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 222

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5878606copy number variation1nstd209human GRCh38 chr2: 102,492,658-102,492,745 , GRCh37.p13 chr2: 103,109,117-103,109,204 SLC9A4
    nsv5874380copy number variation1nstd209human GRCh38 chr2: 102,493,191-102,494,435 , GRCh37.p13 chr2: 103,109,650-103,110,894 SLC9A4
    nsv5871866copy number variation1nstd209human GRCh38 chr2: 102,488,904-102,489,037 , GRCh37.p13 chr2: 103,105,363-103,105,496 SLC9A4
    nsv5558142mobile element insertion1nstd206human GRCh38 chr2: 102,295,972-141,288,199 , GRCh37.p13 chr2: 102,912,432-142,045,768 , LOC105373587, 623 more genes
    nsv5554214mobile element insertion1nstd206human GRCh38 chr2: 43,826,578-177,947,868 , GRCh37.p13 chr2: 44,053,717-178,812,595 , POLR1B, 2149 more genes
    nsv5452993copy number variation1nstd206human GRCh38 chr2: 102,493,191-102,494,436 , GRCh37.p13 chr2: 103,109,650-103,110,895 SLC9A4
    nsv5445282copy number variation1nstd206human GRCh38 chr2: 102,492,658-102,492,749 , GRCh37.p13 chr2: 103,109,117-103,109,208 SLC9A4
    nsv5360953translocation1nstd200human GRCh38 chr2: 102,492,749-102,492,749 , GRCh38 chr2: 102,492,658-102,492,658 , GRCh37.p13 chr2: 103,109,117-103,109,117 , GRCh37.p13 chr2: 103,109,208-103,109,208 SLC9A4
    nsv5035923inversion1nstd200human GRCh38 chr2: 83,726,586-172,391,178 , GRCh37.p13 chr2: 83,953,710-173,255,906 , MTND2P21, 1427 more genes
    nsv4894871copy number variation1nstd200human GRCh38 chr2: 102,492,304-102,492,921 , GRCh37.p13 chr2: 103,108,763-103,109,380 SLC9A4
    nsv4892997copy number variation1nstd200human GRCh38 chr2: 102,505,932-102,506,007 , GRCh37.p13 chr2: 103,122,391-103,122,466 SLC9A4
    nsv4892996copy number variation1nstd200human GRCh38 chr2: 102,493,191-102,494,436 , GRCh37.p13 chr2: 103,109,650-103,110,895 SLC9A4
    nsv4786673copy number variation1nstd200human GRCh37 chr2: 103,109,650-103,110,895 , GRCh38.p12 chr2: 102,493,191-102,494,436 SLC9A4
    nsv4786672copy number variation1nstd200human GRCh37 chr2: 103,109,117-103,109,208 , GRCh38.p12 chr2: 102,492,658-102,492,749 SLC9A4
    nsv4766632inversion1nstd199human GRCh37 chr2: 87,997,505-112,010,501 , GRCh38.p12 chr1: 125,085,511-144,884,066 , GRCh38.p12 chr2: 87,697,986-111,252,924 , GRCh38.p12 chr9: 40,649,907-63,450,751 , GRCh38.p12 chr9: 40,649,751-63,450,622 , ADRA2B, 706 more genes
    nsv4752571inversion1nstd199human GRCh37 chr2: 87,550,795-112,295,517 , GRCh38.p12 chr1: 125,085,511-144,884,066 , GRCh38.p12 chr2: 87,323,672-111,537,940 , GRCh38.p12 chr9: 40,649,907-63,450,751 , GRCh38.p12 chr9: 40,649,751-63,450,622 , ADRA2B, 723 more genes
    nsv4743379copy number variation1nstd199human GRCh37 chr2: 88,481,090-124,440,189 , GRCh38.p12 chr9: 40,649,751-63,450,622 , GRCh38.p12 chr9: 40,649,907-63,450,751 , GRCh38.p12 chr1: 125,085,511-144,884,066 , GRCh38.p12 chr2: 88,181,571-123,682,613 , EIF2AK3, 861 more genes
    nsv4737534copy number variation1nstd199human GRCh37 chr2: 103,109,116-103,109,204 , GRCh38.p12 chr2: 102,492,657-102,492,745 SLC9A4
    nsv4660619copy number variation1nstd186human GRCh37 chr2: 103,109,650-103,110,895 , GRCh38.p12 chr2: 102,493,191-102,494,436 SLC9A4
    nsv4639705copy number variation3nstd186human GRCh37 chr2: 103,109,650-103,110,895 , GRCh38.p12 chr2: 102,493,191-102,494,436 SLC9A4
    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