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 32

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3874640copy number variation1nstd102humanBenign GRCh37 chr1: 17,213,883-17,285,244 , GRCh38.p12 chr1: 16,887,388-16,958,749 CROCC, LOC107985101, 3 more genes
    nsv3872169copy number variation1nstd102humanBenign GRCh37 chr1: 17,209,369-17,279,470 , GRCh38.p12 chr1: 16,882,874-16,952,975 CROCC, LOC105376805, 3 more genes
    nsv6290672copy number variation1nstd102humanPathogenic GRCh37 chr1: 849,466-17,525,065 , GRCh38.p12 chr1: 914,086-17,198,570 CROCC, RPL9P11, 466 more genes
    nsv7098827copy number variation1nstd102humanPathogenic GRCh37 chr1: 4,481,271-20,530,242 , GRCh38.p12 chr1: 4,421,211-20,203,749 CROCC, LOC107985467, 386 more genes
    nsv3900501copy number variation1nstd102humanPathogenic GRCh38 chr1: 3,006,193-17,688,934 , GRCh37 chr1: 2,922,757-18,015,429 , NCBI36 chr1: 2,912,617-17,888,016 CROCC, MFFP1, 364 more genes
    nsv3900236copy number variation1nstd102humanPathogenic GRCh38 chr1: 5,363,826-18,360,302 , GRCh37 chr1: 5,423,886-18,686,796 , NCBI36 chr1: 5,323,746-18,559,383 CROCC, PDPN, 333 more genes
    nsv6636785copy number variation1nstd102humanPathogenic GRCh37 chr1: 6,758,933-19,287,770 , GRCh38.p12 chr1: 6,698,873-18,961,276 CROCC, GPR157, 313 more genes
    nsv6137724copy number variation1nstd102humanPathogenic GRCh37 chr1: 16,785,250-23,491,592 , GRCh38.p12 chr1: 16,458,755-23,165,099 CROCC, PADI1, 176 more genes
    nsv3899287copy number variation1nstd102humanPathogenic GRCh37 chr1: 15,711,763-21,306,842 , NCBI36 chr1: 15,584,350-21,179,429 , GRCh38 chr1: 15,385,267-20,980,349 CROCC, EMC1-AS1, 166 more genes
    nsv4728309copy number variation1nstd102humanPathogenic GRCh37 chr1: 16,041,431-21,295,864 , GRCh38.p12 chr1: 15,714,936-20,969,371 CROCC, RNU1-6P, 150 more genes
    nsv4728344copy number variation1nstd102humanPathogenic GRCh37 chr1: 17,284,906-21,778,495 , GRCh38.p12 chr1: 16,958,411-21,452,002 CROCC, NBL1, 98 more genes
    nsv3898082copy number variation1nstd102humanPathogenic GRCh37 chr1: 16,008,307-19,988,832 , NCBI36 chr1: 15,880,894-19,861,419 , GRCh38 chr1: 15,681,812-19,662,339 CROCC, ESPNP, 114 more genes
    nsv6290472copy number variation1nstd102humanPathogenic GRCh37 chr1: 16,773,001-20,221,073 , GRCh38.p12 chr1: 16,446,506-19,894,580 CROCC, MIR1290, 92 more genes
    nsv6290458copy number variation1nstd102humanPathogenic GRCh37 chr1: 17,284,531-17,770,100 , GRCh38.p12 chr1|NW_011332688.1: 1-288,827 , GRCh38.p12 chr1: 16,958,036-17,443,604 CROCC, PADI2, 12 more genes
    nsv3877365copy number variation1nstd102humanPathogenic GRCh37 chr1: 47,851-249,228,449 , GRCh38.p12 chr1: 47,851-248,934,250 CROCC, MARK1, 4930 more genes
    nsv3885206copy number variation1nstd102humanPathogenic GRCh37 chr1: 82,154-249,218,992 , GRCh38.p12 chr1: 82,154-248,924,793 CROCC, SNAP47, 4927 more genes
    nsv3884414copy number variation2nstd102humanPathogenic GRCh37 chr1: 849,467-249,224,684 , GRCh38.p12 chr1: 914,087-248,930,485 CROCC, RNU1-153P, 4887 more genes
    nsv3909483copy number variation1nstd102humanPathogenic NCBI36 chr1: 13,819,061-18,665,253 , GRCh38 chr1: 13,619,979-18,466,172 , GRCh37 chr1: 13,946,474-18,792,666 CROCC, TMEM51, 117 more genes
    nsv3875728copy number variation1nstd102humanBenign GRCh37 chr1: 17,277,995-17,397,704 , GRCh38.p12 chr1: 16,951,500-17,071,209 CROCC, MFAP2, 4 more genes
    nsv3910768copy number variation1nstd102humanBenign NCBI36 chr1: 16,722,216-17,157,376 , GRCh37.p13 chr1|NW_003871056.3: 519,502-907,580 , GRCh37.p13 chr1: 16,849,629-17,284,789 , GRCh38.p12 chr1: 16,523,134-16,958,294 CROCC, RNU1-6P, 31 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