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 231

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5914081copy number variation1nstd209human GRCh38 chr7: 123,704,494-123,704,549 , GRCh37.p13 chr7: 123,344,548-123,344,603 WASL
    nsv5730625mobile element insertion1nstd211human GRCh38 chr7: 123,724,615-123,724,615 , GRCh37.p13 chr7: 123,364,669-123,364,669 WASL
    nsv5720492mobile element insertion1nstd211human GRCh38 chr7: 123,699,703-123,699,703 , GRCh37.p13 chr7: 123,339,757-123,339,757 WASL
    nsv5559918mobile element insertion1nstd206human GRCh38 chr7: 123,724,615-123,724,666 , GRCh37.p13 chr7: 123,364,669-123,364,720 WASL
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5381759copy number variation1nstd102humanPathogenic GRCh37 chr7: 116,297,277-126,370,694 , GRCh38.p12 chr7: 116,657,223-126,730,640 TMEM229A, ST7-OT3, 110 more genes
    nsv5378801translocation1nstd200human GRCh38 chr7: 123,751,010-123,751,010 , GRCh38 chr7: 123,686,484-123,686,484 , GRCh37.p13 chr7: 123,326,538-123,326,538 , GRCh37.p13 chr7: 123,391,064-123,391,064 WASL
    nsv5378800translocation1nstd200human GRCh38 chr7: 123,588,759-123,588,759 , GRCh38 chr7: 123,687,637-123,687,637 , GRCh37.p13 chr7: 123,228,813-123,228,813 , GRCh37.p13 chr7: 123,327,691-123,327,691 NDUFA5, WASL, 1 more genes
    nsv5371143translocation1nstd200human GRCh38 chr7: 123,739,569-123,739,569 , GRCh38 chr7: 123,739,631-123,739,631 , GRCh37.p13 chr7: 123,379,623-123,379,623 , GRCh37.p13 chr7: 123,379,685-123,379,685 WASL
    nsv5326600inversion1nstd204human GRCh37.p13 chr7: 97,320,865-141,491,704 , GRCh38.p13 chr7: 97,691,553-141,791,904 , ARF5, 752 more genes
    nsv5039775inversion1nstd200human GRCh38 chr7: 22,938,090-134,148,361 , GRCh37.p13 chr7: 22,977,709-133,833,114 , NFE4, 1832 more genes
    nsv5029742inversion1nstd200human GRCh38 chr7: 79,688,546-147,673,588 , GRCh37.p13 chr7: 79,317,862-147,370,680 , LOC100533722, 1168 more genes
    nsv4968687copy number variation1nstd200human GRCh38 chr7: 123,313,906-124,175,429 , GRCh37.p13 chr7: 122,953,960-123,815,483 RNU6-11P, TMEM229A, 11 more genes
    nsv4958052copy number variation1nstd200human GRCh38 chr7: 123,725,314-123,725,441 , GRCh37.p13 chr7: 123,365,368-123,365,495 WASL
    nsv4880762inversion1nstd200human GRCh37 chr7: 79,317,862-147,370,680 , GRCh38.p12 chr7: 79,688,546-147,673,588 , RN7SKP277, 1168 more genes
    nsv4820374copy number variation1nstd200human GRCh37 chr7: 123,365,368-123,365,495 , GRCh38.p12 chr7: 123,725,314-123,725,441 WASL
    nsv4729428copy number variation1nstd102humanUncertain significance GRCh37 chr7: 122,963,176-123,347,717 , GRCh38.p12 chr7: 123,323,122-123,707,663 LMOD2, RNU6-296P, 5 more genes
    nsv4675620copy number variation1nstd102humanPathogenic GRCh37 chr7: 109,251,060-159,119,707 , GRCh38.p12 chr7: 109,611,003-159,327,017 RPL26P23, ST13P17, 887 more genes
    nsv4674894copy number variation1nstd102humanLikely benign GRCh37 chr7: 122,637,357-123,574,829 , GRCh38.p12 chr7: 122,997,303-123,934,775 HYAL4, RNU6-11P, 11 more genes
    nsv4615926copy number variation1nstd183human GRCh37 chr7: 123,321,975-123,322,525 , GRCh38.p12 chr7: 123,681,921-123,682,471 WASL
    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