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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097863copy number variation1nstd102humanUncertain significance GRCh37 chr7: 130,020,362-130,667,121 , GRCh38.p12 chr7: 130,380,521-130,982,362 LINC-PINT, COPG2, 17 more genes
    nsv7048362inversion1nstd229human GRCh38 chr7: 130,572,248-130,572,328 , GRCh37.p13 chr7|NW_003871065.1: 251,479-251,559 , GRCh37.p13 chr7: 130,256,521-130,256,601 COPG2
    nsv7046115inversion1nstd229human GRCh38 chr7: 128,204,685-135,838,306 , GRCh37.p13 chr7: 127,844,738-135,523,054 RPL37P16, BPGM, 155 more genes
    nsv7043190inversion1nstd229human GRCh38 chr7: 123,472,699-130,834,800 , GRCh37.p13 chr7: 123,112,753-129,984,423 KCP, LINC01000, 138 more genes
    nsv6837905copy number variation1nstd229human GRCh38 chr7: 130,601,133-130,677,938 , GRCh37.p13 chr7: 130,286,011-130,362,778 , GRCh37.p13 chr7|NW_003871065.1: 280,364-357,169 COPG2, RNA5SP246, 1 more genes
    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
    nsv6837372copy number variation1nstd229human GRCh38 chr7: 130,555,631-130,556,209 , GRCh37.p13 chr7|NW_003871065.1: 234,854-235,432 COPG2
    nsv6836075copy number variation1nstd229human GRCh38 chr7: 130,536,911-130,541,315 , GRCh37.p13 chr: NaN-NaN COPG2
    nsv6835761copy number variation1nstd229human GRCh38 chr7: 130,504,160-130,517,305 , GRCh37.p13 chr7: 130,144,001-130,154,523 , GRCh37.p13 chr7|NW_003871065.1: 159,578-170,100 COPG2, MEST
    nsv6834244copy number variation1nstd229human GRCh38 chr7: 130,633,501-130,639,100 , GRCh37.p13 chr7: 130,318,370-130,323,969 , GRCh37.p13 chr7|NW_003871065.1: 312,732-318,331 COPG2
    nsv6833244copy number variation1nstd229human GRCh38 chr7: 130,580,801-130,587,600 , GRCh37.p13 chr7: 130,265,072-130,271,869 , GRCh37.p13 chr7|NW_003871065.1: 260,032-266,831 COPG2
    nsv6833068copy number variation1nstd229human GRCh38 chr7: 130,667,646-130,667,813 , GRCh37.p13 chr7|NW_003871065.1: 346,877-347,044 , GRCh37.p13 chr7: 130,352,486-130,352,653 COPG2, TSGA13
    nsv6823732copy number variation1nstd229human GRCh38 chr7: 130,507,109-130,507,155 , GRCh37.p13 chr7|NW_003871065.1: 162,527-162,573 , GRCh37.p13 chr7: 130,146,950-130,146,996 COPG2
    nsv6821929copy number variation1nstd229human GRCh38 chr7: 130,665,874-130,666,026 , GRCh37.p13 chr7: 130,350,714-130,350,866 , GRCh37.p13 chr7|NW_003871065.1: 345,105-345,257 COPG2
    nsv6818969copy number variation1nstd229human GRCh38 chr7: 130,654,408-130,654,890 , GRCh37.p13 chr7: 130,339,248-130,339,730 , GRCh37.p13 chr7|NW_003871065.1: 333,639-334,121 COPG2
    nsv6818720copy number variation1nstd229human GRCh38 chr7: 130,616,224-130,618,489 , GRCh37.p13 chr7|NW_003871065.1: 295,455-297,720 , GRCh37.p13 chr7: 130,301,095-130,303,360 COPG2
    nsv6818142copy number variation1nstd229human GRCh38 chr7: 130,541,383-130,541,884 , GRCh37.p13 chr7|NW_003871065.1: 220,610-221,111 COPG2IT1, COPG2
    nsv6636929copy number variation1nstd102humanUncertain significance GRCh37 chr7: 129,147,455-132,777,678 , GRCh38.p12 chr7: 129,507,614-133,092,918 LINC03008, TMEM209, 60 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
    nsv6575188inversion1nstd223human GRCh38 chr7: 130,663,761-130,665,092 , GRCh37.p13 chr7|NW_003871065.1: 342,992-344,323 , GRCh37.p13 chr7: 130,348,601-130,349,932 COPG2
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