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 1019

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv993413mobile element insertion52nstd94human GRCh37 chr21: 15,652,854-15,652,854 , GRCh38.p12 chr21: 14,280,533-14,280,533 ABCC13
    nsv993404mobile element insertion133nstd94human GRCh37 chr18: 54,706,181-54,706,181 , GRCh38.p12 chr18: 57,038,950-57,038,950 WDR7-OT1
    nsv993353mobile element insertion161nstd94human GRCh37 chr18: 63,487,270-63,487,270 , GRCh38.p12 chr18: 65,820,034-65,820,034 CDH7
    nsv993291mobile element insertion89nstd94human GRCh37 chr18: 59,713,734-59,713,734 , GRCh38.p12 chr18: 62,046,501-62,046,501 PIGN
    nsv993281mobile element insertion108nstd94human GRCh37 chr18: 47,147,441-47,147,441 , GRCh38.p12 chr18: 49,621,071-49,621,071 LOC105372112
    nsv993248mobile element insertion32nstd94human GRCh37 chr22: 32,827,425-32,827,425 , GRCh38.p12 chr22: 32,431,438-32,431,438 BPIFC
    nsv993247mobile element insertion7nstd94human GRCh37 chr22: 28,455,916-28,455,916 , GRCh38.p12 chr22: 28,059,928-28,059,928 TTC28
    nsv993228mobile element insertion30nstd94human GRCh37 chr19: 35,073,552-35,073,552 , GRCh38.p12 chr19: 34,582,647-34,582,647 SCGB1B2P
    nsv993227mobile element insertion14nstd94human GRCh37 chrX: 84,390,728-84,390,728 , GRCh38.p12 chrX: 85,135,722-85,135,722 SATL1
    nsv993222mobile element insertion157nstd94human GRCh37 chr19: 24,011,286-24,011,286 , GRCh38.p12 chr19: 23,828,484-23,828,484 RPSA2
    nsv993210mobile element insertion113nstd94human GRCh37 chr22: 23,872,669-23,872,669 , GRCh38.p12 chr22: 23,530,482-23,530,482 LOC107985580
    nsv993202mobile element insertion115nstd94human GRCh37 chr19: 56,966,034-56,966,034 , GRCh38.p12 chr19: 56,454,665-56,454,665 ZNF667
    nsv993184mobile element insertion45nstd94human GRCh37 chrX: 111,557,758-111,557,758 , GRCh38.p12 chrX: 112,314,530-112,314,530 RTL4
    nsv993113mobile element insertion173nstd94human GRCh37 chr18: 66,399,175-66,399,175 , GRCh38.p12 chr18: 68,731,938-68,731,938 CCDC102B
    nsv993107mobile element insertion15nstd94human GRCh37 chrX: 11,182,003-11,182,003 , GRCh38.p12 chrX: 11,163,883-11,163,883 ARHGAP6
    nsv992917mobile element insertion66nstd94human GRCh37 chr22: 22,715,588-22,715,588 , GRCh38.p12 chr22: 22,361,240-22,361,240 IGL
    nsv992894mobile element insertion133nstd94human GRCh37 chr20: 8,670,617-8,670,617 , GRCh38.p12 chr20: 8,689,970-8,689,970 PLCB1
    nsv992886mobile element insertion136nstd94human GRCh37 chr22: 34,430,612-34,430,612 , GRCh38.p12 chr22: 34,034,623-34,034,623 LINC01643
    nsv992880mobile element insertion146nstd94human GRCh37 chr18: 66,572,511-66,572,511 , GRCh38.p12 chr18: 68,905,274-68,905,274 CCDC102B
    nsv992869mobile element insertion11nstd94human GRCh37 chr18: 32,226,992-32,226,992 , GRCh38.p12 chr18: 34,647,028-34,647,028 DTNA
    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