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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112678copy number variation1nstd102humanPathogenic GRCh37 chr1: 16,370,960-16,383,841 , GRCh38.p12 chr1: 16,044,465-16,057,346 FAM131C, CLCNKB
    nsv5967286insertion1nstd209human GRCh38 chr1: 16,050,023-16,050,023 , GRCh37.p13 chr1: 16,376,518-16,376,518 CLCNKB
    nsv5878588copy number variation1nstd209human GRCh38 chr1: 16,037,298-16,060,502 , GRCh37.p13 chr1: 16,363,793-16,386,997 CLCNKB, FAM131C, 1 more genes
    nsv5874151copy number variation1nstd209human GRCh38 chr1: 13,714,112-20,623,728 , GRCh37.p13 chr1: 14,040,607-20,950,221 , TRV-CAC11-1, 171 more genes
    nsv5872444copy number variation1nstd209human GRCh38 chr1: 16,040,228-16,062,667 , GRCh37.p13 chr1: 16,366,723-16,389,162 CLCNKB, FAM131C, 1 more genes
    nsv5867713copy number variation1nstd209human GRCh38 chr1: 16,032,248-16,046,348 , GRCh37.p13 chr1: 16,358,743-16,372,843 CLCNKA, CLCNKB, 1 more genes
    nsv5828264copy number variation2nstd209human GRCh38 chr1: 16,038,184-16,043,827 , GRCh37.p13 chr1: 16,364,679-16,370,322 FAM131C2P, CLCNKB
    nsv5828176copy number variation2nstd209human GRCh38 chr1: 16,038,084-16,044,759 , GRCh37.p13 chr1: 16,364,579-16,371,254 FAM131C2P, CLCNKB
    nsv5828058copy number variation2nstd209human GRCh38 chr1: 16,042,962-16,057,197 , GRCh37.p13 chr1: 16,369,457-16,383,692 CLCNKB, FAM131C
    nsv5624041insertion1nstd207human GRCh38 chr1: 16,050,023-16,050,023 , GRCh37.p13 chr1: 16,376,518-16,376,518 CLCNKB
    nsv5556728sequence alteration1nstd206human GRCh38 chr1: 16,050,023-16,050,023 , GRCh37.p13 chr1: 16,376,518-16,376,518 CLCNKB
    nsv5427283copy number variation1nstd206human GRCh38 chr1: 16,026,587-16,048,556 , GRCh37.p13 chr1: 16,353,082-16,375,051 FAM131C2P, CLCNKA, 1 more genes
    nsv5373274translocation1nstd200human GRCh38 chr1: 16,050,023-16,050,023 , GRCh38 chr1: 16,059,839-16,059,839 , GRCh37.p13 chr1: 16,386,334-16,386,334 , GRCh37.p13 chr1: 16,376,518-16,376,518 CLCNKB, FAM131C
    nsv5347999translocation1nstd200human GRCh38 chr1: 16,050,023-16,050,023 , GRCh38 chr1: 16,059,762-16,059,762 , GRCh37.p13 chr1: 16,376,518-16,376,518 , GRCh37.p13 chr1: 16,386,257-16,386,257 CLCNKB, FAM131C
    nsv5344261translocation1nstd200human GRCh37 chr1: 16,386,257-16,386,257 , GRCh37 chr1: 16,376,518-16,376,518 , GRCh38.p12 chr1: 16,059,762-16,059,762 , GRCh38.p12 chr1: 16,050,023-16,050,023 CLCNKB, FAM131C
    nsv5332319translocation1nstd200human GRCh37 chr1: 16,372,844-16,372,844 , GRCh37 chr1: 16,358,744-16,358,744 , GRCh38.p12 chr1: 16,046,349-16,046,349 , GRCh38.p12 chr1: 16,032,249-16,032,249 CLCNKB, CLCNKA
    nsv5323817translocation1nstd204human GRCh37.p13 chr1: 16,376,518-16,376,518 , GRCh37.p13 chr1: 16,386,257-16,386,257 , GRCh38.p13 chr1: 16,059,762-16,059,762 , GRCh38.p13 chr1: 16,050,023-16,050,023 CLCNKB, FAM131C
    nsv5322043translocation1nstd204human GRCh37.p13 chr1: 16,376,518-16,376,518 , GRCh37.p13 chr1: 16,386,334-16,386,334 , GRCh38.p13 chr1: 16,050,023-16,050,023 , GRCh38.p13 chr1: 16,059,839-16,059,839 CLCNKB, FAM131C
    nsv5293185copy number variation1nstd204human GRCh38.p13 chr1: 16,023,318-16,045,746 , GRCh37.p13 chr1: 16,349,813-16,372,241 FAM131C2P, CLCNKB, 1 more genes
    nsv5292282copy number variation1nstd204human GRCh38.p13 chr1: 16,020,315-16,042,789 , GRCh37.p13 chr1: 16,346,810-16,369,284 FAM131C2P, CLCNKA, 1 more genes
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