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Items: 1 to 20 of 223

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7077137inversion1nstd229human GRCh38 chr9: 97,438,342-97,438,449 , GRCh37.p13 chr9: 100,200,624-100,200,731 TDRD7
    nsv7075365inversion1nstd229human GRCh38 chr9: 94,549,389-100,549,990 , GRCh37.p13 chr9: 97,311,671-103,312,272 PCAT7, ANKS6, 128 more genes
    nsv7071969inversion1nstd229human GRCh38 chr9: 97,446,526-97,456,702 , GRCh37.p13 chr9: 100,208,808-100,218,984 TDRD7
    nsv7066937inversion1nstd229human GRCh38 chr9: 97,486,079-97,488,021 , GRCh37.p13 chr9: 100,248,361-100,250,303 TDRD7
    nsv7063607inversion1nstd229human GRCh38 chr9: 97,419,407-97,419,442 , GRCh37.p13 chr9: 100,181,689-100,181,724 TDRD7
    nsv6872147copy number variation1nstd229human GRCh38 chr9: 97,479,835-97,486,301 , GRCh37.p13 chr9: 100,242,117-100,248,583 TDRD7
    nsv6871795copy number variation1nstd229human GRCh38 chr9: 97,415,694-97,420,543 , GRCh37.p13 chr9: 100,177,976-100,182,825 TDRD7
    nsv6868487copy number variation1nstd229human GRCh38 chr9: 97,486,397-97,486,566 , GRCh37.p13 chr9: 100,248,679-100,248,848 TDRD7
    nsv6865689copy number variation1nstd229human GRCh38 chr9: 97,454,455-97,461,088 , GRCh37.p13 chr9: 100,216,737-100,223,370 TDRD7
    nsv6865688copy number variation1nstd229human GRCh38 chr9: 97,435,541-97,436,655 , GRCh37.p13 chr9: 100,197,823-100,198,937 TDRD7
    nsv6860722copy number variation1nstd229human GRCh38 chr9: 97,415,701-97,420,500 , GRCh37.p13 chr9: 100,177,983-100,182,782 TDRD7
    nsv6634454copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-131,603,223 , GRCh38.p12 chr9: 203,861-128,840,944 HNRNPA1P41, GAS1RR, 1868 more genes
    nsv6558659inversion1nstd223human GRCh38 chr9: 97,449,474-97,451,198 , GRCh37.p13 chr9: 100,211,756-100,213,480 TDRD7
    nsv6452922copy number variation1nstd223human GRCh38 chr9: 97,411,501-97,412,900 , GRCh37.p13 chr9: 100,173,783-100,175,182 TDRD7
    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
    nsv6440330copy number variation1nstd223human GRCh38 chr9: 97,458,471-97,459,167 , GRCh37.p13 chr9: 100,220,753-100,221,449 TDRD7
    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
    nsv6314530complex chromosomal rearrangement4nstd102humanPathogenic GRCh37 chr9: 100,194,180-100,194,180 , GRCh37 chr9: 100,195,366-100,195,366 , GRCh37 chr9: 126,738,625-126,738,625 , GRCh37 chr9: 126,741,394-126,741,394 , GRCh37 chr9: 126,753,305-126,753,305 , GRCh37 chr9: 126,756,206-126,756,206 , GRCh37 chr9: 127,266,258-127,266,258 , GRCh37 chr9: 127,266,339-127,266,339 , GRCh38.p12 chr9: 97,431,898-97,431,898 , GRCh38.p12 chr9: 97,433,084-97,433,084 , GRCh38.p12 chr9: 123,976,346-123,976,346 , GRCh38.p12 chr9: 123,979,115-123,979,115 , GRCh38.p12 chr9: 123,991,026-123,991,026 , GRCh38.p12 chr9: 123,993,927-123,993,927 , GRCh38.p12 chr9: 124,503,979-124,503,979 , GRCh38.p12 chr9: 124,504,060-124,504,060 NR5A1, TDRD7, 1 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
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