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 180

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5977361inversion1nstd209human GRCh38 chr7: 5,132,403-5,833,612 , GRCh37.p13 chr7: 5,172,034-5,873,243 , ACTB, 15 more genes
    nsv5562206sequence alteration1nstd206human GRCh38 chr7: 4,983,711-5,730,820 , GRCh37.p13 chr7: 5,023,342-5,770,451 , FSCN1, 21 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
    nsv5554692sequence alteration1nstd206human GRCh38 chr7: 5,142,858-5,773,733 , GRCh37.p13 chr7: 5,182,489-5,813,364 , FSCN1, 14 more genes
    nsv5467937copy number variation1nstd206human GRCh38 chr7: 5,527,506-5,527,588 , GRCh37.p13 chr7: 5,567,137-5,567,219 ACTB
    nsv5455838copy number variation1nstd206human GRCh38 chr7: 5,529,404-5,529,533 , GRCh37.p13 chr7: 5,569,035-5,569,164 ACTB
    nsv5352682translocation1nstd200human GRCh38 chr7: 5,526,894-5,526,894 , GRCh38 chr1: 65,722,520-65,722,520 , GRCh37.p13 chr7: 5,566,525-5,566,525 , GRCh37.p13 chr1: 66,188,203-66,188,203 ACTB
    nsv5310278copy number variation1nstd204human GRCh37.p13 chr7: 5,563,394-5,564,874 , GRCh38.p13 chr7: 5,523,763-5,525,243 LOC221946, ACTB
    nsv5235653copy number variation1nstd204human GRCh37.p13 chr7: 5,239,332-5,603,931 , GRCh38.p13 chr7: 5,199,701-5,564,300 ACTB, WIPI2, 7 more genes
    nsv4953291copy number variation1nstd200human GRCh38 chr7: 5,503,256-5,528,311 , GRCh37.p13 chr7: 5,542,887-5,567,942 LOC221946, FBXL18, 1 more genes
    nsv4949911copy number variation1nstd200human GRCh38 chr7: 5,529,666-5,530,523 , GRCh37.p13 chr7: 5,569,297-5,570,154 ACTB
    nsv4949910copy number variation1nstd200human GRCh38 chr7: 5,523,789-5,525,214 , GRCh37.p13 chr7: 5,563,420-5,564,845 LOC221946, ACTB
    nsv4818564copy number variation1nstd200human GRCh37 chr7: 5,563,422-5,564,845 , GRCh38.p12 chr7: 5,523,791-5,525,214 ACTB, LOC221946
    nsv4768306copy number variation1nstd102humanLikely pathogenic GRCh37 chr7: 5,567,327-5,567,689 , GRCh38 chr7: 5,527,696-5,528,058 ACTB
    nsv4675817copy number variation1nstd102humanPathogenic GRCh37 chr7: 1,648,373-10,627,513 , GRCh38.p12 chr7: 1,608,737-10,587,886 TTYH3, UNC93B2, 150 more genes
    nsv4648450copy number variation1nstd186human GRCh37 chr7: 5,567,000-5,573,000 , GRCh38.p12 chr7: 5,527,369-5,533,369 ACTB
    nsv4608399copy number variation1nstd183human GRCh37 chr7: 5,569,277-5,569,323 , GRCh38.p12 chr7: 5,529,646-5,529,692 ACTB
    nsv4605190copy number variation1nstd183human GRCh37 chr7: 5,569,019-5,570,322 , GRCh38.p12 chr7: 5,529,388-5,530,691 ACTB
    nsv4603112copy number variation2nstd183human GRCh37 chr7: 5,569,108-5,570,673 , GRCh38.p12 chr7: 5,529,477-5,531,042 ACTB
    nsv4601244copy number variation1nstd183human GRCh37 chr7: 5,567,803-5,573,530 , GRCh38.p12 chr7: 5,528,172-5,533,899 ACTB
    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