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Items: 1 to 20 of 122

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148134copy number variation1nstd102humanPathogenic GRCh37 chr8: 61,121,294-63,502,403 , GRCh38.p12 chr8: 60,208,735-62,589,844 LOC112268028, LOC105375864, 23 more genes
    nsv7071939inversion1nstd229human GRCh38 chr8: 60,205,407-60,499,435 , GRCh37.p13 chr8: 61,117,966-61,411,994 CA8, PDCL3P1, 2 more genes
    nsv6853933copy number variation1nstd229human GRCh38 chr8: 59,153,072-60,491,960 , GRCh37.p13 chr8: 60,065,631-61,404,519 SLC2A13P1, LOC105375859, 10 more genes
    nsv6568995inversion1nstd223human GRCh38 chr8: 60,386,525-60,386,626 , GRCh37.p13 chr8: 61,299,084-61,299,185 PDCL3P1
    nsv6426457copy number variation1nstd223human GRCh38 chr8: 60,387,675-60,390,823 , GRCh37.p13 chr8: 61,300,234-61,303,382 PDCL3P1
    nsv6312729copy number variation1nstd102humanUncertain significance GRCh37 chr8: 61,121,344-62,626,930 , GRCh38.p12 chr8: 60,208,785-61,714,371 NPM1P6, PDCL3P1, 15 more genes
    nsv6246050mobile element insertion1nstd215human GRCh38 chr8: 60,386,636-60,386,636 , GRCh37.p13 chr8: 61,299,195-61,299,195 PDCL3P1
    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
    nsv6136061copy number variation1nstd213human GRCh37 chr8: 54,780,000-63,060,001 , GRCh38.p12 chr8: 53,867,440-62,147,442 RAB2A, SDCBP, 117 more genes
    nsv4960522copy number variation1nstd200human GRCh38 chr8: 60,387,678-60,390,823 , GRCh37.p13 chr8: 61,300,237-61,303,382 PDCL3P1
    nsv4729323copy number variation1nstd102humanUncertain significance GRCh37 chr8: 60,717,207-61,303,622 , GRCh38.p12 chr8: 59,804,648-60,391,063 LOC105375864, CA8, 4 more genes
    nsv4716589copy number variation1nstd102humanLikely pathogenic GRCh37 chr8: 60,026,663-63,779,735 , GRCh38.p12 chr8: 59,114,104-62,867,176 ASPH, CA8, 36 more genes
    nsv4456871copy number variation1nstd102humanPathogenic GRCh37 chr8: 39,555,657-64,049,089 , GRCh38.p12 chr8: 39,698,138-63,136,530 CRIPTOP5, TRIM60P15, 297 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
    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
    nsv3923501copy number variation1nstd102humanPathogenic NCBI36 chr8: 55,896,471-62,221,415 , GRCh38 chr8: 54,821,357-61,146,302 , GRCh37 chr8: 55,733,917-62,058,861 NUDT15P1, LINC01301, 83 more genes
    nsv3923310copy number variation1nstd102humanPathogenic NCBI36 chr8: 166,452-146,264,902 , GRCh38 chr8: 226,452-145,068,712 , GRCh37 chr8: 176,452-146,294,098 LOC112268023, RPL23AP96, 2105 more genes
    nsv3923110copy number variation1nstd102humanPathogenic GRCh37 chr8: 57,838,371-62,604,418 , NCBI36 chr8: 58,000,925-62,766,972 , GRCh38 chr8: 56,925,812-61,691,859 LOC105375855, LOC105375858, 50 more genes
    nsv3919282copy number variation1nstd102humanPathogenic GRCh37 chr8: 191,530-146,280,020 , GRCh38 chr8: 241,530-145,054,634 , NCBI36 chr8: 181,530-146,250,824 MIR4662B, LOC101927845, 2104 more genes
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