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 270

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5970582insertion1nstd209human GRCh38 chr11: 13,288,394-13,288,394 , GRCh37.p13 chr11: 13,309,941-13,309,941 BMAL1
    nsv5915617copy number variation1nstd209human GRCh38 chr11: 13,331,501-13,334,148 , GRCh37.p13 chr11: 13,353,048-13,355,695 BMAL1
    nsv5862026copy number variation1nstd209human GRCh38 chr11: 13,331,465-13,334,564 , GRCh37.p13 chr11: 13,353,012-13,356,111 BMAL1
    nsv5644891insertion1nstd207human GRCh38 chr11: 13,288,417-13,288,417 , GRCh37.p13 chr11: 13,309,964-13,309,964 BMAL1
    nsv5599448copy number variation1nstd207human GRCh38 chr11: 13,284,196-13,284,247 , GRCh37.p13 chr11: 13,305,743-13,305,794 BMAL1
    nsv5548899insertion1nstd206human GRCh38 chr11: 13,387,036-13,387,073 , GRCh37.p13 chr11: 13,408,583-13,408,620 BTBD10, BMAL1
    nsv5511498copy number variation1nstd206human GRCh38 chr11: 13,291,271-13,292,984 , GRCh37.p13 chr11: 13,312,818-13,314,531 BMAL1
    nsv5511275copy number variation1nstd206human GRCh38 chr11: 13,331,501-13,334,149 , GRCh37.p13 chr11: 13,353,048-13,355,696 BMAL1
    nsv5504418copy number variation1nstd206human GRCh38 chr11: 13,370,664-13,371,973 , GRCh37.p13 chr11: 13,392,211-13,393,520 BMAL1
    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
    nsv5354754translocation1nstd200human GRCh38 chr11: 13,371,973-13,371,973 , GRCh38 chr11: 13,370,664-13,370,664 , GRCh37.p13 chr11: 13,392,211-13,392,211 , GRCh37.p13 chr11: 13,393,520-13,393,520 BMAL1
    nsv5259499copy number variation1nstd204human GRCh38.p13 chr11: 13,373,901-13,382,800 , GRCh37.p13 chr11: 13,395,448-13,404,347 BMAL1
    nsv4984212copy number variation1nstd200human GRCh38 chr11: 13,304,784-13,306,943 , GRCh37.p13 chr11: 13,326,331-13,328,490 BMAL1
    nsv4978310copy number variation1nstd200human GRCh38 chr11: 13,316,264-13,316,404 , GRCh37.p13 chr11: 13,337,811-13,337,951 BMAL1
    nsv4978309copy number variation1nstd200human GRCh38 chr11: 13,296,293-13,299,274 , GRCh37.p13 chr11: 13,317,840-13,320,821 BMAL1
    nsv4843108copy number variation1nstd200human GRCh37 chr11: 13,317,840-13,320,821 , GRCh38.p12 chr11: 13,296,293-13,299,274 BMAL1
    nsv4840557copy number variation1nstd200human GRCh37 chr11: 13,337,811-13,337,951 , GRCh38.p12 chr11: 13,316,264-13,316,404 BMAL1
    nsv4831560copy number variation1nstd200human GRCh37 chr11: 13,326,331-13,328,490 , GRCh38.p12 chr11: 13,304,784-13,306,943 BMAL1
    nsv4751865inversion1nstd199human GRCh37 chr11: 1,620,303-71,272,233 , GRCh38.p12 chr11: 1,599,073-71,561,187 , ACP2, 1686 more genes
    nsv4743742copy number variation1nstd199human GRCh37 chr11: 13,305,635-13,305,702 , GRCh38.p12 chr11: 13,284,088-13,284,155 BMAL1
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Recent activity

    You are here: NCBI > Variation > Database of Genomic Structural Variation (dbVar)
    Support Center