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Items: 1 to 20 of 246

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7062610inversion1nstd229human GRCh38 chr8: 60,977,244-66,075,546 , GRCh37.p13 chr8: 61,889,803-66,987,781 LOC105375870, LINC01289, 55 more genes
    nsv6857727copy number variation1nstd229human GRCh38 chr8: 65,628,368-65,631,353 , GRCh37.p13 chr8: 66,540,603-66,543,588 ARMC1
    nsv6852611copy number variation1nstd229human GRCh38 chr8: 64,552,298-65,913,335 , GRCh37.p13 chr8: 65,464,855-66,825,570 LOC105375880, PDE7A, 14 more genes
    nsv6852273copy number variation1nstd229human GRCh38 chr8: 61,996,129-66,319,713 , GRCh37.p13 chr8: 62,908,688-67,231,948 LOC112268028, LOC105375873, 52 more genes
    nsv6840500copy number variation1nstd229human GRCh38 chr8: 65,630,939-65,649,515 , GRCh37.p13 chr8: 66,543,174-66,561,750 ARMC1, MTFR1
    nsv6636356copy number variation1nstd102humanUncertain significance GRCh37 chr8: 64,049,070-66,671,663 , GRCh38.p12 chr8: 63,136,511-65,759,428 LOC107986949, LOC107986878, 31 more genes
    nsv6570666inversion1nstd223human GRCh38 chr8: 65,617,909-65,618,534 , GRCh37.p13 chr8: 66,530,144-66,530,769 ARMC1
    nsv6565281inversion1nstd223human GRCh38 chr8: 65,610,204-65,610,785 , GRCh37.p13 chr8: 66,522,439-66,523,020 ARMC1
    nsv6564302inversion1nstd223human GRCh38 chr8: 65,619,945-65,620,309 , GRCh37.p13 chr8: 66,532,180-66,532,544 ARMC1
    nsv6562639inversion1nstd223human GRCh38 chr8: 65,611,919-65,612,582 , GRCh37.p13 chr8: 66,524,154-66,524,817 ARMC1
    nsv6426951copy number variation1nstd223human GRCh38 chr8: 65,628,344-65,631,328 , GRCh37.p13 chr8: 66,540,579-66,543,563 ARMC1
    nsv6290731copy number variation1nstd102humanPathogenic GRCh37 chr8: 66,045,954-69,807,260 , GRCh38.p12 chr8: 65,133,719-68,895,025 LINC00967, LOC107986950, 64 more genes
    nsv6136690copy number variation1nstd213human GRCh37 chr8: 64,070,000-66,540,001 , GRCh38.p12 chr8: 63,157,441-65,627,766 ARMC1, LINC01289, 27 more genes
    nsv6136681copy number variation1nstd213human GRCh37 chr8: 46,860,000-86,550,001 , GRCh38.p12 chr8: 45,948,378-85,637,772 CEBPD, EYA1, 519 more genes
    nsv6136592copy number variation1nstd213human GRCh37 chr8: 66,160,000-66,610,001 , GRCh38.p12 chr8: 65,247,765-65,697,766 MTFR1, ARMC1, 2 more genes
    nsv5575899copy number variation1nstd207human GRCh38 chr8: 65,616,970-65,617,092 , GRCh37.p13 chr8: 66,529,205-66,529,327 ARMC1
    nsv5490854copy number variation1nstd206human GRCh38 chr8: 65,616,977-65,617,064 , GRCh37.p13 chr8: 66,529,212-66,529,299 ARMC1
    nsv5485566copy number variation1nstd206human GRCh38 chr8: 65,622,746-65,623,393 , GRCh37.p13 chr8: 66,534,981-66,535,628 ARMC1
    nsv5303383copy number variation1nstd204human GRCh38.p13 chr8: 65,629,025-65,629,636 , GRCh37.p13 chr8: 66,541,260-66,541,871 ARMC1
    nsv5180496mobile element insertion1nstd203human GRCh38 chr8: 65,627,706-65,627,723 , GRCh37.p13 chr8: 66,539,941-66,539,958 ARMC1
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