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 282

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112685copy number variation1nstd102humannot provided GRCh37 chr1: 2,420,003-8,155,935 , GRCh38.p12 chr1: 2,488,564-8,095,875 LINC02780, C1orf174, 100 more genes
    nsv5868669copy number variation1nstd209human GRCh38 chr1: 3,900,758-3,916,502 , GRCh37.p13 chr1|NW_004070864.2: 1-9,483 , GRCh37.p13 chr1: 3,823,584-3,833,066 C1orf174, LINC01134
    nsv5830192copy number variation1nstd209human GRCh38 chr1: 3,900,717-3,909,641 , GRCh37.p13 chr1: 3,817,281-3,823,583 LINC01134, C1orf174
    nsv5605557insertion1nstd207human GRCh38 chr1: 3,906,468-3,906,468 , GRCh37.p13 chr1: 3,823,032-3,823,032 LINC01134
    nsv5428297copy number variation1nstd206human GRCh38 chr1: 3,585,575-4,260,086 , GRCh37.p13 chr1: 3,502,139-4,320,146 , LINC02780, 19 more genes
    nsv5427829copy number variation1nstd206human GRCh38 chr1: 3,900,738-3,916,525 , GRCh37.p13 chr1|NW_004070864.2: 1-9,506 , GRCh37.p13 chr1: 3,823,564-3,833,089 C1orf174, LINC01134
    nsv5422583copy number variation1nstd206human GRCh38 chr1: 3,821,016-4,289,147 , GRCh37.p13 chr1: 3,737,580-4,349,207 , DFFB, 7 more genes
    nsv5377545translocation1nstd200human GRCh38 chr1: 3,912,999-3,912,999 , GRCh38 chr1: 3,918,317-3,918,317 , GRCh37.p13 chr1|NW_004070864.2: 5,980-5,980 , GRCh37.p13 chr1: 3,829,563-3,829,563 , GRCh37.p13 chr1|NW_004070864.2: 11,298-11,298 , GRCh37.p13 chr1: 3,834,881-3,834,881 LINC01134
    nsv5346086translocation1nstd200human GRCh38 chr1: 3,918,326-3,918,326 , GRCh38 chr1: 3,913,231-3,913,231 , GRCh37.p13 chr1|NW_004070864.2: 11,307-11,307 , GRCh37.p13 chr1: 3,834,890-3,834,890 , GRCh37.p13 chr1|NW_004070864.2: 6,212-6,212 , GRCh37.p13 chr1: 3,829,795-3,829,795 LINC01134
    nsv5323481inversion1nstd204human GRCh37.p13 chr1: 3,438,482-4,249,593 , GRCh38.p13 chr1: 3,521,918-4,189,533 , CCDC27, 21 more genes
    nsv5071716mobile element insertion1nstd203human GRCh38 chr1: 3,901,896-3,901,926 , GRCh37.p13 chr1: 3,818,460-3,818,490 LINC01134
    nsv5066272mobile element insertion1nstd203human GRCh38 chr1: 3,901,879-3,901,896 , GRCh37.p13 chr1: 3,818,443-3,818,460 LINC01134
    nsv5030662inversion1nstd200human GRCh38 chr1: 3,521,920-4,189,533 , GRCh37.p13 chr1: 3,438,484-4,249,593 , TP73-AS3, 21 more genes
    nsv4894276copy number variation1nstd200human GRCh38 chr1: 2,989,984-4,291,637 , GRCh37.p13 chr1: 2,906,548-4,351,697 , LINC02780, 31 more genes
    nsv4889504copy number variation1nstd200human GRCh38 chr1: 3,903,239-3,908,536 , GRCh37.p13 chr1: 3,819,803-3,823,583 LINC01134
    nsv4873243inversion1nstd200human GRCh37 chr1: 3,438,484-4,249,593 , GRCh38.p12 chr1: 3,521,920-4,189,533 , LINC01346, 21 more genes
    nsv4772109copy number variation1nstd200human GRCh37 chr1: 3,817,322-3,833,069 , GRCh38.p12 chr1: 3,900,758-3,916,505 C1orf174, LINC01134
    nsv4728461copy number variation1nstd102humanUncertain significance GRCh37 chr1: 3,202,162-4,143,527 , GRCh38.p12 chr1: 3,285,598-4,083,467 LOC105378608, WRAP73, 20 more genes
    nsv4728187copy number variation1nstd102humanPathogenic GRCh37 chr1: 1-5,592,835 , GRCh38.p12 chr1: 10,001-5,532,775 UBE2J2, MRPL20, 196 more genes
    nsv4685972copy number variation1nstd102humanLikely pathogenic GRCh37 chr1: 762,080-7,309,686 , GRCh38.p12 chr1: 826,700-7,249,626 CDK11B, DFFB, 184 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