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Items: 1 to 20 of 148

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099241copy number variation1nstd231human GRCh38.p12 chr1: 161,703,753-165,575,316 , GRCh37 chr1: 161,673,543-165,544,553 LMX1A, DDR2, 49 more genes
    nsv7095487copy number variation1nstd102humanUncertain significance GRCh37 chr1: 161,279,609-161,751,809 , GRCh38.p12 chr1: 161,309,819-161,782,019 FCGR2C, RNU6-481P, 56 more genes
    nsv7057537inversion1nstd229human GRCh38 chr1: 161,493,525-166,518,262 , GRCh37.p13 chr1: 161,463,315-166,487,499 LOC107985451, ALDH9A1, 88 more genes
    nsv7046634inversion1nstd229human GRCh38 chr1: 161,724,713-161,728,493 , GRCh37.p13 chr1: 161,694,503-161,698,283 FCRLB
    nsv7042802inversion1nstd229human GRCh38 chr1: 159,324,839-163,640,188 , GRCh37.p13 chr1: 159,294,629-163,609,919 TRG-GCC2-1, LOC107985220, 178 more genes
    nsv7039884inversion1nstd229human GRCh38 chr1: 159,817,036-167,858,499 , GRCh37.p13 chr1: 159,786,826-167,827,737 TRP-AGG2-1, FCGR2C, 228 more genes
    nsv6643393copy number variation1nstd229human GRCh38 chr1: 161,726,193-161,726,225 , GRCh37.p13 chr1: 161,695,983-161,696,015 FCRLB
    nsv6332269copy number variation1nstd223human GRCh38 chr1: 160,388,767-162,811,116 , GRCh37.p13 chr1: 160,358,557-162,780,906 ATF6-DT, RPS23P10, 119 more genes
    nsv6326199copy number variation1nstd223human GRCh38 chr1: 161,604,876-161,741,092 , GRCh37.p13 chr1: 161,574,666-161,710,882 FCRLB, TRL-CAA6-1, 7 more genes
    nsv6313604copy number variation1nstd102humanPathogenic GRCh37 chr1: 160,417,296-166,197,042 , GRCh38.p12 chr1: 160,447,506-166,227,805 USF1, TRE-CTC1-3, 161 more genes
    nsv6310598copy number variation1nstd102humanUncertain significance GRCh37 chr1: 161,645,027-161,772,082 , GRCh38.p12 chr1: 161,675,237-161,802,292 FCGR2B, FCRLB, 6 more genes
    nsv6310595copy number variation2nstd102humanUncertain significance GRCh37 chr1: 158,581,054-162,750,036 , GRCh38.p12 chr1: 158,611,264-162,780,246 IGSF8, SETP9, 193 more genes
    nsv6133934copy number variation1nstd213human GRCh37 chr1: 161,630,000-164,240,001 , GRCh38.p12 chr1: 161,660,210-164,270,764 FCGR2B, NOS1AP, 35 more genes
    nsv6133933copy number variation1nstd213human GRCh37 chr1: 161,620,000-196,730,001 , GRCh38.p12 chr1: 161,650,210-196,760,871 FASLG, SERPINC1, 510 more genes
    nsv6133590copy number variation1nstd213human GRCh37 chr1: 161,630,000-161,880,001 , GRCh38.p12 chr1: 161,660,210-161,910,211 FCGR2B, DUSP12, 7 more genes
    nsv5981898copy number variation1nstd212human GRCh38 chr1: 161,726,280-161,726,454 , GRCh37.p13 chr1: 161,696,070-161,696,244 FCRLB
    nsv5969343inversion1nstd209human GRCh38 chr1: 161,566,673-161,918,703 , GRCh37.p13 chr1: 161,536,463-161,888,493 FCGR2B, FCGR3B, 12 more genes
    nsv5881058copy number variation1nstd209human GRCh38 chr1: 161,697,901-161,830,547 , GRCh37.p13 chr1: 161,667,691-161,800,337 DUSP12, ATF6, 4 more genes
    nsv5381285copy number variation2nstd102humanUncertain significance GRCh37 chr1: 130,980,840-248,900,000 , GRCh38.p12 chr1: 120,324,463-248,736,699 , DCST1, 2428 more genes
    nsv4903969copy number variation1nstd200human GRCh38 chr1: 161,726,991-161,748,682 , GRCh37.p13 chr1: 161,696,781-161,718,472 DUSP12, FCRLB, 1 more genes
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