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Items: 1 to 20 of 496

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112780copy number variation1nstd102humanPathogenic GRCh37 chr15: 92,335,751-102,399,741 , GRCh38.p12 chr15: 91,792,521-101,859,538 LOC105371009, ST8SIA2, 149 more genes
    nsv5927971copy number variation1nstd209human GRCh38 chr15: 92,640,901-92,643,222 , GRCh37.p13 chr15: 93,184,131-93,186,452 FAM174B
    nsv5878949copy number variation1nstd209human GRCh38 chr15: 92,640,835-92,643,209 , GRCh37.p13 chr15: 93,184,065-93,186,439 FAM174B
    nsv5714257mobile element insertion1nstd211human GRCh38 chr15: 92,666,550-92,666,550 , GRCh37.p13 chr15: 93,209,780-93,209,780 FAM174B
    nsv5663894insertion1nstd207human GRCh38 chr15: 92,631,357-92,631,357 , GRCh37.p13 chr15: 93,174,587-93,174,587 FAM174B
    nsv5663194insertion1nstd207human GRCh38 chr15: 92,669,219-92,669,219 , GRCh37.p13 chr15: 93,212,449-93,212,449 FAM174B
    nsv5659177insertion1nstd207human GRCh38 chr15: 92,630,873-92,630,873 , GRCh37.p13 chr15: 93,174,103-93,174,103 FAM174B
    nsv5658541insertion1nstd207human GRCh38 chr15: 92,631,082-92,631,082 , GRCh37.p13 chr15: 93,174,312-93,174,312 FAM174B
    nsv5653233insertion1nstd207human GRCh38 chr15: 92,631,000-92,631,000 , GRCh37.p13 chr15: 93,174,230-93,174,230 FAM174B
    nsv5650805insertion1nstd207human GRCh38 chr15: 92,631,242-92,631,242 , GRCh37.p13 chr15: 93,174,472-93,174,472 FAM174B
    nsv5602205copy number variation1nstd207human GRCh38 chr15: 92,630,954-92,631,168 , GRCh37.p13 chr15: 93,174,184-93,174,398 FAM174B
    nsv5601677copy number variation1nstd207human GRCh38 chr15: 92,631,245-92,631,315 , GRCh37.p13 chr15: 93,174,475-93,174,545 FAM174B
    nsv5591137copy number variation1nstd207human GRCh38 chr15: 92,630,786-92,630,854 , GRCh37.p13 chr15: 93,174,016-93,174,084 FAM174B
    nsv5588831copy number variation1nstd207human GRCh38 chr15: 92,669,219-92,669,273 , GRCh37.p13 chr15: 93,212,449-93,212,503 FAM174B
    nsv5532979copy number variation1nstd206human GRCh38 chr15: 92,650,357-92,655,702 , GRCh37.p13 chr15: 93,193,587-93,198,932 FAM174B
    nsv5531067copy number variation1nstd206human GRCh38 chr15: 92,402,520-97,547,707 , GRCh37.p13 chr15: 92,945,750-98,090,937 , LOC105371004, 71 more genes
    nsv5514392copy number variation1nstd206human GRCh38 chr15: 92,730,301-92,732,803 , GRCh37.p13 chr15: 93,273,531-93,276,033 H2AZ2P1, FAM174B
    nsv5433767mobile element insertion1nstd206human GRCh38 chr15: 92,666,550-92,666,601 , GRCh37.p13 chr15: 93,209,780-93,209,831 FAM174B
    nsv5184350mobile element insertion1nstd203human GRCh38 chr15: 92,724,668-92,724,676 , GRCh37.p13 chr15: 93,267,898-93,267,906 FAM174B
    nsv5158139mobile element insertion1nstd203human GRCh38 chr15: 92,626,139-92,626,139 , GRCh37.p13 chr15: 93,169,369-93,169,369 FAM174B
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