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 134

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5919512copy number variation1nstd209human GRCh38 chr7: 26,509,679-33,120,288 , GRCh37.p13 chr7: 26,549,298-33,159,900 , CPVL-AS1, 126 more genes
    nsv5914132copy number variation1nstd209human GRCh38 chr7: 26,936,027-36,716,695 , GRCh37.p13 chr7: 26,975,646-36,756,300 , HOXA7, 162 more genes
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5489413copy number variation1nstd206human GRCh38 chr7: 30,627,469-30,627,832 , GRCh37.p13 chr7: 30,667,085-30,667,448 GARS1
    nsv5477561copy number variation1nstd206human GRCh38 chr7: 30,631,178-30,631,295 , GRCh37.p13 chr7: 30,670,794-30,670,911 GARS1
    nsv5378634translocation1nstd200human GRCh38 chr7: 30,631,178-30,631,178 , GRCh38 chr7: 30,631,295-30,631,295 , GRCh37.p13 chr7: 30,670,794-30,670,794 , GRCh37.p13 chr7: 30,670,911-30,670,911 GARS1
    nsv5114768mobile element insertion1nstd203human GRCh38 chr7: 30,599,082-30,599,099 , GRCh37.p13 chr7: 30,638,698-30,638,715 GARS1
    nsv5039775inversion1nstd200human GRCh38 chr7: 22,938,090-134,148,361 , GRCh37.p13 chr7: 22,977,709-133,833,114 , NFE4, 1832 more genes
    nsv4956217copy number variation1nstd200human GRCh38 chr7: 30,600,093-30,600,957 , GRCh37.p13 chr7: 30,639,709-30,640,573 GARS1
    nsv4953552copy number variation1nstd200human GRCh38 chr7: 30,612,963-31,127,528 , GRCh37.p13 chr7: 30,652,579-31,167,142 , INMT-MINDY4, 12 more genes
    nsv4882608inversion1nstd200human GRCh37 chr7: 6,326,174-37,121,976 , GRCh38.p12 chr7: 6,286,543-37,082,371 , HOXA13, 435 more genes
    nsv4811216copy number variation1nstd200human GRCh37 chr7: 30,670,794-30,670,911 , GRCh38.p12 chr7: 30,631,178-30,631,295 GARS1
    nsv4729079copy number variation1nstd102humanLikely pathogenic GRCh37 chr7: 29,758,030-31,318,843 , GRCh38.p12 chr7: 29,718,414-31,279,229 ADCYAP1R1, AQP1, 33 more genes
    nsv4681522copy number variation1nstd102humanUncertain significance GRCh37 chr7: 30,655,502-30,673,486 , GRCh38.p12 chr7: 30,615,886-30,633,870 GARS1
    nsv4676067copy number variation1nstd102humanUncertain significance GRCh37 chr7: 30,502,942-30,888,964 , GRCh38.p12 chr7: 30,463,326-30,849,348 GARS1-DT, NOD1, 9 more genes
    nsv4675863copy number variation1nstd102humanLikely pathogenic GRCh37 chr7: 28,487,175-32,037,495 , GRCh38.p12 chr7: 28,447,557-31,997,883 ADCYAP1R1, AQP1, 55 more genes
    nsv4675226copy number variation1nstd102humanUncertain significance GRCh37 chr7: 30,463,886-30,674,061 , GRCh38.p12 chr7: 30,424,270-30,634,445 LOC100287825, GARS1, 3 more genes
    nsv4674822copy number variation1nstd102humanPathogenic GRCh37 chr7: 23,877,135-33,139,446 , GRCh38.p12 chr7: 23,837,516-33,099,834 RP9P, LINC00997, 156 more genes
    nsv4491774mobile element insertion1nstd166human GRCh37.p13 chr7: 30,638,698-30,638,698 , GRCh38.p12 chr7: 30,599,082-30,599,082 GARS1
    nsv4455091copy number variation1nstd102humanPathogenic GRCh37 chr7: 10,365-159,119,707 , GRCh38.p12 chr7: 10,365-159,327,017 RPL23AP51, FLJ40288, 2684 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