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 107

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7145159insertion1nstd232human GRCh37.p13 chr12: 57,036,617-57,036,617 , GRCh38.p12 chr12: 56,642,833-56,642,833 ATP5F1B, SNORD59B
    nsv7138307insertion1nstd232human GRCh38.p12 chr12: 56,643,957-56,643,957 , GRCh37.p13 chr12: 57,037,741-57,037,741 ATP5F1B, SNORD59A, 1 more genes
    nsv7137979copy number variation1nstd232human GRCh37.p13 chr12: 57,036,362-57,036,453 , GRCh38.p12 chr12: 56,642,578-56,642,669 ATP5F1B, SNORD59B
    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
    nsv6933923copy number variation1nstd229human GRCh38 chr12: 56,640,194-56,642,456 , GRCh37.p13 chr12: 57,033,978-57,036,240 ATP5F1B, SNORD59B
    nsv6925004copy number variation1nstd229human GRCh38 chr12: 56,642,601-56,649,600 , GRCh37.p13 chr12: 57,036,385-57,043,384 SNORD59B, ATP5F1B, 1 more genes
    nsv6924218copy number variation1nstd229human GRCh38 chr12: 55,714,201-56,819,900 , GRCh37.p13 chr12: 56,107,985-57,213,684 ESYT1, STAT2, 66 more genes
    nsv6921524copy number variation1nstd229human GRCh38 chr12: 56,643,960-56,644,773 , GRCh37.p13 chr12: 57,037,744-57,038,557 ATP5F1B, SNORD59A, 1 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
    nsv6591698inversion1nstd223human GRCh38 chr12: 56,641,069-56,642,005 , GRCh37.p13 chr12: 57,034,853-57,035,789 SNORD59B, ATP5F1B
    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
    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
    nsv6315199copy number variation1nstd102humanUncertain significance GRCh38 chr12: 55,986,511-56,885,590 , GRCh37.p13 chr12: 56,380,295-57,279,374 ERBB3, APOF, 47 more genes
    nsv6143026copy number variation1nstd206human GRCh38 chr12: 48,500,915-111,724,058 , GRCh37.p13 chr12: 48,894,698-112,161,862 , LINC00592, 1206 more genes
    nsv5853668copy number variation1nstd209human GRCh38 chr12: 56,643,122-56,645,356 , GRCh37.p13 chr12: 57,036,906-57,039,140 SNORD59A, SNORD59B, 1 more genes
    nsv5040224inversion1nstd200human GRCh38 chr12: 47,213,128-71,357,206 , GRCh37.p13 chr12: 47,606,911-71,750,986 , NR4A1, 686 more genes
    nsv5036282inversion1nstd200human GRCh38 chr12: 52,338,357-95,425,642 , GRCh37.p13 chr12: 52,732,141-95,819,418 , MIR6502, 769 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