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Items: 1 to 20 of 138

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094815copy number variation1nstd102humanUncertain significance GRCh37 chr16: 18,794,331-19,089,480 , GRCh38.p12 chr16: 18,783,009-19,078,158 SMG1-DT, TMC7, 7 more genes
    nsv7076939inversion1nstd229human GRCh38 chr16: 15,569,413-22,730,334 , GRCh37.p13 chr16: 15,663,270-22,741,655 ACSM5P1, RNU6-213P, 154 more genes
    nsv7062654inversion1nstd229human GRCh38 chr16: 16,571,414-18,782,671 , GRCh37.p13 chr16: 16,665,271-18,793,993 PKD1P4-NPIPA8, LOC102723692, 28 more genes
    nsv7058379inversion1nstd229human GRCh38 chr16: 16,196,635-18,896,827 , GRCh37.p13 chr16: 16,290,492-18,908,149 LOC105376751, NOMO3, 46 more genes
    nsv6996672copy number variation1nstd229human GRCh38 chr16: 18,789,136-18,789,225 , GRCh37.p13 chr16: 18,800,458-18,800,547 RPS15A
    nsv6996648copy number variation1nstd229human GRCh38 chr16: 18,782,364-18,782,672 , GRCh37.p13 chr16: 18,793,686-18,793,994 RPS15A
    nsv6966433copy number variation1nstd229human GRCh38 chr16: 17,335,724-19,726,946 , GRCh37.p13 chr16: 17,429,581-19,738,268 MIR3179-4, GDE1, 45 more genes
    nsv6637429copy number variation1nstd102humanPathogenic GRCh37 chr16: 4,380,767-30,445,350 , GRCh38.p12 chr16: 4,330,766-30,434,029 MIR6511B2, ACSM5, 535 more genes
    nsv6502607copy number variation1nstd223human GRCh38 chr16: 18,784,377-18,799,306 , GRCh37.p13 chr16: 18,795,699-18,810,628 ARL6IP1, RPS15A
    nsv6133258copy number variation1nstd213human GRCh37 chr16: 16,530,000-21,500,001 , GRCh38.p12 chr16: 16,436,143-21,488,680 CRYM, GP2, 93 more genes
    nsv6133007copy number variation1nstd213human GRCh37 chr16: 16,560,000-19,410,001 , GRCh38.p12 chr16: 16,466,143-19,398,679 RPS15A, COQ7, 43 more genes
    nsv5967951inversion1nstd209human GRCh38 chr16: 13,469,401-22,726,308 , GRCh37.p13 chr16: 13,563,258-22,737,629 , ABCC6, 214 more genes
    nsv5273048copy number variation1nstd204human GRCh38.p13 chr16: 18,763,201-18,782,300 , GRCh37.p13 chr16: 18,774,523-18,793,622 RPS15A
    nsv5271054copy number variation1nstd204human GRCh38.p13 chr16: 18,704,901-18,782,200 , GRCh37.p13 chr16: 18,716,223-18,793,522 RPS15A
    nsv5260976copy number variation1nstd204human GRCh38.p13 chr16: 18,763,645-18,782,340 , GRCh37.p13 chr16: 18,774,967-18,793,662 RPS15A
    nsv4994515copy number variation1nstd200human GRCh38 chr16: 18,784,377-18,799,306 , GRCh37.p13 chr16: 18,795,699-18,810,628 RPS15A, ARL6IP1
    nsv4994513copy number variation1nstd200human GRCh38 chr16: 18,581,483-18,803,775 , GRCh37.p13 chr16: 18,592,805-18,815,097 SMG1, ABCC6P1, 2 more genes
    nsv4730208inversion9nstd198human GRCh38 chr16: 16,118,120-18,828,979 , GRCh37.p13 chr16: 16,211,977-18,840,301 , ABCC6, 48 more genes
    nsv4729901copy number variation1nstd102humanPathogenic GRCh37 chr16: 2,959,279-30,190,593 , GRCh38.p12 chr16: 2,909,278-30,179,272 NPIPB9, TMEM219, 597 more genes
    nsv4685985copy number variation1nstd102humanPathogenic GRCh37 chr16: 5,805,001-34,230,001 , GRCh38.p12 chr16: 5,755,000-34,995,630 LOC105371069, PKD1P6-NPIPP1, 654 more genes
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