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 95

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7075420inversion1nstd229human GRCh38 chr12: 94,829,509-94,861,959 , GRCh37.p13 chr12: 95,223,285-95,255,735 MIR492, KRT19P2
    nsv7065284inversion1nstd229human GRCh38 chr12: 94,129,761-97,319,471 , GRCh37.p13 chr12: 94,523,537-97,713,249 AMDHD1, TMCC3, 62 more genes
    nsv6923025copy number variation1nstd229human GRCh38 chr12: 94,830,842-94,845,307 , GRCh37.p13 chr12: 95,224,618-95,239,083 MIR492, KRT19P2
    nsv6474519copy number variation1nstd223human GRCh38 chr12: 94,835,496-94,836,330 , GRCh37.p13 chr12: 95,229,272-95,230,106 KRT19P2
    nsv6465379copy number variation1nstd223human GRCh38 chr12: 94,686,219-94,882,731 , GRCh37.p13 chr12: 95,079,995-95,276,507 KRT19P2, MIR492
    nsv6143026copy number variation1nstd206human GRCh38 chr12: 48,500,915-111,724,058 , GRCh37.p13 chr12: 48,894,698-112,161,862 , LINC00592, 1206 more genes
    nsv6132721copy number variation1nstd213human GRCh37 chr12: 94,820,000-97,270,001 , GRCh38.p12 chr12: 94,426,224-96,876,223 ELK3, METAP2, 50 more genes
    nsv5943627copy number variation1nstd209human GRCh38 chr12: 94,835,496-94,836,329 , GRCh37.p13 chr12: 95,229,272-95,230,105 KRT19P2
    nsv5563821inversion1nstd206human GRCh38 chr12: 94,829,509-94,861,959 , GRCh37.p13 chr12: 95,223,285-95,255,735 KRT19P2, MIR492
    nsv5041318inversion1nstd200human GRCh38 chr12: 94,829,509-94,861,959 , GRCh37.p13 chr12: 95,223,285-95,255,735 MIR492, KRT19P2
    nsv5037136inversion1nstd200human GRCh38 chr12: 69,787,024-109,882,221 , GRCh37.p13 chr12: 70,180,804-110,320,026 , RPL23AP68, 540 more genes
    nsv5036282inversion1nstd200human GRCh38 chr12: 52,338,357-95,425,642 , GRCh37.p13 chr12: 52,732,141-95,819,418 , MIR6502, 769 more genes
    nsv4993572copy number variation1nstd200human GRCh38 chr12: 94,686,219-94,882,731 , GRCh37.p13 chr12: 95,079,995-95,276,507 MIR492, KRT19P2
    nsv4886161inversion1nstd200human GRCh37 chr12: 70,180,810-110,320,027 , GRCh38.p12 chr12: 69,787,030-109,882,222 , LOC728739, 540 more genes
    nsv4883504inversion1nstd200human GRCh37 chr12: 52,732,141-95,819,418 , GRCh38.p12 chr12: 52,338,357-95,425,642 , MYL6B, 769 more genes
    nsv4880145inversion1nstd200human GRCh37 chr12: 95,223,285-95,255,735 , GRCh38.p12 chr12: 94,829,509-94,861,959 KRT19P2, MIR492
    nsv4755205inversion1nstd199human GRCh37 chr12: 25,956,127-125,801,151 , GRCh38.p12 chr12: 25,803,193-125,316,605 , ACACB, 1787 more genes
    nsv4736781copy number variation1nstd199human GRCh37 chr12: 25,957,322-125,801,148 , GRCh38.p12 chr12: 25,804,388-125,316,602 , RNA5SP368, 1787 more genes
    nsv4345788sequence alteration1nstd166human GRCh37.p13 chr12: 59,785,153-101,478,055 , GRCh38.p12 chr12: 59,391,372-101,084,277 , APAF1, 538 more genes
    nsv4325802inversion1nstd166human GRCh37.p13 chr12: 70,180,810-110,320,028 , GRCh38.p12 chr12: 69,787,030-109,882,223 , APAF1, 540 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