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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5948295insertion1nstd209human GRCh38 chr10: 102,885,500-102,885,500 , GRCh37.p13 chr10: 104,645,257-104,645,257 BORCS7-ASMT, AS3MT
    nsv5927460copy number variation1nstd209human GRCh38 chr10: 102,891,952-102,892,984 , GRCh37.p13 chr10: 104,651,709-104,652,741 BORCS7-ASMT, AS3MT
    nsv5910104copy number variation1nstd209human GRCh38 chr10: 102,852,051-102,871,611 , GRCh37.p13 chr10: 104,611,808-104,631,368 AS3MT, BORCS7, 1 more genes
    nsv5848261copy number variation1nstd209human GRCh38 chr10: 102,855,181-102,871,240 , GRCh37.p13 chr10: 104,614,938-104,630,997 BORCS7-ASMT, BORCS7, 1 more genes
    nsv5711617mobile element insertion1nstd211human GRCh38 chr10: 102,888,868-102,888,868 , GRCh37.p13 chr10: 104,648,625-104,648,625 AS3MT, BORCS7-ASMT
    nsv5596322copy number variation1nstd207human GRCh38 chr10: 102,885,490-102,885,828 , GRCh37.p13 chr10: 104,645,247-104,645,585 AS3MT, RPL22P17, 1 more genes
    nsv5508628copy number variation1nstd206human GRCh38 chr10: 102,876,000-102,882,368 , GRCh37.p13 chr10: 104,635,757-104,642,125 BORCS7-ASMT, AS3MT
    nsv5502954copy number variation1nstd206human GRCh38 chr10: 102,885,500-102,885,829 , GRCh37.p13 chr10: 104,645,257-104,645,586 RPL22P17, AS3MT, 1 more genes
    nsv5501677copy number variation1nstd206human GRCh38 chr10: 102,877,751-102,877,802 , GRCh37.p13 chr10: 104,637,508-104,637,559 AS3MT, BORCS7-ASMT
    nsv5499745copy number variation1nstd206human GRCh38 chr10: 102,891,812-102,892,943 , GRCh37.p13 chr10: 104,651,569-104,652,700 AS3MT, BORCS7-ASMT
    nsv5496771copy number variation1nstd206human GRCh38 chr10: 102,884,048-102,886,394 , GRCh37.p13 chr10: 104,643,805-104,646,151 RPL22P17, BORCS7-ASMT, 1 more genes
    nsv5383046mobile element deletion1nstd186human GRCh37 chr10: 104,645,257-104,645,586 , GRCh38.p12 chr10: 102,885,500-102,885,829 AS3MT, RPL22P17, 1 more genes
    nsv5373277translocation1nstd200human GRCh38 chr10: 102,871,890-102,871,890 , GRCh38 chr10: 102,870,571-102,870,571 , GRCh37.p13 chr10: 104,630,328-104,630,328 , GRCh37.p13 chr10: 104,631,647-104,631,647 BORCS7-ASMT, AS3MT
    nsv5348059translocation1nstd200human GRCh38 chr10: 102,871,919-102,871,919 , GRCh38 chr10: 102,870,959-102,870,959 , GRCh37.p13 chr10: 104,630,716-104,630,716 , GRCh37.p13 chr10: 104,631,676-104,631,676 BORCS7-ASMT, AS3MT
    nsv5341705translocation1nstd200human GRCh37 chr10: 104,645,199-104,645,199 , GRCh37 chr10: 104,645,566-104,645,566 , GRCh38.p12 chr10: 102,885,442-102,885,442 , GRCh38.p12 chr10: 102,885,809-102,885,809 AS3MT, RPL22P17, 1 more genes
    nsv5309933copy number variation1nstd204human GRCh37.p13 chr10: 104,643,836-104,645,045 , GRCh38.p13 chr10: 102,884,079-102,885,288 AS3MT, BORCS7-ASMT
    nsv5203119mobile element deletion1nstd204human GRCh37.p13 chr10: 104,645,257-104,645,586 , GRCh38.p13 chr10: 102,885,500-102,885,829 AS3MT, RPL22P17, 1 more genes
    nsv5138395mobile element insertion1nstd203human GRCh38 chr10: 102,885,478-102,885,500 , GRCh37.p13 chr10: 104,645,235-104,645,257 BORCS7-ASMT, AS3MT
    nsv5137613mobile element insertion1nstd203human GRCh38 chr10: 102,894,228-102,894,261 , GRCh37.p13 chr10: 104,653,985-104,654,018 AS3MT, BORCS7-ASMT
    nsv5137245mobile element insertion1nstd203human GRCh38 chr10: 102,885,500-102,885,522 , GRCh37.p13 chr10: 104,645,257-104,645,279 AS3MT, BORCS7-ASMT
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