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 95

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7076407inversion1nstd229human GRCh38 chr11: 46,405,448-49,855,596 , GRCh37.p13 chr11: 46,426,998-49,862,647 KBTBD4, MADD-AS1, 89 more genes
    nsv7061528inversion1nstd229human GRCh38 chr11: 47,146,905-49,892,579 , GRCh37.p13 chr11: 47,168,456-49,862,647 YPEL5P2, MADD, 76 more genes
    nsv6911457copy number variation1nstd229human GRCh38 chr11: 47,540,000-47,635,415 , GRCh37.p13 chr11: 47,561,552-47,656,967 C1QTNF4, MTCH2, 7 more genes
    nsv6904724copy number variation1nstd229human GRCh38 chr11: 47,562,601-47,612,800 , GRCh37.p13 chr11: 47,584,153-47,634,352 RNU5E-10P, NDUFS3, 6 more genes
    nsv6470626copy number variation1nstd223human GRCh38 chr11: 47,559,316-47,587,912 , GRCh37.p13 chr11: 47,580,868-47,609,464 CELF1, KBTBD4, 5 more genes
    nsv6466290copy number variation1nstd223human GRCh38 chr11: 47,563,410-47,608,683 , GRCh37.p13 chr11: 47,584,962-47,630,235 MTCH2, KBTBD4, 6 more genes
    nsv6464518copy number variation1nstd223human GRCh38 chr11: 47,584,858-47,585,286 , GRCh37.p13 chr11: 47,606,410-47,606,838 FAM180B, NDUFS3
    nsv6459298copy number variation1nstd223human GRCh38 chr11: 47,589,401-47,591,300 , GRCh37.p13 chr11: 47,610,953-47,612,852 C1QTNF4, FAM180B
    nsv6315537copy number variation1nstd102humanPathogenic GRCh37 chr11: 32,799,481-134,938,470 , GRCh38.p12 chr11: 32,777,935-135,068,576 PYGM, ATL3, 2125 more genes
    nsv6315474copy number variation1nstd102humanPathogenic GRCh37 chr11: 43,607,886-61,466,671 , GRCh38.p12 chr11: 43,586,336-61,699,199 TRR-TCT3-2, OR4A41P, 494 more genes
    nsv6132367copy number variation1nstd213human GRCh37 chr11: 46,660,000-47,930,001 , GRCh38.p12 chr11: 46,638,450-47,908,449 ACP2, ARHGAP1, 39 more genes
    nsv6132266copy number variation1nstd213human GRCh37 chr11: 47,180,000-47,890,001 , GRCh38.p12 chr11: 47,158,449-47,868,449 ACP2, DDB2, 28 more genes
    nsv6132180copy number variation1nstd213human GRCh37 chr11: 47,180,000-47,880,001 , GRCh38.p12 chr11: 47,158,449-47,858,449 ACP2, DDB2, 28 more genes
    nsv5380796copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397 FAUP4, MMP7, 2031 more genes
    nsv5380725copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chr11: 45,827,353-47,804,770 , GRCh38.p12 chr11: 45,805,802-47,783,218 MIR4688, LOC112268075, 58 more genes
    nsv4984480copy number variation1nstd200human GRCh38 chr11: 47,563,410-47,608,721 , GRCh37.p13 chr11: 47,584,962-47,630,273 CELF1, KBTBD4, 6 more genes
    nsv4848564copy number variation1nstd200human GRCh37 chr11: 47,606,392-47,607,205 , GRCh38.p12 chr11: 47,584,840-47,585,653 , GRCh38.p12 chr11|NW_019805496.1: 12,666-13,479 NDUFS3, FAM180B
    nsv4751865inversion1nstd199human GRCh37 chr11: 1,620,303-71,272,233 , GRCh38.p12 chr11: 1,599,073-71,561,187 , ACP2, 1686 more genes
    nsv4741272copy number variation1nstd199human GRCh37 chr11: 3,487,146-67,605,076 , GRCh38.p12 chr11: 3,465,916-67,837,605 , DRAP1, 1535 more genes
    nsv3924778copy number variation1nstd102humanPathogenic GRCh38 chr11: 41,118,322-48,643,003 , GRCh37 chr11: 41,139,872-48,664,555 , NCBI36 chr11: 41,096,448-48,621,131 F2, PSMC3, 140 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