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 146

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5930748copy number variation1nstd209human GRCh38 chr19: 41,682,333-41,687,710 , GRCh37.p13 chr19|NW_004775434.1: 251,372-256,749 , GRCh37.p13 chr19: 42,186,264-42,191,639 CEACAM7
    nsv5872359copy number variation1nstd209human GRCh38 chr19: 41,682,352-41,687,153 , GRCh37.p13 chr19|NW_004775434.1: 251,391-256,192 , GRCh37.p13 chr19: 42,186,283-42,191,084 CEACAM7
    nsv5529795copy number variation1nstd206human GRCh38 chr19: 41,681,963-41,683,075 , GRCh37.p13 chr19: 42,185,894-42,187,006 , GRCh37.p13 chr19|NW_004775434.1: 251,002-252,114 CEACAM7
    nsv5520217copy number variation1nstd206human GRCh38 chr19: 41,682,333-41,687,711 , GRCh37.p13 chr19: 42,186,264-42,191,640 , GRCh37.p13 chr19|NW_004775434.1: 251,372-256,750 CEACAM7
    nsv5293732copy number variation1nstd204human GRCh38.p13 chr19: 41,614,001-41,747,800 , GRCh37.p13 chr19|NW_004775434.1: 183,040-316,839 , GRCh37.p13 chr19: 42,120,357-42,251,720 LOC105372405, CEACAM5, 3 more genes
    nsv5289503copy number variation1nstd204human GRCh38.p13 chr19: 41,682,202-41,687,437 , GRCh37.p13 chr19|NW_004775434.1: 251,241-256,476 , GRCh37.p13 chr19: 42,186,133-42,191,366 CEACAM7
    nsv5283164copy number variation1nstd204human GRCh38.p13 chr19: 41,653,344-41,692,340 , GRCh37.p13 chr19: 42,157,269-42,196,261 , GRCh37.p13 chr19|NW_004775434.1: 222,383-261,379 CEACAM7, LOC105372405
    nsv5024656copy number variation1nstd200human GRCh38 chr19: 41,682,333-41,687,711 , GRCh37.p13 chr19: 42,186,264-42,191,640 , GRCh37.p13 chr19|NW_004775434.1: 251,372-256,750 CEACAM7
    nsv5020495copy number variation1nstd200human GRCh38 chr19: 41,681,963-41,683,075 , GRCh37.p13 chr19|NW_004775434.1: 251,002-252,114 , GRCh37.p13 chr19: 42,185,894-42,187,006 CEACAM7
    nsv4865181copy number variation1nstd200human GRCh37 chr19: 42,186,264-42,191,640 , GRCh38.p12 chr19: 41,682,333-41,687,711 CEACAM7
    nsv4712399tandem duplication1nstd195human GRCh37 chr19: 42,186,260-42,186,261 , GRCh38.p12 chr19: 41,682,329-41,682,330 CEACAM7
    nsv4711282inversion1nstd195human GRCh37 chr19: 42,188,032-42,188,033 , GRCh38.p12 chr19: 41,684,101-41,684,101 CEACAM7
    nsv4702641copy number variation1nstd195human GRCh37 chr19: 41,998,201-42,367,401 , GRCh38.p12 chr19: 41,492,293-41,863,329 , GRCh38.p12 chr19|NT_187620.1: 1-198,050 CEACAM5, CEACAM7, 20 more genes
    nsv4676231copy number variation1nstd102humanUncertain significance GRCh37 chr19: 41,889,319-42,338,832 , GRCh38.p12 chr19: 41,383,414-41,834,777 , GRCh38.p12 chr19|NT_187620.1: 1-233,762 CEACAM7, LYPD4, 25 more genes
    nsv4667272copy number variation1nstd186human GRCh37 chr19: 42,186,492-42,191,707 , GRCh38.p12 chr19: 41,682,561-41,687,778 CEACAM7
    nsv4630236copy number variation2nstd183human GRCh37 chr19: 42,186,492-42,191,707 , GRCh38.p12 chr19: 41,682,561-41,687,778 CEACAM7
    nsv4457372copy number variation1nstd102humanPathogenic GRCh37 chr19: 28,271,106-49,213,832 , GRCh38.p12 chr19: 27,780,198-48,710,575 ZNF461, LOC101927572, 735 more genes
    nsv4415351copy number variation1nstd174human GRCh37 chr19: 42,186,335-42,191,707 , GRCh38.p12 chr19: 41,682,404-41,687,778 CEACAM7
    nsv4259529copy number variation1nstd166human GRCh37.p13 chr19: 42,186,264-42,191,640 , GRCh38.p12 chr19: 41,682,333-41,687,711 CEACAM7
    nsv3967626copy number variation1nstd168human GRCh38 chr19: 41,606,861-41,683,076 , GRCh37.p13 chr19|NW_004775434.1: 175,900-252,115 , GRCh37.p13 chr19: 42,113,216-42,187,007 CEACAM4, LOC105372405, 2 more genes
    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