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Items: 1 to 20 of 182

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137735insertion1nstd232human GRCh37.p13 chr22: 32,802,756-32,802,756 , GRCh38.p12 chr22: 32,406,769-32,406,769 RTCB
    nsv7095832copy number variation1nstd102humanUncertain significance GRCh37 chr22: 32,500,753-32,894,517 , GRCh38.p12 chr22: 32,104,766-32,498,530 IGLCOR22-2, AP1B1P2, 16 more genes
    nsv7078067inversion1nstd229human GRCh38 chr22: 30,287,061-38,012,264 , GRCh37.p13 chr22: 30,683,050-38,408,271 LINC02885, RN7SL20P, 203 more genes
    nsv7068065inversion1nstd229human GRCh38 chr22: 27,585,838-32,538,391 , GRCh37.p13 chr22: 27,981,799-32,934,377 LOC105372995, NEFH, 147 more genes
    nsv7065500inversion1nstd229human GRCh38 chr22: 29,260,563-37,652,385 , GRCh37.p13 chr22: 29,656,552-38,048,392 RFPL1, PATZ1, 217 more genes
    nsv7064427inversion1nstd229human GRCh38 chr22: 32,257,546-32,480,102 , GRCh37.p13 chr22: 32,653,533-32,876,089 RFPL3S, BPIFC, 10 more genes
    nsv7037825copy number variation1nstd229human GRCh38 chr22: 32,412,477-32,416,398 , GRCh37.p13 chr22: 32,808,464-32,812,385 BPIFC, RTCB
    nsv7027946copy number variation1nstd229human GRCh38 chr22: 32,353,729-32,409,889 , GRCh37.p13 chr22: 32,749,716-32,805,876 RFPL3S, SLC5A4, 5 more genes
    nsv7019053copy number variation1nstd229human GRCh38 chr22: 32,402,561-32,402,702 , GRCh37.p13 chr22: 32,798,548-32,798,689 RTCB
    nsv6627452copy number variation1nstd224human GRCh37 chr22: 32,744,045-32,786,217 , GRCh38.p12 chr22: 32,348,058-32,390,230 SLC5A4, RFPL3S, 5 more genes
    nsv6554139copy number variation1nstd223human GRCh38 chr22: 32,409,910-32,449,827 , GRCh37.p13 chr22: 32,805,897-32,845,814 RTCB, BPIFC
    nsv6550876copy number variation1nstd223human GRCh38 chr22: 32,353,734-32,409,835 , GRCh37.p13 chr22: 32,749,721-32,805,822 RFPL3S, IGLCOR22-2, 5 more genes
    nsv6550513copy number variation1nstd223human GRCh38 chr22: 32,412,477-32,416,395 , GRCh37.p13 chr22: 32,808,464-32,812,382 RTCB, BPIFC
    nsv6546338copy number variation1nstd223human GRCh38 chr22: 32,378,398-32,423,332 , GRCh37.p13 chr22: 32,774,385-32,819,319 LOC339666, RGL4P1, 2 more genes
    nsv6543835copy number variation1nstd223human GRCh38 chr22: 32,379,646-32,387,011 , GRCh37.p13 chr22: 32,775,633-32,782,998 RGL4P1, LOC339666, 1 more genes
    nsv6536117copy number variation1nstd223human GRCh38 chr22: 32,402,561-32,402,702 , GRCh37.p13 chr22: 32,798,548-32,798,689 RTCB
    nsv6311321copy number variation1nstd102humanUncertain significance GRCh37 chr22: 32,232,938-34,157,463 , GRCh38.p12 chr22: 31,836,952-33,761,476 SYN3, DEPDC5, 36 more genes
    nsv6311263copy number variation1nstd102humanUncertain significance GRCh37 chr22: 29,083,885-34,046,674 , GRCh38.p12 chr22: 28,687,897-33,650,688 SNORD125, LOC107985533, 145 more genes
    nsv6307412copy number variation1nstd186human GRCh37 chr22: 32,798,553-32,798,688 , GRCh38.p12 chr22: 32,402,566-32,402,701 RTCB
    nsv6223746copy number variation1nstd214human GRCh38 chr22: 32,402,561-32,402,700 , GRCh37.p13 chr22: 32,798,548-32,798,687 RTCB
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