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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3109761copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr8: 12,490,999-146,295,771 , GRCh38 (hg38) chr8: 12,633,490-145,070,385 , NCBI36 (hg18) chr8: 12,535,370-146,266,575 SNAI2, MIR3150BHG, 1863 more genes
    esv4010899copy number variation1estd233human GRCh37 (hg19) chr8: 49,421,000-50,368,000 , GRCh38 (hg38) chr8: 48,508,440-49,455,441 SNAI2, EFCAB1, 11 more genes
    nsv2778159copy number variation1nstd37humanUncertain significance NCBI36 (hg18) chr8: 47,858,050-50,929,098 , GRCh37 (hg19) chr8: 47,738,885-50,766,545 , GRCh38 (hg38) chr8: 46,827,263-49,853,985 SNAI2, SPIDR, 56 more genes
    nsv2776038copy number variation1nstd37humanPathogenic NCBI36 (hg18) chr8: 3,938-146,274,826 , GRCh37 (hg19) chr8: 13,938-146,304,022 , GRCh38 (hg38) chr8: 63,938-145,078,636 SNAI2, ADRB3, 2163 more genes
    nsv2775835copy number variation1nstd37humanUncertain significance GRCh37 (hg19) chr8: 46,912,309-50,818,801 , GRCh38 (hg38) chr8: 46,000,687-49,906,241 , NCBI36 (hg18) chr8: 47,031,474-50,981,354 SNAI2, PRKDC, 63 more genes
    nsv2774782copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr8: 158,991-146,280,828 , GRCh38 (hg38) chr8: 208,991-145,055,442 , NCBI36 (hg18) chr8: 148,991-146,251,632 SNAI2, NATP, 2159 more genes
    nsv2771806copy number variation5nstd37humanPathogenic GRCh37 (hg19) chr8: 158,049-146,295,771 , GRCh38 (hg38) chr8: 208,049-145,070,385 , NCBI36 (hg18) chr8: 148,049-146,266,575 SNAI2, FAM90A17P, 2160 more genes
    nsv2770008copy number variation1nstd37humanUncertain significance GRCh37 (hg19) chr8: 24,772,064-56,509,566 , GRCh38 (hg38) chr8: 24,914,551-55,597,007 , NCBI36 (hg18) chr8: 24,827,969-56,672,120 SNAI2, ADAM3A, 439 more genes
    nsv2769186copy number variation1nstd37humanUncertain significance NCBI36 (hg18) chr8: 49,913,673-50,119,577 , GRCh37 (hg19) chr8: 49,751,120-49,957,024 , GRCh38 (hg38) chr8: 48,838,561-49,044,465 SNAI2, LOC107986942
    esv3853708copy number variation1estd219human GRCh37 (hg19) chr8: 49,824,053-49,830,049 , GRCh38 (hg38) chr8: 48,911,494-48,917,490 SNAI2
    nsv2580807short tandem repeat3nstd128human GRCh37 (hg19) chr8: 49,831,213-49,831,251 , GRCh38 (hg38) chr8: 48,918,654-48,918,692 SNAI2
    nsv2580806short tandem repeat5nstd128human GRCh37 (hg19) chr8: 49,828,714-49,828,730 , GRCh38 (hg38) chr8: 48,916,155-48,916,171 SNAI2
    nsv2557163short tandem repeat1nstd128human GRCh37 (hg19) chr8: 49,830,744-49,830,762 , GRCh38 (hg38) chr8: 48,918,185-48,918,203 SNAI2
    nsv1195513copy number variation1nstd113human NCBI36 (hg18) chr8: 48,862,265-60,701,695 , GRCh37 (hg19) chr8: 48,699,712-60,539,141 , GRCh38 (hg38) chr8: 47,787,151-59,626,582 SNAI2, SDCBP, 154 more genes
    nsv1189709copy number variation1nstd113human NCBI36 (hg18) chr8: 35,999,817-50,360,931 , GRCh37 (hg19) chr8: 35,880,275-50,198,378 , GRCh38 (hg38) chr8: 36,022,757-49,285,819 SNAI2, ADAM2, 201 more genes
    esv3815464copy number variation1estd192human GRCh37 (hg19) chr8: 39,995,604-126,537,271 , GRCh38 (hg38) chr8: 40,138,085-125,525,029 SNAI2, JPH1, 1120 more genes
    esv3815616tandem duplication1estd192human GRCh37 (hg19) chr8: 39,008,684-54,189,644 , GRCh38 (hg38) chr8: 39,151,165-53,277,084 SNAI2, ATP6V1G1P2, 169 more genes
    esv3815709copy number variation1estd192human GRCh37 (hg19) chr8: 47,220,819-121,441,475 , GRCh38 (hg38) chr8: 46,309,197-120,429,235 SNAI2, LOC105375826, 970 more genes
    esv3795253inversion1estd192human GRCh37 (hg19) chr8: 42,395,999-57,119,083 , GRCh38 (hg38) chr8: 42,540,856-56,206,524 SNAI2, MTCYBP20, 169 more genes
    esv3807786tandem duplication1estd192human GRCh37 (hg19) chr8: 35,546,577-111,013,217 , GRCh38 (hg38) chr8: 35,689,059-110,000,988 SNAI2, ADAM2, 1029 more genes
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