1, 170 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