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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148263copy number variation1nstd102humanPathogenic GRCh38 chr9: 102,995,214-108,903,040 , GRCh37.p13 chr9: 105,757,496-111,665,320 ACTL7B, OR13C3, 88 more genes
    nsv7145274copy number variation1nstd232human GRCh37.p13 chr9: 107,624,919-107,625,023 , GRCh38.p12 chr9: 104,862,638-104,862,742 ABCA1
    nsv7141857copy number variation1nstd232human GRCh37.p13 chr9: 107,637,039-107,637,130 , GRCh38.p12 chr9: 104,874,758-104,874,849 ABCA1
    nsv7098191copy number variation1nstd102humanUncertain significance GRCh37 chr9: 107,546,596-108,536,361 , GRCh38.p12 chr9: 104,784,315-105,774,080 TMEM38B, CT70, 14 more genes
    nsv7097678copy number variation1nstd102humanLikely pathogenic GRCh37 chr9: 107,547,657-107,550,868 , GRCh38.p12 chr9: 104,785,376-104,788,587 ABCA1
    nsv7070748inversion1nstd229human GRCh38 chr9: 104,877,831-104,877,974 , GRCh37.p13 chr9: 107,640,112-107,640,255 ABCA1
    nsv6877356copy number variation1nstd229human GRCh38 chr9: 104,914,153-104,916,451 , GRCh37.p13 chr9: 107,676,434-107,678,732 ABCA1
    nsv6876364copy number variation1nstd229human GRCh38 chr9: 104,791,907-104,792,583 , GRCh37.p13 chr9: 107,554,188-107,554,864 ABCA1
    nsv6875457copy number variation1nstd229human GRCh38 chr9: 104,918,978-105,002,057 , GRCh37.p13 chr9: 107,681,259-107,764,338 CT70, LOC105376196, 1 more genes
    nsv6873599copy number variation1nstd229human GRCh38 chr9: 104,863,701-104,867,200 , GRCh37.p13 chr9: 107,625,982-107,629,481 ABCA1
    nsv6873544copy number variation1nstd229human GRCh38 chr9: 104,825,729-104,826,087 , GRCh37.p13 chr9: 107,588,010-107,588,368 ABCA1
    nsv6869199copy number variation1nstd229human GRCh38 chr9: 104,859,395-104,859,460 , GRCh37.p13 chr9: 107,621,676-107,621,741 ABCA1
    nsv6867275copy number variation1nstd229human GRCh38 chr9: 104,833,909-104,834,826 , GRCh37.p13 chr9: 107,596,190-107,597,107 ABCA1
    nsv6864571copy number variation1nstd229human GRCh38 chr9: 104,913,872-104,920,521 , GRCh37.p13 chr9: 107,676,153-107,682,802 ABCA1
    nsv6861414copy number variation1nstd229human GRCh38 chr9: 104,873,901-104,881,389 , GRCh37.p13 chr9: 107,636,182-107,643,670 ABCA1
    nsv6861301copy number variation1nstd229human GRCh38 chr9: 104,803,039-104,803,211 , GRCh37.p13 chr9: 107,565,320-107,565,492 ABCA1
    nsv6859413copy number variation1nstd229human GRCh38 chr9: 104,763,473-104,779,785 , GRCh37.p13 chr9: 107,525,754-107,542,066 NIPSNAP3B, ABCA1
    nsv6634454copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-131,603,223 , GRCh38.p12 chr9: 203,861-128,840,944 HNRNPA1P41, GAS1RR, 1868 more genes
    nsv6565843inversion1nstd223human GRCh38 chr9: 104,913,798-104,914,520 , GRCh37.p13 chr9: 107,676,079-107,676,801 ABCA1
    nsv6562843inversion1nstd223human GRCh38 chr9: 104,859,980-104,860,703 , GRCh37.p13 chr9: 107,622,261-107,622,984 ABCA1
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