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Items: 1 to 20 of 243

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5937790copy number variation1nstd209human GRCh38 chr17: 30,668,045-32,084,125 , GRCh37.p13 chr17: 28,995,063-30,411,144 , OMG, 39 more genes
    nsv5937217copy number variation1nstd209human GRCh38 chr17: 30,601,695-31,009,572 , GRCh37.p13 chr17: 28,928,713-29,336,590 LOC107984974, CRLF3, 16 more genes
    nsv5526153copy number variation1nstd206human GRCh38 chr17: 30,957,674-30,962,763 , GRCh37.p13 chr17: 29,284,692-29,289,781 RN7SL138P, ADAP2
    nsv5514320copy number variation1nstd206human GRCh38 chr17: 30,938,910-30,948,204 , GRCh37.p13 chr17: 29,265,928-29,275,222 ADAP2
    nsv5029019copy number variation1nstd200human GRCh38 chr17: 30,928,498-31,045,499 , GRCh37.p13 chr17: 29,255,516-29,372,517 LOC107984974, ADAP2, 4 more genes
    nsv5015984copy number variation1nstd200human GRCh38 chr17: 30,920,000-30,923,517 , GRCh37.p13 chr17: 29,247,018-29,250,535 ADAP2
    nsv4858552copy number variation1nstd200human GRCh37 chr17: 29,247,044-29,250,570 , GRCh38.p12 chr17: 30,920,026-30,923,552 ADAP2
    nsv4762422inversion1nstd199human GRCh37 chr17: 151-36,202,676 , GRCh38.p12 chr17: 150,358-36,446,544 , ABR, 1046 more genes
    nsv4729986copy number variation1nstd102humanUncertain significance GRCh37 chr17: 28,931,870-29,336,853 , GRCh38.p12 chr17: 30,604,852-31,009,835 RN7SL138P, LOC107984974, 16 more genes
    nsv4729791copy number variation1nstd102humanPathogenic GRCh37 chr17: 29,039,844-30,412,788 , GRCh38.p12 chr17: 30,712,826-32,085,769 ADAP2, TEFM, 37 more genes
    nsv4729745copy number variation1nstd102humanUncertain significance GRCh37 chr17: 29,061,631-29,305,516 , GRCh38.p12 chr17: 30,734,613-30,978,498 SUZ12P1, RPS17P3, 8 more genes
    nsv4675286copy number variation1nstd102humanPathogenic GRCh37 chr17: 29,088,218-30,159,137 , GRCh38.p12 chr17: 30,761,200-31,832,118 CRLF3, RN7SL45P, 30 more genes
    nsv4578269copy number variation1nstd102humanPathogenic GRCh37 chr17: 28,941,066-30,326,958 , GRCh38.p12 chr17: 30,614,048-31,999,939 LOC105371723, MIR4724, 41 more genes
    nsv4576722mobile element insertion1nstd166human GRCh37.p13 chr17: 29,275,294-29,275,294 , GRCh38.p12 chr17: 30,948,276-30,948,276 ADAP2
    nsv4568424sequence alteration1nstd166human GRCh37.p13 chr17: 29,237,973-29,247,166 , GRCh38.p12 chr17: 30,910,955-30,920,148 ADAP2
    nsv4457831copy number variation1nstd102humanPathogenic GRCh37 chr17: 21,690,653-38,772,647 , GRCh38.p12 chr17: 22,164,047-40,616,395 LOC105371753, TAOK1, 474 more genes
    nsv4457734copy number variation1nstd102humanUncertain significance GRCh37 chr17: 28,999,903-29,336,050 , GRCh38.p12 chr17: 30,672,885-31,009,032 SUZ12P1, RN7SL138P, 11 more genes
    nsv4457704copy number variation1nstd102humanPathogenic GRCh37 chr17: 29,054,315-30,409,336 , GRCh38.p12 chr17: 30,727,297-32,082,317 SH3GL1P1, LOC646030, 36 more genes
    nsv4457608copy number variation1nstd102humanUncertain significance GRCh37 chr17: 29,210,100-29,327,116 , GRCh38.p12 chr17: 30,883,082-31,000,098 ADAP2, TEFM, 4 more genes
    nsv4457605copy number variation1nstd102humanUncertain significance GRCh37 chr17: 29,214,423-29,327,116 , GRCh38.p12 chr17: 30,887,405-31,000,098 RN7SL138P, ATAD5, 4 more genes
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