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 901

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5884312copy number variation1nstd209human GRCh38 chr1: 1,296,791-1,296,852 , GRCh37.p13 chr1: 1,232,171-1,232,232 ACAP3
    nsv5881509copy number variation1nstd209human GRCh38 chr1: 1,264,791-1,546,719 , GRCh37.p13 chr1: 1,200,171-1,482,099 , MRPL20-AS1, 30 more genes
    nsv5870872copy number variation1nstd209human GRCh38 chr1: 1,298,948-1,299,159 , GRCh37.p13 chr1: 1,234,328-1,234,539 ACAP3
    nsv5869237copy number variation1nstd209human GRCh38 chr1: 1,297,141-1,297,320 , GRCh37.p13 chr1: 1,232,521-1,232,700 ACAP3
    nsv5868523copy number variation1nstd209human GRCh38 chr1: 1,297,574-1,297,751 , GRCh37.p13 chr1: 1,232,954-1,233,131 ACAP3
    nsv5827761copy number variation1nstd209human GRCh38 chr1: 1,294,166-1,296,965 , GRCh37.p13 chr1: 1,229,546-1,232,345 MIR6726, ACAP3
    nsv5827651copy number variation1nstd209human GRCh38 chr1: 1,298,475-1,315,259 , GRCh37.p13 chr1: 1,233,855-1,250,639 MIR6727, INTS11, 3 more genes
    nsv5609398insertion1nstd207human GRCh38 chr1: 1,296,332-1,296,332 , GRCh37.p13 chr1: 1,231,712-1,231,712 ACAP3, MIR6726
    nsv5605988insertion1nstd207human GRCh38 chr1: 1,293,731-1,293,731 , GRCh37.p13 chr1: 1,229,111-1,229,111 ACAP3
    nsv5583325copy number variation1nstd207human GRCh38 chr1: 1,297,193-1,297,688 , GRCh37.p13 chr1: 1,232,573-1,233,068 ACAP3
    nsv5577074copy number variation1nstd207human GRCh38 chr1: 1,297,619-1,297,750 , GRCh37.p13 chr1: 1,232,999-1,233,130 ACAP3
    nsv5567059copy number variation1nstd207human GRCh38 chr1: 1,297,141-1,297,274 , GRCh37.p13 chr1: 1,232,521-1,232,654 ACAP3
    nsv5428946copy number variation1nstd206human GRCh38 chr1: 1,305,329-1,305,411 , GRCh37.p13 chr1: 1,240,709-1,240,791 ACAP3
    nsv5384351copy number variation1nstd186human GRCh37 chr1: 1,232,467-1,233,132 , GRCh38.p12 chr1: 1,297,087-1,297,752 ACAP3
    nsv5384163copy number variation1nstd186human GRCh37 chr1: 1,232,482-1,232,820 , GRCh38.p12 chr1: 1,297,102-1,297,440 ACAP3
    nsv5383148copy number variation1nstd186human GRCh37 chr1: 1,232,716-1,233,046 , GRCh38.p12 chr1: 1,297,336-1,297,666 ACAP3
    nsv5382798copy number variation1nstd186human GRCh37 chr1: 1,232,763-1,233,141 , GRCh38.p12 chr1: 1,297,383-1,297,761 ACAP3
    nsv5381304copy number variation2nstd102humanUncertain significance GRCh37 chr1: 948,954-1,284,445 , GRCh38.p12 chr1: 1,013,574-1,349,065 LOC100288175, UBE2J2, 28 more genes
    nsv5361468translocation1nstd200human GRCh38 chr1: 1,156,214-1,156,214 , GRCh38 chr1: 1,304,767-1,304,767 , GRCh37.p13 chr1: 1,091,594-1,091,594 , GRCh37.p13 chr1: 1,240,147-1,240,147 ACAP3, SNORD167
    nsv5290017copy number variation1nstd204human GRCh38.p13 chr1: 1,297,089-1,297,807 , GRCh37.p13 chr1: 1,232,469-1,233,187 ACAP3
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Recent activity

    You are here: NCBI > Variation > Database of Genomic Structural Variation (dbVar)
    Support Center