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Items: 1 to 20 of 95

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096524copy number variation1nstd102humanPathogenic GRCh37 chr2: 85,766,411-86,564,633 , GRCh38.p12 chr2: 85,539,288-86,337,510 GPR160P1, USP39, 27 more genes
    nsv7042863inversion1nstd229human GRCh38 chr2: 85,463,758-85,729,166 , GRCh37.p13 chr2: 85,690,881-85,956,289 PARTICL, RNF181, 14 more genes
    nsv6681244copy number variation1nstd229human GRCh38 chr2: 85,286,438-85,844,313 , GRCh37.p13 chr2: 85,513,561-86,071,436 RETSAT, SH2D6, 30 more genes
    nsv6636862copy number variation1nstd102humanUncertain significance GRCh37 chr2: 85,786,007-86,559,358 , GRCh38.p12 chr2: 85,558,884-86,332,235 MIR4779, RN7SKP83, 25 more genes
    nsv6634330copy number variation1nstd102humanPathogenic GRCh37 chr2: 11,504,318-111,365,996 , GRCh38.p12 chr2: 11,364,192-110,608,419 CYP1B1-AS1, LOC107985771, 1649 more genes
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 more genes
    nsv6314726copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 40,607,042-146,902,764 , GRCh38.p12 chr2: 40,379,902-146,145,196 ACTG2, ACYP2, 1713 more genes
    nsv6313890copy number variation1nstd102humanPathogenic GRCh37 chr2: 82,486,900-87,322,042 , GRCh38.p12 chr2: 82,259,776-87,094,919 LOC105374836, LOC105374833, 93 more genes
    nsv6112750copy number variation1nstd102humanPathogenic GRCh37 chr2: 81,209,244-86,688,030 , GRCh38.p12 chr2: 80,982,120-86,460,907 VAMP8, TMSB10, 86 more genes
    nsv5554214mobile element insertion1nstd206human GRCh38 chr2: 43,826,578-177,947,868 , GRCh37.p13 chr2: 44,053,717-178,812,595 , POLR1B, 2149 more genes
    nsv5452687copy number variation1nstd206human GRCh38 chr2: 85,577,131-85,578,543 , GRCh37.p13 chr2: 85,804,254-85,805,666 VAMP8
    nsv5451542copy number variation1nstd206human GRCh38 chr2: 85,577,130-85,579,682 , GRCh37.p13 chr2: 85,804,253-85,806,805 VAMP8
    nsv5436982copy number variation1nstd206human GRCh38 chr2: 85,539,948-89,142,574 , GRCh37.p13 chr2: 85,767,071-89,442,057 , IGKV2-18, 129 more genes
    nsv5360873translocation1nstd200human GRCh38 chr2: 85,578,543-85,578,543 , GRCh38 chr2: 85,577,131-85,577,131 , GRCh37.p13 chr2: 85,805,666-85,805,666 , GRCh37.p13 chr2: 85,804,254-85,804,254 VAMP8
    nsv5035923inversion1nstd200human GRCh38 chr2: 83,726,586-172,391,178 , GRCh37.p13 chr2: 83,953,710-173,255,906 , MTND2P21, 1427 more genes
    nsv4908903copy number variation1nstd200human GRCh38 chr2: 85,577,130-85,579,682 , GRCh37.p13 chr2: 85,804,253-85,806,805 VAMP8
    nsv4728539copy number variation1nstd102humanUncertain significance GRCh37 chr2: 85,786,006-86,559,358 , GRCh38.p12 chr2: 85,558,883-86,332,235 ST3GAL5-AS1, TMEM150A, 25 more genes
    nsv4595820copy number variation1nstd183human GRCh37 chr2: 85,505,867-85,911,446 , GRCh38.p12 chr2: 85,278,744-85,684,323 , RN7SL251P, 23 more genes
    nsv4584593copy number variation1nstd183human GRCh37 chr2: 85,508,825-85,911,677 , GRCh38.p12 chr2: 85,281,702-85,684,554 , USP39, 24 more genes
    nsv4451607copy number variation1nstd102humanPathogenic GRCh37 chr2: 77,907,114-87,330,965 , GRCh38.p12 chr2: 77,679,988-87,103,842 REEP1, RBX1P1, 134 more genes
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