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Items: 1 to 20 of 76

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv6702494copy number variation1nstd229human GRCh38 chr3: 42,741,525-42,892,852 , GRCh37.p13 chr3: 42,783,017-42,934,344 ACKR2, CYP8B1, 6 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
    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
    nsv4572219sequence alteration1nstd166human GRCh37.p13 chr3: 42,912,314-42,912,315 , GRCh38.p12 chr3: 42,870,822-42,870,823 CYP8B1
    nsv4564128inversion1nstd166human GRCh37.p13 chr3: 3,474,047-77,824,459 , GRCh38.p12 chr3: 3,432,363-77,775,308 , ACY1, 1205 more genes
    nsv4086495copy number variation1nstd166human GRCh37.p13 chr3: 42,860,000-42,994,200 , GRCh38.p12 chr3: 42,818,508-42,952,708 ACKR2, CYP8B1, 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
    nsv3883164copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 37,028,313-49,929,220 , GRCh38.p12 chr3: 36,986,822-49,891,787 ACAA1, ACVR2B, 344 more genes
    nsv3881275copy number variation1nstd102humanPathogenic GRCh37 chr3: 41,104,508-44,636,698 , GRCh38.p12 chr3: 41,063,017-44,595,206 LOC107986077, LOC105377052, 69 more genes
    nsv3880617copy number variation1nstd102humanPathogenic GRCh37 chr3: 61,495-197,838,262 , GRCh38.p12 chr3: 19,817-198,111,391 RPL23AP49, DLEC1, 2875 more genes
    nsv3168877copy number variation1nstd158human GRCh37 chr3: 38,483,456-71,473,806 , GRCh38.p12 chr3: 38,441,965-71,424,655 , ACVR2B, 646 more genes
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