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Items: 1 to 20 of 1648

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097556copy number variation1nstd102humanUncertain significance GRCh37 chr5: 95,743,907-95,768,746 , GRCh38.p12 chr5: 96,408,203-96,433,042 LOC102724070, PCSK1, 1 more genes
    nsv7097553copy number variation1nstd102humanPathogenic GRCh37 chr5: 94,800,311-96,107,383 , GRCh38.p12 chr5: 95,464,607-96,771,679 LOC105379675, GPR150, 27 more genes
    nsv7097302copy number variation1nstd102humanPathogenic GRCh37 chr5: 95,728,705-95,765,041 , GRCh38.p12 chr5: 96,393,001-96,429,337 PCSK1, LOC101929710
    nsv7058036inversion1nstd229human GRCh38 chr5: 94,195,543-97,660,538 , GRCh37.p13 chr5: 93,531,248-96,996,242 RIOK2, SPATA9, 51 more genes
    nsv7057702inversion1nstd229human GRCh38 chr5: 96,147,327-96,274,378 , GRCh37.p13 chr5: 95,483,031-95,610,082 LOC101929710, MIR583HG, 2 more genes
    nsv7056617inversion1nstd229human GRCh38 chr5: 96,120,723-96,120,746 , GRCh37.p13 chr5: 95,456,427-95,456,450 MIR583HG, LOC101929710
    nsv7055396inversion1nstd229human GRCh38 chr5: 96,167,047-97,983,533 , GRCh37.p13 chr5: 95,502,751-97,319,237 MTCYBP40, LINC02234, 22 more genes
    nsv7053255inversion1nstd229human GRCh38 chr5: 96,077,435-96,088,981 , GRCh37.p13 chr5: 95,413,139-95,424,685 MIR583HG, MIR583, 1 more genes
    nsv7050733inversion1nstd229human GRCh38 chr5: 96,036,253-96,036,346 , GRCh37.p13 chr5: 95,371,957-95,372,050 LOC105379096, LOC101929710
    nsv7048524inversion1nstd229human GRCh38 chr5: 96,571,317-96,571,371 , GRCh37.p13 chr5: 95,907,021-95,907,075 LOC101929710
    nsv7046728inversion1nstd229human GRCh38 chr5: 96,630,172-96,630,192 , GRCh37.p13 chr5: 95,965,876-95,965,896 LOC101929710
    nsv7045809inversion1nstd229human GRCh38 chr5: 96,054,263-96,058,693 , GRCh37.p13 chr5: 95,389,967-95,394,397 LOC101929710, LOC105379096, 1 more genes
    nsv7044198inversion1nstd229human GRCh38 chr5: 93,856,097-99,790,151 , GRCh37.p13 chr5: 93,191,803-99,125,855 FAM81B, LOC107986365, 78 more genes
    nsv7038366inversion1nstd229human GRCh38 chr5: 96,419,105-96,419,232 , GRCh37.p13 chr5: 95,754,809-95,754,936 LOC101929710, PCSK1
    nsv6777943copy number variation1nstd229human GRCh38 chr5: 96,261,921-96,267,887 , GRCh37.p13 chr5: 95,597,625-95,603,591 LOC101929710
    nsv6777848copy number variation1nstd229human GRCh38 chr5: 95,962,898-95,994,509 , GRCh37.p13 chr5: 95,298,602-95,330,213 LOC105379096, FABP5P5, 1 more genes
    nsv6777572copy number variation1nstd229human GRCh38 chr5: 96,611,884-96,641,456 , GRCh37.p13 chr5: 95,947,588-95,977,160 LOC101929710
    nsv6777147copy number variation1nstd229human GRCh38 chr5: 96,231,356-96,327,826 , GRCh37.p13 chr5: 95,567,060-95,663,530 LOC101929710, LOC107986365
    nsv6776948copy number variation1nstd229human GRCh38 chr5: 96,206,847-96,206,911 , GRCh37.p13 chr5: 95,542,551-95,542,615 LOC101929710, MIR583HG
    nsv6776830copy number variation1nstd229human GRCh38 chr5: 96,130,519-96,130,710 , GRCh37.p13 chr5: 95,466,223-95,466,414 LOC101929710, MIR583HG
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