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 514

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7142497insertion1nstd232human GRCh37.p13 chr4: 73,990,777-73,990,777 , GRCh38.p12 chr4: 73,125,060-73,125,060 ANKRD17
    nsv7051444inversion1nstd229human GRCh38 chr4: 70,947,675-74,191,821 , GRCh37.p13 chr4: 71,813,392-75,057,538 , COX18, 44 more genes
    nsv7045939inversion1nstd229human GRCh38 chr4: 69,867,306-75,844,103 , GRCh37.p13 chr4: 70,733,024-76,765,256 , PF4V1, 99 more genes
    nsv7044416inversion1nstd229human GRCh38 chr4: 73,234,467-73,234,483 , GRCh37.p13 chr4: 74,100,184-74,100,200 ANKRD17
    nsv7041687inversion1nstd229human GRCh38 chr4: 73,174,448-73,174,478 , GRCh37.p13 chr4: 74,040,165-74,040,195 ANKRD17
    nsv7040415inversion1nstd229human GRCh38 chr4: 72,183,424-80,893,316 , GRCh37.p13 chr4: 73,049,141-81,814,470 , KPNA2P1, 148 more genes
    nsv6757277copy number variation1nstd229human GRCh38 chr4: 73,217,647-73,224,238 , GRCh37.p13 chr4: 74,083,364-74,089,955 ANKRD17
    nsv6756277copy number variation1nstd229human GRCh38 chr4: 73,242,479-73,252,543 , GRCh37.p13 chr4: 74,108,196-74,118,260 ANKRD17
    nsv6754937copy number variation1nstd229human GRCh38 chr4: 73,125,001-73,134,600 , GRCh37.p13 chr4: 73,990,718-74,000,317 ANKRD17
    nsv6753524copy number variation1nstd229human GRCh38 chr4: 73,224,216-73,228,369 , GRCh37.p13 chr4: 74,089,933-74,094,086 ANKRD17
    nsv6749524copy number variation1nstd229human GRCh38 chr4: 73,238,740-73,245,071 , GRCh37.p13 chr4: 74,104,457-74,110,788 ANKRD17
    nsv6749244copy number variation1nstd229human GRCh38 chr4: 71,830,854-79,510,197 , GRCh37.p13 chr4: 72,696,571-80,431,351 , COX18, 134 more genes
    nsv6748406copy number variation1nstd229human GRCh38 chr4: 73,179,834-73,179,904 , GRCh37.p13 chr4: 74,045,551-74,045,621 ANKRD17
    nsv6747862copy number variation1nstd229human GRCh38 chr4: 72,931,936-73,155,410 , GRCh37.p13 chr4: 73,797,653-74,021,127 LOC105377273, COX18, 6 more genes
    nsv6747527copy number variation1nstd229human GRCh38 chr4: 73,090,101-73,115,600 , GRCh37.p13 chr4: 73,955,818-73,981,317 ANKRD17, HMGA1P2
    nsv6746970copy number variation1nstd229human GRCh38 chr4: 73,076,201-73,102,300 , GRCh37.p13 chr4: 73,941,918-73,968,017 ANKRD17, HMGA1P2
    nsv6746769copy number variation1nstd229human GRCh38 chr4: 69,087,431-73,565,096 , GRCh37.p13 chr4: 69,953,149-74,430,813 LOC642496, CSN2, 76 more genes
    nsv6746703copy number variation1nstd229human GRCh38 chr4: 73,165,239-73,175,439 , GRCh37.p13 chr4: 74,030,956-74,041,156 ANKRD17
    nsv6740221copy number variation1nstd229human GRCh38 chr4: 71,124,425-74,382,728 , GRCh37.p13 chr4: 71,990,142-75,248,445 , ALB, 45 more genes
    nsv6739745copy number variation1nstd229human GRCh38 chr4: 73,167,975-73,174,650 , GRCh37.p13 chr4: 74,033,692-74,040,367 ANKRD17
    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