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Items: 1 to 20 of 84

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7051996inversion1nstd229human GRCh38 chr3: 43,186,996-45,060,828 , GRCh37.p13 chr3: 43,228,488-45,102,320 ABHD5, CLEC3B, 44 more genes
    nsv7045350inversion1nstd229human GRCh38 chr3: 42,956,971-43,487,783 , GRCh37.p13 chr3: 42,998,463-43,529,275 GASK1A, LOC105377052, 8 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
    nsv6706862copy number variation1nstd229human GRCh38 chr3: 43,255,168-44,930,739 , GRCh37.p13 chr3: 43,296,660-44,972,231 LOC101928529, ANO10, 40 more genes
    nsv6313629copy number variation1nstd102humanUncertain significance GRCh37 chr3: 42,984,620-43,656,876 , GRCh38.p12 chr3: 42,943,128-43,615,384 RN7SL517P, LOC107986079, 9 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
    nsv6134849copy number variation1nstd213human GRCh37 chr3: 42,800,000-43,600,001 , GRCh38.p12 chr3: 42,758,508-43,558,509 ACKR2, CYP8B1, 18 more genes
    nsv5437305copy number variation1nstd206human GRCh38 chr3: 43,303,325-43,358,138 , GRCh37.p13 chr3: 43,344,817-43,399,630 SNRK, SNRK-AS1, 1 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
    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
    nsv4728435copy number variation1nstd102humanUncertain significance GRCh37 chr3: 43,230,722-43,933,855 , GRCh38.p12 chr3: 43,189,230-43,892,363 LOC105377052, ANO10, 7 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
    nsv4340778sequence alteration1nstd166human GRCh37.p13 chr3: 43,194,655-44,018,771 , GRCh38.p12 chr3: 43,153,163-43,977,279 , SNRK, 10 more genes
    nsv4077684copy number variation1nstd166human GRCh37.p13 chr3: 43,234,481-43,504,990 , GRCh38.p12 chr3: 43,192,989-43,463,498 , SNRK, 4 more genes
    nsv3889228copy number variation2nstd102humanPathogenic GRCh37 chr3: 61,892-197,851,986 , GRCh38.p12 chr3: 20,214-198,125,115 NDUFB4, LOC105374108, 2876 more genes
    nsv3885606copy number variation1nstd102humanPathogenic GRCh37 chr3: 60,174-197,948,027 , GRCh38.p12 chr3: 18,496-198,221,156 RNU4-62P, SEMA3B-AS1, 2880 more genes
    nsv3885169copy number variation1nstd102humanPathogenic GRCh37 chr3: 16,923,595-45,249,923 , GRCh38.p12 chr3: 16,884,818-45,208,431 RNU6-243P, ZNF385D, 382 more genes
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