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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5855384copy number variation1nstd209human GRCh38 chr7: 149,854,641-149,867,768 , GRCh37.p13 chr7: 149,551,730-149,564,857 ZNF862, ATP6V0E2-AS1
    nsv5566464copy number variation1nstd207human GRCh38 chr7: 149,865,834-149,865,917 , GRCh37.p13 chr7: 149,562,923-149,563,006 ATP6V0E2-AS1, ZNF862
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5486183copy number variation1nstd206human GRCh38 chr7: 149,854,804-150,129,000 , GRCh37.p13 chr7: 149,551,893-149,826,089 , ATP6V0E2, 4 more genes
    nsv5344690translocation1nstd200human GRCh37 chr7: 149,562,989-149,562,989 , GRCh37 chr7: 149,563,082-149,563,082 , GRCh38.p12 chr7: 149,865,900-149,865,900 , GRCh38.p12 chr7: 149,865,993-149,865,993 ATP6V0E2-AS1, ZNF862
    nsv5253066copy number variation1nstd204human GRCh38.p13 chr7: 149,854,601-149,997,600 , GRCh37.p13 chr7: 149,551,690-149,694,689 ATP6V0E2-AS1, ACTR3C, 2 more genes
    nsv5246981copy number variation1nstd204human GRCh38.p13 chr7: 149,852,841-149,907,726 , GRCh37.p13 chr7: 149,549,930-149,604,815 ATP6V0E2-AS1, ACTR3C, 2 more genes
    nsv5244131copy number variation1nstd204human GRCh37.p13 chr7: 149,551,690-149,861,689 , GRCh38.p13 chr7: 149,854,601-150,164,600 , ATP6V0E2, 4 more genes
    nsv5243561copy number variation1nstd204human GRCh38.p13 chr7: 149,856,901-149,997,300 , GRCh37.p13 chr7: 149,553,990-149,694,389 ATP6V0E2, ACTR3C, 2 more genes
    nsv5241142copy number variation1nstd204human GRCh38.p13 chr7: 149,854,801-149,950,100 , GRCh37.p13 chr7: 149,551,890-149,647,189 ZNF862, ATP6V0E2-AS1, 2 more genes
    nsv4741804copy number variation1nstd199human GRCh37 chr7: 149,562,976-149,563,055 , GRCh38.p12 chr7: 149,865,887-149,865,966 ATP6V0E2-AS1, ZNF862
    nsv4729103copy number variation1nstd102humanUncertain significance GRCh37 chr7: 149,365,302-149,863,491 , GRCh38.p12 chr7: 149,668,211-150,166,402 SSPOP, TRC-GCA9-4, 8 more genes
    nsv4685723copy number variation1nstd102humannot provided GRCh37 chr7: 147,897,705-149,874,566 , GRCh38.p12 chr7: 148,200,613-150,177,477 CUL1, RNY1, 63 more genes
    nsv4685715copy number variation1nstd102humannot provided GRCh37 chr7: 143,107,740-156,886,246 , GRCh38.p12 chr7: 143,410,647-157,093,552 CTAGE4, CDK5, 277 more genes
    nsv4680264copy number variation1nstd189human GRCh37.p13 chr7: 149,362,570-149,673,044 , GRCh38.p12 chr7: 149,665,479-149,975,955 SSPOP, KRBA1, 7 more genes
    nsv4680018copy number variation1nstd189human GRCh37.p13 chr7: 149,362,570-149,722,674 , GRCh38.p12 chr7: 149,665,479-150,025,585 SSPOP, KRBA1, 7 more genes
    nsv4679998copy number variation1nstd189human GRCh37.p13 chr7: 149,362,570-149,710,146 , GRCh38.p12 chr7: 149,665,479-150,013,057 SSPOP, KRBA1, 7 more genes
    nsv4678914copy number variation1nstd189human GRCh37.p13 chr7: 149,362,570-149,697,294 , GRCh38.p12 chr7: 149,665,479-150,000,205 SSPOP, KRBA1, 7 more genes
    nsv4675620copy number variation1nstd102humanPathogenic GRCh37 chr7: 109,251,060-159,119,707 , GRCh38.p12 chr7: 109,611,003-159,327,017 RPL26P23, ST13P17, 887 more genes
    nsv4675615copy number variation1nstd102humanPathogenic GRCh37 chr7: 131,414,604-159,126,310 , GRCh38.p12 chr7: 131,729,845-159,333,620 ATG9B, OR10AC1, 603 more genes
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