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 324

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7142127copy number variation1nstd232human GRCh37.p13 chr22: 44,232,415-44,232,492 , GRCh38.p12 chr22: 43,836,535-43,836,612 SULT4A1
    nsv7063046inversion1nstd229human GRCh38 chr22: 43,798,624-43,898,271 , GRCh37.p13 chr22: 44,194,504-44,294,151 SULT4A1, PNPLA5, 3 more genes
    nsv7061959inversion1nstd229human GRCh38 chr22: 36,818,005-44,993,640 , GRCh37.p13 chr22: 37,214,049-45,389,520 SMIM45, A4GALT, 271 more genes
    nsv7035668copy number variation1nstd229human GRCh38 chr22: 43,796,171-43,824,291 , GRCh37.p13 chr22: 44,192,051-44,220,171 HMGN2P9, EFCAB6-DT, 2 more genes
    nsv7033359copy number variation1nstd229human GRCh38 chr22: 43,847,225-43,851,722 , GRCh37.p13 chr22: 44,243,105-44,247,602 SULT4A1
    nsv7030452copy number variation1nstd229human GRCh38 chr22: 43,463,348-44,099,240 , GRCh37.p13 chr22: 43,859,242-44,495,120 RPL35AP36, EFCAB6-DT, 12 more genes
    nsv7029692copy number variation1nstd229human GRCh38 chr22: 43,843,066-43,851,164 , GRCh37.p13 chr22: 44,238,946-44,247,044 SULT4A1
    nsv7028343copy number variation1nstd229human GRCh38 chr22: 43,852,019-43,856,312 , GRCh37.p13 chr22: 44,247,899-44,252,192 SULT4A1
    nsv7027741copy number variation1nstd229human GRCh38 chr22: 39,432,386-49,047,389 , GRCh37.p13 chr22: 39,828,391-49,443,201 LOC105373064, ACO2, 233 more genes
    nsv7026986copy number variation1nstd229human GRCh38 chr22: 43,771,301-43,918,600 , GRCh37.p13 chr22: 44,167,181-44,314,480 SULT4A1, EFCAB6, 3 more genes
    nsv6638073copy number variation1nstd102humanPathogenic GRCh37 chr22: 43,436,847-51,188,164 , GRCh38.p12 chr22: 43,040,841-50,749,736 SCUBE1-AS1, MIR6821, 165 more genes
    nsv6637969copy number variation1nstd102humanPathogenic GRCh37 chr22: 44,178,749-51,183,840 , GRCh38.p12 chr22: 43,782,869-50,745,412 LOC105373081, RPL35AP36, 148 more genes
    nsv6597991inversion1nstd223human GRCh38 chr22: 43,335,838-45,080,470 , GRCh37.p13 chr22: 43,731,844-45,476,351 , LOC105373060, 35 more genes
    nsv6596723inversion1nstd223human GRCh38 chr22: 43,336,006-45,080,499 , GRCh37.p13 chr22: 43,732,012-45,476,380 , PNPLA5, 35 more genes
    nsv6554560copy number variation1nstd223human GRCh38 chr22: 43,836,153-43,836,489 , GRCh37.p13 chr22: 44,232,033-44,232,369 SULT4A1
    nsv6543666copy number variation1nstd223human GRCh38 chr22: 43,846,805-43,860,052 , GRCh37.p13 chr22: 44,242,685-44,255,932 SULT4A1
    nsv6537550copy number variation1nstd223human GRCh38 chr22: 43,835,729-43,849,647 , GRCh37.p13 chr22: 44,231,609-44,245,527 SULT4A1
    nsv6535893copy number variation1nstd223human GRCh38 chr22: 41,572,303-44,198,988 , GRCh37.p13 chr22: 41,968,307-44,594,868 , RPS25P10, 87 more genes
    nsv6314059copy number variation1nstd102humanPathogenic GRCh37 chr22: 42,972,719-51,197,838 , GRCh38.p12 chr22: 42,576,713-50,759,410 TRABD, LOC100422416, 181 more genes
    nsv6313968copy number variation1nstd102humanPathogenic GRCh37 chr22: 43,451,316-46,662,660 , GRCh38.p12 chr22: 43,055,310-46,266,763 EFCAB6-DT, LOC107985535, 82 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