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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098788copy number variation1nstd102humanUncertain significance GRCh37 chr4: 101,947,022-107,268,849 , GRCh38.p12 chr4: 101,025,865-106,347,692 LOC107986297, LOC100288914, 60 more genes
    nsv7097220copy number variation1nstd102humanPathogenic GRCh37 chr4: 101,947,022-106,061,534 , GRCh38.p12 chr4: 101,025,865-105,140,377 LOC100419096, LOC105377347, 41 more genes
    nsv7096821copy number variation1nstd102humanLikely pathogenic GRCh37 chr4: 103,635,575-103,635,738 , GRCh38.p12 chr4: 102,714,418-102,714,581 MANBA
    nsv7096485copy number variation1nstd102humanPathogenic GRCh37 chr4: 102,001,669-103,806,607 , GRCh38.p12 chr4: 101,080,512-102,885,450 SLC9B1, MIR8066, 24 more genes
    nsv7093528insertion1nstd102humanPathogenic GRCh37 chr4: 103,557,077-103,557,077 , GRCh38 chr4: 102,635,920-102,635,920 MANBA
    nsv7093277copy number variation1nstd102humanUncertain significance GRCh37 chr4: 103,681,940-103,682,064 , GRCh38 chr4: 102,760,783-102,760,907 MANBA
    nsv7054609inversion1nstd229human GRCh38 chr4: 95,257,712-104,152,159 , GRCh37.p13 chr4: 96,178,863-105,073,316 SLC39A8, PABPC1P7, 96 more genes
    nsv7052661inversion1nstd229human GRCh38 chr4: 96,912,053-103,991,076 , GRCh37.p13 chr4: 97,833,204-104,912,233 MIR1255A, LOC107986297, 86 more genes
    nsv7048086inversion1nstd229human GRCh38 chr4: 100,058,481-107,564,371 , GRCh37.p13 chr4: 100,979,638-108,485,528 ACTR6P1, INTS12, 79 more genes
    nsv7046928inversion1nstd229human GRCh38 chr4: 95,051,434-103,882,549 , GRCh37.p13 chr4: 95,972,585-104,803,706 PABPC1P7, RN7SL728P, 95 more genes
    nsv7044544inversion1nstd229human GRCh38 chr4: 98,964,941-108,185,877 , GRCh37.p13 chr4: 99,886,092-109,107,033 LOC102725220, TACR3, 117 more genes
    nsv6757240copy number variation1nstd229human GRCh38 chr4: 102,678,477-102,678,522 , GRCh37.p13 chr4: 103,599,634-103,599,679 MANBA
    nsv6755724copy number variation1nstd229human GRCh38 chr4: 102,654,401-102,682,300 , GRCh37.p13 chr4: 103,575,558-103,603,457 MANBA, RPL21P49
    nsv6750670copy number variation1nstd229human GRCh38 chr4: 102,664,455-102,676,729 , GRCh37.p13 chr4: 103,585,612-103,597,886 MANBA
    nsv6749077copy number variation1nstd229human GRCh38 chr4: 102,709,560-102,719,108 , GRCh37.p13 chr4: 103,630,717-103,640,265 MANBA
    nsv6748525copy number variation1nstd229human GRCh38 chr4: 102,609,242-102,641,695 , GRCh37.p13 chr4: 103,530,399-103,562,852 NFKB1, MANBA, 1 more genes
    nsv6747774copy number variation1nstd229human GRCh38 chr4: 102,639,873-102,740,399 , GRCh37.p13 chr4: 103,561,030-103,661,556 KRT8P46, LRRC37A15P, 3 more genes
    nsv6744048copy number variation1nstd229human GRCh38 chr4: 102,562,601-102,713,400 , GRCh37.p13 chr4: 103,483,758-103,634,557 MANBA, NFKB1, 2 more genes
    nsv6738806copy number variation1nstd229human GRCh38 chr4: 102,712,178-102,714,768 , GRCh37.p13 chr4: 103,633,335-103,635,925 MANBA
    nsv6738428copy number variation1nstd229human GRCh38 chr4: 102,629,209-102,636,824 , GRCh37.p13 chr4: 103,550,366-103,557,981 MANBA
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