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 109

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7054087inversion1nstd229human GRCh38 chr3: 45,220,999-45,223,022 , GRCh37.p13 chr3: 45,262,491-45,264,514 TMEM158
    nsv7049375inversion1nstd229human GRCh38 chr3: 45,009,134-45,392,115 , GRCh37.p13 chr3: 45,050,626-45,433,607 LOC105377061, LOC101928636, 8 more genes
    nsv6704139copy number variation1nstd229human GRCh38 chr3: 45,201,485-45,248,810 , GRCh37.p13 chr3: 45,242,977-45,290,302 TMEM158, LOC101928636
    nsv6370436copy number variation1nstd223human GRCh38 chr3: 45,223,901-45,227,100 , GRCh37.p13 chr3: 45,265,393-45,268,592 TMEM158
    nsv6369235copy number variation1nstd223human GRCh38 chr3: 45,225,201-45,228,300 , GRCh37.p13 chr3: 45,266,693-45,269,792 TMEM158
    nsv6315166copy number variation1nstd102humanPathogenic GRCh37 chr3: 44,948,482-49,115,809 , GRCh38.p12 chr3: 44,906,990-49,078,376 TMEM89, TGM4, 129 more genes
    nsv6134813copy number variation1nstd213human GRCh37 chr3: 44,650,000-45,860,001 , GRCh38.p12 chr3: 44,608,508-45,818,509 TGM4, CLEC3B, 35 more genes
    nsv5377484translocation1nstd200human GRCh38 chr3: 45,221,007-45,221,007 , GRCh38 chr3: 45,222,626-45,222,626 , GRCh37.p13 chr3: 45,262,499-45,262,499 , GRCh37.p13 chr3: 45,264,118-45,264,118 TMEM158
    nsv5377483translocation1nstd200human GRCh38 chr3: 45,223,026-45,223,026 , GRCh38 chr3: 45,220,999-45,220,999 , GRCh37.p13 chr3: 45,262,491-45,262,491 , GRCh37.p13 chr3: 45,264,518-45,264,518 TMEM158
    nsv5037434inversion1nstd200human GRCh38 chr3: 5,031,119-56,902,223 , GRCh37.p13 chr3: 5,072,804-56,936,251 , IRAK2, 925 more genes
    nsv5030280inversion1nstd200human GRCh38 chr3: 3,432,416-77,775,308 , GRCh37.p13 chr3: 3,474,100-77,824,459 , BHLHE40, 1198 more genes
    nsv4888770inversion1nstd200human GRCh37 chr3: 3,474,100-77,824,459 , GRCh38.p12 chr3: 3,432,416-77,775,308 , ATRIP, 1198 more genes
    nsv4877503inversion1nstd200human GRCh37 chr3: 24,885,632-100,711,157 , GRCh38.p12 chr3: 24,844,141-100,992,313 , LINC00692, 1088 more genes
    nsv4674744copy number variation1nstd102humanUncertain significance GRCh37 chr3: 44,444,902-45,413,927 , GRCh38.p12 chr3: 44,403,410-45,372,435 RPL12P44, TMEM42, 37 more genes
    nsv4564128inversion1nstd166human GRCh37.p13 chr3: 3,474,047-77,824,459 , GRCh38.p12 chr3: 3,432,363-77,775,308 , ACY1, 1205 more genes
    nsv4373432copy number variation1nstd173human GRCh37 chr3: 45,243,355-45,285,935 , GRCh38.p12 chr3: 45,201,863-45,244,443 TMEM158, LOC101928636
    nsv4368843copy number variation1nstd173human GRCh37 chr3: 45,241,165-45,285,935 , GRCh38.p12 chr3: 45,199,673-45,244,443 TMEM158, LOC101928636
    nsv4365275copy number variation2nstd173human GRCh37 chr3: 45,243,355-45,285,947 , GRCh38.p12 chr3: 45,201,863-45,244,455 TMEM158, LOC101928636
    nsv4347762copy number variation1nstd102humanPathogenic GRCh37 chr3: 45,153,770-53,878,616 , GRCh38.p12 chr3: 45,112,278-53,844,589 UQCRC1, DHX30, 291 more genes
    nsv4090166copy number variation1nstd166human GRCh37.p13 chr3: 45,267,729-45,267,791 , GRCh38.p12 chr3: 45,226,237-45,226,299 TMEM158
    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