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Items: 1 to 20 of 233

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095480copy number variation4nstd102humanUncertain significance GRCh37 chr19: 39,904,727-42,931,301 , GRCh38.p12 chr19: 39,414,087-42,427,149 CYP2B6, EID2B, 140 more genes
    nsv7095281copy number variation1nstd102humanUncertain significance GRCh37 chr19: 41,725,298-41,737,223 , GRCh38.p12 chr19: 41,219,393-41,231,318 AXL
    nsv7071361inversion1nstd229human GRCh38 chr19: 39,004,066-42,402,005 , GRCh37.p13 chr19: 39,494,706-42,906,157 RAB4B, RABAC1, 160 more genes
    nsv7068288inversion1nstd229human GRCh38 chr19: 39,023,970-42,945,419 , GRCh37.p13 chr19: 39,514,610-43,449,571 MIR4530, RNU6-195P, 178 more genes
    nsv7066709inversion1nstd229human GRCh38 chr19: 40,109,835-46,893,669 , GRCh37.p13 chr19: 40,615,742-47,396,926 LOC105372405, RNU6-611P, 305 more genes
    nsv7014204copy number variation1nstd229human GRCh38 chr19: 41,250,264-41,255,833 , GRCh37.p13 chr19: 41,756,169-41,761,738 AXL
    nsv7009629copy number variation1nstd229human GRCh38 chr19: 41,137,056-41,302,288 , GRCh37.p13 chr19: 41,642,961-41,808,193 RN7SL718P, CYP2S1, 6 more genes
    nsv7008156copy number variation1nstd229human GRCh38 chr19: 36,851,242-46,031,790 , GRCh37.p13 chr19: 37,342,144-46,535,048 LOC105372390, LOC107985291, 396 more genes
    nsv7004672copy number variation1nstd229human GRCh38 chr19: 41,224,627-41,227,732 , GRCh37.p13 chr19: 41,730,532-41,733,637 AXL
    nsv6598416inversion1nstd223human GRCh38 chr19: 40,109,815-44,449,696 , GRCh37.p13 chr19: 40,615,722-44,953,884 , SERTAD1, 188 more genes
    nsv6529238copy number variation1nstd223human GRCh38 chr19: 41,229,413-41,246,127 , GRCh37.p13 chr19: 41,735,318-41,752,032 AXL, TRK-TTT10-1
    nsv6523347copy number variation1nstd223human GRCh38 chr19: 41,222,598-41,223,213 , GRCh37.p13 chr19: 41,728,503-41,729,118 AXL
    nsv6523224copy number variation1nstd223human GRCh38 chr19: 41,217,867-41,221,527 , GRCh37.p13 chr19: 41,723,772-41,727,432 AXL
    nsv6287113insertion1nstd214human GRCh38 chr19: 41,240,419-41,240,419 , GRCh37.p13 chr19: 41,746,324-41,746,324 TRK-TTT10-1, AXL
    nsv6251050mobile element insertion1nstd215human GRCh38 chr19: 41,246,825-41,246,825 , GRCh37.p13 chr19: 41,752,730-41,752,730 AXL
    nsv6251049mobile element insertion1nstd215human GRCh38 chr19: 41,218,726-41,218,726 , GRCh37.p13 chr19: 41,724,631-41,724,631 AXL
    nsv6214438copy number variation1nstd214human GRCh38 chr19: 41,243,045-41,243,125 , GRCh37.p13 chr19: 41,748,950-41,749,030 AXL
    nsv6133703copy number variation1nstd213human GRCh37 chr19: 41,220,000-49,640,001 , GRCh38.p12 chr19: 40,714,095-49,136,744 , APOC1, 402 more genes
    nsv6133523copy number variation1nstd213human GRCh37 chr19: 34,000,000-42,200,001 , GRCh38.p12 chr19: 33,509,094-41,696,083 , ACTN4, 345 more genes
    nsv5933353copy number variation1nstd209human GRCh38 chr19: 41,240,131-41,240,294 , GRCh37.p13 chr19: 41,746,036-41,746,199 AXL, TRK-TTT10-1
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