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 325

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7145755copy number variation1nstd232human GRCh37.p13 chr12: 102,314,060-102,314,161 , GRCh38.p12 chr12: 101,920,282-101,920,383 DRAM1
    nsv7143020insertion1nstd232human GRCh37.p13 chr12: 102,284,253-102,284,253 , GRCh38.p12 chr12: 101,890,475-101,890,475 DRAM1
    nsv7141383insertion1nstd232human GRCh37.p13 chr12: 102,284,830-102,284,830 , GRCh38.p12 chr12: 101,891,052-101,891,052 DRAM1
    nsv7074674inversion1nstd229human GRCh38 chr12: 100,072,817-104,989,567 , GRCh37.p13 chr12: 100,466,595-105,383,345 SYCP3, GOLGA2P5, 84 more genes
    nsv7068612inversion1nstd229human GRCh38 chr12: 100,083,131-104,989,539 , GRCh37.p13 chr12: 100,476,909-105,383,317 EID3, RNU6-1068P, 84 more genes
    nsv6937243copy number variation1nstd229human GRCh38 chr12: 101,767,778-101,962,494 , GRCh37.p13 chr12: 102,161,556-102,356,272 NENFP2, GNPTAB, 9 more genes
    nsv6933971copy number variation1nstd229human GRCh38 chr12: 101,806,546-101,944,077 , GRCh37.p13 chr12: 102,200,324-102,337,855 HSPE1P4, RPL9P24, 4 more genes
    nsv6929112copy number variation1nstd229human GRCh38 chr12: 101,886,801-101,898,300 , GRCh37.p13 chr12: 102,280,579-102,292,078 DRAM1
    nsv6928120copy number variation1nstd229human GRCh38 chr12: 101,779,786-101,995,724 , GRCh37.p13 chr12: 102,173,564-102,389,502 RNU6-172P, DRAM1, 8 more genes
    nsv6926679copy number variation1nstd229human GRCh38 chr12: 101,785,450-101,956,134 , GRCh37.p13 chr12: 102,179,228-102,349,912 RNU6-1183P, LOC107984548, 6 more genes
    nsv6923081copy number variation1nstd229human GRCh38 chr12: 101,889,923-102,037,281 , GRCh37.p13 chr12: 102,283,701-102,431,059 DRAM1, WASHC3, 3 more genes
    nsv6922635copy number variation1nstd229human GRCh38 chr12: 96,115,345-104,800,221 , GRCh37.p13 chr12: 96,509,123-105,193,999 RNY1P16, CHST11, 121 more genes
    nsv6922193copy number variation1nstd229human GRCh38 chr12: 101,882,017-101,882,783 , GRCh37.p13 chr12: 102,275,795-102,276,561 DRAM1
    nsv6920707copy number variation1nstd229human GRCh38 chr12: 101,920,302-101,920,384 , GRCh37.p13 chr12: 102,314,080-102,314,162 DRAM1
    nsv6621483copy number variation1nstd224human GRCh37 chr12: 102,288,465-102,430,806 , GRCh38.p12 chr12: 101,894,687-102,037,028 RPL9P24, DRAM1, 3 more genes
    nsv6593197inversion1nstd223human GRCh38 chr12: 101,889,668-101,890,476 , GRCh37.p13 chr12: 102,283,446-102,284,254 DRAM1
    nsv6588517inversion1nstd223human GRCh38 chr12: 101,912,886-101,913,701 , GRCh37.p13 chr12: 102,306,664-102,307,479 DRAM1
    nsv6585473inversion1nstd223human GRCh38 chr12: 101,913,032-101,913,739 , GRCh37.p13 chr12: 102,306,810-102,307,517 DRAM1
    nsv6577900inversion1nstd223human GRCh38 chr12: 101,883,470-101,883,945 , GRCh37.p13 chr12: 102,277,248-102,277,723 DRAM1
    nsv6575959inversion1nstd223human GRCh38 chr12: 101,905,446-101,906,721 , GRCh37.p13 chr12: 102,299,224-102,300,499 DRAM1
    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