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Items: 1 to 20 of 202

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5899906copy number variation1nstd209human GRCh38 chr5: 163,434,767-163,436,284 , GRCh37.p13 chr5: 162,861,773-162,863,290 LOC105377700, CCNG1
    nsv5841553copy number variation1nstd209human GRCh38 chr5: 163,434,738-163,436,271 , GRCh37.p13 chr5: 162,861,744-162,863,277 LOC105377700, CCNG1
    nsv5686477mobile element insertion1nstd211human GRCh38 chr5: 163,438,306-163,438,306 , GRCh37.p13 chr5: 162,865,312-162,865,312 CCNG1
    nsv5677194mobile element insertion1nstd211human GRCh38 chr5: 163,448,274-163,448,274 , GRCh37.p13 chr5: 162,875,280-162,875,280 CCNG1, NUDCD2
    nsv5675980mobile element insertion2nstd211human GRCh38 chr5: 163,446,471-163,446,471 , GRCh37.p13 chr5: 162,873,477-162,873,477 NUDCD2, CCNG1
    nsv5640507insertion1nstd207human GRCh38 chr5: 163,446,457-163,446,457 , GRCh37.p13 chr5: 162,873,463-162,873,463 CCNG1, NUDCD2
    nsv5584111copy number variation1nstd207human GRCh38 chr5: 163,434,776-163,436,282 , GRCh37.p13 chr5: 162,861,782-162,863,288 CCNG1, LOC105377700
    nsv5456275copy number variation1nstd206human GRCh38 chr5: 163,434,767-163,436,285 , GRCh37.p13 chr5: 162,861,773-162,863,291 LOC105377700, CCNG1
    nsv5403695mobile element insertion1nstd206human GRCh38 chr5: 163,446,471-163,446,522 , GRCh37.p13 chr5: 162,873,477-162,873,528 CCNG1, NUDCD2
    nsv5400732mobile element insertion1nstd206human GRCh38 chr5: 163,448,274-163,448,325 , GRCh37.p13 chr5: 162,875,280-162,875,331 CCNG1, NUDCD2
    nsv5369054translocation1nstd200human GRCh38 chr5: 163,444,316-163,444,316 , GRCh38 chr5: 163,444,417-163,444,417 , GRCh37.p13 chr5: 162,871,322-162,871,322 , GRCh37.p13 chr5: 162,871,423-162,871,423 CCNG1
    nsv5338125translocation1nstd200human GRCh37 chr4: 129,638,064-129,638,064 , GRCh37 chr5: 162,871,417-162,871,417 , GRCh38.p12 chr4: 128,716,909-128,716,909 , GRCh38.p12 chr5: 163,444,411-163,444,411 CCNG1
    nsv5317882copy number variation1nstd204human GRCh37.p13 chr5: 162,861,773-162,863,291 , GRCh38.p13 chr5: 163,434,767-163,436,285 CCNG1, LOC105377700
    nsv5301541copy number variation1nstd204human GRCh38.p13 chr5: 163,429,687-163,899,395 , GRCh37.p13 chr5: 162,856,693-163,326,401 CCNG1, HMMR-AS1, 8 more genes
    nsv5238056copy number variation1nstd204human GRCh38.p13 chr5: 163,435,672-163,459,185 , GRCh37.p13 chr5: 162,862,678-162,886,191 LOC105377700, NUDCD2, 2 more genes
    nsv5237067copy number variation1nstd204human GRCh38.p13 chr5: 163,434,801-163,436,300 , GRCh37.p13 chr5: 162,861,807-162,863,306 CCNG1, LOC105377700
    nsv5233702copy number variation1nstd204human GRCh38.p13 chr5: 163,434,788-163,436,321 , GRCh37.p13 chr5: 162,861,794-162,863,327 LOC105377700, CCNG1
    nsv5230067copy number variation1nstd204human GRCh38.p13 chr5: 163,434,601-163,438,400 , GRCh37.p13 chr5: 162,861,607-162,865,406 LOC105377700, CCNG1
    nsv5227453copy number variation1nstd204human GRCh38.p13 chr5: 163,433,401-163,436,300 , GRCh37.p13 chr5: 162,860,407-162,863,306 LOC105377700, CCNG1
    nsv5220639copy number variation1nstd204human GRCh38.p13 chr5: 163,430,401-163,899,400 , GRCh37.p13 chr5: 162,857,407-163,326,406 HMMR, CCNG1, 8 more genes
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