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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148253copy number variation1nstd102humanPathogenic GRCh38 chr8: 449,893-23,854,904 , GRCh37.p13 chr8: 399,893-23,712,417 ENTPD4, LOC100421446, 447 more genes
    nsv7148131copy number variation1nstd102humanPathogenic GRCh37 chr8: 10,501-11,142,629 , GRCh38.p12 chr8: 60,501-11,285,120 XKR6, FAM90A11, 224 more genes
    nsv7148128copy number variation1nstd102humanLikely pathogenic GRCh37 chr8: 10,501-6,614,959 , GRCh38.p12 chr8: 60,501-6,757,438 ANGPT2, CLN8, 67 more genes
    nsv7097906copy number variation1nstd102humanUncertain significance GRCh37 chr8: 6,372,178-6,500,570 , GRCh38.p12 chr8: 6,514,657-6,643,049 ANGPT2, MIR8055, 2 more genes
    nsv7097802copy number variation1nstd102humanPathogenic GRCh37 chr8: 6,264,189-6,500,570 , GRCh38.p12 chr8: 6,406,668-6,643,049 ANGPT2, MCPH1, 4 more genes
    nsv7097666copy number variation1nstd102humanUncertain significance GRCh37 chr8: 6,357,353-6,357,470 , GRCh38.p12 chr8: 6,499,832-6,499,949 MCPH1, ANGPT2
    nsv6857766copy number variation1nstd229human GRCh38 chr8: 6,550,301-6,555,500 , GRCh37.p13 chr8: 6,407,822-6,413,021 MCPH1, ANGPT2
    nsv6857600copy number variation1nstd229human GRCh38 chr8: 6,492,017-6,953,289 , GRCh37.p13 chr8: 6,349,538-6,810,811 MIR4659B, MCPH1-AS1, 14 more genes
    nsv6857217copy number variation1nstd229human GRCh38 chr8: 6,563,596-6,595,496 , GRCh37.p13 chr8: 6,421,117-6,453,017 MCPH1, ANGPT2
    nsv6856140copy number variation1nstd229human GRCh38 chr8: 6,522,101-6,531,600 , GRCh37.p13 chr8: 6,379,622-6,389,121 ANGPT2, MCPH1
    nsv6855375copy number variation1nstd229human GRCh38 chr8: 6,495,901-6,558,900 , GRCh37.p13 chr8: 6,353,422-6,416,421 MCPH1, ANGPT2
    nsv6855191copy number variation1nstd229human GRCh38 chr8: 6,381,726-6,719,102 , GRCh37.p13 chr8: 6,239,247-6,576,623 MCPH1-DT, LOC100422495, 6 more genes
    nsv6854192copy number variation1nstd229human GRCh38 chr8: 6,549,101-6,550,900 , GRCh37.p13 chr8: 6,406,622-6,408,421 MCPH1, ANGPT2
    nsv6852460copy number variation1nstd229human GRCh38 chr8: 6,542,645-6,558,114 , GRCh37.p13 chr8: 6,400,166-6,415,635 ANGPT2, MCPH1
    nsv6850377copy number variation1nstd229human GRCh38 chr8: 6,329,983-6,576,699 , GRCh37.p13 chr8: 6,187,504-6,434,220 LOC101928016, MCPH1-DT, 2 more genes
    nsv6849446copy number variation1nstd229human GRCh38 chr8: 6,471,669-6,497,974 , GRCh37.p13 chr8: 6,329,190-6,355,495 MCPH1, LOC101928016, 1 more genes
    nsv6846361copy number variation1nstd229human GRCh38 chr8: 6,547,610-6,550,097 , GRCh37.p13 chr8: 6,405,131-6,407,618 ANGPT2, MCPH1
    nsv6845189copy number variation1nstd229human GRCh38 chr8: 6,539,576-6,552,083 , GRCh37.p13 chr8: 6,397,097-6,409,604 MCPH1, ANGPT2
    nsv6843588copy number variation1nstd229human GRCh38 chr8: 6,543,513-6,915,947 , GRCh37.p13 chr8: 6,401,034-6,773,469 ANGPT2, XKR5, 11 more genes
    nsv6842872copy number variation1nstd229human GRCh38 chr8: 6,527,501-6,569,400 , GRCh37.p13 chr8: 6,385,022-6,426,921 MCPH1, ANGPT2
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