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Items: 1 to 20 of 151

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7077729inversion1nstd229human GRCh38 chr9: 94,417,509-96,970,614 , GRCh37.p13 chr9: 97,179,791-99,732,896 HSD17B3-AS1, ERCC6L2, 60 more genes
    nsv7075365inversion1nstd229human GRCh38 chr9: 94,549,389-100,549,990 , GRCh37.p13 chr9: 97,311,671-103,312,272 PCAT7, ANKS6, 128 more genes
    nsv7058325inversion1nstd229human GRCh38 chr9: 96,940,841-96,943,803 , GRCh37.p13 chr9: 99,703,123-99,706,085 NUTM2G, MFSD14CP
    nsv6877577copy number variation1nstd229human GRCh38 chr9: 96,755,585-97,161,429 , GRCh37.p13 chr9: 99,517,867-99,923,711 ZNF782, YRDCP2, 15 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
    nsv6452438copy number variation1nstd223human GRCh38 chr9: 96,914,411-96,933,269 , GRCh37.p13 chr9: 99,676,693-99,695,551 NUTM2G, LOC107987024, 1 more genes
    nsv6447755copy number variation1nstd223human GRCh38 chr9: 92,901,749-100,255,234 , GRCh37.p13 chr9: 95,664,031-103,017,516 EIF4BP3, VN1R51P, 162 more genes
    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
    nsv6315179copy number variation1nstd102humanPathogenic GRCh37 chr9: 93,864,974-106,661,581 , GRCh38.p12 chr9: 91,102,692-103,899,300 SUGT1P4-STRA6LP, NR4A3, 255 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
    nsv6313546copy number variation1nstd102humanPathogenic GRCh37 chr9: 353,349-141,020,389 , GRCh38.p12 chr9: 353,349-138,125,937 FAM27C, DPM2, 2166 more genes
    nsv6304003copy number variation1nstd186human GRCh37 chr9: 99,694,951-99,747,246 , GRCh38.p12 chr9: 96,932,669-96,984,964 MFSD14CP, NUTM2G, 1 more genes
    nsv6301497copy number variation1nstd186human GRCh37 chr9: 99,682,834-99,701,382 , GRCh38.p12 chr9: 96,920,552-96,939,100 NUTM2G, MFSD14CP
    nsv6290004inversion1nstd102humanLikely pathogenic GRCh38.p12 chr9: 12,246,100-98,797,096 , GRCh37 chr9: 12,246,100-101,559,378 ACO1, PLIN2, 1215 more genes
    nsv6142676copy number variation1nstd206human GRCh38 chr9: 96,906,000-96,939,000 , GRCh37.p13 chr9: 99,668,282-99,701,282 MFSD14CP, PTMAP11, 2 more genes
    nsv6136402copy number variation1nstd213human GRCh37 chr9: 99,490,000-99,740,001 , GRCh38.p12 chr9: 96,727,718-96,977,719 ZNF510, MFSD14CP, 7 more genes
    nsv6016767copy number variation1nstd212human GRCh38 chr9: 96,930,389-96,930,501 , GRCh37.p13 chr9: 99,692,671-99,692,783 MFSD14CP, NUTM2G
    nsv6012387copy number variation1nstd212human GRCh38 chr9: 96,930,973-96,931,045 , GRCh37.p13 chr9: 99,693,255-99,693,327 NUTM2G, MFSD14CP
    nsv5493365copy number variation1nstd206human GRCh38 chr9: 96,920,552-96,939,100 , GRCh37.p13 chr9: 99,682,834-99,701,382 NUTM2G, MFSD14CP
    nsv5485310copy number variation1nstd206human GRCh38 chr9: 96,856,726-96,974,338 , GRCh37.p13 chr9: 99,619,008-99,736,620 MFSD14CP, ZNF782, 5 more genes
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