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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv1194680copy number variation1nstd113human NCBI36 (hg18) chr8: 63,796,919-64,855,685 , GRCh37 (hg19) chr8: 63,634,365-64,693,131 , GRCh38 (hg38) chr8: 62,721,806-63,780,574 YTHDF3-AS1, YTHDF3, 5 more genes
    esv3617422mobile element insertion62estd214human GRCh37 (hg19) chr8: 63,988,913-63,988,913 , GRCh38 (hg38) chr8: 63,076,354-63,076,354 TTPA
    nsv1067689copy number variation2nstd101humanPathogenic NCBI36 (hg18) chr8: 181,530-146,250,824 , GRCh37 (hg19) chr8: 191,530-146,280,020 , GRCh38 (hg38) chr8: 241,530-145,054,634 NAT2, MIR875, 914 more genes
    nsv1033527copy number variation1nstd100human NCBI36 (hg18) chr8: 63,836,469-64,236,289 , GRCh37 (hg19) chr8: 63,673,915-64,073,735 , GRCh38 (hg38) chr8: 62,761,356-63,161,176 NKAIN3, UG0898H09, 2 more genes
    nsv1029869copy number variation1nstd100human NCBI36 (hg18) chr8: 58,900,523-67,994,870 , GRCh37 (hg19) chr8: 58,737,969-67,832,316 , GRCh38 (hg38) chr8: 57,825,410-66,920,081 MIR124-2HG, TRY-GTA5-5, 46 more genes
    nsv1025509copy number variation1nstd100human NCBI36 (hg18) chr8: 52,087,277-65,794,084 , GRCh37 (hg19) chr8: 51,924,724-65,631,530 , GRCh38 (hg38) chr8: 51,012,164-64,718,973 MIR124-2HG, T1560, 56 more genes
    nsv1023233copy number variation1nstd100human NCBI36 (hg18) chr8: 47,963,295-67,971,643 , GRCh37 (hg19) chr8: 47,844,130-67,809,089 , GRCh38 (hg38) chr8: 46,932,508-66,896,854 MIR124-2HG, TRY-GTA5-5, 87 more genes
    nsv1022800copy number variation1nstd100human NCBI36 (hg18) chr8: 43,943,193-146,264,292 , GRCh37 (hg19) chr8: 43,824,036-146,293,488 , GRCh38 (hg38) chr8: 43,968,893-145,068,102 MIR875, MIR937, 566 more genes
    nsv1015430copy number variation1nstd100human NCBI36 (hg18) chr8: 63,869,692-65,646,141 , GRCh37 (hg19) chr8: 63,707,138-65,483,587 , GRCh38 (hg38) chr8: 62,794,579-64,571,030 MIR124-2HG, YTHDF3-AS1, 7 more genes
    nsv995731copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr8: 21,149,033-146,295,771 , GRCh38 (hg38) chr8: 21,291,522-145,070,385 , NCBI36 (hg18) chr8: 21,193,313-146,266,575 MIR875, MIR937, 761 more genes
    nsv995405copy number variation2nstd37humanPathogenic GRCh37 (hg19) chr8: 158,048-146,295,771 , GRCh38 (hg38) chr8: 208,048-145,070,385 , NCBI36 (hg18) chr8: 148,048-146,266,575 NAT2, MIR875, 914 more genes
    nsv984843copy number variation10nstd11humannot provided NCBI36 (hg18) chr8: 21,254-146,268,959 , GRCh37 (hg19) chr8: 31,254-146,298,155 , GRCh38 (hg38) chr8: 81,254-145,072,769 NAT2, MIR875, 900 more genes
    esv3445521copy number variation1estd59human NCBI36 (hg18) chr8: 64,152,001-64,179,824 , GRCh37 (hg19) chr8: 63,989,447-64,017,270 , GRCh38 (hg38) chr8: 63,076,888-63,104,711 TTPA
    esv3445164copy number variation1estd59human NCBI36 (hg18) chr8: 64,160,352-64,162,200 , GRCh37 (hg19) chr8: 63,997,798-63,999,646 , GRCh38 (hg38) chr8: 63,085,239-63,087,087 TTPA
    esv3435382copy number variation1estd59human NCBI36 (hg18) chr8: 50,869,325-130,813,208 , GRCh37 (hg19) chr8: 50,706,772-130,744,026 , GRCh38 (hg38) chr8: 49,794,212-129,731,780 MIR875, C8orf88, 414 more genes
    esv3373017copy number variation3estd59human NCBI36 (hg18) chr8: 64,152,001-64,176,804 , GRCh37 (hg19) chr8: 63,989,447-64,014,250 , GRCh38 (hg38) chr8: 63,076,888-63,101,691 TTPA
    esv3345424copy number variation1estd59human NCBI36 (hg18) chr8: 583,634-144,106,346 , GRCh37 (hg19) chr8: 593,634-144,034,971 , GRCh38 (hg38) chr8: 643,634-142,953,554 NAT2, MIR875, 813 more genes
    esv3115114copy number variation1estd209human GRCh37 (hg19) chr8: 63,978,658-63,978,659 , GRCh38 (hg38) chr8: 63,066,099-63,066,100 TTPA
    esv2854257insertion1estd209human GRCh37 (hg19) chr8: 63,980,099-63,980,099 , GRCh38 (hg38) chr8: 63,067,540-63,067,540 TTPA
    nsv948582copy number variation2nstd85human NCBI35 (hg17) chr8: 180,568-146,263,538 , GRCh37 (hg19) chr8: 190,568-146,292,734 , GRCh38 (hg38) chr8: 240,568-145,067,348 NAT2, MIR875, 899 more genes
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