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Items: 1 to 20 of 147

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6861191copy number variation1nstd229human GRCh38 chr9: 93,066,829-93,079,895 , GRCh37.p13 chr9: 95,829,111-95,842,177 SUSD3
    nsv6637944copy number variation1nstd102humanPathogenic GRCh37 chr9: 95,711,603-98,469,214 , GRCh38.p12 chr9: 92,949,321-95,706,932 MIRLET7D, MIR24-1, 60 more genes
    nsv6637275copy number variation1nstd102humanUncertain significance GRCh37 chr9: 95,649,997-95,850,428 , GRCh38.p12 chr9: 92,887,715-93,088,146 ALOX15P2, LOC101927954, 4 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
    nsv6634025copy number variation1nstd224human GRCh37 chr9: 95,830,197-95,918,643 , GRCh38.p12 chr9: 93,067,915-93,156,361 LOC101927993, CARD19, 2 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
    nsv6440614copy number variation1nstd223human GRCh38 chr9: 93,066,829-93,079,892 , GRCh37.p13 chr9: 95,829,111-95,842,174 SUSD3
    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
    nsv6290004inversion1nstd102humanLikely pathogenic GRCh38.p12 chr9: 12,246,100-98,797,096 , GRCh37 chr9: 12,246,100-101,559,378 ACO1, PLIN2, 1215 more genes
    nsv6257911mobile element insertion1nstd215human GRCh38 chr9: 93,075,434-93,075,434 , GRCh37.p13 chr9: 95,837,716-95,837,716 SUSD3
    nsv6136400copy number variation1nstd213human GRCh37 chr9: 95,630,000-96,300,001 , GRCh38.p12 chr9: 92,867,718-93,537,719 NINJ1, ZNF484, 15 more genes
    nsv5478423copy number variation1nstd206human GRCh38 chr9: 93,064,464-93,065,627 , GRCh37.p13 chr9: 95,826,746-95,827,909 SUSD3
    nsv5343380translocation1nstd200human GRCh37 chr9: 95,842,674-95,842,674 , GRCh37 chr9: 95,843,541-95,843,541 , GRCh38.p12 chr9: 93,080,392-93,080,392 , GRCh38.p12 chr9: 93,081,259-93,081,259 SUSD3
    nsv4973213copy number variation1nstd200human GRCh38 chr9: 93,080,392-93,081,259 , GRCh37.p13 chr9: 95,842,674-95,843,541 SUSD3
    nsv4973212copy number variation1nstd200human GRCh38 chr9: 93,066,829-93,079,892 , GRCh37.p13 chr9: 95,829,111-95,842,174 SUSD3
    nsv4887530inversion1nstd200human GRCh37 chr9: 90,662,371-96,951,001 , GRCh38.p12 chr9: 88,047,456-94,188,719 , MTATP6P29, 125 more genes
    nsv4673659copy number variation1nstd186human GRCh37 chr9: 95,826,667-95,827,851 , GRCh38.p12 chr9: 93,064,385-93,065,569 SUSD3
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