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Items: 1 to 20 of 129

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7065303inversion1nstd229human GRCh38 chr9: 71,473,712-72,923,816 , GRCh37.p13 chr9: 74,088,628-75,538,732 LOC101927234, GDA, 21 more genes
    nsv6875084copy number variation1nstd229human GRCh38 chr9: 72,057,426-72,058,361 , GRCh37.p13 chr9: 74,672,342-74,673,277 LOC101927108, C9orf57
    nsv6869926copy number variation1nstd229human GRCh38 chr9: 71,942,601-72,080,400 , GRCh37.p13 chr9: 74,557,517-74,695,316 C9orf85, LOC101927108, 2 more genes
    nsv6866934copy number variation1nstd229human GRCh38 chr9: 72,042,462-72,053,998 , GRCh37.p13 chr9: 74,657,378-74,668,914 C9orf57, LOC101927108
    nsv6866352copy number variation1nstd229human GRCh38 chr9: 71,933,756-72,130,667 , GRCh37.p13 chr9: 74,548,672-74,745,583 LOC101927108, GDA, 4 more genes
    nsv6862173copy number variation1nstd229human GRCh38 chr9: 71,987,301-72,248,100 , GRCh37.p13 chr9: 74,602,217-74,863,016 GDA, LOC101927108, 3 more genes
    nsv6637502copy number variation1nstd102humanUncertain significance GRCh37 chr9: 70,966,262-76,901,382 , GRCh38.p12 chr9: 68,351,346-74,286,466 RPS20P24, MAMDC2-AS1, 77 more genes
    nsv6634454copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-131,603,223 , GRCh38.p12 chr9: 203,861-128,840,944 HNRNPA1P41, GAS1RR, 1868 more genes
    nsv6564952inversion1nstd223human GRCh38 chr9: 72,047,663-72,050,481 , GRCh37.p13 chr9: 74,662,579-74,665,397 LOC101927108, C9orf57
    nsv6563970inversion1nstd223human GRCh38 chr9: 71,164,626-72,130,108 , GRCh37.p13 chr9: 73,779,542-74,745,024 ABHD17B, C9orf57, 10 more genes
    nsv6557691inversion1nstd223human GRCh38 chr9: 72,059,620-72,060,200 , GRCh37.p13 chr9: 74,674,536-74,675,116 C9orf57, LOC101927108
    nsv6451126copy number variation1nstd223human GRCh38 chr9: 72,050,588-72,071,019 , GRCh37.p13 chr9: 74,665,504-74,685,935 LOC101927108, C9orf57
    nsv6442209copy number variation1nstd223human GRCh38 chr9: 72,057,408-72,058,322 , GRCh37.p13 chr9: 74,672,324-74,673,238 LOC101927108, C9orf57
    nsv6315405copy number variation1nstd102humanUncertain significance GRCh37 chr9: 19,356,861-119,513,311 , GRCh38.p12 chr9: 19,356,863-116,751,032 RNU6-156P, GDA, 1425 more genes
    nsv6313900copy number variation1nstd102humanLikely pathogenic GRCh37 chr9: 71,349,994-122,603,410 , GRCh38.p12 chr9: 68,735,078-119,841,132 ABCA1, ALAD, 793 more genes
    nsv6313827copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-84,155,399 , GRCh38.p12 chr9: 203,861-81,540,484 RPSAP75, ANKRD20A2P, 1008 more genes
    nsv6313546copy number variation1nstd102humanPathogenic GRCh37 chr9: 353,349-141,020,389 , GRCh38.p12 chr9: 353,349-138,125,937 FAM27C, DPM2, 2166 more genes
    nsv6290004inversion1nstd102humanLikely pathogenic GRCh38.p12 chr9: 12,246,100-98,797,096 , GRCh37 chr9: 12,246,100-101,559,378 ACO1, PLIN2, 1215 more genes
    nsv6137094copy number variation1nstd213human GRCh37 chr9: 71,840,000-78,800,001 , GRCh38.p12 chr9: 69,225,084-76,185,085 KLF9, PCSK5, 83 more genes
    nsv5854586copy number variation1nstd209human GRCh38 chr9: 72,057,299-72,058,498 , GRCh37.p13 chr9: 74,672,215-74,673,414 LOC101927108, C9orf57
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