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Items: 1 to 20 of 101

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7054895inversion1nstd229human GRCh38 chr2: 229,787,965-232,576,060 , GRCh37.p13 chr2: 230,652,681-233,440,770 GPR55, RN7SL834P, 80 more genes
    nsv7045289inversion1nstd229human GRCh38 chr2: 231,331,222-231,542,017 , GRCh37.p13 chr2: 232,195,934-232,406,728 SNORD20, NCL, 12 more genes
    nsv7044524inversion1nstd229human GRCh38 chr2: 231,260,277-231,483,600 , GRCh37.p13 chr2: 232,124,990-232,348,311 SNORA75, SNORD20, 8 more genes
    nsv6697310copy number variation1nstd229human GRCh38 chr2: 231,016,947-231,455,744 , GRCh37.p13 chr2: 231,881,662-232,320,455 B3GNT7, RPS28P4, 13 more genes
    nsv6687979copy number variation1nstd229human GRCh38 chr2: 231,400,801-231,409,500 , GRCh37.p13 chr2: 232,265,512-232,274,211 B3GNT7
    nsv6687695copy number variation1nstd229human GRCh38 chr2: 231,332,801-231,398,700 , GRCh37.p13 chr2: 232,197,513-232,263,411 MIR4777, B3GNT7, 1 more genes
    nsv6338025copy number variation1nstd223human GRCh38 chr2: 231,400,767-231,408,396 , GRCh37.p13 chr2: 232,265,478-232,273,107 B3GNT7
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 more genes
    nsv6313683copy number variation1nstd102humanPathogenic GRCh37 chr2: 228,807,574-235,475,892 , GRCh38.p12 chr2: 227,942,858-234,567,248 RNU7-9P, SCARNA5, 143 more genes
    nsv6313668copy number variation1nstd102humanPathogenic GRCh37 chr2: 219,606,537-239,217,703 , GRCh38.p12 chr2: 218,741,814-238,309,062 LOC105373947, RN7SL764P, 357 more genes
    nsv6311650copy number variation2nstd102humanUncertain significance GRCh37 chr2: 231,033,840-234,978,657 , GRCh38.p12 chr2: 230,169,124-234,070,013 SP110, LINC00471, 112 more genes
    nsv6134539copy number variation1nstd213human GRCh37 chr2: 231,850,000-233,400,001 , GRCh38.p12 chr2: 230,985,285-232,535,291 ALPI, ALPP, 47 more genes
    nsv5447756copy number variation1nstd206human GRCh38 chr2: 231,400,935-231,408,572 , GRCh37.p13 chr2: 232,265,646-232,273,283 B3GNT7
    nsv5210239copy number variation1nstd204human GRCh38.p13 chr2: 231,191,801-231,414,900 , GRCh37.p13 chr2: 232,056,515-232,279,611 B3GNT7, MIR4777, 2 more genes
    nsv5208702copy number variation1nstd204human GRCh38.p13 chr2: 231,354,696-231,414,884 , GRCh37.p13 chr2: 232,219,408-232,279,595 ARMC9, MIR4777, 1 more genes
    nsv4917353copy number variation1nstd200human GRCh38 chr2: 231,400,816-231,408,416 , GRCh37.p13 chr2: 232,265,527-232,273,127 B3GNT7
    nsv4806251copy number variation1nstd200human GRCh37 chr2: 232,265,476-232,273,109 , GRCh38.p12 chr2: 231,400,765-231,408,398 B3GNT7
    nsv4728725copy number variation1nstd102humanPathogenic GRCh37 chr2: 178,397,959-243,007,457 , GRCh38.p12 chr2: 177,533,231-242,065,306 LOC105376755, FZD7, 1013 more genes
    nsv4673913copy number variation1nstd102humanPathogenic GRCh37 chr2: 230,814,690-242,783,384 , GRCh38.p12 chr2: 229,949,974-241,841,232 MIR2467, D2HGDH, 270 more genes
    nsv4595385copy number variation1nstd183human GRCh37 chr2: 232,264,786-232,265,892 , GRCh38.p12 chr2: 231,400,075-231,401,181 B3GNT7
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