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 479

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099215copy number variation1nstd231human GRCh38.p12 chr1: 84,991,383-97,594,649 , GRCh37 chr1: 85,457,066-98,060,205 ABCA4, BRDT, 220 more genes
    nsv7050257inversion1nstd229human GRCh38 chr1: 90,043,458-91,855,366 , GRCh37.p13 chr1: 90,509,016-92,320,923 SNORD3G, LINC01763, 24 more genes
    nsv7045277inversion1nstd229human GRCh38 chr1: 89,219,136-91,269,986 , GRCh37.p13 chr1: 89,684,819-91,735,543 LOC105378847, CAPNS1P1, 33 more genes
    nsv7043892inversion1nstd229human GRCh38 chr1: 90,652,907-91,933,179 , GRCh37.p13 chr1: 91,118,464-92,398,736 ZNF644, RPL5P6, 17 more genes
    nsv6657146copy number variation1nstd229human GRCh38 chr1: 91,379,051-91,385,876 , GRCh37.p13 chr1: 91,844,608-91,851,433 HFM1
    nsv6657145copy number variation1nstd229human GRCh38 chr1: 91,287,809-91,291,638 , GRCh37.p13 chr1: 91,753,366-91,757,195 HFM1
    nsv6657070copy number variation1nstd229human GRCh38 chr1: 91,399,366-91,401,205 , GRCh37.p13 chr1: 91,864,923-91,866,762 HFM1
    nsv6657068copy number variation1nstd229human GRCh38 chr1: 91,366,401-91,372,800 , GRCh37.p13 chr1: 91,831,958-91,838,357 HFM1
    nsv6657064copy number variation1nstd229human GRCh38 chr1: 91,159,650-91,619,553 , GRCh37.p13 chr1: 91,625,207-92,085,110 HFM1, LOC107985417, 6 more genes
    nsv6657058copy number variation1nstd229human GRCh38 chr1: 91,366,292-92,033,167 , GRCh37.p13 chr1: 91,831,849-92,498,724 LOC102723436, EPHX4, 10 more genes
    nsv6657057copy number variation1nstd229human GRCh38 chr1: 91,309,662-91,315,241 , GRCh37.p13 chr1: 91,775,219-91,780,798 HFM1
    nsv6657056copy number variation1nstd229human GRCh38 chr1: 91,287,729-91,291,638 , GRCh37.p13 chr1: 91,753,286-91,757,195 HFM1
    nsv6657055copy number variation1nstd229human GRCh38 chr1: 91,282,006-91,578,137 , GRCh37.p13 chr1: 91,747,563-92,043,694 FEN1P1, LOC102723436, 5 more genes
    nsv6656277copy number variation1nstd229human GRCh38 chr1: 91,400,059-91,410,433 , GRCh37.p13 chr1: 91,865,616-91,875,990 HFM1
    nsv6656276copy number variation1nstd229human GRCh38 chr1: 91,393,847-91,393,943 , GRCh37.p13 chr1: 91,859,404-91,859,500 HFM1
    nsv6656275copy number variation1nstd229human GRCh38 chr1: 91,332,401-91,337,200 , GRCh37.p13 chr1: 91,797,958-91,802,757 HFM1
    nsv6656274copy number variation1nstd229human GRCh38 chr1: 91,293,264-91,302,003 , GRCh37.p13 chr1: 91,758,821-91,767,560 HFM1
    nsv6656272copy number variation1nstd229human GRCh38 chr1: 91,254,795-91,268,203 , GRCh37.p13 chr1: 91,720,352-91,733,760 HFM1
    nsv6656260copy number variation1nstd229human GRCh38 chr1: 91,027,708-91,370,033 , GRCh37.p13 chr1: 91,493,265-91,835,590 FEN1P1, HFM1
    nsv6626409copy number variation1nstd224human GRCh37 chr1: 91,809,014-91,845,778 , GRCh38.p12 chr1: 91,343,457-91,380,221 HFM1
    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