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Items: 1 to 20 of 226

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099240copy number variation1nstd231human GRCh38.p12 chr1: 159,722,599-161,418,916 , GRCh37 chr1: 159,692,389-161,388,706 APOA2, ATP1A2, 87 more genes
    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
    nsv7038321inversion1nstd229human GRCh38 chr1: 161,256,421-161,292,178 , GRCh37.p13 chr1: 161,226,211-161,261,968 LOC107985221, PCP4L1, 1 more genes
    nsv6643578copy number variation1nstd229human GRCh38 chr1: 161,276,336-161,282,066 , GRCh37.p13 chr1: 161,246,126-161,251,856 LOC105371472, PCP4L1
    nsv6643577copy number variation1nstd229human GRCh38 chr1: 161,263,878-161,268,804 , GRCh37.p13 chr1: 161,233,668-161,238,594 PCP4L1
    nsv6643375copy number variation1nstd229human GRCh38 chr1: 161,265,744-161,271,142 , GRCh37.p13 chr1: 161,235,534-161,240,932 PCP4L1
    nsv6643151copy number variation1nstd229human GRCh38 chr1: 161,056,580-161,363,232 , GRCh37.p13 chr1: 161,026,370-161,333,022 NR1I3, FCER1G, 23 more genes
    nsv6637016copy number variation1nstd102humanUncertain significance GRCh37 chr1: 161,207,985-161,437,998 , GRCh38.p12 chr1: 161,238,195-161,468,208 TRL-CAG1-4, TRD-GTC2-2, 34 more genes
    nsv6634338copy number variation1nstd102humanLikely pathogenic GRCh37 chr1: 161,216,755-161,409,359 , GRCh38.p12 chr1: 161,246,965-161,439,569 MPZ, RRM2P2, 15 more genes
    nsv6625891copy number variation1nstd224human GRCh37 chr1: 161,239,471-161,261,041 , GRCh38.p12 chr1: 161,269,681-161,291,251 LOC107985221, PCP4L1, 1 more genes
    nsv6625853copy number variation1nstd224human GRCh37 chr1: 161,239,471-161,596,027 , GRCh38.p12 chr1: 161,269,681-161,626,237 FCGR3A, SDHC, 51 more genes
    nsv6625852copy number variation1nstd224human GRCh37 chr1: 161,211,678-161,398,477 , GRCh38.p12 chr1: 161,241,888-161,428,687 SDHC, LOC148430, 12 more genes
    nsv6535849inversion1nstd223human GRCh38 chr1: 161,263,875-161,264,543 , GRCh37.p13 chr1: 161,233,665-161,234,333 PCP4L1
    nsv6333389copy number variation1nstd223human GRCh38 chr1: 161,265,736-161,271,141 , GRCh37.p13 chr1: 161,235,526-161,240,931 PCP4L1
    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
    nsv6315425copy number variation1nstd102humanPathogenic GRCh37 chr1: 161,224,742-161,429,290 , GRCh38.p12 chr1: 161,254,952-161,459,500 CFAP126, TRL-CAG1-1, 26 more genes
    nsv6313872copy number variation1nstd102humanLikely pathogenic GRCh37 chr1: 161,207,984-161,404,272 , GRCh38.p12 chr1: 161,238,194-161,434,482 MPZ, RRM2P2, 13 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
    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
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