U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Search results

Items: 1 to 20 of 89

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3884698copy number variation1nstd102humanBenign GRCh37 chr2: 1,706,794-1,708,472 , GRCh38.p12 chr2: 1,703,022-1,704,700 PXDN
    nsv6137787copy number variation1nstd102humanBenign GRCh38 chr2: 1,639,032-1,639,083 , GRCh37 chr2: 1,642,804-1,642,855 PXDN
    nsv3914145copy number variation1nstd102humanUncertain significance NCBI36 chr2: 1,547,171-1,734,592 , GRCh37.p13 chr2: 1,568,164-1,755,585 , GRCh38.p12 chr2: 1,564,392-1,751,813 PXDN
    nsv7096105copy number variation1nstd102humanUncertain significance GRCh37 chr2: 1,748,008-1,748,227 , GRCh38.p12 chr2: 1,744,236-1,744,455 PXDN
    nsv7093359copy number variation1nstd102humanlow penetrance, Pathogenic GRCh37 chr2: 1,618,581-1,856,549 , GRCh38.p12 chr2: 1,614,809-1,852,777 PXDN, MYT1L, 1 more genes
    nsv7093368copy number variation1nstd102humanlow penetrance, Pathogenic GRCh37 chr2: 1,742,240-1,848,126 , GRCh38.p12 chr2: 1,738,468-1,844,354 PXDN, MYT1L, 1 more genes
    nsv7093364copy number variation1nstd102humanlow penetrance, Pathogenic GRCh37 chr2: 1,742,241-1,848,126 , GRCh38.p12 chr2: 1,738,469-1,844,354 PXDN, MYT1L, 1 more genes
    nsv3882486copy number variation1nstd102humanLikely pathogenic GRCh38.p12 chr2: 1,730,766-2,299,873 , GRCh37 chr2: 1,734,538-2,303,645 PXDN, MYT1L, 1 more genes
    nsv3874398copy number variation1nstd102humanLikely pathogenic GRCh38.p12 chr2: 1,540,993-1,956,170 , GRCh37 chr2: 1,544,765-1,959,942 TPO, PXDN, 3 more genes
    nsv3886051copy number variation1nstd102humanLikely pathogenic GRCh38.p12 chr2: 1,607,919-1,857,776 , GRCh37 chr2: 1,611,691-1,861,548 PXDN, MYT1L, 1 more genes
    nsv3878138copy number variation1nstd102humanLikely benign GRCh37 chr2: 1,383,123-1,812,894 , GRCh38.p12 chr2: 1,379,351-1,809,122 LOC102723730, TPO, 2 more genes
    nsv4674703copy number variation1nstd102humanLikely benign GRCh37 chr2: 1,364,047-1,727,590 , GRCh38.p12 chr2: 1,360,275-1,723,818 PXDN, TPO, 2 more genes
    nsv3907650copy number variation1nstd102humanLikely benign NCBI36 chr2: 1,597,588-1,827,074 , GRCh37 chr2: 1,618,581-1,848,067 , GRCh38 chr2: 1,614,809-1,844,295 MYT1L, PXDN, 1 more genes
    nsv6637129copy number variation1nstd102humanUncertain significance GRCh37 chr2: 1,544,766-2,315,044 , GRCh38.p12 chr2: 1,540,994-2,311,272 TPO, PXDN, 3 more genes
    nsv4728166copy number variation1nstd102humanUncertain significance GRCh37 chr2: 1,492,690-2,204,279 , GRCh38.p12 chr2: 1,488,918-2,200,507 LOC102723730, TPO, 3 more genes
    nsv6290671copy number variation1nstd102humanUncertain significance GRCh37 chr2: 1,492,690-2,203,775 , GRCh38.p12 chr2: 1,488,918-2,200,003 LOC102723730, TPO, 3 more genes
    nsv6290554copy number variation1nstd102humanUncertain significance GRCh37 chr2: 1,625,269-2,315,044 , GRCh38.p12 chr2: 1,621,497-2,311,272 LOC107985838, MYT1L, 1 more genes
    nsv4674726copy number variation1nstd102humanUncertain significance GRCh37 chr2: 959,840-1,655,144 , GRCh38.p12 chr2: 964,154-1,651,372 LOC102723730, LOC105373359, 3 more genes
    nsv3917259copy number variation1nstd102humanUncertain significance NCBI36 chr2: 1,421,110-2,107,469 , GRCh37.p13 chr2: 1,442,103-2,128,462 , GRCh38.p12 chr2: 1,438,331-2,124,690 LOC102723730, LOC107985838, 3 more genes
    nsv3886740copy number variation1nstd102humanUncertain significance GRCh37 chr2: 995,005-1,670,069 , GRCh38.p12 chr2: 999,319-1,666,297 LOC105373359, LOC102723730, 3 more genes
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Search details

    See more...

    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