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Items: 1 to 20 of 136

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097202copy number variation1nstd102humanUncertain significance GRCh37 chr3: 49,866,536-50,540,854 , GRCh38.p12 chr3: 49,829,103-50,503,423 HYAL2, MON1A, 32 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
    nsv6368900copy number variation1nstd223human GRCh38 chr3: 50,236,772-50,288,786 , GRCh37.p13 chr3|NW_003871059.1: 6,620-58,634 , GRCh37.p13 chr3: 50,274,204-50,326,217 IFRD2, SEMA3B, 4 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
    nsv5210825copy number variation1nstd204human GRCh38.p13 chr3: 50,089,801-50,648,000 , GRCh37.p13 chr3: 50,127,234-50,685,431 C3orf18, GNAI2, 30 more genes
    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
    nsv4914330copy number variation1nstd200human GRCh38 chr3: 50,236,772-50,288,787 , GRCh37.p13 chr3|NW_003871059.1: 6,620-58,635 , GRCh37.p13 chr3: 50,274,204-50,326,218 GNAI2, SEMA3B-AS1, 4 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
    nsv4790656copy number variation1nstd200human GRCh37 chr3: 50,303,882-50,307,672 , GRCh38.p12 chr3: 50,266,450-50,270,241 SEMA3B, SEMA3B-AS1
    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
    nsv4588763copy number variation1nstd183human GRCh37 chr3: 50,065,789-50,352,458 , GRCh38.p12 chr3: 50,028,356-50,315,027 , SLC38A3, 16 more genes
    nsv4564128inversion1nstd166human GRCh37.p13 chr3: 3,474,047-77,824,459 , GRCh38.p12 chr3: 3,432,363-77,775,308 , ACY1, 1205 more genes
    nsv4409984copy number variation1nstd174human GRCh37 chr3: 50,189,901-50,476,600 , GRCh38.p12 chr3: 50,152,468-50,439,169 , RNA5SP131, 23 more genes
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