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 133

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5901394copy number variation1nstd209human GRCh38 chr3: 173,919,154-173,919,219 , GRCh37.p13 chr3: 173,636,944-173,637,009 NLGN1-AS1, NLGN1
    nsv5896500copy number variation1nstd209human GRCh38 chr3: 171,525,972-180,293,041 , GRCh37.p13 chr3: 171,243,761-180,010,829 , RNU6-1120P, 95 more genes
    nsv5453639copy number variation1nstd206human GRCh38 chr3: 163,047,000-198,226,000 , GRCh37.p13 chr3: 162,764,788-197,952,871 , MIR922, 587 more genes
    nsv5437821copy number variation1nstd206human GRCh38 chr3: 173,919,157-173,919,220 , GRCh37.p13 chr3: 173,636,947-173,637,010 NLGN1-AS1, NLGN1
    nsv5033132inversion1nstd200human GRCh38 chr3: 147,205,794-180,217,342 , GRCh37.p13 chr3: 146,923,581-179,935,130 , LOC105374154, 433 more genes
    nsv4924865copy number variation1nstd200human GRCh38 chr3: 173,880,377-174,253,847 , GRCh37.p13 chr3: 173,598,167-173,971,637 RN7SKP234, NLGN1, 1 more genes
    nsv4920776copy number variation1nstd200human GRCh38 chr3: 173,914,395-173,914,550 , GRCh37.p13 chr3: 173,632,185-173,632,340 NLGN1-AS1, NLGN1
    nsv4674680copy number variation1nstd102humanPathogenic GRCh37 chr3: 169,617,690-190,593,854 , GRCh38.p12 chr3: 169,899,902-190,876,065 RNU6-1120P, LOC105374262, 323 more genes
    nsv4596225copy number variation1nstd183human GRCh37 chr3: 173,629,229-173,703,057 , GRCh38.p12 chr3: 173,911,439-173,985,267 NLGN1, NLGN1-AS1
    nsv4587873copy number variation1nstd183human GRCh37 chr3: 173,625,352-173,703,844 , GRCh38.p12 chr3: 173,907,562-173,986,054 NLGN1, NLGN1-AS1
    nsv4585586copy number variation1nstd183human GRCh37 chr3: 173,593,088-173,965,591 , GRCh38.p12 chr3: 173,875,298-174,247,801 RN7SKP234, NLGN1-AS1, 1 more genes
    nsv4405345copy number variation1nstd174human GRCh37 chr3: 173,625,340-173,711,210 , GRCh38.p12 chr3: 173,907,550-173,993,420 NLGN1, NLGN1-AS1
    nsv4390811copy number variation1nstd171human GRCh37 chr3: 173,636,945-173,637,010 , GRCh38.p12 chr3: 173,919,155-173,919,220 NLGN1, NLGN1-AS1
    nsv4327395inversion1nstd166human GRCh37.p13 chr3: 126,265,569-194,265,571 , GRCh38.p12 chr3: 126,546,726-194,544,842 , ACTG1P1, 1039 more genes
    nsv4107044copy number variation1nstd166human GRCh37.p13 chr3: 173,631,276-173,631,743 , GRCh38.p12 chr3: 173,913,486-173,913,953 NLGN1, NLGN1-AS1
    nsv4106627copy number variation1nstd166human GRCh37.p13 chr3: 173,637,441-173,637,587 , GRCh38.p12 chr3: 173,919,651-173,919,797 NLGN1-AS1, NLGN1
    nsv4098764copy number variation1nstd166human GRCh37.p13 chr3: 173,598,167-173,971,658 , GRCh38.p12 chr3: 173,880,377-174,253,868 NLGN1-AS1, RN7SKP234, 1 more genes
    nsv4097700copy number variation1nstd166human GRCh37.p13 chr3: 173,636,947-173,637,010 , GRCh38.p12 chr3: 173,919,157-173,919,220 NLGN1, NLGN1-AS1
    nsv4093660copy number variation1nstd166human GRCh37.p13 chr3: 173,632,185-173,632,340 , GRCh38.p12 chr3: 173,914,395-173,914,550 NLGN1-AS1, NLGN1
    nsv3918982copy number variation1nstd102humanPathogenic GRCh37 chr3: 167,885,356-197,837,049 , NCBI36 chr3: 169,368,050-199,321,446 , GRCh38 chr3: 168,167,568-198,110,178 EIF4G1, LOC105374248, 515 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