U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Search results

Items: 1 to 20 of 438

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv514191copy number variation161nstd46human NCBI36 chr3: 190,846,768-191,021,280 , GRCh37.p13 chr3: 189,364,074-189,538,586 , GRCh38.p12 chr3: 189,646,285-189,820,797 TP63
    nsv514610copy number variation488nstd46human NCBI36 chr11: 38,206,020-38,246,792 , GRCh37.p13 chr11: 38,249,444-38,290,216 , GRCh38.p12 chr11: 38,227,894-38,268,666 LOC105376634
    nsv514350copy number variation488nstd46human NCBI36 chr6: 32,563,216-32,601,108 , GRCh37.p13 chr6: 32,455,238-32,493,130 , GRCh38.p12 chr6: 32,487,461-32,525,353 HLA-DRB5
    nsv514648copy number variation421nstd46human NCBI36 chr12: 11,396,685-11,433,740 , GRCh37.p13 chr12: 11,505,418-11,542,473 , GRCh38.p12 chr12: 11,352,484-11,389,539 , GRCh38.p12 chr12|NT_187658.1: 547,447-572,349 PRB1
    nsv514453copy number variation89nstd46human NCBI36 chr7: 141,416,096-141,440,400 , GRCh37.p13 chr7|NW_003571040.1: 211,778-236,082 , GRCh37.p13 chr7: 141,769,627-141,793,931 , GRCh38.p12 chr7: 142,069,827-142,094,131 , GRCh38.p12 chr7|NT_187562.1: 31,707-56,011 MGAM
    nsv514932copy number variation478nstd46human NCBI36 chr20: 1,511,631-1,531,931 , GRCh37.p13 chr20: 1,563,631-1,583,931 , GRCh38.p12 chr20: 1,582,985-1,603,285 SIRPB1
    nsv514989copy number variation488nstd46human NCBI36 chr2: 77,830,224-77,847,872 , GRCh37.p13 chr2: 77,976,716-77,994,364 , GRCh38.p12 chr2: 77,749,590-77,767,238 LOC101927967
    nsv514611copy number variation488nstd46human NCBI36 chr11: 38,251,456-38,268,496 , GRCh37.p13 chr11: 38,294,880-38,311,920 , GRCh38.p12 chr11: 38,273,330-38,290,370 LOC105376634
    nsv514825copy number variation30nstd46human NCBI36 chr17: 14,985,258-14,999,389 , GRCh37.p13 chr17: 15,044,533-15,058,664 , GRCh38.p12 chr17: 15,141,216-15,155,347 LOC107984976
    nsv514452copy number variation215nstd46human NCBI36 chr7: 133,435,896-133,448,328 , GRCh37.p13 chr7: 133,785,356-133,797,788 , GRCh38.p12 chr7: 134,100,603-134,113,035
    nsv514007copy number variation341nstd46human NCBI36 chr1: 150,838,880-150,850,880 , GRCh37.p13 chr1: 152,572,256-152,584,256 , GRCh38.p12 chr1: 152,599,780-152,611,780 LCE3C
    nsv514997copy number variation487nstd46human NCBI36 chr3: 156,963,760-156,974,432 , GRCh37.p13 chr3: 155,481,066-155,491,738 , GRCh38.p12 chr3: 155,763,277-155,773,949 C3orf33
    nsv514083copy number variation72nstd46human NCBI36 chr2: 89,867,504-89,878,056 , GRCh37.p13 chr2: 90,230,199-90,240,751 , GRCh38.p12 chr2: 90,191,347-90,201,885 IGK
    nsv514884copy number variation40nstd46human NCBI36 chr18: 64,897,288-64,907,444 , GRCh37.p13 chr18: 66,746,308-66,756,464 , GRCh38.p12 chr18: 69,079,071-69,089,227 CCDC102B
    nsv514990copy number variation142nstd46human NCBI36 chr2: 87,219,744-87,229,552 , GRCh37.p13 chr2: 87,366,233-87,376,041 , GRCh38.p12 chr2: 87,139,110-87,148,918 LOC102724642
    nsv514982copy number variation488nstd46human NCBI36 chr2: 195,022,992-195,032,480 , GRCh37.p13 chr2: 195,314,747-195,324,235 , GRCh38.p12 chr2: 194,450,023-194,459,511 LOC100419812
    nsv514952copy number variation68nstd46human NCBI36 chr21: 22,577,780-22,586,534 , GRCh37.p13 chr21|NW_003315968.1: 187,819-196,573 , GRCh37.p13 chr21: 23,655,909-23,664,663 , GRCh38.p12 chr21: 22,283,589-22,292,343 , GRCh38.p12 chr21|NW_003315968.2: 187,818-196,572 LOC107985508
    nsv514754copy number variation109nstd46human NCBI36 chr14: 79,175,888-79,184,280 , GRCh37.p13 chr14: 80,106,135-80,114,527 , GRCh38.p12 chr14: 79,639,792-79,648,184 NRXN3
    nsv514403copy number variation54nstd46human NCBI36 chr7: 246,785-254,873 , GRCh37.p13 chr7: 151,702-159,790 , GRCh38.p12 chr7: 151,702-159,790 , GRCh38.p12 chr7|NT_187558.1: 107,507-115,596 , GRCh38.p12 chr7|NT_187653.1: 144,023-152,111 LINC03014
    nsv514201copy number variation134nstd46human NCBI36 chr4: 20,978,244-20,986,012 , GRCh37.p13 chr4: 21,369,146-21,376,914 , GRCh38.p12 chr4: 21,367,523-21,375,291 KCNIP4
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Search details

    See more...

    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