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Items: 1 to 20 of 18455

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3110105copy number variation1nstd37humanPathogenic GRCh37 (hg19) chrX: 168,547-112,474,026 , GRCh38 (hg38) chrX: 251,880-113,230,799 , NCBI36 (hg18) chrX: 108,547-112,360,682 GAGE12F, GS1-600G8.3, 710 more genes
    nsv3110084copy number variation1nstd37humanUncertain significance NCBI36 (hg18) chr9: 127,143,251-128,083,810 , GRCh37 (hg19) chr9: 128,103,430-129,043,989 , GRCh38 (hg38) chr9: 125,341,151-126,281,710 GAPVD1, PBX3, 1 more genes
    nsv3110082copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr8: 86,841,154-146,295,771 , GRCh38 (hg38) chr8: 85,828,925-145,070,385 , NCBI36 (hg18) chr8: 86,910,442-146,266,575 MIR875, MIR937, 395 more genes
    nsv3110080copy number variation1nstd37humanPathogenic NCBI36 (hg18) chr8: 181,530-22,460,928 , GRCh37 (hg19) chr8: 191,530-22,404,983 , GRCh38 (hg38) chr8: 241,530-22,547,470 NAT2, DEFB131C, 178 more genes
    nsv3110077copy number variation1nstd37humanPathogenic NCBI36 (hg18) chr8: 131,751,745-146,250,824 , GRCh37 (hg19) chr8: 131,682,563-146,280,020 , GRCh38 (hg38) chr8: 130,670,317-145,054,634 MIR937, MIR939, 151 more genes
    nsv3110075copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr7: 72,677,301-74,143,240 , GRCh38 (hg38) chr7: 73,280,574-75,129,258 , NCBI36 (hg18) chr7: 72,315,237-73,781,176 MIR4284, RNA5SP233, 33 more genes
    nsv3110063copy number variation1nstd37humanPathogenic NCBI36 (hg18) chr5: 164,323,950-180,629,412 , GRCh37 (hg19) chr5: 164,391,372-180,696,806 , GRCh38 (hg38) chr5: 164,964,366-181,269,805 TRV-CAC1-5, SUMO2P6, 185 more genes
    nsv3110045copy number variation1nstd37humanLikely benign GRCh37 (hg19) chr20: 7,106,057-8,586,513 , GRCh38 (hg38) chr20: 7,125,410-8,605,866 , NCBI36 (hg18) chr20: 7,054,057-8,534,513 PLCB1-IT1, LINC01428, 6 more genes
    nsv3110043copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr20: 2,463,101-8,185,680 , GRCh38 (hg38) chr20: 2,482,455-8,205,033 , NCBI36 (hg18) chr20: 2,411,101-8,133,680 UBOX5-AS1, TMEM239, 80 more genes
    nsv3110041copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr1: 849,466-8,901,938 , GRCh38 (hg38) chr1: 914,086-8,841,879 , NCBI36 (hg18) chr1: 839,329-8,824,525 LINC01134, TTC34, 131 more genes
    nsv3110040copy number variation1nstd37humanPathogenic NCBI36 (hg18) chr1: 836,543-3,987,287 , GRCh37 (hg19) chr1: 846,680-4,087,427 , GRCh38 (hg38) chr1: 911,300-4,027,367 LINC01134, TTC34, 92 more genes
    nsv3109973copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr7: 72,718,277-74,141,494 , GRCh38 (hg38) chr7: 73,304,280-74,727,156 , NCBI36 (hg18) chr7: 72,356,213-73,779,430 MIR4284, RNA5SP233, 27 more genes
    nsv3109972copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr7: 72,702,149-74,141,746 , GRCh38 (hg38) chr7: 73,288,147-74,727,408 , NCBI36 (hg18) chr7: 72,340,085-73,779,682 MIR4284, RNA5SP233, 27 more genes
    nsv3109949copy number variation1nstd37humanUncertain significance GRCh37 (hg19) chr3: 178,853,769-179,369,934 , GRCh38 (hg38) chr3: 179,135,981-179,652,146 , NCBI36 (hg18) chr3: 180,336,463-180,852,628 KCNMB3, NDUFB5, 6 more genes
    nsv3109948copy number variation1nstd37humanPathogenic NCBI36 (hg18) chr3: 175,313,014-183,652,825 , GRCh37 (hg19) chr3: 173,830,320-182,170,131 , GRCh38 (hg38) chr3: 174,112,530-182,452,343 LINC01208, LINC00578, 38 more genes
    nsv3109927copy number variation1nstd37humanLikely pathogenic GRCh37 (hg19) chr20: 61,568-10,486,106 , GRCh38 (hg38) chr20: 80,927-10,505,458 , NCBI36 (hg18) chr20: 9,568-10,434,106 SNORD119, SNAP25-AS1, 137 more genes
    nsv3109924copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr1: 849,466-2,330,338 , GRCh38 (hg38) chr1: 914,086-2,398,899 , NCBI36 (hg18) chr1: 839,329-2,320,198 TTLL10-AS1, PRKCZ-AS1, 63 more genes
    nsv3109923copy number variation1nstd37humanPathogenic NCBI36 (hg18) chr1: 836,543-3,394,283 , GRCh37 (hg19) chr1: 846,680-3,404,423 , GRCh38 (hg38) chr1: 911,300-3,487,859 TTC34, MIR4251, 77 more genes
    nsv3109860copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr8: 11,945,855-34,875,355 , GRCh38 (hg38) chr8: 12,088,346-35,017,837 , NCBI36 (hg18) chr8: 11,983,264-34,994,897 NAT2, RBPMS-AS1, 167 more genes
    nsv3109828copy number variation1nstd37humanPathogenic NCBI36 (hg18) chr3: 178,729,187-199,321,446 , GRCh37 (hg19) chr3: 177,246,493-197,837,049 , GRCh38 (hg38) chr3: 177,528,705-198,110,178 MIR922, MIR944, 230 more genes
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