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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
    nsv5937037copy number variation1nstd209human GRCh38 chr17: 4,774,428-4,778,125 , GRCh37.p13 chr17: 4,677,723-4,681,420 TM4SF5
    nsv5935586copy number variation1nstd209human GRCh38 chr17: 4,777,084-4,777,749 , GRCh37.p13 chr17: 4,680,379-4,681,044 TM4SF5
    nsv5930070copy number variation1nstd209human GRCh38 chr17: 4,777,060-4,777,846 , GRCh37.p13 chr17: 4,680,355-4,681,141 TM4SF5
    nsv5928082copy number variation1nstd209human GRCh38 chr17: 4,763,992-4,780,332 , GRCh37.p13 chr17: 4,667,287-4,683,627 TM4SF5
    nsv5879533copy number variation1nstd209human GRCh38 chr17: 4,774,338-4,780,537 , GRCh37.p13 chr17: 4,677,633-4,683,832 TM4SF5
    nsv5878783copy number variation1nstd209human GRCh38 chr17: 4,775,181-4,790,868 , GRCh37.p13 chr17: 4,678,476-4,694,163 GLTPD2, TM4SF5, 1 more genes
    nsv5874166copy number variation1nstd209human GRCh38 chr17: 4,767,115-4,772,287 , GRCh37.p13 chr17: 4,670,410-4,675,582 TM4SF5
    nsv5299082copy number variation1nstd204human GRCh37.p13 chr17: 4,627,696-4,727,995 , GRCh38.p13 chr17: 4,724,401-4,824,700 PLD2, PSMB6, 6 more genes
    nsv5015600copy number variation1nstd200human GRCh38 chr17: 4,780,609-4,782,622 , GRCh37.p13 chr17: 4,683,904-4,685,917 TM4SF5
    nsv5015599copy number variation1nstd200human GRCh38 chr17: 4,772,991-4,776,307 , GRCh37.p13 chr17: 4,676,286-4,679,602 TM4SF5
    nsv5015598copy number variation1nstd200human GRCh38 chr17: 4,765,337-4,780,209 , GRCh37.p13 chr17: 4,668,632-4,683,504 TM4SF5
    nsv5015597copy number variation1nstd200human GRCh38 chr17: 4,765,636-4,770,552 , GRCh37.p13 chr17: 4,668,931-4,673,847 TM4SF5
    nsv4857828copy number variation1nstd200human GRCh37 chr17: 4,668,932-4,673,804 , GRCh38.p12 chr17: 4,765,637-4,770,509 TM4SF5
    nsv4762422inversion1nstd199human GRCh37 chr17: 151-36,202,676 , GRCh38.p12 chr17: 150,358-36,446,544 , ABR, 1046 more genes
    nsv4674912copy number variation1nstd102humanPathogenic GRCh37 chr17: 8,547-5,627,408 , GRCh38.p12 chr17: 158,756-5,724,088 SRR, DBIL5P, 196 more genes
    nsv4630208copy number variation1nstd183human GRCh37 chr17: 4,486,568-5,620,052 , GRCh38.p12 chr17: 4,583,273-5,716,732 , ARRB2, 59 more genes
    nsv4620129copy number variation1nstd183human GRCh37 chr17: 4,684,047-4,685,959 , GRCh38.p12 chr17: 4,780,752-4,782,664 TM4SF5
    nsv4532650copy number variation1nstd166human GRCh37.p13 chr17: 4,684,611-4,684,735 , GRCh38.p12 chr17: 4,781,316-4,781,440 TM4SF5
    nsv4457587copy number variation1nstd102humanUncertain significance GRCh37 chr17: 3,759,126-6,128,911 , GRCh38.p12 chr17: 3,855,832-6,225,591 DERL2, ZZEF1, 82 more genes
    nsv4350781copy number variation1nstd102humanPathogenic GRCh37 chr17: 47,546-6,287,620 , GRCh38.p12 chr17: 197,755-6,384,300 SERPINF1, UBE2G1, 201 more genes
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