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Items: 1 to 20 of 192

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5951716insertion1nstd209human GRCh38 chr9: 97,449,116-97,449,116 , GRCh37.p13 chr9: 100,211,398-100,211,398 TDRD7
    nsv5702160mobile element insertion1nstd211human GRCh38 chr9: 97,450,586-97,450,586 , GRCh37.p13 chr9: 100,212,868-100,212,868 TDRD7
    nsv5701357mobile element insertion1nstd211human GRCh38 chr9: 97,449,132-97,449,132 , GRCh37.p13 chr9: 100,211,414-100,211,414 TDRD7
    nsv5694384mobile element insertion1nstd211human GRCh38 chr9: 97,473,318-97,473,318 , GRCh37.p13 chr9: 100,235,600-100,235,600 TDRD7
    nsv5594549copy number variation1nstd207human GRCh38 chr9: 97,410,969-97,411,080 , GRCh37.p13 chr9: 100,173,251-100,173,362 TDRD7
    nsv5478624copy number variation1nstd206human GRCh38 chr9: 97,441,989-97,442,046 , GRCh37.p13 chr9: 100,204,271-100,204,328 TDRD7
    nsv5475150copy number variation1nstd206human GRCh38 chr9: 97,445,834-97,447,795 , GRCh37.p13 chr9: 100,208,116-100,210,077 TDRD7
    nsv5400113mobile element insertion1nstd206human GRCh38 chr9: 97,473,318-97,473,369 , GRCh37.p13 chr9: 100,235,600-100,235,651 TDRD7
    nsv5399829mobile element insertion1nstd206human GRCh38 chr9: 97,450,586-97,450,637 , GRCh37.p13 chr9: 100,212,868-100,212,919 TDRD7
    nsv5395861mobile element insertion1nstd206human GRCh38 chr9: 97,449,132-97,449,183 , GRCh37.p13 chr9: 100,211,414-100,211,465 TDRD7
    nsv5381561copy number variation1nstd102humanPathogenic GRCh37 chr9: 97,834,573-107,199,088 , GRCh38.p12 chr9: 95,072,291-104,436,807 TBC1D2, ZNF782, 170 more genes
    nsv5125705mobile element insertion1nstd203human GRCh38 chr9: 97,446,172-97,446,176 , GRCh37.p13 chr9: 100,208,454-100,208,458 TDRD7
    nsv4824174copy number variation1nstd200human GRCh37 chr9: 100,187,584-100,188,208 , GRCh38.p12 chr9: 97,425,302-97,425,926 TDRD7
    nsv4746976copy number variation1nstd199human GRCh37 chr9: 100,173,264-100,173,374 , GRCh38.p12 chr9: 97,410,982-97,411,092 TDRD7
    nsv4684256copy number variation1nstd102humanPathogenic GRCh37 chr9: 96,126,075-108,535,272 , GRCh38.p12 chr9: 93,363,793-105,772,991 RPS26P37, MIR27B, 238 more genes
    nsv4683944copy number variation1nstd102humanUncertain significance GRCh37 chr9: 100,190,728-101,558,793 , GRCh38.p12 chr9: 97,428,446-98,796,511 TRMO, RNU6-918P, 20 more genes
    nsv4676103copy number variation1nstd102humanPathogenic NCBI36 chr9: 95,946,863-99,986,314 , GRCh37.p13 chr9: 96,907,042-100,946,493 , GRCh38.p12 chr9: 94,144,760-98,184,211 MIR3074, LOC112268039, 108 more genes
    nsv4547659insertion1nstd166human GRCh37.p13 chr9: 100,235,584-100,235,584 , GRCh38.p12 chr9: 97,473,302-97,473,302 TDRD7
    nsv4493740mobile element insertion1nstd166human GRCh37.p13 chr9: 100,199,298-100,199,298 , GRCh38.p12 chr9: 97,437,016-97,437,016 TDRD7
    nsv4489362mobile element insertion1nstd166human GRCh37.p13 chr9: 100,211,398-100,211,398 , GRCh38.p12 chr9: 97,449,116-97,449,116 TDRD7
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