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 370

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6130884insertion1nstd186human GRCh37 chr21: 10,697,897-44,966,043 , GRCh38.p12 chr21: 12,965,809-43,546,162 , APP, 533 more genes
    nsv6129836insertion1nstd186human GRCh37 chr21: 44,316,447-44,316,474 , GRCh38.p12 chr21: 42,896,337-42,896,364 NDUFV3
    nsv5974556insertion1nstd209human GRCh38 chr21: 42,896,313-42,896,313 , GRCh37.p13 chr21: 44,316,423-44,316,423 NDUFV3
    nsv5967998insertion1nstd209human GRCh38 chr21: 42,894,362-42,894,362 , GRCh37.p13 chr21: 44,314,472-44,314,472 NDUFV3
    nsv5964146copy number variation1nstd209human GRCh38 chr21: 42,910,510-42,910,623 , GRCh37.p13 chr21: 44,330,620-44,330,733 NDUFV3
    nsv5953817copy number variation1nstd209human GRCh38 chr21: 42,905,595-42,908,437 , GRCh37.p13 chr21: 44,325,705-44,328,547 NDUFV3
    nsv5868062copy number variation1nstd209human GRCh38 chr21: 42,905,595-42,908,444 , GRCh37.p13 chr21: 44,325,705-44,328,554 NDUFV3
    nsv5671553insertion1nstd207human GRCh38 chr21: 42,894,401-42,894,401 , GRCh37.p13 chr21: 44,314,511-44,314,511 NDUFV3
    nsv5668719insertion1nstd207human GRCh38 chr21: 42,896,313-42,896,313 , GRCh37.p13 chr21: 44,316,423-44,316,423 NDUFV3
    nsv5664759insertion1nstd207human GRCh38 chr21: 42,894,362-42,894,362 , GRCh37.p13 chr21: 44,314,472-44,314,472 NDUFV3
    nsv5590675copy number variation1nstd207human GRCh38 chr21: 42,908,564-42,908,638 , GRCh37.p13 chr21: 44,328,674-44,328,748 NDUFV3
    nsv5546752copy number variation1nstd206human GRCh38 chr21: 42,894,119-42,902,068 , GRCh37.p13 chr21: 44,314,229-44,322,178 NDUFV3
    nsv5545894insertion1nstd206human GRCh38 chr21: 42,896,337-42,896,364 , GRCh37.p13 chr21: 44,316,447-44,316,474 NDUFV3
    nsv5540252copy number variation1nstd206human GRCh38 chr21: 42,893,617-42,894,482 , GRCh37.p13 chr21: 44,313,727-44,314,592 NDUFV3
    nsv5537279copy number variation1nstd206human GRCh38 chr21: 42,901,677-42,901,931 , GRCh37.p13 chr21: 44,321,787-44,322,041 NDUFV3
    nsv5188815mobile element insertion1nstd203human GRCh38 chr21: 42,907,961-42,907,978 , GRCh37.p13 chr21: 44,328,071-44,328,088 NDUFV3
    nsv5179822mobile element insertion1nstd203human GRCh38 chr21: 42,896,314-42,896,337 , GRCh37.p13 chr21: 44,316,424-44,316,447 NDUFV3
    nsv5177909mobile element insertion1nstd203human GRCh38 chr21: 42,896,316-42,896,337 , GRCh37.p13 chr21: 44,316,426-44,316,447 NDUFV3
    nsv5175274mobile element insertion1nstd203human GRCh38 chr21: 42,896,323-42,896,337 , GRCh37.p13 chr21: 44,316,433-44,316,447 NDUFV3
    nsv5173890mobile element insertion1nstd203human GRCh38 chr21: 42,896,317-42,896,337 , GRCh37.p13 chr21: 44,316,427-44,316,447 NDUFV3
    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