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Items: 1 to 20 of 167

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6714292copy number variation1nstd229human GRCh38 chr3: 49,677,236-49,697,278 , GRCh37.p13 chr3: 49,714,669-49,734,711 MST1, RNF123, 1 more genes
    nsv6710416copy number variation1nstd229human GRCh38 chr3: 49,713,201-49,721,200 , GRCh37.p13 chr3: 49,750,634-49,758,633 AMIGO3, RNF123, 1 more genes
    nsv6709766copy number variation1nstd229human GRCh38 chr3: 49,646,889-49,769,072 , GRCh37.p13 chr3: 49,684,322-49,806,505 BSN, MST1, 6 more genes
    nsv6700836copy number variation1nstd229human GRCh38 chr3: 48,056,801-51,204,000 , GRCh37.p13 chr3: 48,098,291-51,241,431 APEH, SLC26A6, 129 more genes
    nsv6311990copy number variation1nstd102humanPathogenic GRCh37 chr3: 49,547,968-50,685,477 , GRCh38.p12 chr3: 49,510,535-50,648,046 APEH, RNA5SP131, 52 more genes
    nsv6135016copy number variation1nstd213human GRCh37 chr3: 48,760,000-52,290,001 , GRCh38.p12 chr3: 48,722,567-52,255,985 ACY1, ALAS1, 128 more genes
    nsv6134694copy number variation1nstd213human GRCh37 chr3: 46,170,000-52,140,001 , GRCh38.p12 chr3: 46,128,508-52,105,985 ACY1, AMT, 210 more genes
    nsv5891025copy number variation1nstd209human GRCh38 chr3: 49,693,626-52,462,904 , GRCh37.p13 chr3: 49,731,059-52,496,920 , SEMA3G, 106 more genes
    nsv5673729copy number variation1nstd102humanPathogenic GRCh37 chr3: 48,507,870-50,340,407 , GRCh38.p12 chr3: 48,466,471-50,302,976 SEMA3B-AS1, GNAT1, 87 more genes
    nsv5561912sequence alteration1nstd206human GRCh38 chr3: 46,623,292-58,677,536 , GRCh37.p13 chr3: 46,664,782-58,663,263 , CDC25A, 327 more genes
    nsv5070090mobile element insertion1nstd203human GRCh38 chr3: 49,710,079-49,710,079 , GRCh37.p13 chr3: 49,747,512-49,747,512 RNF123
    nsv5063887mobile element insertion1nstd203human GRCh38 chr3: 49,710,082-49,710,082 , GRCh37.p13 chr3: 49,747,515-49,747,515 RNF123
    nsv5037434inversion1nstd200human GRCh38 chr3: 5,031,119-56,902,223 , GRCh37.p13 chr3: 5,072,804-56,936,251 , IRAK2, 925 more genes
    nsv5030280inversion1nstd200human GRCh38 chr3: 3,432,416-77,775,308 , GRCh37.p13 chr3: 3,474,100-77,824,459 , BHLHE40, 1198 more genes
    nsv4888770inversion1nstd200human GRCh37 chr3: 3,474,100-77,824,459 , GRCh38.p12 chr3: 3,432,416-77,775,308 , ATRIP, 1198 more genes
    nsv4877503inversion1nstd200human GRCh37 chr3: 24,885,632-100,711,157 , GRCh38.p12 chr3: 24,844,141-100,992,313 , LINC00692, 1088 more genes
    nsv4728146copy number variation1nstd102humanPathogenic GRCh37 chr3: 48,807,193-51,363,558 , GRCh38.p12 chr3: 48,769,760-51,326,127 APEH, MIR5193, 90 more genes
    nsv4665229copy number variation1nstd186human GRCh37 chr3: 49,724,812-49,728,909 , GRCh38.p12 chr3: 49,687,379-49,691,476 MST1, RNF123
    nsv4664969copy number variation1nstd186human GRCh37 chr3: 49,722,148-49,734,498 , GRCh38.p12 chr3: 49,684,715-49,697,065 MST1, RNF123
    nsv4662390copy number variation2nstd186human GRCh37 chr3: 49,721,852-49,725,911 , GRCh38.p12 chr3: 49,684,419-49,688,478 APEH, MST1, 1 more genes
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