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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7141666copy number variation1nstd232human GRCh37.p13 chr5: 179,540,304-179,540,512 , GRCh38.p12 chr5: 180,113,304-180,113,512 RASGEF1C
    nsv7049819inversion1nstd229human GRCh38 chr5: 179,951,229-180,200,012 , GRCh37.p13 chr5: 179,378,229-179,627,012 RNF130, LOC646058, 2 more genes
    nsv7045408inversion1nstd229human GRCh38 chr5: 180,190,212-180,191,515 , GRCh37.p13 chr5: 179,617,212-179,618,515 RASGEF1C
    nsv6797255copy number variation1nstd229human GRCh38 chr5: 180,169,042-180,169,094 , GRCh37.p13 chr5: 179,596,042-179,596,094 RASGEF1C
    nsv6796769copy number variation1nstd229human GRCh38 chr5: 180,203,724-180,206,265 , GRCh37.p13 chr5: 179,630,724-179,633,265 RASGEF1C
    nsv6795649copy number variation1nstd229human GRCh38 chr5: 180,111,501-180,197,100 , GRCh37.p13 chr5: 179,538,501-179,624,100 RASGEF1C
    nsv6795562copy number variation1nstd229human GRCh38 chr5: 180,110,030-180,111,522 , GRCh37.p13 chr5: 179,537,030-179,538,522 RASGEF1C
    nsv6795545copy number variation1nstd229human GRCh38 chr5: 180,071,401-180,508,100 , GRCh37.p13 chr5: 179,498,401-179,935,100 MAPK9, CNOT6, 8 more genes
    nsv6793961copy number variation1nstd229human GRCh38 chr5: 180,131,677-180,610,761 , GRCh37.p13 chr5: 179,558,677-180,037,761 LOC102725231, CNOT6, 9 more genes
    nsv6792684copy number variation1nstd229human GRCh38 chr5: 180,195,486-180,200,653 , GRCh37.p13 chr5: 179,622,486-179,627,653 RASGEF1C
    nsv6791358copy number variation1nstd229human GRCh38 chr5: 180,143,763-180,159,043 , GRCh37.p13 chr5: 179,570,763-179,586,043 RASGEF1C
    nsv6790734copy number variation1nstd229human GRCh38 chr5: 180,153,171-180,153,280 , GRCh37.p13 chr5: 179,580,171-179,580,280 RASGEF1C
    nsv6788934copy number variation1nstd229human GRCh38 chr5: 180,095,318-180,100,009 , GRCh37.p13 chr5: 179,522,318-179,527,009 RASGEF1C
    nsv6788929copy number variation1nstd229human GRCh38 chr5: 180,180,680-180,184,217 , GRCh37.p13 chr5: 179,607,680-179,611,217 RASGEF1C
    nsv6788632copy number variation1nstd229human GRCh38 chr5: 180,096,401-180,286,200 , GRCh37.p13 chr5: 179,523,401-179,713,200 RASGEF1C, RPS8P7, 2 more genes
    nsv6788369copy number variation1nstd229human GRCh38 chr5: 180,209,427-180,212,858 , GRCh37.p13 chr5: 179,636,427-179,639,858 RASGEF1C
    nsv6787720copy number variation1nstd229human GRCh38 chr5: 180,189,070-180,222,509 , GRCh37.p13 chr5: 179,616,070-179,649,509 RASGEF1C
    nsv6787529copy number variation1nstd229human GRCh38 chr5: 180,197,568-180,225,556 , GRCh37.p13 chr5: 179,624,568-179,652,556 RPS8P7, RASGEF1C
    nsv6786157copy number variation1nstd229human GRCh38 chr5: 180,160,735-180,165,978 , GRCh37.p13 chr5: 179,587,735-179,592,978 RASGEF1C
    nsv6786117copy number variation1nstd229human GRCh38 chr5: 179,803,021-180,143,476 , GRCh37.p13 chr5: 179,230,021-179,570,476 RASGEF1C, MIR340, 10 more genes
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