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Items: 1 to 20 of 147

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148056copy number variation1nstd102humanPathogenic GRCh37 chr2: 186,698,504-223,918,111 , GRCh38.p12 chr2: 185,833,777-223,053,393 DNAJB1P1, MTCO2P17, 580 more genes
    nsv7048316inversion1nstd229human GRCh38 chr2: 217,690,925-222,070,373 , GRCh37.p13 chr2: 218,555,648-222,935,092 LOC105373895, CXCR2P1, 119 more genes
    nsv6692448copy number variation1nstd229human GRCh38 chr2: 218,161,129-218,162,496 , GRCh37.p13 chr2: 219,025,852-219,027,219 CXCR1
    nsv6685864copy number variation1nstd229human GRCh38 chr2: 216,932,763-218,687,760 , GRCh37.p13 chr2: 217,797,486-219,552,483 LOC105373872, IGFBP-AS1, 45 more genes
    nsv6346688copy number variation1nstd223human GRCh38 chr2: 218,161,128-218,162,494 , GRCh37.p13 chr2: 219,025,851-219,027,217 CXCR1
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 more genes
    nsv6313768copy number variation1nstd102humanUncertain significance GRCh37 chr2: 218,210,665-220,141,650 , GRCh38.p12 chr2: 217,345,942-219,276,928 PNKD, RNU6-136P, 73 more genes
    nsv6313686copy number variation1nstd102humanPathogenic GRCh37 chr2: 215,108,009-221,679,980 , GRCh38.p12 chr2: 214,243,285-220,815,260 BCS1L, LOC105373880, 160 more genes
    nsv6311374copy number variation2nstd102humanUncertain significance GRCh37 chr2: 218,999,525-220,435,954 , GRCh38.p12 chr2: 218,134,802-219,571,232 CHPF, WNT6, 83 more genes
    nsv6298058copy number variation1nstd186human GRCh37 chr2: 219,007,178-219,091,349 , GRCh38.p12 chr2: 218,142,455-218,226,626 CXCR1, ARPC2, 2 more genes
    nsv5904443copy number variation1nstd209human GRCh38 chr2: 218,161,128-218,162,493 , GRCh37.p13 chr2: 219,025,851-219,027,216 CXCR1
    nsv5832503copy number variation1nstd209human GRCh38 chr2: 218,161,093-218,162,506 , GRCh37.p13 chr2: 219,025,816-219,027,229 CXCR1
    nsv5581952copy number variation1nstd207human GRCh38 chr2: 218,161,128-218,162,493 , GRCh37.p13 chr2: 219,025,851-219,027,216 CXCR1
    nsv5560580sequence alteration1nstd206human GRCh38 chr2: 151,447,581-231,256,535 , GRCh37.p13 chr2: 152,304,095-232,121,248 , ATIC, 1163 more genes
    nsv5452099copy number variation1nstd206human GRCh38 chr2: 218,161,129-218,162,494 , GRCh37.p13 chr2: 219,025,852-219,027,217 CXCR1
    nsv5441156copy number variation1nstd206human GRCh38 chr2: 218,142,455-218,226,626 , GRCh37.p13 chr2: 219,007,178-219,091,349 CXCR1, LOC101928487, 2 more genes
    nsv5303662copy number variation1nstd204human GRCh38.p13 chr2: 218,142,430-218,226,652 , GRCh37.p13 chr2: 219,007,153-219,091,375 LOC101928487, CXCR1, 2 more genes
    nsv5303363copy number variation1nstd204human GRCh38.p13 chr2: 218,161,119-218,162,503 , GRCh37.p13 chr2: 219,025,842-219,027,226 CXCR1
    nsv5218966copy number variation1nstd204human GRCh38.p13 chr2: 218,162,907-218,187,654 , GRCh37.p13 chr2: 219,027,630-219,052,377 CXCR1
    nsv5211147copy number variation1nstd204human GRCh38.p13 chr2: 218,161,093-218,162,506 , GRCh37.p13 chr2: 219,025,816-219,027,229 CXCR1
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