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Items: 1 to 20 of 93

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097194copy number variation1nstd102humanUncertain significance GRCh37 chr3: 42,733,354-42,733,485 , GRCh38.p12 chr3: 42,691,862-42,691,993 KLHL40, HHATL
    nsv7096719copy number variation1nstd102humanUncertain significance GRCh37 chr3: 42,727,111-42,733,485 , GRCh38.p12 chr3: 42,685,619-42,691,993 KLHL40, HHATL
    nsv7056995inversion1nstd229human GRCh38 chr3: 42,690,687-42,822,483 , GRCh37.p13 chr3: 42,732,179-42,863,975 MIX23P4, HIGD1A, 7 more genes
    nsv7040447inversion1nstd229human GRCh38 chr3: 42,182,224-43,567,375 , GRCh37.p13 chr3: 42,223,716-43,608,867 VIPR1-AS1, SALL4P6, 38 more genes
    nsv7038909inversion1nstd229human GRCh38 chr3: 40,520,096-45,093,302 , GRCh37.p13 chr3: 40,561,587-45,134,794 ABHD5, ZKSCAN7, 97 more genes
    nsv6711902copy number variation1nstd229human GRCh38 chr3: 38,527,947-43,061,183 , GRCh37.p13 chr3: 38,569,438-43,102,675 ZBTB47, VIPR1-AS1, 90 more genes
    nsv6708396copy number variation1nstd229human GRCh38 chr3: 42,693,337-42,693,416 , GRCh37.p13 chr3: 42,734,829-42,734,908 HHATL
    nsv6708181copy number variation1nstd229human GRCh38 chr3: 42,668,343-42,699,971 , GRCh37.p13 chr3: 42,709,835-42,741,463 HHATL, RN7SL567P, 1 more genes
    nsv6698463copy number variation1nstd229human GRCh38 chr3: 42,695,416-42,704,386 , GRCh37.p13 chr3: 42,736,908-42,745,878 HHATL, HHATL-AS1, 1 more genes
    nsv6365416copy number variation1nstd223human GRCh38 chr3: 42,668,343-42,699,971 , GRCh37.p13 chr3: 42,709,835-42,741,463 KLHL40, HHATL, 1 more genes
    nsv6311795copy number variation1nstd102humanUncertain significance GRCh37 chr3: 40,924,962-43,760,024 , GRCh38.p12 chr3: 40,883,471-43,718,532 VIPR1, SNRK-AS1, 52 more genes
    nsv5887754copy number variation1nstd209human GRCh38 chr3: 42,700,008-42,700,079 , GRCh37.p13 chr3: 42,741,500-42,741,571 HHATL
    nsv5617979insertion1nstd207human GRCh38 chr3: 42,700,275-42,700,275 , GRCh37.p13 chr3: 42,741,767-42,741,767 HHATL
    nsv5536952insertion1nstd206human GRCh38 chr3: 42,700,297-42,700,334 , GRCh37.p13 chr3: 42,741,789-42,741,826 HHATL
    nsv5381497copy number variation1nstd102humanUncertain significance GRCh37 chr3: 42,727,101-42,733,495 , GRCh38.p12 chr3: 42,685,609-42,692,003 HHATL, KLHL40
    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
    nsv4790447copy number variation1nstd200human GRCh37 chr3: 42,732,517-42,732,999 , GRCh38.p12 chr3: 42,691,025-42,691,507 HHATL, KLHL40
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