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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097483copy number variation1nstd102humanPathogenic GRCh37 chr7: 128,480,619-128,486,474 , GRCh38.p12 chr7: 128,840,565-128,846,420 FLNC
    nsv7097481copy number variation1nstd102humanPathogenic GRCh37 chr7: 128,475,360-128,478,877 , GRCh38.p12 chr7: 128,835,306-128,838,823 FLNC
    nsv6312526copy number variation1nstd102humanPathogenic GRCh37 chr7: 128,487,731-128,488,142 , GRCh38.p12 chr7: 128,847,677-128,848,088 FLNC
    nsv5673787copy number variation1nstd102humanLikely pathogenic GRCh37 chr7: 128,475,370-128,478,867 , GRCh38.p12 chr7: 128,835,316-128,838,813 FLNC
    nsv7097482copy number variation1nstd102humanLikely pathogenic GRCh37 chr7: 128,480,199-128,481,774 , GRCh38.p12 chr7: 128,840,145-128,841,720 FLNC
    nsv7097862copy number variation1nstd102humanUncertain significance GRCh37 chr7: 128,470,692-128,482,448 , GRCh38.p12 chr7: 128,830,638-128,842,394 FLNC
    nsv6829719copy number variation1nstd229human GRCh38 chr7: 128,840,751-128,840,786 , GRCh37.p13 chr7: 128,480,805-128,480,840 FLNC
    nsv4658851copy number variation1nstd186human GRCh37 chr7: 128,469,851-128,474,907 , GRCh38.p12 chr7: 128,829,797-128,834,853 FLNC
    nsv4599648copy number variation1nstd183human GRCh37 chr7: 128,469,851-128,474,907 , GRCh38.p12 chr7: 128,829,797-128,834,853 FLNC
    esv3106471copy number variation1estd209human GRCh37 chr7: 128,473,672-128,473,673 , GRCh38.p12 chr7: 128,833,618-128,833,619 FLNC
    esv3542416copy number variation1estd215human GRCh37 chr7: 128,480,791-128,480,828 , GRCh38.p12 chr7: 128,840,737-128,840,774 FLNC
    esv2675111copy number variation86estd199human GRCh37 chr7: 128,469,645-128,475,192 , GRCh38.p12 chr7: 128,829,591-128,835,138 FLNC
    esv3433126copy number variation2estd59human NCBI36 chr7: 128,267,992-128,268,320 , GRCh37.p13 chr7: 128,480,756-128,481,084 , GRCh38.p12 chr7: 128,840,702-128,841,030 FLNC
    esv2200592copy number variation1estd194human NCBI36 chr7: 128,260,909-128,260,910 , GRCh37.p13 chr7: 128,473,673-128,473,674 , GRCh38.p12 chr7: 128,833,619-128,833,620 FLNC
    esv1317997copy number variation1estd22human NCBI36 chr7: 128,260,908-128,260,909 , GRCh37.p13 chr7: 128,473,672-128,473,673 , GRCh38.p12 chr7: 128,833,618-128,833,619 FLNC
    nsv4165552copy number variation1nstd166human GRCh37.p13 chr7: 128,463,000-128,479,000 , GRCh38.p12 chr7: 128,822,946-128,838,946 FLNC
    nsv3124530copy number variation1nstd151human GRCh37 chr7: 128,477,688-128,481,029 , GRCh38.p12 chr7: 128,837,634-128,840,975 FLNC
    nsv3130418copy number variation1nstd151human GRCh37 chr7: 128,480,074-128,481,626 , GRCh38.p12 chr7: 128,840,020-128,841,572 FLNC
    esv2845175insertion1estd209human GRCh37 chr7: 128,474,736-128,474,736 , GRCh38.p12 chr7: 128,834,682-128,834,682 FLNC
    esv2845174insertion1estd209human GRCh37 chr7: 128,474,365-128,474,365 , GRCh38.p12 chr7: 128,834,311-128,834,311 FLNC
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