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Items: 1 to 20 of 339

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6118611copy number variation1nstd186human GRCh37 chr4: 6,624,531-6,626,655 , GRCh38.p12 chr4: 6,622,804-6,624,928 MAN2B2
    nsv6112761copy number variation1nstd102humanPathogenic GRCh37 chr4: 69,671-29,702,595 , GRCh38.p12 chr4: 69,779-29,700,973 LOC101928306, PDE6B-AS1, 460 more genes
    nsv6112747copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,598-18,912,995 , GRCh38.p12 chr4: 68,706-18,911,372 GPR78, LOC105374510, 362 more genes
    nsv5979532inversion1nstd209human GRCh38 chr4: 4,147,913-9,493,295 , GRCh37.p13 chr4: 4,149,640-9,494,939 , CRMP1, 130 more genes
    nsv5974394inversion1nstd209human GRCh38 chr4: 4,005,086-9,639,734 , GRCh37.p13 chr4: 4,006,813-9,641,358 , CRMP1, 142 more genes
    nsv5973087inversion1nstd209human GRCh38 chr4: 3,883,398-8,956,544 , GRCh37.p13 chr4: 3,885,125-8,958,270 , CRMP1, 102 more genes
    nsv5954479insertion1nstd209human GRCh38 chr4: 6,611,558-6,611,558 , GRCh37.p13 chr4: 6,613,285-6,613,285 MAN2B2
    nsv5840027copy number variation1nstd209human GRCh38 chr4: 6,622,443-6,624,942 , GRCh37.p13 chr4: 6,624,170-6,626,669 MAN2B2
    nsv5686362mobile element insertion2nstd211human GRCh38 chr4: 6,622,760-6,622,760 , GRCh37.p13 chr4: 6,624,487-6,624,487 MAN2B2
    nsv5623525insertion1nstd207human GRCh38 chr4: 6,579,111-6,579,111 , GRCh37.p13 chr4: 6,580,838-6,580,838 MAN2B2
    nsv5621696insertion1nstd207human GRCh38 chr4: 6,579,298-6,579,298 , GRCh37.p13 chr4: 6,581,025-6,581,025 MAN2B2
    nsv5617724insertion1nstd207human GRCh38 chr4: 6,579,189-6,579,189 , GRCh37.p13 chr4: 6,580,916-6,580,916 MAN2B2
    nsv5611445insertion1nstd207human GRCh38 chr4: 6,611,558-6,611,558 , GRCh37.p13 chr4: 6,613,285-6,613,285 MAN2B2
    nsv5610850insertion1nstd207human GRCh38 chr4: 6,579,126-6,579,126 , GRCh37.p13 chr4: 6,580,853-6,580,853 MAN2B2
    nsv5583812copy number variation1nstd207human GRCh38 chr4: 6,622,759-6,624,510 , GRCh37.p13 chr4: 6,624,486-6,626,237 MAN2B2
    nsv5577136copy number variation1nstd207human GRCh38 chr4: 6,579,102-6,579,246 , GRCh37.p13 chr4: 6,580,829-6,580,973 MAN2B2
    nsv5571089copy number variation1nstd207human GRCh38 chr4: 6,579,243-6,579,300 , GRCh37.p13 chr4: 6,580,970-6,581,027 MAN2B2
    nsv5553550insertion1nstd206human GRCh38 chr4: 6,611,572-6,611,609 , GRCh37.p13 chr4: 6,613,299-6,613,336 MAN2B2
    nsv5536726insertion1nstd206human GRCh38 chr4: 6,579,543-6,579,551 , GRCh37.p13 chr4: 6,581,270-6,581,278 MAN2B2
    nsv5453796copy number variation1nstd206human GRCh38 chr4: 4,427,625-9,008,826 , GRCh37.p13 chr4: 4,429,352-9,010,552 , CPZ, 81 more genes
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