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 97

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5370451translocation1nstd200human GRCh38 chr7: 25,949,892-25,949,892 , GRCh38 chr7: 25,945,279-25,945,279 , GRCh37.p13 chr7: 25,989,512-25,989,512 , GRCh37.p13 chr7: 25,984,899-25,984,899 MIR148A, LOC105375199, 1 more genes
    nsv5039775inversion1nstd200human GRCh38 chr7: 22,938,090-134,148,361 , GRCh37.p13 chr7: 22,977,709-133,833,114 , NFE4, 1832 more genes
    nsv4956078copy number variation1nstd200human GRCh38 chr7: 25,950,066-25,953,059 , GRCh37.p13 chr7: 25,989,686-25,992,679 LOC105375199, MIR148A
    nsv4953510copy number variation1nstd200human GRCh38 chr7: 25,907,996-26,242,888 , GRCh37.p13 chr7: 25,947,616-26,282,508 MIR148A, LOC105375199, 5 more genes
    nsv4882608inversion1nstd200human GRCh37 chr7: 6,326,174-37,121,976 , GRCh38.p12 chr7: 6,286,543-37,082,371 , HOXA13, 435 more genes
    nsv4729033copy number variation1nstd102humanUncertain significance GRCh37 chr7: 25,753,007-26,217,383 , GRCh38.p12 chr7: 25,713,387-26,177,763 NFE2L3, LINC03007, 5 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
    nsv4455091copy number variation1nstd102humanPathogenic GRCh37 chr7: 10,365-159,119,707 , GRCh38.p12 chr7: 10,365-159,327,017 RPL23AP51, FLJ40288, 2684 more genes
    nsv4435897copy number variation1nstd102humanPathogenic GRCh37 chr7: 23,236,782-30,690,453 , GRCh38.p12 chr7: 23,197,163-30,650,837 CCDC126, LOC389473, 138 more genes
    nsv4352523inversion1nstd102humanPathogenic GRCh37 chr7: 20,954,043-114,556,605 , GRCh38.p12 chr7: 20,914,424-114,916,550 ACHE, ADCY1, 1532 more genes
    nsv4144596copy number variation1nstd166human GRCh37.p13 chr7: 25,949,175-26,101,422 , GRCh38.p12 chr7: 25,909,555-26,061,802 MIR148A, LOC105375200, 1 more genes
    nsv3922885copy number variation1nstd102humanPathogenic GRCh38 chr7: 20,561,456-32,005,143 , GRCh37 chr7: 20,601,079-32,044,755 , NCBI36 chr7: 20,567,604-32,011,280 IL6-AS1, HOXA10-AS, 195 more genes
    nsv3922329copy number variation1nstd102humanPathogenic GRCh37 chr7: 43,360-27,236,023 , GRCh38 chr7: 43,360-27,196,404 , NCBI36 chr7: 138,443-27,202,548 LOC401312, IQCE, 411 more genes
    nsv3920590copy number variation1nstd102humanLikely pathogenic NCBI36 chr7: 25,909,533-27,028,642 , GRCh37 chr7: 25,943,008-27,062,117 , GRCh38 chr7: 25,903,388-27,022,498 HNRNPA2B1, SKAP2, 18 more genes
    nsv3919826copy number variation1nstd102humanPathogenic GRCh37 chr7: 54,185-159,075,079 , GRCh38 chr7: 54,185-159,282,390 , NCBI36 chr7: 149,268-158,767,840 RNU6-438P, LOC105375300, 2682 more genes
    nsv3918785copy number variation1nstd102humanPathogenic GRCh37 chr7: 54,185-37,129,317 , NCBI36 chr7: 149,268-37,095,842 , GRCh38 chr7: 54,185-37,089,712 MMD2, ICA1-AS1, 554 more genes
    nsv3916683copy number variation1nstd102humanPathogenic GRCh37 chr7: 54,185-26,867,253 , NCBI36 chr7: 149,268-26,833,778 , GRCh38 chr7: 54,185-26,827,634 ZNF12, LOC105375183, 389 more genes
    nsv3916518copy number variation1nstd102humanPathogenic GRCh37 chr7: 1,737,760-27,246,914 , NCBI36 chr7: 1,704,286-27,213,439 , GRCh38 chr7: 1,698,124-27,207,295 LOC105375156, LOC105375133, 365 more genes
    nsv3916054copy number variation1nstd102humanPathogenic NCBI36 chr7: 20,217,060-27,855,544 , GRCh37 chr7: 20,250,535-27,889,019 , GRCh38 chr7: 20,210,912-27,849,400 MIR148A, NFE2L3, 139 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