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Items: 1 to 20 of 122

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7057842inversion1nstd229human GRCh38 chr3: 74,001,158-74,001,254 , GRCh37.p13 chr3: 74,050,309-74,050,405 LINC02047
    nsv7057718inversion1nstd229human GRCh38 chr3: 73,943,893-83,492,461 , GRCh37.p13 chr3: 73,993,044-83,541,612 RN7SL647P, CNTN3, 70 more genes
    nsv7041748inversion1nstd229human GRCh38 chr3: 72,070,390-75,778,215 , GRCh37.p13 chr3: 72,119,541-75,827,366 FTH1P23, LOC107986099, 66 more genes
    nsv7040307inversion1nstd229human GRCh38 chr3: 73,728,944-74,437,847 , GRCh37.p13 chr3: 73,778,095-74,486,998 AKR1B1P2, HSP90AB5P, 3 more genes
    nsv6714552copy number variation1nstd229human GRCh38 chr3: 73,824,901-74,437,800 , GRCh37.p13 chr3: 73,874,052-74,486,951 AKR1B1P2, CNTN3, 3 more genes
    nsv6707159copy number variation1nstd229human GRCh38 chr3: 73,870,368-74,007,763 , GRCh37.p13 chr3: 73,919,519-74,056,914 LINC02047, LINC02005
    nsv6705361copy number variation1nstd229human GRCh38 chr3: 74,004,642-74,004,955 , GRCh37.p13 chr3: 74,053,793-74,054,106 LINC02047
    nsv6700513copy number variation1nstd229human GRCh38 chr3: 73,991,854-73,999,641 , GRCh37.p13 chr3: 74,041,005-74,048,792 LINC02047
    nsv6628874copy number variation1nstd224human GRCh37 chr3: 74,033,442-74,805,509 , GRCh38.p12 chr3: 73,984,291-74,756,358 HSP90AB5P, AKR1B1P2, 3 more genes
    nsv6540174inversion1nstd223human GRCh38 chr3: 74,002,927-74,003,733 , GRCh37.p13 chr3: 74,052,078-74,052,884 LINC02047
    nsv6372193copy number variation1nstd223human GRCh38 chr3: 74,006,022-74,006,597 , GRCh37.p13 chr3: 74,055,173-74,055,748 LINC02047
    nsv6364664copy number variation1nstd223human GRCh38 chr3: 73,870,368-74,007,763 , GRCh37.p13 chr3: 73,919,519-74,056,914 LINC02047, LINC02005
    nsv6314751copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 72,488,757-99,614,758 , GRCh38.p12 chr3: 72,439,606-99,895,914 AKR1B1P2, COL8A1, 231 more genes
    nsv6134705copy number variation1nstd213human GRCh37 chr3: 66,270,000-87,730,001 , GRCh38.p12 chr3: 66,219,846-87,680,851 , AKR1B1P2, 187 more genes
    nsv5902904copy number variation1nstd209human GRCh38 chr3: 66,803,410-74,489,186 , GRCh37.p13 chr3: 66,853,834-74,538,337 , LOC105377160, 83 more genes
    nsv5033386inversion1nstd200human GRCh38 chr3: 66,830,019-82,426,887 , GRCh37.p13 chr3: 66,880,443-82,476,038 , HNRNPA3P6, 150 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
    nsv4728221copy number variation1nstd102humanUncertain significance GRCh37 chr3: 70,938,608-74,660,846 , GRCh38.p12 chr3: 70,889,457-74,611,695 CCDC137P1, LINC02047, 45 more genes
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