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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5925537copy number variation1nstd209human GRCh38 chr9: 86,321,136-86,321,511 , GRCh37.p13 chr9: 88,936,051-88,936,426 TUT7
    nsv5036269inversion1nstd200human GRCh38 chr9: 79,108,237-87,224,469 , GRCh37.p13 chr9: 81,723,153-89,839,384 , RMI1, 100 more genes
    nsv4972943copy number variation1nstd200human GRCh38 chr9: 86,291,758-86,294,311 , GRCh37.p13 chr9: 88,906,673-88,909,226 TUT7
    nsv4814331copy number variation1nstd200human GRCh37 chr9: 88,906,673-88,909,226 , GRCh38.p12 chr9: 86,291,758-86,294,311 TUT7
    nsv4675092copy number variation1nstd102humanUncertain significance GRCh37 chr9: 88,622,823-88,951,838 , GRCh38.p12 chr9: 86,007,908-86,336,923 GOLM1, NAA35, 6 more genes
    nsv4671564copy number variation2nstd186human GRCh37 chr9: 88,896,976-88,911,047 , GRCh38.p12 chr9: 86,282,061-86,296,132 ISCA1, TUT7
    nsv4610280copy number variation1nstd183human GRCh37 chr9: 88,902,619-88,902,999 , GRCh38.p12 chr9: 86,287,704-86,288,084 TUT7
    nsv4607767copy number variation2nstd183human GRCh37 chr9: 88,896,976-88,911,047 , GRCh38.p12 chr9: 86,282,061-86,296,132 TUT7, ISCA1
    nsv4572670mobile element insertion1nstd166human GRCh37.p13 chr9: 88,960,977-88,960,977 , GRCh38.p12 chr9: 86,346,062-86,346,062 TUT7
    nsv4488930mobile element insertion1nstd166human GRCh37.p13 chr9: 88,961,067-88,961,067 , GRCh38.p12 chr9: 86,346,152-86,346,152 TUT7
    nsv4457273copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-141,020,388 , GRCh38.p12 chr9: 203,861-138,125,936 CDRT15P14, MIR548AW, 2167 more genes
    nsv4455186copy number variation1nstd102humanPathogenic GRCh37 chr9: 71,416,475-141,020,389 , GRCh38.p12 chr9: 68,801,559-138,125,937 LOC105376327, ENG, 1304 more genes
    nsv4349215copy number variation1nstd102humanPathogenic GRCh37 chr9: 79,520,825-97,201,274 , GRCh38.p12 chr9: 76,905,909-94,438,992 SPATA31C1, LINC02893, 280 more genes
    nsv4314197inversion1nstd166human GRCh37.p13 chr9: 88,968,744-90,042,303 , GRCh38.p12 chr9: 86,353,829-87,427,388 , TUT7, 14 more genes
    nsv4189525copy number variation1nstd166human GRCh37.p13 chr9: 88,963,185-88,965,972 , GRCh38.p12 chr9: 86,348,270-86,351,057 TUT7
    nsv4177066copy number variation1nstd166human GRCh37.p13 chr9: 88,922,688-88,922,752 , GRCh38.p12 chr9: 86,307,773-86,307,837 TUT7
    nsv3955380insertion1nstd168human GRCh38 chr9: 86,293,914-86,296,630 , GRCh37.p13 chr9: 88,908,829-88,911,545 TUT7
    nsv3922684copy number variation2nstd102humanPathogenic NCBI36 chr9: 194,193-140,193,718 , GRCh38 chr9: 193,412-138,179,445 , GRCh37 chr9: 204,193-141,073,897 TDRD7, CDK9, 2170 more genes
    nsv3921598copy number variation1nstd102humanPathogenic GRCh38 chr9: 203,861-138,125,937 , NCBI36 chr9: 193,861-140,140,210 , GRCh37 chr9: 203,861-141,020,389 PGAP4, ECPAS, 2167 more genes
    nsv3920713copy number variation1nstd102humanPathogenic NCBI36 chr9: 193,862-140,140,210 , GRCh38 chr9: 203,862-138,125,937 , GRCh37 chr9: 203,862-141,020,389 ABHD17B, LOC100533707, 2167 more genes
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