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Items: 1 to 20 of 387

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7144307insertion1nstd232human GRCh37.p13 chr4: 101,390,637-101,390,637 , GRCh38.p12 chr4: 100,469,480-100,469,480 EMCN
    nsv7142429insertion1nstd232human GRCh37.p13 chr4: 101,390,638-101,390,638 , GRCh38.p12 chr4: 100,469,481-100,469,481 EMCN
    nsv7056495inversion1nstd229human GRCh38 chr4: 100,393,677-100,393,744 , GRCh37.p13 chr4: 101,314,834-101,314,901 SNORA101A, EMCN
    nsv7054609inversion1nstd229human GRCh38 chr4: 95,257,712-104,152,159 , GRCh37.p13 chr4: 96,178,863-105,073,316 SLC39A8, PABPC1P7, 96 more genes
    nsv7052845inversion1nstd229human GRCh38 chr4: 97,450,222-102,053,198 , GRCh37.p13 chr4: 98,371,373-102,974,355 RNU6-462P, LOC105377345, 58 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
    nsv6756321copy number variation1nstd229human GRCh38 chr4: 100,460,322-100,460,378 , GRCh37.p13 chr4: 101,381,479-101,381,535 EMCN
    nsv6750958copy number variation1nstd229human GRCh38 chr4: 100,385,284-100,409,402 , GRCh37.p13 chr4: 101,306,441-101,330,559 SNORA101A, EMCN
    nsv6750469copy number variation1nstd229human GRCh38 chr4: 100,471,013-100,487,727 , GRCh37.p13 chr4: 101,392,170-101,408,884 EMCN
    nsv6749570copy number variation1nstd229human GRCh38 chr4: 100,468,053-100,487,581 , GRCh37.p13 chr4: 101,389,210-101,408,738 EMCN
    nsv6749308copy number variation1nstd229human GRCh38 chr4: 100,511,701-100,514,800 , GRCh37.p13 chr4: 101,432,858-101,435,957 EMCN
    nsv6748751copy number variation1nstd229human GRCh38 chr4: 100,509,673-100,536,819 , GRCh37.p13 chr4: 101,430,830-101,457,976 EMCN, LOC105377345
    nsv6746015copy number variation1nstd229human GRCh38 chr4: 100,430,101-100,437,500 , GRCh37.p13 chr4: 101,351,258-101,358,657 EMCN
    nsv6744098copy number variation1nstd229human GRCh38 chr4: 100,511,644-100,516,719 , GRCh37.p13 chr4: 101,432,801-101,437,876 EMCN
    nsv6741646copy number variation1nstd229human GRCh38 chr4: 100,424,001-100,437,600 , GRCh37.p13 chr4: 101,345,158-101,358,757 EMCN
    nsv6739522copy number variation1nstd229human GRCh38 chr4: 100,469,479-100,469,655 , GRCh37.p13 chr4: 101,390,636-101,390,812 EMCN
    nsv6738567copy number variation1nstd229human GRCh38 chr4: 100,451,584-100,551,972 , GRCh37.p13 chr4: 101,372,741-101,473,129 LOC105377345, EMCN
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