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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137082copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 74,807,864-74,810,388 , GRCh38 chr16: 74,773,966-74,776,490 FA2H
    nsv7095096copy number variation1nstd102humanPathogenic GRCh37 chr16: 74,808,364-74,808,653 , GRCh38.p12 chr16: 74,774,466-74,774,755 FA2H
    nsv7095041copy number variation1nstd102humanUncertain significance GRCh37 chr16: 74,485,954-75,339,100 , GRCh38.p12 chr16: 74,452,056-75,305,202 CTRB1, CTRB2, 19 more genes
    nsv7076339inversion1nstd229human GRCh38 chr16: 70,122,272-74,889,687 , GRCh37.p13 chr16: 70,156,175-74,923,585 SNORD111B, HCCAT5, 96 more genes
    nsv7066185inversion1nstd229human GRCh38 chr16: 71,798,581-75,423,466 , GRCh37.p13 chr16: 71,832,484-75,457,364 TMPOP2, RPSAP56, 57 more genes
    nsv7061930inversion1nstd229human GRCh38 chr16: 71,759,694-75,426,750 , GRCh37.p13 chr16: 71,793,597-75,460,648 BCAR1, LOC105371343, 57 more genes
    nsv7058675inversion1nstd229human GRCh38 chr16: 67,667,666-75,720,241 , GRCh37.p13 chr16: 67,701,569-75,754,139 RNU6-898P, DPEP2, 199 more genes
    nsv6994899copy number variation1nstd229human GRCh38 chr16: 74,719,488-74,784,762 , GRCh37.p13 chr16: 74,753,386-74,818,660 FA2H
    nsv6993219copy number variation1nstd229human GRCh38 chr16: 74,768,001-74,826,983 , GRCh37.p13 chr16: 74,801,899-74,860,881 FA2H
    nsv6992527copy number variation1nstd229human GRCh38 chr16: 74,767,117-74,771,705 , GRCh37.p13 chr16: 74,801,015-74,805,603 FA2H
    nsv6991745copy number variation1nstd229human GRCh38 chr16: 74,743,201-75,242,700 , GRCh37.p13 chr16: 74,777,099-75,276,598 RPS4Y1P1, BCAR1, 9 more genes
    nsv6990498copy number variation1nstd229human GRCh38 chr16: 74,773,631-74,773,909 , GRCh37.p13 chr16: 74,807,529-74,807,807 FA2H
    nsv6990121copy number variation1nstd229human GRCh38 chr16: 74,579,142-74,773,977 , GRCh37.p13 chr16: 74,613,040-74,807,875 FA2H, MLKL, 4 more genes
    nsv6989483copy number variation1nstd229human GRCh38 chr16: 74,727,928-74,848,310 , GRCh37.p13 chr16: 74,761,826-74,882,208 LOC105371343, FA2H
    nsv6987859copy number variation1nstd229human GRCh38 chr16: 74,533,101-74,779,800 , GRCh37.p13 chr16: 74,566,999-74,813,698 RPS10P23, HSPE1P7, 5 more genes
    nsv6986917copy number variation1nstd229human GRCh38 chr16: 74,719,502-74,723,060 , GRCh37.p13 chr16: 74,753,400-74,756,958 FA2H
    nsv6985498copy number variation1nstd229human GRCh38 chr16: 74,757,434-74,757,619 , GRCh37.p13 chr16: 74,791,332-74,791,517 FA2H
    nsv6983408copy number variation1nstd229human GRCh38 chr16: 74,048,861-75,393,024 , GRCh37.p13 chr16: 74,082,760-75,426,922 PSMD7, RNU6-237P, 28 more genes
    nsv6980836copy number variation1nstd229human GRCh38 chr16: 74,661,158-74,759,631 , GRCh37.p13 chr16: 74,695,056-74,793,529 MLKL, TMPOP2, 2 more genes
    nsv6637595copy number variation1nstd102humanUncertain significance GRCh37 chr16: 73,673,334-78,137,887 , GRCh38.p12 chr16: 73,639,435-78,103,990 CNTNAP4, WDR59, 73 more genes
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