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 334

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112802copy number variation1nstd102humanPathogenic GRCh37 chr18: 23,626,739-78,014,976 , GRCh38.p12 chr18: 26,046,775-80,257,093 RPL9P31, LINC02582, 595 more genes
    nsv5970228inversion1nstd209human GRCh38 chr18: 42,666,448-47,133,105 , GRCh37.p13 chr18: 40,246,413-44,659,476 , ATP5F1A, 50 more genes
    nsv5969506insertion1nstd209human GRCh38 chr18: 46,113,033-46,113,033 , GRCh37.p13 chr18: 43,692,999-43,692,999 HAUS1
    nsv5943213copy number variation1nstd209human GRCh38 chr18: 46,106,417-46,109,018 , GRCh37.p13 chr18: 43,686,383-43,688,984 HAUS1
    nsv5935331copy number variation1nstd209human GRCh38 chr18: 46,126,045-46,127,473 , GRCh37.p13 chr18: 43,706,011-43,707,439 HAUS1
    nsv5932522copy number variation1nstd209human GRCh38 chr18: 46,115,370-46,117,856 , GRCh37.p13 chr18: 43,695,336-43,697,822 HAUS1
    nsv5884504copy number variation1nstd209human GRCh38 chr18: 46,115,628-46,117,527 , GRCh37.p13 chr18: 43,695,594-43,697,493 HAUS1
    nsv5875016copy number variation1nstd209human GRCh38 chr18: 46,105,810-46,108,559 , GRCh37.p13 chr18: 43,685,776-43,688,525 HAUS1
    nsv5663057insertion1nstd207human GRCh38 chr18: 46,113,035-46,113,035 , GRCh37.p13 chr18: 43,693,001-43,693,001 HAUS1
    nsv5662769insertion1nstd207human GRCh38 chr18: 46,112,386-46,112,386 , GRCh37.p13 chr18: 43,692,352-43,692,352 HAUS1
    nsv5660407insertion1nstd207human GRCh38 chr18: 46,112,820-46,112,820 , GRCh37.p13 chr18: 43,692,786-43,692,786 HAUS1
    nsv5655369insertion1nstd207human GRCh38 chr18: 46,112,780-46,112,780 , GRCh37.p13 chr18: 43,692,746-43,692,746 HAUS1
    nsv5600686copy number variation1nstd207human GRCh38 chr18: 46,112,886-46,112,961 , GRCh37.p13 chr18: 43,692,852-43,692,927 HAUS1
    nsv5587917copy number variation1nstd207human GRCh38 chr18: 46,112,332-46,112,407 , GRCh37.p13 chr18: 43,692,298-43,692,373 HAUS1
    nsv5530188copy number variation1nstd206human GRCh38 chr18: 46,112,517-46,113,000 , GRCh37.p13 chr18: 43,692,483-43,692,966 HAUS1
    nsv5528298copy number variation1nstd206human GRCh38 chr18: 46,119,725-46,129,052 , GRCh37.p13 chr18: 43,699,691-43,709,018 HAUS1, RNU6-1278P
    nsv5526627copy number variation1nstd206human GRCh38 chr18: 46,126,025-46,127,502 , GRCh37.p13 chr18: 43,705,991-43,707,468 HAUS1
    nsv5525222copy number variation1nstd206human GRCh38 chr18: 45,996,443-46,209,010 , GRCh37.p13 chr18: 43,576,409-43,788,976 ATP5F1A, PSTPIP2, 6 more genes
    nsv5517919copy number variation1nstd206human GRCh38 chr18: 46,105,551-46,105,645 , GRCh37.p13 chr18: 43,685,517-43,685,611 HAUS1
    nsv5514966copy number variation1nstd206human GRCh38 chr18: 46,115,376-46,116,060 , GRCh37.p13 chr18: 43,695,342-43,696,026 HAUS1
    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