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 272

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099215copy number variation1nstd231human GRCh38.p12 chr1: 84,991,383-97,594,649 , GRCh37 chr1: 85,457,066-98,060,205 ABCA4, BRDT, 220 more genes
    nsv7055288inversion1nstd229human GRCh38 chr1: 89,551,392-89,593,013 , GRCh37.p13 chr1: 90,016,951-90,058,572 LRRC8B
    nsv7051476inversion1nstd229human GRCh38 chr1: 87,647,529-89,769,769 , GRCh37.p13 chr1: 88,113,212-90,235,328 RBMXL1, PTGES3P1, 35 more genes
    nsv7050556inversion1nstd229human GRCh38 chr1: 89,590,432-89,590,505 , GRCh37.p13 chr1: 90,055,991-90,056,064 LRRC8B
    nsv7049179inversion1nstd229human GRCh38 chr1: 89,529,471-89,535,916 , GRCh37.p13 chr1: 89,995,030-90,001,475 LRRC8B
    nsv7046056inversion1nstd229human GRCh38 chr1: 89,560,452-89,585,972 , GRCh37.p13 chr1: 90,026,011-90,051,531 LRRC8B
    nsv7045277inversion1nstd229human GRCh38 chr1: 89,219,136-91,269,986 , GRCh37.p13 chr1: 89,684,819-91,735,543 LOC105378847, CAPNS1P1, 33 more genes
    nsv7042360inversion1nstd229human GRCh38 chr1: 89,189,894-89,972,465 , GRCh37.p13 chr1: 89,655,577-90,438,024 LRRC8B, LRRC8C-DT, 16 more genes
    nsv7041808inversion1nstd229human GRCh38 chr1: 89,551,224-89,595,600 , GRCh37.p13 chr1: 90,016,783-90,061,159 LRRC8B
    nsv6657001copy number variation1nstd229human GRCh38 chr1: 89,586,424-89,586,740 , GRCh37.p13 chr1: 90,051,983-90,052,299 LRRC8B
    nsv6657000copy number variation1nstd229human GRCh38 chr1: 89,577,375-89,581,460 , GRCh37.p13 chr1: 90,042,934-90,047,019 LRRC8B
    nsv6656864copy number variation1nstd229human GRCh38 chr1: 89,542,350-89,546,709 , GRCh37.p13 chr1: 90,007,909-90,012,268 LRRC8B
    nsv6655971copy number variation1nstd229human GRCh38 chr1: 89,361,450-89,597,492 , GRCh37.p13 chr1: 89,827,009-90,063,051 LOC105378844, CAPNS1P1, 3 more genes
    nsv6626480copy number variation1nstd224human GRCh37 chr1: 89,587,610-90,005,132 , GRCh38.p12 chr1: 89,121,927-89,539,573 GBP5, LOC100421401, 12 more genes
    nsv6542421inversion1nstd223human GRCh38 chr1: 85,951,963-92,104,665 , GRCh37.p13 chr1: 86,417,646-92,570,222 LOC105378844, LINC01773, 104 more genes
    nsv6335206copy number variation1nstd223human GRCh38 chr1: 89,521,101-89,527,600 , GRCh37.p13 chr1: 89,986,660-89,993,159 LRRC8B
    nsv6334204copy number variation1nstd223human GRCh38 chr1: 89,533,526-89,538,042 , GRCh37.p13 chr1: 89,999,085-90,003,601 LRRC8B
    nsv6330296copy number variation1nstd223human GRCh38 chr1: 89,594,401-89,597,900 , GRCh37.p13 chr1: 90,059,960-90,063,459 LRRC8B
    nsv6328194copy number variation1nstd223human GRCh38 chr1: 89,567,401-89,569,100 , GRCh37.p13 chr1: 90,032,960-90,034,659 LRRC8B
    nsv6327515copy number variation1nstd223human GRCh38 chr1: 89,542,360-89,546,708 , GRCh37.p13 chr1: 90,007,919-90,012,267 LRRC8B
    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