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Items: 1 to 20 of 141

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv7032810copy number variation1nstd229human GRCh38 chr22: 31,969,896-32,152,510 , GRCh37.p13 chr22: 32,365,883-32,548,497 RN7SL305P, RPS17P16, 6 more genes
    nsv7027394copy number variation1nstd229human GRCh38 chr22: 32,133,342-32,154,991 , GRCh37.p13 chr22: 32,529,329-32,550,978 C22orf42, AP1B1P2, 1 more genes
    nsv7026386copy number variation1nstd229human GRCh38 chr22: 32,069,077-32,384,600 , GRCh37.p13 chr22: 32,465,064-32,780,587 SLC5A1, CPSF1P1, 12 more genes
    nsv7025023copy number variation1nstd229human GRCh38 chr22: 32,132,680-32,307,112 , GRCh37.p13 chr22: 32,528,667-32,703,099 RFPL2, AP1B1P2, 5 more genes
    nsv7024287copy number variation1nstd229human GRCh38 chr22: 32,121,585-32,131,152 , GRCh37.p13 chr22: 32,517,572-32,527,139 LOC105373000, AP1B1P1
    nsv7021456copy number variation1nstd229human GRCh38 chr22: 32,115,263-32,120,481 , GRCh37.p13 chr22: 32,511,250-32,516,468 LOC105373000, AP1B1P1
    nsv7018427copy number variation1nstd229human GRCh38 chr22: 32,127,759-32,138,012 , GRCh37.p13 chr22: 32,523,746-32,533,999 AP1B1P1, AP1B1P2
    nsv6627398copy number variation1nstd224human GRCh37 chr22: 32,509,440-32,699,673 , GRCh38.p12 chr22: 32,113,453-32,303,686 SLC5A1, SLC5A4, 7 more genes
    nsv6627397copy number variation1nstd224human GRCh37 chr22: 32,479,102-32,777,364 , GRCh38.p12 chr22: 32,083,115-32,381,377 SLC5A4, AP1B1P1, 12 more genes
    nsv6597782inversion1nstd223human GRCh38 chr22: 32,121,142-32,122,814 , GRCh37.p13 chr22: 32,517,129-32,518,801 LOC105373000, AP1B1P1
    nsv6597607inversion1nstd223human GRCh38 chr22: 32,120,722-32,122,366 , GRCh37.p13 chr22: 32,516,709-32,518,353 LOC105373000, AP1B1P1
    nsv6554001copy number variation1nstd223human GRCh38 chr22: 32,128,701-32,130,071 , GRCh37.p13 chr22: 32,524,688-32,526,058 AP1B1P1
    nsv6544706copy number variation1nstd223human GRCh38 chr22: 32,069,077-32,384,596 , GRCh37.p13 chr22: 32,465,064-32,780,583 SLC5A4, C22orf42, 12 more genes
    nsv6538705copy number variation1nstd223human GRCh38 chr22: 32,130,290-32,170,601 , GRCh37.p13 chr22: 32,526,277-32,566,588 AP1B1P2, AP1B1P1, 1 more genes
    nsv6537413copy number variation1nstd223human GRCh38 chr22: 32,117,615-32,131,057 , GRCh37.p13 chr22: 32,513,602-32,527,044 LOC105373000, AP1B1P1
    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
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