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 317

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5970490inversion1nstd209human GRCh38 chr2: 240,811,836-241,011,847 , GRCh37.p13 chr2: 241,751,253-241,951,264 AGXT, KIF1A, 7 more genes
    nsv5890162copy number variation1nstd209human GRCh38 chr2: 240,892,569-240,892,622 , GRCh37.p13 chr2: 241,831,986-241,832,039 MAB21L4
    nsv5833131copy number variation1nstd209human GRCh38 chr2: 240,872,481-240,905,899 , GRCh37.p13 chr2: 241,811,898-241,845,316 CROCC2, AGXT, 1 more genes
    nsv5567396copy number variation1nstd207human GRCh38 chr2: 240,892,569-240,892,622 , GRCh37.p13 chr2: 241,831,986-241,832,039 MAB21L4
    nsv5381323copy number variation1nstd102humanPathogenic GRCh37 chr2: 237,201,756-243,048,760 , GRCh38.p12 chr2: 236,293,113-242,106,609 LRRFIP1, GPR35, 133 more genes
    nsv4910444copy number variation1nstd200human GRCh38 chr2: 240,888,498-240,888,667 , GRCh37.p13 chr2: 241,827,915-241,828,084 MAB21L4
    nsv4768328copy number variation1nstd102humanPathogenic GRCh37 chr2: 233,110,452-243,028,452 , GRCh38.p12 chr2: 232,245,742-242,086,301 LOC107985836, LOC105373980, 217 more genes
    nsv4728725copy number variation1nstd102humanPathogenic GRCh37 chr2: 178,397,959-243,007,457 , GRCh38.p12 chr2: 177,533,231-242,065,306 LOC105376755, FZD7, 1013 more genes
    nsv4684239copy number variation1nstd102humanUncertain significance GRCh37 chr2: 238,863,455-243,048,760 , GRCh38.p12 chr2: 237,954,813-242,106,609 LOC285191, MTERF4, 103 more genes
    nsv4684149copy number variation1nstd102humanUncertain significance GRCh37 chr2: 241,791,028-242,842,568 , GRCh38.p12 chr2: 240,851,611-241,900,417 LOC105373978, ANO7, 39 more genes
    nsv4684141copy number variation1nstd102humanUncertain significance GRCh37 chr2: 241,810,850-243,048,760 , GRCh38.p12 chr2: 240,871,433-242,106,609 LOC105373974, LINC01238, 44 more genes
    nsv4682411copy number variation1nstd102humanPathogenic GRCh37 chr2: 241,808,273-242,708,241 , GRCh38.p12 chr2: 240,868,856-241,768,826 MIR3133, SNED1, 30 more genes
    nsv4674624copy number variation1nstd102humanPathogenic GRCh37 chr2: 234,791,927-242,783,384 , GRCh38.p12 chr2: 233,883,281-241,841,232 LOC93463, DUSP28, 151 more genes
    nsv4674620copy number variation1nstd102humanPathogenic GRCh37 chr2: 237,265,271-242,783,384 , GRCh38.p12 chr2: 236,356,628-241,841,232 OR6B2, COPS8, 122 more genes
    nsv4674409copy number variation1nstd102humanPathogenic GRCh37 chr2: 239,914,717-242,783,384 , GRCh38.p12 chr2: 238,993,021-241,841,232 GAL3ST2, UICLM, 68 more genes
    nsv4673913copy number variation1nstd102humanPathogenic GRCh37 chr2: 230,814,690-242,783,384 , GRCh38.p12 chr2: 229,949,974-241,841,232 MIR2467, D2HGDH, 270 more genes
    nsv4673906copy number variation1nstd102humanPathogenic GRCh37 chr2: 240,112,450-242,783,384 , GRCh38.p12 chr2: 239,190,754-241,841,232 HDLBP-AS1, MIR4786, 66 more genes
    nsv4578473copy number variation1nstd102humanUncertain significance GRCh37 chr2: 241,404,033-242,684,292 , GRCh38.p12 chr2: 240,464,616-241,744,877 SEPTIN2, CROCC2, 42 more genes
    nsv4519672copy number variation1nstd166human GRCh37.p13 chr2: 241,831,937-241,832,027 , GRCh38.p12 chr2: 240,892,520-240,892,610 MAB21L4
    nsv4452859copy number variation1nstd102humanUncertain significance GRCh37 chr2: 241,582,582-242,285,265 , GRCh38.p12 chr2: 240,643,165-241,345,850 MAB21L4, AQP12B, 20 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