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Items: 1 to 20 of 5002

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5311452copy number variation1nstd204human GRCh38.p13 chr13: 108,530,675-109,109,344 , GRCh37.p13 chr13: 109,183,023-109,761,692 MYO16
    nsv5313073copy number variation1nstd204human GRCh38.p13 chr4: 178,681,713-179,242,922 , GRCh37.p13 chr4: 179,602,867-180,164,076 LOC105377563
    nsv5300871copy number variation1nstd204human GRCh38.p13 chr6: 161,567,717-162,085,662 , GRCh37.p13 chr6: 161,988,749-162,506,694 PRKN
    nsv5303733copy number variation1nstd204human GRCh38.p13 chr9: 15,788,082-16,126,279 , GRCh37.p13 chr9: 15,788,080-16,126,277 CCDC171
    nsv5322240copy number variation1nstd204human GRCh38.p13 chr18: 67,136,133-67,472,693 , GRCh37.p13 chr18: 64,803,370-65,139,930 RPL31P9
    nsv5289769copy number variation1nstd204human GRCh38.p13 chr1: 175,460,977-175,792,706 , GRCh37.p13 chr1: 175,430,113-175,761,842 TNR
    nsv5305570copy number variation1nstd204human GRCh38.p13 chr4: 130,945,854-131,243,605 , GRCh37.p13 chr4: 131,867,009-132,164,760 LOC105377422
    nsv5309226copy number variation1nstd204human GRCh38.p13 chr7: 52,188,031-52,483,597 , GRCh37.p13 chr7: 52,255,727-52,551,293 LOC107986796
    nsv5315850copy number variation1nstd204human GRCh38.p13 chr5: 61,837,817-62,131,033 , GRCh37.p13 chr5: 61,133,644-61,426,860 LOC105378998
    nsv5310934copy number variation1nstd204human GRCh38.p13 chr7: 80,791,011-81,070,927 , GRCh37.p13 chr7: 80,420,327-80,700,243 SEMA3C
    nsv5307937copy number variation1nstd204human GRCh38.p13 chr5: 7,505,014-7,781,819 , GRCh37.p13 chr5: 7,505,127-7,781,932 ADCY2
    nsv5318416copy number variation1nstd204human GRCh38.p13 chr13: 88,626,595-88,871,726 , GRCh37.p13 chr13: 89,278,849-89,523,980 LINC00560
    nsv5315603copy number variation1nstd204human GRCh38.p13 chr8: 946,144-1,191,480 , GRCh37.p13 chr8: 896,144-1,141,480 DLGAP2
    nsv5300375copy number variation1nstd204human GRCh38.p13 chr2: 1,003,524-1,214,443 , GRCh37.p13 chr2: 999,210-1,210,129 SNTG2
    nsv5296854copy number variation1nstd204human GRCh38.p13 chr1: 4,120,379-4,312,118 , GRCh37.p13 chr1: 4,180,439-4,372,178 EEF1DP6
    nsv5314716copy number variation1nstd204human GRCh38.p13 chr4: 57,366,287-57,547,670 , GRCh37.p13 chr4: 58,232,453-58,413,836 LINC02380
    nsv5315728copy number variation1nstd204human GRCh38.p13 chr10: 101,379,435-101,552,631 , GRCh37.p13 chr10: 103,139,192-103,312,388 BTRC
    nsv5304937copy number variation1nstd204human GRCh38.p13 chr4: 32,246,848-32,418,308 , GRCh37.p13 chr4: 32,248,470-32,419,930 LINC02353
    nsv5301431copy number variation1nstd204human GRCh38.p13 chr11: 96,564,349-96,735,323 , GRCh37.p13 chr11: 96,437,576-96,606,323 AKTIPP3
    nsv5314893copy number variation1nstd204human GRCh38.p13 chr7: 101,323,450-101,492,808 , GRCh37.p13 chr7: 100,966,731-101,136,089 COL26A1
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