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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094667copy number variation1nstd102humanUncertain significance GRCh37 chr16: 31,332,542-31,332,968 , GRCh38.p12 chr16: 31,321,221-31,321,647 ITGAM
    nsv7094581copy number variation1nstd102humanUncertain significance GRCh37 chr16: 31,340,529-31,340,644 , GRCh38.p12 chr16: 31,329,208-31,329,323 ITGAM
    nsv7094580copy number variation1nstd102humanUncertain significance GRCh37 chr16: 31,338,157-31,343,028 , GRCh38.p12 chr16: 31,326,836-31,331,707 ITGAM
    nsv7074218inversion1nstd229human GRCh38 chr16: 31,272,147-31,275,672 , GRCh37.p13 chr16: 31,283,468-31,286,993 ITGAM
    nsv7068091inversion1nstd229human GRCh38 chr16: 29,736,414-31,610,190 , GRCh37.p13 chr16: 29,747,735-31,621,511 C16orf92, TMEM219, 118 more genes
    nsv7060598inversion1nstd229human GRCh38 chr16: 30,168,175-31,279,114 , GRCh37.p13 chr16: 30,179,496-31,290,435 ZNF629, ZNF771, 72 more genes
    nsv6997111copy number variation1nstd229human GRCh38 chr16: 31,299,201-31,324,700 , GRCh37.p13 chr16: 31,310,522-31,336,021 ITGAM
    nsv6996790copy number variation1nstd229human GRCh38 chr16: 31,311,876-31,320,068 , GRCh37.p13 chr16: 31,323,197-31,331,389 ITGAM
    nsv6993901copy number variation1nstd229human GRCh38 chr16: 31,328,765-31,328,821 , GRCh37.p13 chr16: 31,340,086-31,340,142 ITGAM
    nsv6993768copy number variation1nstd229human GRCh38 chr16: 31,282,286-31,287,891 , GRCh37.p13 chr16: 31,293,607-31,299,212 ITGAM
    nsv6993194copy number variation1nstd229human GRCh38 chr16: 31,331,937-31,331,995 , GRCh37.p13 chr16: 31,343,258-31,343,316 ITGAM
    nsv6991814copy number variation1nstd229human GRCh38 chr16: 31,295,907-31,307,300 , GRCh37.p13 chr16: 31,307,228-31,318,621 ITGAM
    nsv6991338copy number variation1nstd229human GRCh38 chr16: 31,324,840-31,575,158 , GRCh37.p13 chr16: 31,336,161-31,586,479 YBX3P1, COX6A2, 14 more genes
    nsv6986928copy number variation1nstd229human GRCh38 chr16: 31,302,424-31,302,486 , GRCh37.p13 chr16: 31,313,745-31,313,807 ITGAM
    nsv6986468copy number variation1nstd229human GRCh38 chr16: 31,267,849-31,292,450 , GRCh37.p13 chr16: 31,279,170-31,303,771 ITGAM
    nsv6985851copy number variation1nstd229human GRCh38 chr16: 31,269,536-31,271,467 , GRCh37.p13 chr16: 31,280,857-31,282,788 ITGAM
    nsv6985423copy number variation1nstd229human GRCh38 chr16: 31,326,001-31,328,800 , GRCh37.p13 chr16: 31,337,322-31,340,121 ITGAM
    nsv6982267copy number variation1nstd229human GRCh38 chr16: 31,292,901-31,328,700 , GRCh37.p13 chr16: 31,304,222-31,340,021 ITGAM
    nsv6981215copy number variation1nstd229human GRCh38 chr16: 31,300,528-31,304,232 , GRCh37.p13 chr16: 31,311,849-31,315,553 ITGAM
    nsv6980127copy number variation1nstd229human GRCh38 chr16: 31,261,410-31,863,261 , GRCh37.p13 chr16: 31,272,731-31,874,582 ITGAM, FRG2KP, 24 more genes
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