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 332

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6121358copy number variation1nstd186human GRCh37 chr14: 50,287,719-50,288,220 , GRCh38.p12 chr14: 49,821,001-49,821,502 NEMF
    nsv5946878copy number variation1nstd209human GRCh38 chr14: 49,820,974-49,821,501 , GRCh37.p13 chr14: 50,287,692-50,288,219 NEMF
    nsv5938474copy number variation1nstd209human GRCh38 chr14: 49,844,852-49,845,175 , GRCh37.p13 chr14: 50,311,570-50,311,893 NEMF
    nsv5935089copy number variation1nstd209human GRCh38 chr14: 46,941,699-52,127,962 , GRCh37.p13 chr14: 47,410,902-52,594,680 , RNA5SP385, 92 more genes
    nsv5709348mobile element insertion2nstd211human GRCh38 chr14: 49,789,128-49,789,128 , GRCh37.p13 chr14: 50,255,846-50,255,846 NEMF
    nsv5604266copy number variation1nstd207human GRCh38 chr14: 49,820,974-49,821,501 , GRCh37.p13 chr14: 50,287,692-50,288,219 NEMF
    nsv5595324copy number variation1nstd207human GRCh38 chr14: 49,821,592-49,821,641 , GRCh37.p13 chr14: 50,288,310-50,288,359 NEMF
    nsv5512883copy number variation1nstd206human GRCh38 chr14: 49,832,307-49,832,610 , GRCh37.p13 chr14: 50,299,025-50,299,328 NEMF
    nsv5510644copy number variation1nstd206human GRCh38 chr14: 49,821,001-49,821,502 , GRCh37.p13 chr14: 50,287,719-50,288,220 NEMF
    nsv5494694copy number variation1nstd206human GRCh38 chr14: 49,841,379-49,841,857 , GRCh37.p13 chr14: 50,308,097-50,308,575 NEMF
    nsv5414415mobile element insertion1nstd206human GRCh38 chr14: 49,789,128-49,789,179 , GRCh37.p13 chr14: 50,255,846-50,255,897 NEMF
    nsv5391643copy number variation1nstd186human GRCh37 chr14: 50,287,719-50,288,433 , GRCh38.p12 chr14: 49,821,001-49,821,715 NEMF
    nsv5374539translocation1nstd200human GRCh38 chr14: 49,821,256-49,821,256 , GRCh38 chr14: 49,821,483-49,821,483 , GRCh37.p13 chr14: 50,287,974-50,287,974 , GRCh37.p13 chr14: 50,288,201-50,288,201 NEMF
    nsv5357224translocation1nstd200human GRCh38 chr14: 49,821,001-49,821,001 , GRCh38 chr14: 49,821,502-49,821,502 , GRCh37.p13 chr14: 50,287,719-50,287,719 , GRCh37.p13 chr14: 50,288,220-50,288,220 NEMF
    nsv5343793translocation1nstd200human GRCh37 chr14: 50,287,721-50,287,721 , GRCh37 chr14: 50,288,224-50,288,224 , GRCh38.p12 chr14: 49,821,506-49,821,506 , GRCh38.p12 chr14: 49,821,003-49,821,003 NEMF
    nsv5323749translocation1nstd204human GRCh38.p13 chr14: 49,821,001-49,821,001 , GRCh38.p13 chr14: 49,821,532-49,821,532 , GRCh37.p13 chr14: 50,287,719-50,287,719 , GRCh37.p13 chr14: 50,288,250-50,288,250 NEMF
    nsv5319435copy number variation1nstd204human GRCh38.p13 chr14: 49,819,013-49,827,193 , GRCh37.p13 chr14: 50,285,731-50,293,911 NEMF
    nsv5312078copy number variation1nstd204human GRCh38.p13 chr14: 49,793,500-49,793,725 , GRCh37.p13 chr14: 50,260,218-50,260,443 NEMF
    nsv5279497copy number variation1nstd204human GRCh37.p13 chr14: 50,192,319-50,379,318 , GRCh38.p13 chr14: 49,725,601-49,912,600 ARF6, NEMF, 7 more genes
    nsv5275937copy number variation1nstd204human GRCh38.p13 chr14: 49,818,960-49,826,761 , GRCh37.p13 chr14: 50,285,678-50,293,479 NEMF
    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