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 318

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7077118inversion1nstd229human GRCh38 chr13: 29,768,510-29,768,588 , GRCh37.p13 chr13: 30,342,647-30,342,725 UBL3
    nsv7068863inversion1nstd229human GRCh38 chr13: 27,564,614-31,455,391 , GRCh37.p13 chr13: 28,138,751-32,029,528 MFAP1P1, RN7SL272P, 70 more genes
    nsv7058180inversion1nstd229human GRCh38 chr13: 29,278,598-37,954,955 , GRCh37.p13 chr13: 29,852,735-38,529,092 ZAR1L, HSPH1, 116 more genes
    nsv6936533copy number variation1nstd229human GRCh38 chr13: 29,831,101-29,845,300 , GRCh37.p13 chr13: 30,405,238-30,419,437 UBL3
    nsv6930527copy number variation1nstd229human GRCh38 chr13: 29,847,772-29,849,390 , GRCh37.p13 chr13: 30,421,909-30,423,527 UBL3
    nsv6926199copy number variation1nstd229human GRCh38 chr13: 29,820,517-29,825,706 , GRCh37.p13 chr13: 30,394,654-30,399,843 UBL3
    nsv6925573copy number variation1nstd229human GRCh38 chr13: 29,788,064-29,795,027 , GRCh37.p13 chr13: 30,362,201-30,369,164 UBL3
    nsv6924810copy number variation1nstd229human GRCh38 chr13: 29,805,698-29,811,197 , GRCh37.p13 chr13: 30,379,835-30,385,334 UBL3
    nsv6924780copy number variation1nstd229human GRCh38 chr13: 29,847,826-29,855,678 , GRCh37.p13 chr13: 30,421,963-30,429,815 UBL3
    nsv6920551copy number variation1nstd229human GRCh38 chr13: 29,823,083-29,824,439 , GRCh37.p13 chr13: 30,397,220-30,398,576 UBL3
    nsv6919029copy number variation1nstd229human GRCh38 chr13: 29,787,674-29,793,715 , GRCh37.p13 chr13: 30,361,811-30,367,852 UBL3
    nsv6918844copy number variation1nstd229human GRCh38 chr13: 29,787,201-29,790,200 , GRCh37.p13 chr13: 30,361,338-30,364,337 UBL3
    nsv6634431copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,253,848-115,108,937 , GRCh38.p12 chr13: 18,679,708-114,343,462 MTUS2-AS1, LOC105370213, 1330 more genes
    nsv6582661inversion1nstd223human GRCh38 chr13: 29,776,281-29,776,887 , GRCh37.p13 chr13: 30,350,418-30,351,024 UBL3
    nsv6494139copy number variation1nstd223human GRCh38 chr13: 29,809,580-29,810,235 , GRCh37.p13 chr13: 30,383,717-30,384,372 UBL3
    nsv6493133copy number variation1nstd223human GRCh38 chr13: 29,787,737-29,788,252 , GRCh37.p13 chr13: 30,361,874-30,362,389 UBL3
    nsv6485162copy number variation1nstd223human GRCh38 chr13: 29,787,169-29,790,202 , GRCh37.p13 chr13: 30,361,306-30,364,339 UBL3
    nsv6484609copy number variation1nstd223human GRCh38 chr13: 29,778,220-29,778,935 , GRCh37.p13 chr13: 30,352,357-30,353,072 UBL3
    nsv6482196copy number variation1nstd223human GRCh38 chr13: 29,791,322-29,792,070 , GRCh37.p13 chr13: 30,365,459-30,366,207 UBL3
    nsv6481252copy number variation1nstd223human GRCh38 chr13: 29,823,169-29,824,442 , GRCh37.p13 chr13: 30,397,306-30,398,579 UBL3
    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