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Items: 1 to 20 of 172

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5923593copy number variation1nstd209human GRCh38 chr7: 129,201,247-129,201,880 , GRCh37.p13 chr7: 128,841,088-128,841,721 SMO
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5481414copy number variation1nstd206human GRCh38 chr7: 129,201,265-129,201,868 , GRCh37.p13 chr7: 128,841,106-128,841,709 SMO
    nsv5326600inversion1nstd204human GRCh37.p13 chr7: 97,320,865-141,491,704 , GRCh38.p13 chr7: 97,691,553-141,791,904 , ARF5, 752 more genes
    nsv5306836copy number variation1nstd204human GRCh38.p13 chr7: 129,204,365-129,204,807 , GRCh37.p13 chr7: 128,844,206-128,844,648 SMO
    nsv5302852copy number variation1nstd204human GRCh38.p13 chr7: 129,184,430-129,189,687 , GRCh37.p13 chr7: 128,824,271-128,829,528 SMO
    nsv5241297copy number variation1nstd204human GRCh38.p13 chr7: 129,184,465-129,189,001 , GRCh37.p13 chr7: 128,824,306-128,828,842 SMO
    nsv5114702mobile element insertion1nstd203human GRCh38 chr7: 129,204,840-129,204,848 , GRCh37.p13 chr7: 128,844,681-128,844,689 SMO
    nsv5112206mobile element insertion1nstd203human GRCh38 chr7: 129,204,798-129,204,848 , GRCh37.p13 chr7: 128,844,639-128,844,689 SMO
    nsv5110309mobile element insertion1nstd203human GRCh38 chr7: 129,195,562-129,195,568 , GRCh37.p13 chr7: 128,835,403-128,835,409 SMO
    nsv5105333mobile element insertion1nstd203human GRCh38 chr7: 129,204,827-129,204,848 , GRCh37.p13 chr7: 128,844,668-128,844,689 SMO
    nsv5101898mobile element insertion1nstd203human GRCh38 chr7: 129,204,843-129,204,848 , GRCh37.p13 chr7: 128,844,684-128,844,689 SMO
    nsv5039775inversion1nstd200human GRCh38 chr7: 22,938,090-134,148,361 , GRCh37.p13 chr7: 22,977,709-133,833,114 , NFE4, 1832 more genes
    nsv5029742inversion1nstd200human GRCh38 chr7: 79,688,546-147,673,588 , GRCh37.p13 chr7: 79,317,862-147,370,680 , LOC100533722, 1168 more genes
    nsv4880762inversion1nstd200human GRCh37 chr7: 79,317,862-147,370,680 , GRCh38.p12 chr7: 79,688,546-147,673,588 , RN7SKP277, 1168 more genes
    nsv4820523copy number variation1nstd200human GRCh37 chr7: 128,844,215-128,844,641 , GRCh38.p12 chr7: 129,204,374-129,204,800 SMO
    nsv4820522copy number variation1nstd200human GRCh37 chr7: 128,841,075-128,841,690 , GRCh38.p12 chr7: 129,201,234-129,201,849 SMO
    nsv4741728copy number variation1nstd199human GRCh37 chr7: 128,853,714-128,855,110 , GRCh38.p12 chr7: 129,213,873-129,215,269 SMO
    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
    nsv4455826copy number variation1nstd102humanPathogenic GRCh37 chr7: 121,480,906-129,389,003 , GRCh38.p12 chr7: 121,840,852-129,749,163 ASB15, PNPT1P2, 127 more genes
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