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 177

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5921012copy number variation1nstd209human GRCh38 chr7: 106,093,544-106,093,881 , GRCh37.p13 chr7: 105,733,990-105,734,327 SYPL1
    nsv5578105copy number variation1nstd207human GRCh38 chr7: 106,093,544-106,093,881 , GRCh37.p13 chr7: 105,733,990-105,734,327 SYPL1
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5489502copy number variation1nstd206human GRCh38 chr7: 106,101,764-106,104,830 , GRCh37.p13 chr7: 105,742,210-105,745,276 SYPL1
    nsv5478924copy number variation1nstd206human GRCh38 chr7: 106,093,547-106,093,882 , GRCh37.p13 chr7: 105,733,993-105,734,328 SYPL1
    nsv5476411copy number variation1nstd206human GRCh38 chr7: 106,106,317-106,107,964 , GRCh37.p13 chr7: 105,746,763-105,748,410 SYPL1
    nsv5326600inversion1nstd204human GRCh37.p13 chr7: 97,320,865-141,491,704 , GRCh38.p13 chr7: 97,691,553-141,791,904 , ARF5, 752 more genes
    nsv5317042copy number variation1nstd204human GRCh38.p13 chr7: 106,093,547-106,093,882 , GRCh37.p13 chr7: 105,733,993-105,734,328 SYPL1
    nsv5251244copy number variation1nstd204human GRCh38.p13 chr7: 106,093,601-106,093,900 , GRCh37.p13 chr7: 105,734,047-105,734,346 SYPL1
    nsv5215879mobile element deletion1nstd204human GRCh38.p13 chr7: 106,106,263-106,106,565 , GRCh37.p13 chr7: 105,746,709-105,747,011 SYPL1
    nsv5039775inversion1nstd200human GRCh38 chr7: 22,938,090-134,148,361 , GRCh37.p13 chr7: 22,977,709-133,833,114 , NFE4, 1832 more genes
    nsv5029742inversion1nstd200human GRCh38 chr7: 79,688,546-147,673,588 , GRCh37.p13 chr7: 79,317,862-147,370,680 , LOC100533722, 1168 more genes
    nsv4965105copy number variation1nstd200human GRCh38 chr7: 106,089,361-106,121,386 , GRCh37.p13 chr7: 105,729,807-105,761,832 SYPL1
    nsv4950664copy number variation1nstd200human GRCh38 chr7: 106,106,534-106,107,711 , GRCh37.p13 chr7: 105,746,980-105,748,157 SYPL1
    nsv4950663copy number variation1nstd200human GRCh38 chr7: 106,093,547-106,093,882 , GRCh37.p13 chr7: 105,733,993-105,734,328 SYPL1
    nsv4950662copy number variation1nstd200human GRCh38 chr7: 106,083,067-106,269,033 , GRCh37.p13 chr7: 105,723,513-105,909,479 RNU6-392P, SYPL1, 2 more genes
    nsv4880762inversion1nstd200human GRCh37 chr7: 79,317,862-147,370,680 , GRCh38.p12 chr7: 79,688,546-147,673,588 , RN7SKP277, 1168 more genes
    nsv4819911copy number variation1nstd200human GRCh37 chr7: 105,748,039-105,748,460 , GRCh38.p12 chr7: 106,107,593-106,108,014 SYPL1
    nsv4819910copy number variation1nstd200human GRCh37 chr7: 105,746,949-105,748,167 , GRCh38.p12 chr7: 106,106,503-106,107,721 SYPL1
    nsv4819909copy number variation1nstd200human GRCh37 chr7: 105,733,993-105,734,328 , GRCh38.p12 chr7: 106,093,547-106,093,882 SYPL1
    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