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Items: 1 to 20 of 192

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5933890copy number variation1nstd209human GRCh38 chr15: 49,022,510-49,022,570 , GRCh37.p13 chr15: 49,314,707-49,314,767 SECISBP2L
    nsv5703943mobile element insertion1nstd211human GRCh38 chr15: 49,005,588-49,005,588 , GRCh37.p13 chr15: 49,297,785-49,297,785 SECISBP2L
    nsv5517294copy number variation1nstd206human GRCh38 chr15: 49,022,512-49,022,571 , GRCh37.p13 chr15: 49,314,709-49,314,768 SECISBP2L
    nsv5380758copy number variation2nstd102humanUncertain significance GRCh37 chr15: 32,964,879-91,358,519 , GRCh38.p12 chr15: 32,672,678-90,815,289 LOC105370794, HNRNPA1P45, 1173 more genes
    nsv5357904translocation1nstd200human GRCh38 chr15: 49,039,229-49,039,229 , GRCh38 chr15: 49,041,507-49,041,507 , GRCh37.p13 chr15: 49,333,704-49,333,704 , GRCh37.p13 chr15: 49,331,426-49,331,426 SECISBP2L, RN7SL577P
    nsv5357903translocation1nstd200human GRCh38 chr15: 49,024,118-49,024,118 , GRCh38 chr15: 49,024,046-49,024,046 , GRCh37.p13 chr15: 49,316,243-49,316,243 , GRCh37.p13 chr15: 49,316,315-49,316,315 SECISBP2L
    nsv5357902translocation1nstd200human GRCh38 chr15: 49,001,993-49,001,993 , GRCh38 chr15: 49,001,882-49,001,882 , GRCh37.p13 chr15: 49,294,190-49,294,190 , GRCh37.p13 chr15: 49,294,079-49,294,079 SECISBP2L
    nsv5346022translocation1nstd200human GRCh37 chr15: 49,314,709-49,314,709 , GRCh37 chr15: 49,314,768-49,314,768 , GRCh38.p12 chr15: 49,022,512-49,022,512 , GRCh38.p12 chr15: 49,022,571-49,022,571 SECISBP2L
    nsv5341473translocation1nstd200human GRCh37 chr15: 49,316,243-49,316,243 , GRCh37 chr15: 49,316,315-49,316,315 , GRCh38.p12 chr15: 49,024,118-49,024,118 , GRCh38.p12 chr15: 49,024,046-49,024,046 SECISBP2L
    nsv5338953translocation1nstd200human GRCh37 chr15: 49,333,704-49,333,704 , GRCh37 chr15: 49,331,426-49,331,426 , GRCh38.p12 chr15: 49,039,229-49,039,229 , GRCh38.p12 chr15: 49,041,507-49,041,507 RN7SL577P, SECISBP2L
    nsv5317443copy number variation1nstd204human GRCh38.p13 chr15: 48,988,735-48,989,701 , GRCh37.p13 chr15: 49,280,932-49,281,898 SECISBP2L
    nsv5317291copy number variation1nstd204human GRCh38.p13 chr15: 49,022,488-49,022,594 , GRCh37.p13 chr15: 49,314,685-49,314,791 SECISBP2L
    nsv5308769copy number variation1nstd204human GRCh38.p13 chr15: 49,001,873-49,002,001 , GRCh37.p13 chr15: 49,294,070-49,294,198 SECISBP2L
    nsv5302566copy number variation1nstd204human GRCh38.p13 chr15: 49,046,205-49,046,410 , GRCh37.p13 chr15: 49,338,402-49,338,607 SECISBP2L
    nsv5038422inversion1nstd200human GRCh38 chr15: 40,121,948-64,050,807 , GRCh37.p13 chr15: 40,414,149-64,343,006 , EIF4EBP2P2, 475 more genes
    nsv5005369copy number variation1nstd200human GRCh38 chr15: 49,046,215-49,046,401 , GRCh37.p13 chr15: 49,338,412-49,338,598 SECISBP2L
    nsv4872280inversion1nstd200human GRCh37 chr15: 40,414,149-64,343,008 , GRCh38.p12 chr15: 40,121,948-64,050,809 , DNAAF4-CCPG1, 475 more genes
    nsv4866092copy number variation1nstd200human GRCh37 chr15: 49,294,079-49,294,190 , GRCh38.p12 chr15: 49,001,882-49,001,993 SECISBP2L
    nsv4769387copy number variation1nstd102humanPathogenic GRCh37 chr15: 48,744,917-53,851,050 , GRCh38.p12 chr15: 48,452,720-53,558,853 BCL2L10, RNA5SP394, 86 more genes
    nsv4739670copy number variation1nstd199human GRCh37 chr15: 49,314,705-49,314,766 , GRCh38.p12 chr15: 49,022,508-49,022,569 SECISBP2L
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