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 141

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098889copy number variation1nstd102humanLikely pathogenic GRCh37 chr12: 57,064,059-59,314,016 , GRCh38.p12 chr12: 56,670,275-58,920,235 CDK4, CYP27B1, 77 more genes
    nsv7074641inversion1nstd229human GRCh38 chr12: 52,659,002-59,632,575 , GRCh37.p13 chr12: 53,052,786-60,026,356 , LOC105369777, 292 more genes
    nsv7071931inversion1nstd229human GRCh38 chr12: 55,156,710-64,781,897 , GRCh37.p13 chr12: 55,550,494-65,175,677 ZBTB39, MIR548Z, 236 more genes
    nsv7068987inversion1nstd229human GRCh38 chr12: 56,649,721-58,539,946 , GRCh37.p13 chr12: 57,043,505-58,933,729 GIHCG, LOC101927608, 72 more genes
    nsv6933279copy number variation1nstd229human GRCh38 chr12: 57,102,301-57,245,000 , GRCh37.p13 chr12: 57,496,084-57,638,783 STAC3, NDUFA4L2, 6 more genes
    nsv6918954copy number variation1nstd229human GRCh38 chr12: 57,094,930-57,094,995 , GRCh37.p13 chr12: 57,488,713-57,488,778 STAT6, NAB2
    nsv6595151inversion1nstd223human GRCh38 chr12: 56,690,071-66,057,684 , GRCh37.p13 chr12: 57,083,855-66,451,464 HMGA2-AS1, HSD17B6, 166 more genes
    nsv6592643inversion1nstd223human GRCh38 chr12: 56,690,340-66,057,683 , GRCh37.p13 chr12: 57,084,124-66,451,463 MIR10527, HMGA2, 165 more genes
    nsv6592389inversion1nstd223human GRCh38 chr12: 56,202,197-66,057,592 , GRCh37.p13 chr12: 56,595,981-66,451,372 RPL21P103, MIP, 194 more genes
    nsv6590334inversion1nstd223human GRCh38 chr12: 57,052,049-66,057,683 , GRCh37.p13 chr12: 57,445,833-66,451,463 RNU5A-7P, SLC26A10P, 153 more genes
    nsv6584140inversion1nstd223human GRCh38 chr12: 56,381,670-66,057,684 , GRCh37.p13 chr12: 56,775,454-66,451,464 RNU6-879P, KICS2, 180 more genes
    nsv6578359inversion1nstd223human GRCh38 chr12: 56,201,986-66,057,683 , GRCh37.p13 chr12: 56,595,770-66,451,463 AVIL, RPSAP52, 194 more genes
    nsv6577543inversion1nstd223human GRCh38 chr12: 56,676,741-66,057,683 , GRCh37.p13 chr12: 57,070,525-66,451,463 LINC02388, LOC105369795, 166 more genes
    nsv6577024inversion1nstd223human GRCh38 chr12: 56,201,970-66,057,680 , GRCh37.p13 chr12: 56,595,754-66,451,460 AVPR1A, LOC390332, 194 more genes
    nsv6576885inversion1nstd223human GRCh38 chr12: 56,344,988-66,057,676 , GRCh37.p13 chr12: 56,738,772-66,451,456 LOC105369786, MBD6, 184 more genes
    nsv6206479copy number variation1nstd214human GRCh38 chr12: 57,100,638-57,100,711 , GRCh37.p13 chr12: 57,494,421-57,494,494 STAT6
    nsv6203758copy number variation1nstd214human GRCh38 chr12: 57,100,632-57,100,693 , GRCh37.p13 chr12: 57,494,415-57,494,476 STAT6
    nsv6203149copy number variation1nstd214human GRCh38 chr12: 57,100,646-57,100,699 , GRCh37.p13 chr12: 57,494,429-57,494,482 STAT6
    nsv6198176copy number variation1nstd214human GRCh38 chr12: 57,100,642-57,100,699 , GRCh37.p13 chr12: 57,494,425-57,494,482 STAT6
    nsv6192254copy number variation1nstd214human GRCh38 chr12: 57,100,650-57,100,699 , GRCh37.p13 chr12: 57,494,433-57,494,482 STAT6
    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