U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Links from Nucleotide

Items: 1 to 20 of 4068

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6131564mobile element insertion1nstd186human GRCh37 chr17: 43,660,611-43,660,662 , GRCh38.p12 chr17|NT_187663.1: 285,384-285,435 , GRCh38.p12 chr17: 45,583,245-45,583,296 LRRC37A3
    nsv6131352insertion1nstd186human GRCh37 chr17: 43,991,589-43,991,622 , GRCh38.p12 chr17|NT_187663.1: 616,338-616,371 , GRCh38.p12 chr17: 45,914,223-45,914,256 MAPT
    nsv6130594insertion1nstd186human GRCh37 chr17: 43,496,511-43,496,538 , GRCh38.p12 chr17: 45,419,145-45,419,172 , GRCh38.p12 chr17|NT_187663.1: 109,652-109,679 ARHGAP27
    nsv6129852insertion1nstd186human GRCh37 chr17: 44,973,613-44,973,663 , GRCh38.p12 chr17|NT_187663.1: 1,415,664-1,415,714 , GRCh38.p12 chr17: 46,896,247-46,896,297 LRRC37A2
    nsv6129753mobile element insertion1nstd186human GRCh37 chr17: 44,153,977-44,154,015 , GRCh38.p12 chr17: 46,076,611-46,076,649 , GRCh38.p12 chr17|NT_187663.1: 778,710-778,748 KANSL1
    nsv6128663copy number variation1nstd186human GRCh37 chr17: 44,282,819-44,283,064 , GRCh38.p12 chr17: 46,205,453-46,205,698 , GRCh38.p12 chr17|NT_187663.1: 907,555-907,800 KANSL1
    nsv6127092copy number variation1nstd186human GRCh37 chr17: 44,314,882-44,315,607 , GRCh38.p12 chr17: 46,237,516-46,238,241 , GRCh38.p12 chr17|NT_187663.1: 939,692-940,397 0
    nsv6126578copy number variation1nstd186human GRCh37 chr17: 43,637,346-43,650,366 , GRCh38.p12 chr17: 45,559,980-45,573,000 , GRCh38.p12 chr17|NT_187663.1: 262,118-275,139 LOC105369225, LRRC37A3
    nsv6126480copy number variation1nstd186human GRCh37 chr17: 43,637,301-43,655,466 , GRCh38.p12 chr17: 45,559,935-45,578,100 , GRCh38.p12 chr17|NT_187663.1: 262,073-280,239 LOC105369225, LRRC37A3
    nsv6124556copy number variation1nstd186human GRCh37 chr17: 44,282,777-44,286,362 , GRCh38.p12 chr17: 46,205,411-46,208,996 , GRCh38.p12 chr17|NT_187663.1: 907,513-911,098 KANSL1
    nsv6123879copy number variation1nstd186human GRCh37 chr17: 43,575,346-43,589,991 , GRCh38.p12 chr17: 45,497,980-45,512,625 , GRCh38.p12 chr17|NT_187663.1: 188,135-202,780 LRRC37A4P, LRRC37A3, 1 more genes
    nsv6115320copy number variation1nstd186human GRCh37 chr17: 43,609,346-43,619,346 , GRCh38.p12 chr17: 45,531,980-45,541,980 , GRCh38.p12 chr17|NT_187663.1: 234,118-244,118 LRRC37A3, LOC102724345, 1 more genes
    nsv6114998copy number variation1nstd186human GRCh37 chr17: 44,179,739-44,182,307 , GRCh38.p12 chr17: 46,102,373-46,104,941 , GRCh38.p12 chr17|NT_187663.1: 804,478-807,046 KANSL1
    nsv6114862copy number variation1nstd186human GRCh37 chr17: 43,650,611-43,663,346 , GRCh38.p12 chr17: 45,573,245-45,585,980 , GRCh38.p12 chr17|NT_187663.1: 275,384-288,119 LRRC37A3, DND1P1
    nsv6114705mobile element insertion1nstd186human GRCh37 chr17: 43,818,948-43,818,948 , GRCh38.p12 chr17: 45,741,582-45,741,582 , GRCh38.p12 chr17|NT_187663.1: 443,682-443,682 LINC02210-CRHR1
    nsv6113924copy number variation1nstd186human GRCh37 chr17: 44,607,346-44,637,346 , GRCh38.p12 chr17: 46,529,980-46,559,980 , GRCh38.p12 chr17|NT_187663.1: 1,049,667-1,079,682 ARL17A, LRRC37A2, 2 more genes
    nsv6113557copy number variation1nstd186human GRCh37 chr17: 44,775,346-44,780,466 , GRCh38.p12 chr17: 46,697,980-46,703,100 , GRCh38.p12 chr17|NT_187663.1: 1,217,407-1,222,525 , GRCh38.p12 chr17|NT_167251.2: 1,683,869-1,688,989 NSF, LRRC37A2
    nsv5393797mobile element deletion1nstd186human GRCh37 chr17: 44,314,883-44,315,590 , GRCh38.p12 chr17: 46,237,517-46,238,224 , GRCh38.p12 chr17|NT_187663.1: 939,693-940,397 0
    nsv5392462copy number variation2nstd186human GRCh37 chr17: 44,212,772-44,369,547 , GRCh38.p12 chr17: 46,135,406-46,292,181 , GRCh38.p12 chr17|NT_187663.1: 837,513-954,783 KANSL1, KANSL1-AS1, 5 more genes
    nsv5391541copy number variation1nstd186human GRCh37 chr17: 43,655,785-44,366,714 , GRCh38.p12 chr17|NT_187663.1: 280,558-954,783 , GRCh38.p12 chr17: 45,578,419-46,289,348 LINC02210-CRHR1, STH, 22 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