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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5705894mobile element insertion1nstd211human GRCh38 chr9: 72,335,255-72,335,255 , GRCh37.p13 chr9: 74,950,171-74,950,171 LINC01504
    nsv5696405mobile element insertion1nstd211human GRCh38 chr9: 72,320,318-72,320,318 , GRCh37.p13 chr9: 74,935,234-74,935,234 LINC01504
    nsv5550001insertion1nstd206human GRCh38 chr9: 72,335,255-72,335,288 , GRCh37.p13 chr9: 74,950,171-74,950,204 LINC01504
    nsv5139227mobile element insertion1nstd203human GRCh38 chr9: 72,335,236-72,335,255 , GRCh37.p13 chr9: 74,950,152-74,950,171 LINC01504
    nsv5134561mobile element insertion1nstd203human GRCh38 chr9: 72,311,500-72,311,500 , GRCh37.p13 chr9: 74,926,416-74,926,416 LINC01504
    nsv5132742mobile element insertion1nstd203human GRCh38 chr9: 72,335,240-72,335,255 , GRCh37.p13 chr9: 74,950,156-74,950,171 LINC01504
    nsv5122805mobile element insertion1nstd203human GRCh38 chr9: 72,335,237-72,335,255 , GRCh37.p13 chr9: 74,950,153-74,950,171 LINC01504
    nsv4968361copy number variation1nstd200human GRCh38 chr9: 72,339,177-72,342,087 , GRCh37.p13 chr9: 74,954,093-74,957,003 LINC01504
    nsv4954818copy number variation1nstd200human GRCh38 chr9: 72,311,635-72,313,463 , GRCh37.p13 chr9: 74,926,551-74,928,379 LINC01504
    nsv4814781copy number variation1nstd200human GRCh37 chr9: 74,926,551-74,928,376 , GRCh38.p12 chr9: 72,311,635-72,313,460 LINC01504
    nsv4728828copy number variation1nstd102humanUncertain significance GRCh37 chr9: 74,173,350-75,170,163 , GRCh38.p12 chr9: 71,558,434-72,555,247 LOC100289320, TMC1, 16 more genes
    nsv4679980copy number variation1nstd189human GRCh37.p13 chr9: 74,891,446-75,224,013 , GRCh38.p12 chr9: 72,276,530-72,609,097 ZFAND5, TMC1, 6 more genes
    nsv4480078mobile element insertion1nstd166human GRCh37.p13 chr9: 74,950,153-74,950,153 , GRCh38.p12 chr9: 72,335,237-72,335,237 LINC01504
    nsv4457273copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-141,020,388 , GRCh38.p12 chr9: 203,861-138,125,936 CDRT15P14, MIR548AW, 2167 more genes
    nsv4455928copy number variation1nstd102humanPathogenic GRCh37 chr9: 70,974,661-81,829,792 , GRCh38.p12 chr9: 68,359,745-79,214,877 RPL35AP21, LOC105376097, 134 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
    nsv4436161complex substitution1nstd102humanLikely pathogenic GRCh38.p12 chr9: 23,524,428-84,744,973 , GRCh37 chr9: 23,524,426-87,359,888 ACO1, ALDH1A1, 779 more genes
    nsv4183604copy number variation1nstd166human GRCh37.p13 chr9: 74,922,731-74,926,765 , GRCh38.p12 chr9: 72,307,815-72,311,849 LINC01504
    nsv3955587insertion1nstd168human GRCh38 chr9: 72,251,336-72,307,235 , GRCh37.p13 chr9: 74,866,252-74,922,151 GDA, LOC100289320, 2 more genes
    nsv3923526copy number variation1nstd102humanPathogenic NCBI36 chr9: 74,029,084-79,136,863 , GRCh37 chr9: 74,839,264-79,947,043 , GRCh38 chr9: 72,224,348-77,332,127 GCNT1, NMRK1, 65 more genes
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