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 4055

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5329539translocation1nstd204human GRCh38.p13 chr11: 5,226,576-5,226,576 , GRCh38.p13 chr11: 5,225,727-5,225,727 , GRCh37.p13 chr11: 5,247,806-5,247,806 , GRCh37.p13 chr11: 5,246,957-5,246,957 HBB
    nsv5329528translocation1nstd204human GRCh38.p13 chr9: 29,591,759-29,591,759 , GRCh38.p13 chr9: 29,592,459-29,592,459 , GRCh37.p13 chr9: 29,591,757-29,591,757 , GRCh37.p13 chr9: 29,592,457-29,592,457 LOC105376005
    nsv5329524translocation1nstd204human GRCh38.p13 chr16: 77,410,445-77,410,445 , GRCh38.p13 chr16: 77,410,529-77,410,529 , GRCh37.p13 chr16: 77,444,426-77,444,426 , GRCh37.p13 chr16: 77,444,342-77,444,342 ADAMTS18
    nsv5329515translocation1nstd204human GRCh38.p13 chr1: 22,106,241-22,106,241 , GRCh38.p13 chr1: 22,006,431-22,006,431 , GRCh37.p13 chr1: 22,332,924-22,332,924 , GRCh37.p13 chr1: 22,432,734-22,432,734 CELA3A
    nsv5329512translocation1nstd204human GRCh38.p13 chr5: 148,173,476-148,173,476 , GRCh38.p13 chr5: 148,175,043-148,175,043 , GRCh37.p13 chr5: 147,553,039-147,553,039 , GRCh37.p13 chr5: 147,554,606-147,554,606 SPINK14
    nsv5329511translocation1nstd204human GRCh38.p13 chr16: 21,315,659-21,315,659 , GRCh38.p13 chr16: 21,315,866-21,315,866 , GRCh37.p13 chr16: 21,327,187-21,327,187 , GRCh37.p13 chr16: 21,326,980-21,326,980 CRYM-AS1
    nsv5329498translocation1nstd204human GRCh38.p13 chr2: 119,659,503-119,659,503 , GRCh38.p13 chr2: 119,660,919-119,660,919 , GRCh37.p13 chr2: 120,417,079-120,417,079 , GRCh37.p13 chr2: 120,418,495-120,418,495 CFAP221
    nsv5329492translocation1nstd204human GRCh38.p13 chr5: 43,516,380-43,516,380 , GRCh38.p13 chr5: 43,516,447-43,516,447 , GRCh37.p13 chr5: 43,516,482-43,516,482 , GRCh37.p13 chr5: 43,516,549-43,516,549 C5orf34-AS1
    nsv5329482translocation1nstd204human GRCh38.p13 chr12: 106,442,774-106,442,774 , GRCh38.p13 chr12: 106,442,674-106,442,674 , GRCh37.p13 chr12: 106,836,452-106,836,452 , GRCh37.p13 chr12: 106,836,552-106,836,552 POLR3B
    nsv5329478translocation1nstd204human GRCh38.p13 chr9: 136,285,450-136,285,450 , GRCh38.p13 chr9: 136,285,480-136,285,480 , GRCh37.p13 chr9|NW_003315926.1: 40,407-40,407 , GRCh37.p13 chr9|NW_003315926.1: 40,437-40,437 CCDC187
    nsv5329476translocation1nstd204human GRCh38.p13 chr8: 4,249,136-4,249,136 , GRCh38.p13 chr8: 4,248,631-4,248,631 , GRCh37.p13 chr8: 4,106,153-4,106,153 , GRCh37.p13 chr8: 4,106,658-4,106,658 CSMD1
    nsv5329460translocation1nstd204human GRCh38.p13 chr10: 12,078,094-12,078,094 , GRCh38.p13 chr10: 12,082,102-12,082,102 , GRCh37.p13 chr10: 12,120,093-12,120,093 , GRCh37.p13 chr10: 12,124,101-12,124,101 DHTKD1
    nsv5329454translocation1nstd204human GRCh38.p13 chr1: 45,622,759-45,622,759 , GRCh38.p13 chr1: 45,622,124-45,622,124 , GRCh37.p13 chr1: 46,087,796-46,087,796 , GRCh37.p13 chr1: 46,088,431-46,088,431 CCDC17
    nsv5329453translocation1nstd204human GRCh38.p13 chr7: 144,492,133-144,492,133 , GRCh38.p13 chr7: 144,493,769-144,493,769 , GRCh37.p13 chr7: 144,189,226-144,189,226 , GRCh37.p13 chr7: 144,190,862-144,190,862 TPK1
    nsv5329450translocation1nstd204human GRCh38.p13 chr15: 48,460,319-48,460,319 , GRCh38.p13 chr15: 48,463,898-48,463,898 , GRCh37.p13 chr15: 48,752,516-48,752,516 , GRCh37.p13 chr15: 48,756,095-48,756,095 FBN1
    nsv5329439translocation1nstd204human GRCh38.p13 chr17: 15,960,389-15,960,389 , GRCh38.p13 chr17: 15,960,572-15,960,572 , GRCh37.p13 chr17: 15,863,886-15,863,886 , GRCh37.p13 chr17: 15,863,703-15,863,703 ADORA2B
    nsv5329436translocation1nstd204human GRCh38.p13 chr10: 82,106,154-82,106,154 , GRCh38.p13 chr10: 82,106,218-82,106,218 , GRCh37.p13 chr10: 83,865,910-83,865,910 , GRCh37.p13 chr10: 83,865,974-83,865,974 NRG3
    nsv5329430translocation1nstd204human GRCh38.p13 chr8: 30,070,060-30,070,060 , GRCh38.p13 chr8: 30,082,846-30,082,846 , GRCh37.p13 chr8: 29,927,576-29,927,576 , GRCh37.p13 chr8: 29,940,362-29,940,362 SARAF
    nsv5329429translocation1nstd204human GRCh38.p13 chr13: 95,240,944-95,240,944 , GRCh38.p13 chr13: 95,241,783-95,241,783 , GRCh37.p13 chr13: 95,893,198-95,893,198 , GRCh37.p13 chr13: 95,894,037-95,894,037 ABCC4
    nsv5329427translocation1nstd204human GRCh38.p13 chr11: 24,883,328-24,883,328 , GRCh38.p13 chr11: 24,882,867-24,882,867 , GRCh37.p13 chr11: 24,904,413-24,904,413 , GRCh37.p13 chr11: 24,904,874-24,904,874 LUZP2
    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