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 161

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095041copy number variation1nstd102humanUncertain significance GRCh37 chr16: 74,485,954-75,339,100 , GRCh38.p12 chr16: 74,452,056-75,305,202 CTRB1, CTRB2, 19 more genes
    nsv7075290inversion1nstd229human GRCh38 chr16: 75,220,531-75,227,617 , GRCh37.p13 chr16: 75,254,429-75,261,515 CTRB1, BCAR1, 1 more genes
    nsv7071200inversion1nstd229human GRCh38 chr16: 75,204,390-75,231,455 , GRCh37.p13 chr16: 75,238,288-75,265,353 CTRB2, CTRB1, 2 more genes
    nsv7070449inversion1nstd229human GRCh38 chr16: 75,216,555-75,274,303 , GRCh37.p13 chr16: 75,250,453-75,308,201 LOC105371344, BCAR1, 2 more genes
    nsv7066185inversion1nstd229human GRCh38 chr16: 71,798,581-75,423,466 , GRCh37.p13 chr16: 71,832,484-75,457,364 TMPOP2, RPSAP56, 57 more genes
    nsv7061930inversion1nstd229human GRCh38 chr16: 71,759,694-75,426,750 , GRCh37.p13 chr16: 71,793,597-75,460,648 BCAR1, LOC105371343, 57 more genes
    nsv7058675inversion1nstd229human GRCh38 chr16: 67,667,666-75,720,241 , GRCh37.p13 chr16: 67,701,569-75,754,139 RNU6-898P, DPEP2, 199 more genes
    nsv6998053copy number variation1nstd229human GRCh38 chr16: 75,164,533-76,191,896 , GRCh37.p13 chr16: 75,198,431-76,225,794 CTRB2, LOC105371344, 25 more genes
    nsv6996319copy number variation1nstd229human GRCh38 chr16: 75,203,685-75,228,315 , GRCh37.p13 chr16: 75,237,583-75,262,213 CTRB1, CTRB2, 2 more genes
    nsv6991745copy number variation1nstd229human GRCh38 chr16: 74,743,201-75,242,700 , GRCh37.p13 chr16: 74,777,099-75,276,598 RPS4Y1P1, BCAR1, 9 more genes
    nsv6983408copy number variation1nstd229human GRCh38 chr16: 74,048,861-75,393,024 , GRCh37.p13 chr16: 74,082,760-75,426,922 PSMD7, RNU6-237P, 28 more genes
    nsv6982265copy number variation1nstd229human GRCh38 chr16: 75,223,501-75,278,900 , GRCh37.p13 chr16: 75,257,399-75,312,798 CTRB1, LOC105371344, 2 more genes
    nsv6981754copy number variation1nstd229human GRCh38 chr16: 75,173,201-75,337,200 , GRCh37.p13 chr16: 75,207,099-75,371,098 CTRB1, RPS4Y1P1, 6 more genes
    nsv6637595copy number variation1nstd102humanUncertain significance GRCh37 chr16: 73,673,334-78,137,887 , GRCh38.p12 chr16: 73,639,435-78,103,990 CNTNAP4, WDR59, 73 more genes
    nsv6637493copy number variation1nstd102humanUncertain significance GRCh37 chr16: 73,673,334-76,105,189 , GRCh38.p12 chr16: 73,639,435-76,071,291 LOC105371347, LOC105371344, 51 more genes
    nsv6637273copy number variation1nstd102humanUncertain significance GRCh37 chr16: 73,858,079-75,855,162 , GRCh38.p12 chr16: 73,824,180-75,821,264 LOC105371344, CTRB2, 46 more genes
    nsv6634465copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 71,610,276-90,354,753 , GRCh38.p12 chr16: 71,576,373-90,228,345 AP1G1, AFG3L1P, 349 more genes
    nsv6623950copy number variation1nstd224human GRCh37 chr16: 75,239,737-75,261,647 , GRCh38.p12 chr16: 75,205,839-75,227,749 CTRB1, LOC100506281, 2 more genes
    nsv6623753copy number variation1nstd224human GRCh37 chr16: 75,241,024-75,270,782 , GRCh38.p12 chr16: 75,207,126-75,236,884 , GRCh38.p12 chr16|NW_018654723.1: 36,416-52,033 CTRB1, BCAR1, 2 more genes
    nsv6592476inversion1nstd223human GRCh38 chr16: 75,218,015-75,232,004 , GRCh37.p13 chr16: 75,251,913-75,265,902 CTRB1, BCAR1, 1 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