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Items: 1 to 20 of 191

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5977463inversion1nstd209human GRCh38 chr3: 46,449,495-46,450,337 , GRCh37.p13 chr3: 46,490,985-46,491,827 LTF
    nsv5679280mobile element insertion1nstd211human GRCh38 chr3: 46,482,662-46,482,662 , GRCh37.p13 chr3: 46,524,152-46,524,152 LTF
    nsv5443592copy number variation1nstd206human GRCh38 chr3: 46,462,160-46,462,330 , GRCh37.p13 chr3: 46,503,650-46,503,820 LTF
    nsv5211169copy number variation1nstd204human GRCh37.p13 chr3: 46,500,291-46,685,390 , GRCh38.p13 chr3: 46,458,801-46,643,900 LTF, CRIPTO, 4 more genes
    nsv5170047mobile element insertion1nstd203human GRCh38 chr3: 46,448,648-46,448,661 , GRCh37.p13 chr3: 46,490,139-46,490,152 LTF
    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
    nsv4924390copy number variation1nstd200human GRCh38 chr3: 46,433,915-46,659,110 , GRCh37.p13 chr3: 46,475,406-46,700,600 LTF, CRIPTO, 4 more genes
    nsv4911119copy number variation1nstd200human GRCh38 chr3: 46,433,255-46,438,697 , GRCh37.p13 chr3: 46,474,746-46,480,188 LTF
    nsv4911118copy number variation1nstd200human GRCh38 chr3: 46,420,758-46,510,692 , GRCh37.p13 chr3: 46,462,249-46,552,182 RTP3, LTF, 1 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
    nsv4793958copy number variation1nstd200human GRCh37 chr3: 46,500,364-46,685,484 , GRCh38.p12 chr3: 46,458,874-46,643,994 LTF, LRRC2-AS1, 4 more genes
    nsv4727980copy number variation1nstd197human GRCh37 chr3: 46,399,020-46,569,071 , GRCh38.p12 chr3: 46,357,529-46,527,581 CCR5, LTF, 6 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
    nsv4378611copy number variation1nstd173human GRCh37 chr3: 46,462,849-46,549,188 , GRCh38.p12 chr3: 46,421,358-46,507,698 LTF, RTP3, 1 more genes
    nsv4347762copy number variation1nstd102humanPathogenic GRCh37 chr3: 45,153,770-53,878,616 , GRCh38.p12 chr3: 45,112,278-53,844,589 UQCRC1, DHX30, 291 more genes
    nsv4091484copy number variation1nstd166human GRCh37.p13 chr3: 46,482,196-46,484,308 , GRCh38.p12 chr3: 46,440,705-46,442,817 LTF
    nsv4076264copy number variation1nstd166human GRCh37.p13 chr3: 46,503,650-46,503,820 , GRCh38.p12 chr3: 46,462,160-46,462,330 LTF
    nsv3961168insertion1nstd168human GRCh38 chr3: 46,429,392-46,438,497 , GRCh37.p13 chr3: 46,470,883-46,479,988 LTF
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