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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7093619copy number variation1nstd228human GRCh37 chr4: 171,508,974-190,957,473 , GRCh38.p12 chr4: 170,587,823-190,036,318 AGA, SLC25A4, 240 more genes
    nsv7056086inversion1nstd229human GRCh38 chr4: 174,912,619-184,252,538 , GRCh37.p13 chr4: 175,833,770-185,173,691 WDR17, LOC105377580, 84 more genes
    nsv7044269inversion1nstd229human GRCh38 chr4: 174,633,546-175,064,474 , GRCh37.p13 chr4: 175,554,697-175,985,625 LOC105377552, LOC101928551, 4 more genes
    nsv6756230copy number variation1nstd229human GRCh38 chr4: 174,698,194-174,965,158 , GRCh37.p13 chr4: 175,619,345-175,886,309 GLRA3, LOC101928551, 1 more genes
    nsv6753465copy number variation1nstd229human GRCh38 chr4: 174,963,901-174,966,000 , GRCh37.p13 chr4: 175,885,052-175,887,151 ADAM29
    nsv6753170copy number variation1nstd229human GRCh38 chr4: 174,708,501-175,064,400 , GRCh37.p13 chr4: 175,629,652-175,985,551 LOC100131553, GLRA3, 3 more genes
    nsv6752394copy number variation1nstd229human GRCh38 chr4: 174,945,744-174,952,124 , GRCh37.p13 chr4: 175,866,895-175,873,275 ADAM29
    nsv6752205copy number variation1nstd229human GRCh38 chr4: 174,937,016-175,000,477 , GRCh37.p13 chr4: 175,858,167-175,921,628 ADAM29
    nsv6752069copy number variation1nstd229human GRCh38 chr4: 174,914,412-174,916,792 , GRCh37.p13 chr4: 175,835,563-175,837,943 ADAM29
    nsv6751709copy number variation1nstd229human GRCh38 chr4: 174,963,958-174,965,838 , GRCh37.p13 chr4: 175,885,109-175,886,989 ADAM29
    nsv6749025copy number variation1nstd229human GRCh38 chr4: 174,920,601-174,924,300 , GRCh37.p13 chr4: 175,841,752-175,845,451 ADAM29
    nsv6747083copy number variation1nstd229human GRCh38 chr4: 174,944,619-174,949,972 , GRCh37.p13 chr4: 175,865,770-175,871,123 ADAM29
    nsv6746826copy number variation1nstd229human GRCh38 chr4: 174,961,797-174,969,437 , GRCh37.p13 chr4: 175,882,948-175,890,588 ADAM29
    nsv6746056copy number variation1nstd229human GRCh38 chr4: 174,940,159-175,263,141 , GRCh37.p13 chr4: 175,861,310-176,184,292 LOC105377552, LOC100131553, 1 more genes
    nsv6740692copy number variation1nstd229human GRCh38 chr4: 173,724,041-174,933,391 , GRCh37.p13 chr4: 174,645,192-175,854,542 ADAM29, LOC107986204, 16 more genes
    nsv6738148copy number variation1nstd229human GRCh38 chr4: 174,695,784-175,421,722 , GRCh37.p13 chr4: 175,616,935-176,342,873 ADAM29, LOC100129957, 4 more genes
    nsv6634364copy number variation1nstd102humanPathogenic GRCh37 chr4: 167,779,888-190,957,473 , GRCh38.p12 chr4: 166,858,737-190,036,318 LOC101928551, LOC107986330, 279 more genes
    nsv6634351copy number variation1nstd102humanPathogenic GRCh37 chr4: 159,174,483-190,957,473 , GRCh38.p12 chr4: 158,253,331-190,036,318 COPS3P1, LOC339975, 363 more genes
    nsv6570153inversion1nstd223human GRCh38 chr4: 174,953,103-174,953,910 , GRCh37.p13 chr4: 175,874,254-175,875,061 ADAM29
    nsv6570050inversion1nstd223human GRCh38 chr4: 169,780,525-178,315,900 , GRCh37.p13 chr4: 170,701,676-179,237,054 LOC101928409, LOC100131553, 91 more genes
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