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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4360567copy number variation1nstd102humanPathogenic NCBI36 (hg18) chr8: 56,498,527-59,911,866 , GRCh37.p13 chr8: 56,335,973-59,749,312 , GRCh38.p12 chr8: 55,423,413-58,836,753 LYN, LINC00588, 60 more genes
    nsv4359532copy number variation1nstd102humanPathogenic NCBI36 (hg18) chr8: 58,436,356-80,244,868 , GRCh37.p13 chr8: 58,273,802-80,082,313 , GRCh38.p12 chr8: 57,361,243-79,170,078 ASPH, CRH, 269 more genes
    nsv4358507copy number variation1nstd102humanPathogenic NCBI36 (hg18) chr8: 47,062,127-140,366,919 , GRCh37.p13 chr8: 46,942,962-140,297,737 , GRCh38.p12 chr8: 46,031,340-139,285,494 ACTBP6, ADCY8, 1175 more genes
    nsv4357294copy number variation1nstd102humanPathogenic NCBI36 (hg18) chr8: 47,062,121-70,378,576 , GRCh37.p13 chr8: 46,942,956-70,216,022 , GRCh38.p12 chr8: 46,031,334-69,303,787 CYP7A1, NPBWR1, 319 more genes
    nsv4356424copy number variation1nstd102humanPathogenic NCBI36 (hg18) chr8: 56,390,968-66,027,541 , GRCh37.p13 chr8: 56,228,414-65,864,987 , GRCh38.p12 chr8: 55,315,854-64,952,752 ASPH, CYP7A1, 124 more genes
    nsv4355561copy number variation1nstd102humanPathogenic NCBI36 (hg18) chr8: 166,452-146,264,902 , GRCh37.p13 chr8: 176,452-146,294,098 , GRCh38.p12 chr8: 226,452-145,068,712 NAT2, ADRB3, 2159 more genes
    nsv4355415copy number variation1nstd102humanPathogenic NCBI36 (hg18) chr8: 36,556,779-60,694,111 , GRCh37.p13 chr8: 36,437,621-60,531,557 , GRCh38.p12 chr8: 36,580,103-59,618,998 ANK1, CYP7A1, 325 more genes
    nsv4355046copy number variation1nstd102humanPathogenic NCBI36 (hg18) chr8: 55,896,471-62,221,415 , GRCh37.p13 chr8: 55,733,917-62,058,861 , GRCh38.p12 chr8: 54,821,357-61,146,302 CYP7A1, PLAG1, 85 more genes
    nsv4354871copy number variation1nstd102humanPathogenic NCBI36 (hg18) chr8: 181,530-146,250,824 , GRCh37.p13 chr8: 191,530-146,280,020 , GRCh38.p12 chr8: 241,530-145,054,634 NATP, ACTBP6, 2158 more genes
    nsv4354753copy number variation1nstd102humanPathogenic NCBI36 (hg18) chr8: 54,400,502-62,938,131 , GRCh37.p13 chr8: 54,237,949-62,775,577 , GRCh38.p12 chr8: 53,325,389-61,863,018 SDCBP, TOX, 122 more genes
    nsv4354218copy number variation1nstd102humanPathogenic NCBI36 (hg18) chr8: 58,000,925-62,766,972 , GRCh37.p13 chr8: 57,838,371-62,604,418 , GRCh38.p12 chr8: 56,925,812-61,691,859 TOX, LINC00588, 51 more genes
    nsv4353535copy number variation1nstd102humanPathogenic NCBI36 (hg18) chr8: 181,605-146,250,971 , GRCh37.p13 chr8: 191,605-146,280,167 , GRCh38.p12 chr8: 241,605-145,054,781 NATP, ACTBP6, 2158 more genes
    nsv4353127copy number variation1nstd102humanPathogenic NCBI36 (hg18) chr8: 181,530-146,245,639 , GRCh37.p13 chr8: 191,530-146,274,835 , GRCh38.p12 chr8: 241,530-145,049,449 NAT1, ASAH1, 2157 more genes
    nsv4349554copy number variation1nstd102humanPathogenic GRCh37 (hg19) chr8: 158,048-146,295,771 , GRCh38.p12 chr8: 208,048-145,070,385 , NCBI36 (hg18) chr8: 148,048-146,266,575 NAT2, ADRA1A, 2160 more genes
    nsv4349439copy number variation1nstd102humanPathogenic GRCh37 (hg19) chr8: 21,149,033-146,295,771 , GRCh38.p12 chr8: 21,291,522-145,070,385 , NCBI36 (hg18) chr8: 21,193,313-146,266,575 ADRA1A, ANK1, 1756 more genes
    nsv4339796mobile element insertion1nstd166human GRCh37.p13 chr8: 21,879,122-90,710,334 , GRCh38.p12 chr8: 22,021,611-89,698,106 ADRB3, ASPH, 965 more genes
    nsv4331703mobile element insertion1nstd166human GRCh37.p13 chr8: 56,511,244-73,794,025 , GRCh38.p12 chr8: 55,598,685-72,881,790 CYP7A1, PLAG1, 238 more genes
    nsv4322815mobile element insertion1nstd166human GRCh37.p13 chr8: 32,627,412-114,464,823 , GRCh38.p12 chr8: 32,769,894-113,452,594 ANK1, ASPH, 1083 more genes
    nsv4318272inversion1nstd166human GRCh37.p13 chr8: 51,271,211-76,167,888 , GRCh38.p12 chr8: 50,358,651-75,255,653 BTF3P1, CA8, 341 more genes
    nsv4313239mobile element insertion1nstd166human GRCh37.p13 chr8: 19,574,660-129,355,879 , GRCh38.p12 chr8: 19,717,149-128,343,633 ATP6V1B2, POLR3D, 1514 more genes
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