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Items: 1 to 20 of 633

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7145505insertion1nstd232human GRCh37.p13 chr9: 32,883,289-32,883,289 , GRCh38.p12 chr9: 32,883,291-32,883,291 APTX
    nsv7098457copy number variation1nstd102humanUncertain significance GRCh37 chr9: 32,985,949-32,986,048 , GRCh38.p12 chr9: 32,985,951-32,986,050 APTX
    nsv7098455copy number variation6nstd102humanUncertain significance GRCh37 chr9: 32,453,279-37,785,041 , GRCh38.p12 chr9: 32,453,281-37,785,044 TRBVAOR9-2, UBAP2, 197 more genes
    nsv7098080copy number variation1nstd102humanUncertain significance GRCh37 chr9: 32,453,279-35,068,379 , GRCh38.p12 chr9: 32,453,281-35,068,382 SUGT1P1, RNU7-36P, 110 more genes
    nsv6877780copy number variation1nstd229human GRCh38 chr9: 32,991,001-33,024,100 , GRCh37.p13 chr9: 32,990,999-33,024,098 APTX, LAGE3P1, 1 more genes
    nsv6875101copy number variation1nstd229human GRCh38 chr9: 32,955,887-32,960,414 , GRCh37.p13 chr9: 32,955,885-32,960,412 APTX
    nsv6873114copy number variation1nstd229human GRCh38 chr9: 32,950,698-32,954,329 , GRCh37.p13 chr9: 32,950,696-32,954,327 APTX
    nsv6873100copy number variation1nstd229human GRCh38 chr9: 32,914,821-32,921,240 , GRCh37.p13 chr9: 32,914,819-32,921,238 APTX
    nsv6871564copy number variation1nstd229human GRCh38 chr9: 32,948,811-32,953,871 , GRCh37.p13 chr9: 32,948,809-32,953,869 APTX
    nsv6870571copy number variation1nstd229human GRCh38 chr9: 32,925,922-32,929,636 , GRCh37.p13 chr9: 32,925,920-32,929,634 APTX, BOLA3P4
    nsv6867163copy number variation1nstd229human GRCh38 chr9: 32,979,746-32,986,022 , GRCh37.p13 chr9: 32,979,744-32,986,020 APTX
    nsv6866410copy number variation1nstd229human GRCh38 chr9: 32,955,201-33,014,100 , GRCh37.p13 chr9: 32,955,199-33,014,098 APTX, TCEA1P4
    nsv6866310copy number variation1nstd229human GRCh38 chr9: 33,016,101-33,021,300 , GRCh37.p13 chr9: 33,016,099-33,021,298 APTX, LAGE3P1
    nsv6866274copy number variation1nstd229human GRCh38 chr9: 33,015,501-33,023,800 , GRCh37.p13 chr9: 33,015,499-33,023,798 DNAJA1, APTX, 1 more genes
    nsv6865727copy number variation1nstd229human GRCh38 chr9: 32,928,508-32,996,021 , GRCh37.p13 chr9: 32,928,506-32,996,019 ASS1P12, TCEA1P4, 1 more genes
    nsv6861212copy number variation1nstd229human GRCh38 chr9: 32,927,155-32,930,125 , GRCh37.p13 chr9: 32,927,153-32,930,123 APTX
    nsv6858912copy number variation1nstd229human GRCh38 chr9: 32,772,456-32,991,017 , GRCh37.p13 chr9: 32,772,454-32,991,015 BOLA3P4, TMEM215, 5 more genes
    nsv6858860copy number variation1nstd229human GRCh38 chr9: 33,003,217-33,016,131 , GRCh37.p13 chr9: 33,003,215-33,016,129 APTX
    nsv6634454copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-131,603,223 , GRCh38.p12 chr9: 203,861-128,840,944 HNRNPA1P41, GAS1RR, 1868 more genes
    nsv6634409copy number variation1nstd102humanLikely pathogenic GRCh37 chr9: 1-40,036,525 , GRCh38.p12 chr9: 10,001-39,445,729 ACO1, PLIN2, 594 more genes
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