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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5896500copy number variation1nstd209human GRCh38 chr3: 171,525,972-180,293,041 , GRCh37.p13 chr3: 171,243,761-180,010,829 , RNU6-1120P, 95 more genes
    nsv5896060copy number variation1nstd209human GRCh38 chr3: 175,105,827-175,105,923 , GRCh37.p13 chr3: 174,823,617-174,823,713 NAALADL2-AS3, NAALADL2
    nsv5453639copy number variation1nstd206human GRCh38 chr3: 163,047,000-198,226,000 , GRCh37.p13 chr3: 162,764,788-197,952,871 , MIR922, 587 more genes
    nsv5367203translocation1nstd200human GRCh38 chr3: 175,076,185-175,076,185 , GRCh38 chr3: 175,078,076-175,078,076 , GRCh37.p13 chr3: 174,795,866-174,795,866 , GRCh37.p13 chr3: 174,793,975-174,793,975 NAALADL2, NAALADL2-AS3
    nsv5367202translocation1nstd200human GRCh38 chr3: 175,077,998-175,077,998 , GRCh38 chr3: 175,074,298-175,074,298 , GRCh37.p13 chr3: 174,795,788-174,795,788 , GRCh37.p13 chr3: 174,792,088-174,792,088 NAALADL2, NAALADL2-AS3
    nsv5344986translocation1nstd200human GRCh37 chr3: 174,795,788-174,795,788 , GRCh37 chr3: 174,792,088-174,792,088 , GRCh38.p12 chr3: 175,077,998-175,077,998 , GRCh38.p12 chr3: 175,074,298-175,074,298 NAALADL2-AS3, NAALADL2
    nsv5334563translocation1nstd200human GRCh37 chr3: 174,793,975-174,793,975 , GRCh37 chr3: 174,795,866-174,795,866 , GRCh38.p12 chr3: 175,078,076-175,078,076 , GRCh38.p12 chr3: 175,076,185-175,076,185 NAALADL2, NAALADL2-AS3
    nsv5313144copy number variation1nstd204human GRCh38.p13 chr3: 175,091,330-175,093,359 , GRCh37.p13 chr3: 174,809,120-174,811,149 NAALADL2-AS3, NAALADL2
    nsv5090952mobile element insertion1nstd203human GRCh38 chr3: 175,086,902-175,086,915 , GRCh37.p13 chr3: 174,804,692-174,804,705 NAALADL2, NAALADL2-AS3
    nsv5033132inversion1nstd200human GRCh38 chr3: 147,205,794-180,217,342 , GRCh37.p13 chr3: 146,923,581-179,935,130 , LOC105374154, 433 more genes
    nsv4920824copy number variation1nstd200human GRCh38 chr3: 175,085,380-175,089,865 , GRCh37.p13 chr3: 174,803,170-174,807,655 NAALADL2, NAALADL2-AS3
    nsv4920823copy number variation1nstd200human GRCh38 chr3: 175,079,454-175,083,738 , GRCh37.p13 chr3: 174,797,244-174,801,528 NAALADL2, NAALADL2-AS3
    nsv4798648copy number variation1nstd200human GRCh37 chr3: 174,823,423-174,824,567 , GRCh38.p12 chr3: 175,105,633-175,106,777 NAALADL2-AS3, NAALADL2
    nsv4798647copy number variation1nstd200human GRCh37 chr3: 174,803,169-174,807,656 , GRCh38.p12 chr3: 175,085,379-175,089,866 NAALADL2-AS3, NAALADL2
    nsv4674680copy number variation1nstd102humanPathogenic GRCh37 chr3: 169,617,690-190,593,854 , GRCh38.p12 chr3: 169,899,902-190,876,065 RNU6-1120P, LOC105374262, 323 more genes
    nsv4550778insertion1nstd166human GRCh37.p13 chr3: 174,819,836-174,819,836 , GRCh38.p12 chr3: 175,102,046-175,102,046 NAALADL2, NAALADL2-AS3
    nsv4469650mobile element insertion1nstd166human GRCh37.p13 chr3: 174,807,894-174,807,894 , GRCh38.p12 chr3: 175,090,104-175,090,104 NAALADL2, NAALADL2-AS3
    nsv4334621sequence alteration1nstd166human GRCh37.p13 chr3: 174,792,108-174,795,865 , GRCh38.p12 chr3: 175,074,318-175,078,075 NAALADL2, NAALADL2-AS3
    nsv4327395inversion1nstd166human GRCh37.p13 chr3: 126,265,569-194,265,571 , GRCh38.p12 chr3: 126,546,726-194,544,842 , ACTG1P1, 1039 more genes
    nsv4104337copy number variation1nstd166human GRCh37.p13 chr3: 174,828,590-174,828,640 , GRCh38.p12 chr3: 175,110,800-175,110,850 NAALADL2-AS3, NAALADL2
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