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Items: 1 to 20 of 382

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137207copy number variation1nstd102humanPathogenic GRCh37 chr7: 72,718,277-74,142,256 , GRCh38.p12 chr7: 73,304,280-74,727,918 ELN-AS1, CLIP2, 36 more genes
    nsv7137203copy number variation1nstd102humanPathogenic GRCh37 chr7: 72,664,461-74,162,586 , GRCh38.p12 chr7: 73,250,429-74,748,249 VPS37D, ABHD11, 39 more genes
    nsv7137102copy number variation1nstd102humanPathogenic GRCh37 chr7: 72,717,395-74,173,168 , GRCh38.p12 chr7: 73,303,398-74,758,838 MIR10525, MIR590, 38 more genes
    nsv7137028copy number variation1nstd102humanPathogenic GRCh38 chr7: 73,214,501-74,773,500 , GRCh37.p13 chr7|NW_003871064.1: 743,737-2,302,736 , GRCh37.p13 chr7: 72,631,166-74,187,847 LOC105375350, NSUN5, 41 more genes
    nsv7098945copy number variation1nstd102humanPathogenic GRCh38 chr7: 73,229,597-74,727,852 , GRCh37.p13 chr7|NW_003871064.1: 758,833-2,257,088 , GRCh37.p13 chr7: 72,643,631-74,142,190 DNAJC30, MIR10525, 39 more genes
    nsv7053887inversion1nstd229human GRCh38 chr7: 74,171,934-74,839,189 , GRCh37.p13 chr7|NW_003871064.1: 1,701,170-2,368,425 , GRCh37.p13 chr7: 73,586,264-74,223,814 LOC107986742, GTF2IRD1, 13 more genes
    nsv6830166copy number variation1nstd229human GRCh38 chr7: 74,205,053-74,208,399 , GRCh37.p13 chr7|NW_003871064.1: 1,734,289-1,737,635 , GRCh37.p13 chr7: 73,619,383-73,622,729 LAT2
    nsv6818747copy number variation1nstd229human GRCh38 chr7: 74,222,107-74,224,807 , GRCh37.p13 chr7|NW_003871064.1: 1,751,343-1,754,043 , GRCh37.p13 chr7: 73,636,437-73,639,137 LAT2
    nsv6636936copy number variation1nstd102humanPathogenic GRCh37 chr7: 72,718,278-74,142,256 , GRCh38.p12 chr7: 73,304,281-74,727,918 ELN-AS1, FKBP6, 36 more genes
    nsv6636910copy number variation1nstd102humanPathogenic GRCh37 chr7: 72,718,278-74,143,060 , GRCh38.p12 chr7: 73,304,281-74,728,722 RNU6-1080P, ELN-AS1, 36 more genes
    nsv6636745copy number variation1nstd102humanPathogenic GRCh37 chr7: 72,718,278-74,143,240 , GRCh38.p12 chr7: 73,304,281-74,728,902 CLDN3, METTL27, 36 more genes
    nsv6636602copy number variation1nstd102humanPathogenic GRCh37 chr7: 72,643,632-74,143,060 , GRCh38.p12 chr7: 73,229,598-74,728,722 FZD9, WBSCR23, 39 more genes
    nsv6636473copy number variation1nstd102humanPathogenic GRCh37 chr7: 72,654,782-74,142,190 , GRCh38.p12 chr7: 73,240,749-74,727,852 ELN-AS1, FKBP6, 38 more genes
    nsv6634332copy number variation1nstd102humanUncertain significance GRCh37 chr7: 113,371-159,042,325 , GRCh38.p12 chr7: 113,371-159,249,635 RRBP1P1, SLC29A4P1, 2680 more genes
    nsv6619912copy number variation1nstd223human GRCh38 chr7: 74,216,862-74,274,096 , GRCh37.p13 chr7: 73,631,192-73,688,426 , GRCh37.p13 chr7|NW_003871064.1: 1,746,098-1,803,332 RFC2, LAT2
    nsv6610374copy number variation1nstd223human GRCh38 chr7: 74,211,871-74,213,702 , GRCh37.p13 chr7|NW_003871064.1: 1,741,107-1,742,938 , GRCh37.p13 chr7: 73,626,201-73,628,032 LAT2
    nsv6572117inversion1nstd223human GRCh38 chr7: 74,222,114-74,222,799 , GRCh37.p13 chr7|NW_003871064.1: 1,751,350-1,752,035 , GRCh37.p13 chr7: 73,636,444-73,637,129 LAT2
    nsv6315451copy number variation1nstd102humanPathogenic GRCh37 chr7: 72,700,942-74,142,190 , GRCh38.p12 chr7: 73,286,940-74,727,852 STX1A, METTL27, 37 more genes
    nsv6315444copy number variation1nstd102humanPathogenic GRCh37 chr7: 72,718,123-74,142,190 , GRCh38.p12 chr7: 73,304,126-74,727,852 STX1A, LOC105375350, 36 more genes
    nsv6315412copy number variation1nstd102humanPathogenic GRCh37 chr7: 72,700,996-74,142,256 , GRCh38.p12 chr7: 73,286,994-74,727,918 MLXIPL, CLDN4, 37 more genes
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