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Items: 1 to 20 of 104

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6709346copy number variation1nstd229human GRCh38 chr3: 51,803,401-51,836,300 , GRCh37.p13 chr3: 51,837,417-51,870,316 LOC105377087, IQCF4P, 1 more genes
    nsv6371393copy number variation1nstd223human GRCh38 chr3: 51,825,388-51,829,048 , GRCh37.p13 chr3: 51,859,404-51,863,064 IQCF3
    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
    nsv5561912sequence alteration1nstd206human GRCh38 chr3: 46,623,292-58,677,536 , GRCh37.p13 chr3: 46,664,782-58,663,263 , CDC25A, 327 more genes
    nsv5561196sequence alteration1nstd206human GRCh38 chr3: 51,825,676-51,828,371 , GRCh37.p13 chr3: 51,859,692-51,862,387 IQCF3
    nsv5437541copy number variation1nstd206human GRCh38 chr3: 51,825,611-51,828,423 , GRCh37.p13 chr3: 51,859,627-51,862,439 IQCF3
    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
    nsv4911350copy number variation1nstd200human GRCh38 chr3: 51,825,357-51,829,070 , GRCh37.p13 chr3: 51,859,373-51,863,086 IQCF3
    nsv4911347copy number variation1nstd200human GRCh38 chr3: 51,769,352-52,724,007 , GRCh37.p13 chr3: 51,803,368-52,758,023 , ACY1, 55 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
    nsv4790703copy number variation1nstd200human GRCh37 chr3: 51,859,373-51,863,094 , GRCh38.p12 chr3: 51,825,357-51,829,078 IQCF3
    nsv4790701copy number variation1nstd200human GRCh37 chr3: 51,803,368-52,758,023 , GRCh38.p12 chr3: 51,769,352-52,724,007 , SNORD19B, 55 more genes
    nsv4673975copy number variation1nstd102humanUncertain significance GRCh37 chr3: 51,247,306-53,069,942 , GRCh38.p12 chr3: 51,209,875-53,035,926 RRP9, LOC100301990, 76 more genes
    nsv4586446copy number variation1nstd183human GRCh37 chr3: 51,862,200-51,862,784 , GRCh38.p12 chr3: 51,828,184-51,828,768 IQCF3
    nsv4564128inversion1nstd166human GRCh37.p13 chr3: 3,474,047-77,824,459 , GRCh38.p12 chr3: 3,432,363-77,775,308 , ACY1, 1205 more genes
    nsv4520437copy number variation1nstd166human GRCh37.p13 chr3: 51,859,389-51,863,064 , GRCh38.p12 chr3: 51,825,373-51,829,048 IQCF3
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