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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5904246copy number variation1nstd209human GRCh38 chr3: 154,028,749-154,030,075 , GRCh37.p13 chr3: 153,746,538-153,747,864 ARHGEF26-AS1
    nsv5835286copy number variation1nstd209human GRCh38 chr3: 154,028,529-154,030,094 , GRCh37.p13 chr3: 153,746,318-153,747,883 ARHGEF26-AS1
    nsv5723630mobile element insertion2nstd211human GRCh38 chr3: 154,047,322-154,047,322 , GRCh37.p13 chr3: 153,765,111-153,765,111 ARHGEF26-AS1
    nsv5683982mobile element insertion2nstd211human GRCh38 chr3: 154,035,718-154,035,718 , GRCh37.p13 chr3: 153,753,507-153,753,507 ARHGEF26-AS1
    nsv5453067copy number variation1nstd206human GRCh38 chr3: 154,034,864-154,036,095 , GRCh37.p13 chr3: 153,752,653-153,753,884 ARHGEF26-AS1
    nsv5439021copy number variation1nstd206human GRCh38 chr3: 154,028,749-154,030,076 , GRCh37.p13 chr3: 153,746,538-153,747,865 ARHGEF26-AS1
    nsv5381765copy number variation1nstd102humanPathogenic GRCh37 chr3: 138,173,683-162,494,699 , GRCh38.p12 chr3: 138,454,841-162,776,911 MBNL1-AS1, LOC107986138, 339 more genes
    nsv5352059translocation1nstd200human GRCh38 chr3: 154,076,485-154,076,485 , GRCh38 chr3: 154,076,375-154,076,375 , GRCh37.p13 chr3: 153,794,164-153,794,164 , GRCh37.p13 chr3: 153,794,274-153,794,274 ARHGEF26-AS1
    nsv5352058translocation1nstd200human GRCh38 chr3: 154,028,749-154,028,749 , GRCh38 chr3: 154,030,076-154,030,076 , GRCh37.p13 chr3: 153,746,538-153,746,538 , GRCh37.p13 chr3: 153,747,865-153,747,865 ARHGEF26-AS1
    nsv5332089translocation1nstd200human GRCh37 chr3: 153,746,538-153,746,538 , GRCh37 chr3: 153,747,865-153,747,865 , GRCh38.p12 chr3: 154,028,749-154,028,749 , GRCh38.p12 chr3: 154,030,076-154,030,076 ARHGEF26-AS1
    nsv5174325mobile element insertion1nstd203human GRCh38 chr3: 154,047,312-154,047,322 , GRCh37.p13 chr3: 153,765,101-153,765,111 ARHGEF26-AS1
    nsv5161163mobile element insertion1nstd203human GRCh38 chr3: 154,047,307-154,047,322 , GRCh37.p13 chr3: 153,765,096-153,765,111 ARHGEF26-AS1
    nsv5097248mobile element insertion1nstd203human GRCh38 chr3: 154,116,969-154,116,979 , GRCh37.p13 chr3: 153,834,758-153,834,768 ARHGEF26-AS1
    nsv5082296mobile element insertion1nstd203human GRCh38 chr3: 154,035,704-154,035,715 , GRCh37.p13 chr3: 153,753,493-153,753,504 ARHGEF26-AS1
    nsv5033132inversion1nstd200human GRCh38 chr3: 147,205,794-180,217,342 , GRCh37.p13 chr3: 146,923,581-179,935,130 , LOC105374154, 433 more genes
    nsv4914900copy number variation1nstd200human GRCh38 chr3: 154,037,444-154,038,098 , GRCh37.p13 chr3: 153,755,233-153,755,887 ARHGEF26-AS1
    nsv4912483copy number variation1nstd200human GRCh38 chr3: 154,088,637-154,088,690 , GRCh37.p13 chr3: 153,806,426-153,806,479 ARHGEF26-AS1
    nsv4912482copy number variation1nstd200human GRCh38 chr3: 154,054,235-154,055,569 , GRCh37.p13 chr3: 153,772,024-153,773,358 ARHGEF26-AS1
    nsv4912481copy number variation1nstd200human GRCh38 chr3: 154,053,338-154,129,248 , GRCh37.p13 chr3: 153,771,127-153,847,037 ARHGEF26-AS1, ARHGEF26
    nsv4912480copy number variation1nstd200human GRCh38 chr3: 154,034,869-154,036,086 , GRCh37.p13 chr3: 153,752,658-153,753,875 ARHGEF26-AS1
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