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Items: 1 to 20 of 139

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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
    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
    nsv6843109copy number variation1nstd229human GRCh38 chr8: 64,581,901-64,604,300 , GRCh37.p13 chr8: 65,494,458-65,516,857 BHLHE22, CYP7B1, 1 more genes
    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
    nsv6432642copy number variation1nstd223human GRCh38 chr8: 64,562,201-64,580,400 , GRCh37.p13 chr8: 65,474,758-65,492,957 BHLHE22-AS1, BHLHE22
    nsv6415906copy number variation1nstd223human GRCh38 chr8: 64,569,501-64,589,700 , GRCh37.p13 chr8: 65,482,058-65,502,257 BHLHE22-AS1, CYP7B1, 1 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
    nsv5849983copy number variation1nstd209human GRCh38 chr8: 64,577,066-64,579,100 , GRCh37.p13 chr8: 65,489,623-65,491,657 BHLHE22, BHLHE22-AS1
    nsv5478879copy number variation1nstd206human GRCh38 chr8: 64,577,128-64,579,727 , GRCh37.p13 chr8: 65,489,685-65,492,284 BHLHE22-AS1, BHLHE22
    nsv4675964copy number variation1nstd102humanLikely benign GRCh37 chr8: 65,435,916-65,831,159 , GRCh38.p12 chr8: 64,523,359-64,918,924 BHLHE22, LOC105375878, 4 more genes
    nsv4675521copy number variation1nstd102humanUncertain significance GRCh37 chr8: 65,216,452-65,845,271 , GRCh38.p12 chr8: 64,303,895-64,933,036 MIR124-2, LOC107986878, 9 more genes
    nsv4456811copy number variation1nstd102humanPathogenic GRCh37 chr8: 31,936,551-146,295,771 , GRCh38.p12 chr8: 32,079,035-145,070,385 TERF1, LOC107986945, 1511 more genes
    nsv4456190copy number variation1nstd102humanPathogenic GRCh37 chr8: 65,280,508-67,782,846 , GRCh38.p12 chr8: 64,367,951-66,870,611 BHLHE22-AS1, VCPIP1, 41 more genes
    nsv4387546copy number variation1nstd173human GRCh37 chr8: 65,023,339-68,301,135 , GRCh38.p12 chr8: 64,110,782-67,388,900 , LOC105375885, 56 more genes
    nsv4349554copy number variation2nstd102humanPathogenic GRCh37 chr8: 158,048-146,295,771 , GRCh38.p12 chr8: 208,048-145,070,385 LOC101929488, TEX15, 2105 more genes
    nsv4318272inversion1nstd166human GRCh37.p13 chr8: 51,271,211-76,167,888 , GRCh38.p12 chr8: 50,358,651-75,255,653 , ASPH, 341 more genes
    nsv3967261insertion1nstd168human GRCh38 chr8: 64,579,630-64,587,161 , GRCh37.p13 chr8: 65,492,187-65,499,718 CYP7B1, BHLHE22, 1 more genes
    nsv3924415copy number variation1nstd102humanPathogenic GRCh37 chr8: 61,431,781-67,571,260 , GRCh38 chr8: 60,519,222-66,659,025 , NCBI36 chr8: 61,594,335-67,733,814 RN7SKP135, TRIM55, 77 more genes
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