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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7063028inversion1nstd229human GRCh38 chr12: 117,152,016-117,152,122 , GRCh37.p13 chr12: 117,589,821-117,589,927 FBXO21
    nsv6934970copy number variation1nstd229human GRCh38 chr12: 117,168,801-117,172,400 , GRCh37.p13 chr12: 117,606,606-117,610,205 FBXO21
    nsv6918388copy number variation1nstd229human GRCh38 chr12: 117,190,923-117,193,055 , GRCh37.p13 chr12: 117,628,728-117,630,860 FBXO21
    nsv6637830copy number variation1nstd102humanUncertain significance GRCh37 chr12: 116,422,123-117,740,952 , GRCh38.p12 chr12: 115,984,318-117,303,147 ELOCP32, LOC105370010, 23 more genes
    nsv6586460inversion1nstd223human GRCh38 chr12: 117,152,015-117,152,122 , GRCh37.p13 chr12: 117,589,820-117,589,927 FBXO21
    nsv6489919copy number variation1nstd223human GRCh38 chr12: 117,168,814-117,172,443 , GRCh37.p13 chr12: 117,606,619-117,610,248 FBXO21
    nsv6480631copy number variation1nstd223human GRCh38 chr12: 117,190,919-117,193,050 , GRCh37.p13 chr12: 117,628,724-117,630,855 FBXO21
    nsv6479708copy number variation1nstd223human GRCh38 chr12: 117,167,485-117,168,264 , GRCh37.p13 chr12: 117,605,290-117,606,069 FBXO21
    nsv6290239copy number variation1nstd102humanLikely pathogenic GRCh37 chr12: 117,461,902-133,841,395 , GRCh38.p12 chr12: 117,024,097-133,264,809 ACADS, BCL7A, 356 more genes
    nsv6248627mobile element insertion1nstd215human GRCh38 chr12: 117,142,695-117,142,695 , GRCh37.p13 chr12: 117,580,500-117,580,500 FBXO21
    nsv6132216copy number variation1nstd213human GRCh37 chr12: 117,580,000-118,570,001 , GRCh38.p12 chr12: 117,142,195-118,132,196 RFC5, KSR2, 8 more genes
    nsv6131051insertion1nstd186human GRCh37 chr12: 117,589,820-117,589,820 , GRCh38.p12 chr12: 117,152,015-117,152,015 FBXO21
    nsv6110627inversion1nstd212human GRCh38 chr12: 117,152,017-117,152,528 , GRCh37.p13 chr12: 117,589,822-117,590,333 FBXO21
    nsv6090900insertion1nstd212human GRCh38 chr12: 117,152,015-117,152,015 , GRCh37.p13 chr12: 117,589,820-117,589,820 FBXO21
    nsv5979148inversion1nstd209human GRCh38 chr12: 117,152,017-117,152,527 , GRCh37.p13 chr12: 117,589,822-117,590,332 FBXO21
    nsv5864509copy number variation1nstd209human GRCh38 chr12: 117,183,067-117,185,216 , GRCh37.p13 chr12: 117,620,872-117,623,021 FBXO21
    nsv5701880mobile element insertion1nstd211human GRCh38 chr12: 117,175,406-117,175,406 , GRCh37.p13 chr12: 117,613,211-117,613,211 FBXO21
    nsv5661757insertion1nstd207human GRCh38 chr12: 117,150,960-117,150,960 , GRCh37.p13 chr12: 117,588,765-117,588,765 FBXO21
    nsv5655262insertion1nstd207human GRCh38 chr12: 117,152,015-117,152,015 , GRCh37.p13 chr12: 117,589,820-117,589,820 FBXO21
    nsv5563275sequence alteration1nstd206human GRCh38 chr12: 117,152,014-117,152,528 , GRCh37.p13 chr12: 117,589,819-117,590,333 FBXO21
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