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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098428copy number variation1nstd102humanUncertain significance GRCh37 chr9: 133,755,435-133,761,070 , GRCh38.p12 chr9: 130,880,048-130,885,683 ABL1
    nsv7098427copy number variation1nstd102humanUncertain significance GRCh37 chr9: 131,857,676-135,942,612 , GRCh38.p12 chr9: 129,095,397-133,067,225 ASS1, SETX, 86 more genes
    nsv7098062copy number variation1nstd102humanUncertain significance GRCh37 chr9: 133,589,707-133,589,862 , GRCh38.p12 chr9: 130,714,320-130,714,475 ABL1
    nsv7097690copy number variation1nstd102humanUncertain significance GRCh37 chr9: 131,087,402-141,016,451 , GRCh38.p12 chr9: 128,325,123-138,121,999 REXO4, TOR1B, 324 more genes
    nsv7075268inversion1nstd229human GRCh38 chr9: 128,672,751-137,526,572 , GRCh37.p13 chr9: 131,435,030-140,421,024 PNPLA7, NSMF, 293 more genes
    nsv7065210inversion1nstd229human GRCh38 chr9: 130,796,685-130,796,736 , GRCh37.p13 chr9: 133,672,072-133,672,123 ABL1
    nsv6878042copy number variation1nstd229human GRCh38 chr9: 130,835,001-130,835,504 , GRCh37.p13 chr9: 133,710,388-133,710,891 ABL1
    nsv6875797copy number variation1nstd229human GRCh38 chr9: 130,752,641-130,756,874 , GRCh37.p13 chr9: 133,628,028-133,632,261 ABL1
    nsv6874562copy number variation1nstd229human GRCh38 chr9: 130,797,761-130,797,868 , GRCh37.p13 chr9: 133,673,148-133,673,255 ABL1
    nsv6874515copy number variation1nstd229human GRCh38 chr9: 130,862,500-130,862,664 , GRCh37.p13 chr9: 133,737,887-133,738,051 ABL1
    nsv6873238copy number variation1nstd229human GRCh38 chr9: 130,819,511-130,819,551 , GRCh37.p13 chr9: 133,694,898-133,694,938 ABL1
    nsv6872030copy number variation1nstd229human GRCh38 chr9: 130,807,994-130,823,055 , GRCh37.p13 chr9: 133,683,381-133,698,442 ABL1
    nsv6870653copy number variation1nstd229human GRCh38 chr9: 130,842,907-130,843,497 , GRCh37.p13 chr9: 133,718,294-133,718,884 ABL1
    nsv6870237copy number variation1nstd229human GRCh38 chr9: 130,761,501-130,765,100 , GRCh37.p13 chr9: 133,636,888-133,640,487 ABL1
    nsv6870017copy number variation1nstd229human GRCh38 chr9: 130,718,010-130,718,046 , GRCh37.p13 chr9: 133,593,397-133,593,433 ABL1
    nsv6869899copy number variation1nstd229human GRCh38 chr9: 130,745,862-130,748,294 , GRCh37.p13 chr9: 133,621,249-133,623,681 ABL1
    nsv6869399copy number variation1nstd229human GRCh38 chr9: 130,729,682-130,737,146 , GRCh37.p13 chr9: 133,605,069-133,612,533 ABL1
    nsv6867724copy number variation1nstd229human GRCh38 chr9: 130,879,601-130,910,400 , GRCh37.p13 chr9: 133,754,988-133,785,787 FIBCD1, QRFP, 1 more genes
    nsv6867232copy number variation1nstd229human GRCh38 chr9: 130,826,301-131,964,500 , GRCh37.p13 chr9: 133,701,688-134,839,887 SNORD62A, FAM78A, 21 more genes
    nsv6866978copy number variation1nstd229human GRCh38 chr9: 130,724,532-130,729,549 , GRCh37.p13 chr9: 133,599,919-133,604,936 ABL1, RPL37P17
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