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Items: 1 to 20 of 132

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097864copy number variation1nstd102humanPathogenic GRCh37 chr7: 130,781,014-150,301,047 , GRCh38.p12 chr7: 131,096,255-150,603,959 NOBOX, FAM131B, 466 more genes
    nsv7054997inversion1nstd229human GRCh38 chr7: 133,111,037-133,246,350 , GRCh37.p13 chr7: 132,795,797-132,931,106 ST13P7
    nsv7046115inversion1nstd229human GRCh38 chr7: 128,204,685-135,838,306 , GRCh37.p13 chr7: 127,844,738-135,523,054 RPL37P16, BPGM, 155 more genes
    nsv7040506inversion1nstd229human GRCh38 chr7: 133,167,808-133,169,154 , GRCh37.p13 chr7: 132,852,566-132,853,912 ST13P7
    nsv6837835copy number variation1nstd229human GRCh38 chr7: 128,205,538-135,806,503 , GRCh37.p13 chr7: 127,845,591-135,491,251 RN7SL81P, IMP3P2, 155 more genes
    nsv6833402copy number variation1nstd229human GRCh38 chr7: 133,161,683-133,183,967 , GRCh37.p13 chr7: 132,846,441-132,868,725 ST13P7
    nsv6833009copy number variation1nstd229human GRCh38 chr7: 133,167,969-133,168,318 , GRCh37.p13 chr7: 132,852,727-132,853,076 ST13P7
    nsv6823151copy number variation1nstd229human GRCh38 chr7: 133,127,879-133,321,805 , GRCh37.p13 chr7: 132,812,638-133,006,559 RPS15AP23, EXOC4, 2 more genes
    nsv6822762copy number variation1nstd229human GRCh38 chr7: 132,157,507-133,444,065 , GRCh37.p13 chr7: 131,842,266-133,128,819 LOC102724906, LOC729998, 13 more genes
    nsv6820752copy number variation1nstd229human GRCh38 chr7: 133,163,657-133,385,151 , GRCh37.p13 chr7: 132,848,415-133,069,905 MIR6133, RPS15AP23, 2 more genes
    nsv6819654copy number variation1nstd229human GRCh38 chr7: 133,091,217-133,185,868 , GRCh37.p13 chr7: 132,775,977-132,870,626 ST13P7, LOC105375512
    nsv6636458copy number variation1nstd102humanPathogenic GRCh37 chr7: 131,779,213-149,042,734 , GRCh38.p12 chr7: 132,094,454-149,345,643 TRBD2, TRBV5-2, 403 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
    nsv6560945inversion1nstd223human GRCh38 chr7: 129,758,099-137,582,370 , GRCh37.p13 chr7: 129,397,939-137,267,116 LOC100506937, SLC35B4, 115 more genes
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 AOC1, ACHE, 2682 more genes
    nsv6313876copy number variation1nstd102humanPathogenic GRCh37 chr7: 124,103,982-134,693,590 , GRCh38.p12 chr7: 124,463,928-135,008,839 IMPDH1, SSU72L6, 174 more genes
    nsv6135888copy number variation1nstd213human GRCh37 chr7: 130,260,000-136,190,001 , GRCh38.p12 chr7: 130,575,728-136,505,253 AKR1B1, MKLN1, 81 more genes
    nsv6135557copy number variation1nstd213human GRCh37 chr7: 131,800,000-133,210,001 , GRCh38.p12 chr7: 132,115,241-133,525,247 CHCHD3, EXOC4, 13 more genes
    nsv6062462insertion1nstd212human GRCh38 chr7: 133,170,608-133,170,608 , GRCh37.p13 chr7: 132,855,366-132,855,366 ST13P7
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
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