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Items: 1 to 20 of 207

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5936702copy number variation1nstd209human GRCh38 chr17: 4,531,823-4,556,262 , GRCh37.p13 chr17: 4,435,118-4,459,557 MYBBP1A, GGT6, 1 more genes
    nsv5932743copy number variation1nstd209human GRCh38 chr17: 4,540,124-4,540,174 , GRCh37.p13 chr17: 4,443,419-4,443,469 MYBBP1A
    nsv5930741copy number variation1nstd209human GRCh38 chr17: 4,544,154-4,544,213 , GRCh37.p13 chr17: 4,447,449-4,447,508 MYBBP1A
    nsv5878126copy number variation1nstd209human GRCh38 chr17: 4,531,841-4,544,517 , GRCh37.p13 chr17: 4,435,136-4,447,812 MYBBP1A, SPNS2
    nsv5876721copy number variation1nstd209human GRCh38 chr17: 4,538,695-4,540,165 , GRCh37.p13 chr17: 4,441,990-4,443,460 MYBBP1A, SPNS2
    nsv5868246copy number variation1nstd209human GRCh38 chr17: 4,547,215-4,548,614 , GRCh37.p13 chr17: 4,450,510-4,451,909 MYBBP1A
    nsv5650609insertion1nstd207human GRCh38 chr17: 4,544,154-4,544,154 , GRCh37.p13 chr17: 4,447,449-4,447,449 MYBBP1A
    nsv5587499copy number variation1nstd207human GRCh38 chr17: 4,544,154-4,544,213 , GRCh37.p13 chr17: 4,447,449-4,447,508 MYBBP1A
    nsv5532109copy number variation1nstd206human GRCh38 chr17: 4,501,780-4,558,382 , GRCh37.p13 chr17: 4,405,075-4,461,677 MYBBP1A, SPNS2, 1 more genes
    nsv5525567copy number variation1nstd206human GRCh38 chr17: 4,540,102-4,540,168 , GRCh37.p13 chr17: 4,443,397-4,443,463 MYBBP1A
    nsv5023581copy number variation1nstd200human GRCh38 chr17: 4,547,014-4,553,135 , GRCh37.p13 chr17: 4,450,309-4,456,430 MYBBP1A
    nsv5023580copy number variation1nstd200human GRCh38 chr17: 4,411,876-4,581,486 , GRCh37.p13 chr17: 4,315,171-4,484,781 MYBBP1A, SPNS2, 4 more genes
    nsv5023577copy number variation1nstd200human GRCh38 chr17: 4,361,860-4,571,578 , GRCh37.p13 chr17: 4,265,155-4,474,873 GGT6, SPNS2-AS1, 6 more genes
    nsv4786161mobile element deletion1nstd200human GRCh37 chr17: 4,450,211-4,450,502 , GRCh38.p12 chr17: 4,546,916-4,547,207 MYBBP1A
    nsv4762422inversion1nstd199human GRCh37 chr17: 151-36,202,676 , GRCh38.p12 chr17: 150,358-36,446,544 , ABR, 1046 more genes
    nsv4726082insertion1nstd186human GRCh37 chr17: 4,444,219-4,444,219 , GRCh38.p12 chr17: 4,540,924-4,540,924 MYBBP1A
    nsv4675837copy number variation1nstd102humanUncertain significance GRCh37 chr17: 4,245,304-4,581,861 , GRCh38.p12 chr17: 4,342,009-4,678,566 TXNP4, SPNS3, 13 more genes
    nsv4674950copy number variation1nstd102humanUncertain significance GRCh37 chr17: 3,933,998-4,581,861 , GRCh38.p12 chr17: 4,030,704-4,678,566 UBE2G1, PELP1, 20 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
    nsv4630811copy number variation1nstd183human GRCh37 chr17: 4,451,622-4,451,666 , GRCh38.p12 chr17: 4,548,327-4,548,371 MYBBP1A
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