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Items: 1 to 20 of 106

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5929452copy number variation1nstd209human GRCh38 chr17: 6,412,133-13,962,466 , GRCh37.p13 chr17: 6,315,453-13,865,783 , PIK3R5-DT, 226 more genes
    nsv5153827mobile element insertion1nstd203human GRCh38 chr17: 10,827,454-10,827,491 , GRCh37.p13 chr17: 10,730,771-10,730,808 PIRT
    nsv4864521copy number variation1nstd200human GRCh37 chr17: 10,730,360-10,744,073 , GRCh38.p12 chr17: 10,827,043-10,840,756 PIRT
    nsv4762422inversion1nstd199human GRCh37 chr17: 151-36,202,676 , GRCh38.p12 chr17: 150,358-36,446,544 , ABR, 1046 more genes
    nsv4684245copy number variation1nstd102humanUncertain significance GRCh37 chr17: 10,493,837-15,099,023 , GRCh38.p12 chr17: 10,590,520-15,195,706 LOC100506974, MIR1269B, 52 more genes
    nsv4675665copy number variation1nstd102humanUncertain significance GRCh37 chr17: 10,656,332-10,730,021 , GRCh38.p12 chr17: 10,753,015-10,826,704 TMEM220-AS1, PIRT, 1 more genes
    nsv4457480copy number variation1nstd102humanUncertain significance GRCh37 chr17: 10,604,119-10,744,366 , GRCh38.p12 chr17: 10,700,802-10,841,049 ADPRM, TMEM220, 4 more genes
    nsv4436354complex substitution1nstd102humanUncertain significance GRCh37 chr17: 9,586,165-16,325,968 , GRCh38.p12 chr17: 9,682,848-16,422,654 ADORA2B, COX10, 109 more genes
    nsv4250341copy number variation1nstd166human GRCh37.p13 chr17: 10,730,381-10,744,048 , GRCh38.p12 chr17: 10,827,064-10,840,731 PIRT
    nsv3924924copy number variation1nstd102humanUncertain significance GRCh37 chr17: 10,616,809-11,215,859 , NCBI36 chr17: 10,557,534-11,156,584 , GRCh38 chr17: 10,713,492-11,312,542 TMEM220-AS1, TMEM220, 8 more genes
    nsv3922092copy number variation1nstd102humanUncertain significance NCBI36 chr17: 10,288,853-10,894,231 , GRCh37.p13 chr17: 10,348,128-10,953,506 , GRCh38.p12 chr17: 10,444,811-11,050,189 MYH3, RNU6-1065P, 13 more genes
    nsv3921439copy number variation1nstd102humanUncertain significance NCBI36 chr17: 10,520,697-11,183,346 , GRCh37.p13 chr17: 10,579,972-11,242,621 , GRCh38.p12 chr17: 10,676,655-11,339,304 RNU6-1065P, TMEM220, 11 more genes
    nsv3917187copy number variation1nstd102humanPathogenic NCBI36 chr17: 10,178,551-10,744,358 , GRCh37 chr17: 10,237,826-10,803,633 , GRCh38 chr17: 10,334,509-10,900,316 MYH2, MYH8, 14 more genes
    nsv3917059copy number variation1nstd102humanPathogenic GRCh37 chr17: 45,835-12,247,218 , NCBI36 chr17: 11,807-12,187,943 , GRCh38 chr17: 162,016-12,343,901 PSMB6, RNU6-1065P, 409 more genes
    nsv3915354copy number variation1nstd102humanPathogenic GRCh38 chr17: 150,732-14,764,202 , NCBI36 chr17: 525-14,608,244 , GRCh37 chr17: 525-14,667,519 KIF1C-AS1, TMEM107, 433 more genes
    nsv3911050copy number variation1nstd102humanPathogenic GRCh38 chr17: 5,732,953-12,095,349 , GRCh37 chr17: 5,636,273-11,998,666 , NCBI36 chr17: 5,576,997-11,939,391 C17orf49, SPEM1, 209 more genes
    nsv3907261copy number variation2nstd102humanPathogenic GRCh37 chr17: 526-81,041,938 , GRCh38.p12 chr17: 150,733-83,084,062 SMURF2, LOC112268199, 2366 more genes
    nsv3906245copy number variation1nstd102humanPathogenic GRCh37 chr17: 12,344-81,057,996 , GRCh38.p12 chr17: 162,553-83,100,251 MIR21, LOC105371899, 2366 more genes
    nsv3904771copy number variation1nstd102humanPathogenic GRCh37 chr17: 525-11,186,432 , GRCh38.p12 chr17: 150,732-11,283,115 SLC2A4, CCDC92B, 401 more genes
    nsv3903684copy number variation1nstd102humanPathogenic GRCh37 chr17: 8,547-81,060,040 , GRCh38.p12 chr17: 158,756-83,102,004 MIR3185, YWHAEP6, 2366 more genes
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