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 193

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7058001inversion1nstd229human GRCh38 chr6: 47,441,459-48,144,831 , GRCh37.p13 chr6: 47,409,195-48,112,567 ADGRF2, RPL27AP7, 9 more genes
    nsv7047571inversion1nstd229human GRCh38 chr6: 47,471,816-49,526,857 , GRCh37.p13 chr6: 47,439,552-49,494,570 MMUT, RN7SKP116, 19 more genes
    nsv7044146inversion1nstd229human GRCh38 chr6: 47,635,253-48,108,329 , GRCh37.p13 chr6: 47,602,989-48,076,065 OPN5, LOC107986601, 6 more genes
    nsv6791534copy number variation1nstd229human GRCh38 chr6: 47,831,378-47,834,803 , GRCh37.p13 chr6: 47,799,114-47,802,539 OPN5
    nsv6413151copy number variation1nstd223human GRCh38 chr6: 47,808,137-47,824,029 , GRCh37.p13 chr6: 47,775,873-47,791,765 RNU1-105P, OPN5
    nsv6411763copy number variation1nstd223human GRCh38 chr6: 46,841,055-48,021,507 , GRCh37.p13 chr6: 46,808,792-47,989,243 RPL27AP7, LOC105375082, 18 more genes
    nsv6406672copy number variation1nstd223human GRCh38 chr6: 47,796,625-47,797,133 , GRCh37.p13 chr6: 47,764,361-47,764,869 OPN5
    nsv6401941copy number variation1nstd223human GRCh38 chr6: 47,797,201-47,799,700 , GRCh37.p13 chr6: 47,764,937-47,767,436 OPN5
    nsv6314749copy number variation1nstd102humanLikely pathogenic GRCh37 chr6: 43,636,308-64,947,206 , GRCh38.p12 chr6: 43,668,571-64,237,313 ACTG1P9, CRISP1, 245 more genes
    nsv6245112mobile element insertion1nstd215human GRCh38 chr6: 47,784,693-47,784,693 , GRCh37.p13 chr6: 47,752,429-47,752,429 OPN5
    nsv6186261copy number variation1nstd214human GRCh38 chr6: 47,828,671-47,828,720 , GRCh37.p13 chr6: 47,796,407-47,796,456 OPN5
    nsv6135921copy number variation1nstd213human GRCh37 chr6: 34,700,000-52,650,001 , GRCh38.p12 chr6: 34,732,223-52,785,203 ACTG1P9, CRISP1, 361 more genes
    nsv6076831insertion1nstd212human GRCh38 chr6: 47,788,561-47,788,561 , GRCh37.p13 chr6: 47,756,297-47,756,297 OPN5
    nsv6075073insertion1nstd212human GRCh38 chr6: 47,819,336-47,819,336 , GRCh37.p13 chr6: 47,787,072-47,787,072 OPN5
    nsv5725198mobile element insertion1nstd211human GRCh38 chr6: 47,823,279-47,823,279 , GRCh37.p13 chr6: 47,791,015-47,791,015 RNU1-105P, OPN5
    nsv5718992mobile element insertion1nstd211human GRCh38 chr6: 47,815,103-47,815,103 , GRCh37.p13 chr6: 47,782,839-47,782,839 OPN5
    nsv5692092mobile element insertion1nstd211human GRCh38 chr6: 47,784,693-47,784,693 , GRCh37.p13 chr6: 47,752,429-47,752,429 OPN5
    nsv5679758mobile element insertion2nstd211human GRCh38 chr6: 47,810,503-47,810,503 , GRCh37.p13 chr6: 47,778,239-47,778,239 OPN5
    nsv5638761insertion1nstd207human GRCh38 chr6: 47,819,336-47,819,336 , GRCh37.p13 chr6: 47,787,072-47,787,072 OPN5
    nsv5637846insertion1nstd207human GRCh38 chr6: 47,810,489-47,810,489 , GRCh37.p13 chr6: 47,778,225-47,778,225 OPN5
    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