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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6129846insertion1nstd186human GRCh37 chr17: 30,570,449-30,570,449 , GRCh38.p12 chr17: 32,243,430-32,243,430 RHOT1
    nsv6129431insertion1nstd186human GRCh37 chr17: 30,565,028-30,565,028 , GRCh38.p12 chr17: 32,238,009-32,238,009 RHOT1
    nsv6116082copy number variation1nstd186human GRCh37 chr17: 30,505,931-30,507,076 , GRCh38.p12 chr17: 32,178,912-32,180,057 RHOT1
    nsv5977091insertion1nstd209human GRCh38 chr17: 32,243,426-32,243,426 , GRCh37.p13 chr17: 30,570,445-30,570,445 RHOT1
    nsv5946796copy number variation1nstd209human GRCh38 chr17: 32,179,845-32,179,995 , GRCh37.p13 chr17: 30,506,864-30,507,014 RHOT1
    nsv5942530copy number variation1nstd209human GRCh38 chr17: 32,218,424-32,218,730 , GRCh37.p13 chr17: 30,545,443-30,545,749 RHOT1
    nsv5940381copy number variation1nstd209human GRCh38 chr17: 32,151,614-32,154,330 , GRCh37.p13 chr17: 30,478,633-30,481,349 RHOT1, ARGFXP2
    nsv5874158copy number variation1nstd209human GRCh38 chr17: 32,152,866-32,154,215 , GRCh37.p13 chr17: 30,479,885-30,481,234 RHOT1
    nsv5697303mobile element insertion1nstd211human GRCh38 chr17: 32,223,255-32,223,255 , GRCh37.p13 chr17: 30,550,274-30,550,274 RHOT1
    nsv5660178insertion2nstd207human GRCh38 chr17: 32,243,426-32,243,426 , GRCh37.p13 chr17: 30,570,445-30,570,445 RHOT1
    nsv5651235insertion1nstd207human GRCh38 chr17: 32,238,009-32,238,009 , GRCh37.p13 chr17: 30,565,028-30,565,028 RHOT1
    nsv5644554insertion1nstd207human GRCh38 chr17: 32,179,980-32,179,980 , GRCh37.p13 chr17: 30,506,999-30,506,999 RHOT1
    nsv5598013copy number variation1nstd207human GRCh38 chr17: 32,238,779-32,238,846 , GRCh37.p13 chr17: 30,565,798-30,565,865 RHOT1
    nsv5597687copy number variation1nstd207human GRCh38 chr17: 32,179,840-32,179,990 , GRCh37.p13 chr17: 30,506,859-30,507,009 RHOT1
    nsv5561493sequence alteration1nstd206human GRCh37.p13 chr17: 30,380,978-30,536,565 , GRCh38 chr17: 32,053,959-32,209,546 RHOT1, LRRC37B, 4 more genes
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5544808insertion1nstd206human GRCh38 chr17: 32,243,430-32,243,430 , GRCh37.p13 chr17: 30,570,449-30,570,449 RHOT1
    nsv5540369insertion1nstd206human GRCh38 chr17: 32,238,009-32,238,009 , GRCh37.p13 chr17: 30,565,028-30,565,028 RHOT1
    nsv5532625copy number variation1nstd206human GRCh38 chr17: 32,148,559-32,153,464 , GRCh37.p13 chr17: 30,475,578-30,480,483 ARGFXP2, RHOT1
    nsv5522467copy number variation1nstd206human GRCh38 chr17: 32,178,914-32,179,182 , GRCh37.p13 chr17: 30,505,933-30,506,201 RHOT1
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