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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5970408inversion1nstd209human GRCh38 chr19: 2,282,477-7,636,587 , GRCh37.p13 chr19: 2,282,476-7,701,473 , TLE5, 195 more genes
    nsv5942775copy number variation1nstd209human GRCh38 chr19: 2,865,023-7,153,898 , GRCh37.p13 chr19: 2,865,021-7,153,909 , GNA15-DT, 159 more genes
    nsv5299773copy number variation1nstd204human GRCh38.p13 chr19: 3,557,501-3,571,500 , GRCh37.p13 chr19: 3,557,499-3,571,498 HMG20B, MFSD12
    nsv5294162copy number variation1nstd204human GRCh38.p13 chr19: 3,332,801-3,820,800 , GRCh37.p13 chr19: 3,332,799-3,820,798 LOC105372245, LOC105372248, 19 more genes
    nsv5292408copy number variation1nstd204human GRCh38.p13 chr19: 2,552,101-4,875,100 , GRCh37.p13 chr19: 2,552,099-4,875,112 , S1PR4, 93 more genes
    nsv5290913copy number variation1nstd204human GRCh38.p13 chr19: 3,541,601-3,599,100 , GRCh37.p13 chr19: 3,541,599-3,599,098 HMG20B, TEKTIP1, 3 more genes
    nsv5019303copy number variation1nstd200human GRCh38 chr19: 3,574,949-3,580,047 , GRCh37.p13 chr19: 3,574,947-3,580,045 HMG20B
    nsv4907479mobile element deletion1nstd200human GRCh38 chr19: 3,575,670-3,575,972 , GRCh37.p13 chr19: 3,575,668-3,575,970 HMG20B
    nsv4769711mobile element deletion1nstd200human GRCh37 chr19: 3,575,668-3,575,970 , GRCh38.p12 chr19: 3,575,670-3,575,972 HMG20B
    nsv4676189copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,912-4,384,674 , GRCh38.p12 chr19: 260,912-4,384,677 MRPL54, DAZAP1, 198 more genes
    nsv4457843copy number variation1nstd102humanUncertain significance GRCh37 chr19: 3,132,909-3,907,470 , GRCh38.p12 chr19: 3,132,911-3,907,472 LOC105372244, TEKTIP1, 27 more genes
    nsv4457776copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,911-4,788,357 , GRCh38.p12 chr19: 260,911-4,788,345 BSG, LOC100420586, 217 more genes
    nsv4452268copy number variation1nstd102humanUncertain significance GRCh37 chr19: 1,406,030-3,597,207 , GRCh38.p12 chr19: 1,406,031-3,597,209 C19orf25, MIR7108, 92 more genes
    nsv4436611copy number variation1nstd102humanUncertain significance GRCh37 chr19: 2,229,488-4,004,142 , GRCh38.p12 chr19: 2,229,489-4,004,144 LMNB2, SF3A2, 76 more genes
    nsv4350537copy number variation1nstd102humanPathogenic GRCh37 chr19: 3,076,808-4,796,782 , GRCh38.p12 chr19: 3,076,810-4,796,770 FEM1A, MIR7-3, 70 more genes
    nsv3924102copy number variation1nstd102humanPathogenic GRCh38 chr19: 259,395-6,795,611 , GRCh37 chr19: 259,395-6,795,622 , NCBI36 chr19: 210,395-6,746,622 POLR2E, PWWP3A, 283 more genes
    nsv3923561copy number variation1nstd102humanPathogenic NCBI36 chr19: 184,565-4,650,484 , GRCh37 chr19: 233,565-4,699,484 , GRCh38 chr19: 233,565-4,699,472 DAPK3, IZUMO4, 214 more genes
    nsv3923355copy number variation1nstd102humanUncertain significance GRCh38 chr19: 3,080,621-3,730,716 , GRCh37 chr19: 3,080,619-3,730,714 , NCBI36 chr19: 3,031,619-3,681,714 LOC105372245, MFSD12, 21 more genes
    nsv3921957copy number variation1nstd102humanPathogenic GRCh38 chr19: 2,926,238-4,051,635 , NCBI36 chr19: 2,877,236-4,002,633 , GRCh37 chr19: 2,926,236-4,051,633 TEKTIP1, APBA3, 42 more genes
    nsv3915373copy number variation1nstd102humanPathogenic NCBI36 chr19: 1,516,574-4,059,126 , GRCh37 chr19: 1,565,574-4,108,126 , GRCh38 chr19: 1,565,575-4,108,128 LOC100419704, DIRAS1, 104 more genes
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