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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148056copy number variation1nstd102humanPathogenic GRCh37 chr2: 186,698,504-223,918,111 , GRCh38.p12 chr2: 185,833,777-223,053,393 DNAJB1P1, MTCO2P17, 580 more genes
    nsv7096393copy number variation1nstd102humanPathogenic GRCh37 chr2: 208,986,397-209,220,029 , GRCh38.p12 chr2: 208,121,673-208,355,305 PIKFYVE, CRYGA, 11 more genes
    nsv7057573inversion1nstd229human GRCh38 chr2: 207,521,365-209,493,860 , GRCh37.p13 chr2: 208,386,089-210,358,584 CRYGEP, CRYGFP, 40 more genes
    nsv7045025inversion1nstd229human GRCh38 chr2: 208,153,874-208,173,799 , GRCh37.p13 chr2: 209,018,598-209,038,523 LOC100507443, CRYGA, 1 more genes
    nsv6697293copy number variation1nstd229human GRCh38 chr2: 208,164,041-208,187,980 , GRCh37.p13 chr2: 209,028,765-209,052,704 C2orf80, CRYGA
    nsv6694141copy number variation1nstd229human GRCh38 chr2: 208,167,501-208,194,100 , GRCh37.p13 chr2: 209,032,225-209,058,824 C2orf80
    nsv6693751copy number variation1nstd229human GRCh38 chr2: 208,174,901-208,181,500 , GRCh37.p13 chr2: 209,039,625-209,046,224 C2orf80
    nsv6693225copy number variation1nstd229human GRCh38 chr2: 208,168,602-208,193,907 , GRCh37.p13 chr2: 209,033,326-209,058,631 C2orf80
    nsv6690922copy number variation1nstd229human GRCh38 chr2: 208,176,024-208,180,951 , GRCh37.p13 chr2: 209,040,748-209,045,675 C2orf80
    nsv6690726copy number variation1nstd229human GRCh38 chr2: 208,164,901-208,176,900 , GRCh37.p13 chr2: 209,029,625-209,041,624 C2orf80
    nsv6689824copy number variation1nstd229human GRCh38 chr2: 208,168,601-208,195,000 , GRCh37.p13 chr2: 209,033,325-209,059,724 C2orf80
    nsv6688118copy number variation1nstd229human GRCh38 chr2: 208,152,701-208,165,000 , GRCh37.p13 chr2: 209,017,425-209,029,724 CRYGA, C2orf80, 1 more genes
    nsv6688017copy number variation1nstd229human GRCh38 chr2: 208,180,393-208,186,510 , GRCh37.p13 chr2: 209,045,117-209,051,234 C2orf80
    nsv6686148copy number variation1nstd229human GRCh38 chr2: 208,169,001-208,194,000 , GRCh37.p13 chr2: 209,033,725-209,058,724 C2orf80
    nsv6683830copy number variation1nstd229human GRCh38 chr2: 207,947,519-208,320,337 , GRCh37.p13 chr2: 208,812,243-209,185,061 C2orf80, CRYGEP, 18 more genes
    nsv6682132copy number variation1nstd229human GRCh38 chr2: 208,162,608-208,176,966 , GRCh37.p13 chr2: 209,027,332-209,041,690 C2orf80, CRYGA
    nsv6681263copy number variation1nstd229human GRCh38 chr2: 208,173,401-208,181,500 , GRCh37.p13 chr2: 209,038,125-209,046,224 C2orf80
    nsv6680871copy number variation1nstd229human GRCh38 chr2: 208,168,572-208,193,901 , GRCh37.p13 chr2: 209,033,296-209,058,625 C2orf80
    nsv6680762copy number variation1nstd229human GRCh38 chr2: 208,171,412-208,171,466 , GRCh37.p13 chr2: 209,036,136-209,036,190 C2orf80
    nsv6680629copy number variation1nstd229human GRCh38 chr2: 208,167,201-208,194,000 , GRCh37.p13 chr2: 209,031,925-209,058,724 C2orf80
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