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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7093376copy number variation1nstd102humanLikely pathogenic GRCh37 chr5: 156,786,013-162,945,369 , GRCh38.p12 chr5: 157,359,005-163,518,363 ADRA1B, CCNG1, 81 more genes
    nsv7054438inversion1nstd229human GRCh38 chr5: 158,806,124-160,433,845 , GRCh37.p13 chr5: 158,233,132-159,860,852 LINC01845, TTC1, 30 more genes
    nsv6797124copy number variation1nstd229human GRCh38 chr5: 160,429,172-160,433,019 , GRCh37.p13 chr5: 159,856,179-159,860,026 PTTG1
    nsv6796943copy number variation1nstd229human GRCh38 chr5: 160,393,469-160,449,653 , GRCh37.p13 chr5: 159,820,476-159,876,660 FAM200C, PTTG1, 1 more genes
    nsv6794984copy number variation1nstd229human GRCh38 chr5: 159,275,371-163,261,193 , GRCh37.p13 chr5: 158,702,379-162,688,199 LOC105377685, CCNJL, 45 more genes
    nsv6787693copy number variation1nstd229human GRCh38 chr5: 160,428,898-160,432,509 , GRCh37.p13 chr5: 159,855,905-159,859,516 PTTG1
    nsv6784956copy number variation1nstd229human GRCh38 chr5: 160,393,399-160,439,014 , GRCh37.p13 chr5: 159,820,406-159,866,021 PTTG1, SLU7, 1 more genes
    nsv6780899copy number variation1nstd229human GRCh38 chr5: 160,424,506-160,431,171 , GRCh37.p13 chr5: 159,851,513-159,858,178 PTTG1
    nsv6636891copy number variation1nstd102humanPathogenic GRCh37 chr5: 150,535,183-172,906,793 , GRCh38.p12 chr5: 151,155,622-173,479,790 EFCAB9, LOC112267936, 287 more genes
    nsv6636858copy number variation1nstd102humanUncertain significance GRCh37 chr5: 159,535,230-161,656,766 , GRCh38.p12 chr5: 160,108,223-162,229,760 MIR146A, SNRPEP1, 23 more genes
    nsv6406754copy number variation1nstd223human GRCh38 chr5: 160,428,898-160,432,506 , GRCh37.p13 chr5: 159,855,905-159,859,513 PTTG1
    nsv6315448copy number variation1nstd102humanPathogenic GRCh37 chr5: 149,010,383-180,719,789 , GRCh38.p12 chr5: 149,630,820-181,292,788 GRM6, MIR1229, 554 more genes
    nsv6315317copy number variation1nstd102humanUncertain significance GRCh38 chr5: 158,887,731-164,722,046 , GRCh37.p13 chr5: 158,314,739-164,149,052 LINC03000, SNRPEP1, 64 more genes
    nsv6290966copy number variation1nstd102humannot provided GRCh37 chr5: 155,970,607-162,450,579 , GRCh38.p12 chr5: 156,543,597-163,023,573 C1QTNF2, MED7, 86 more genes
    nsv6135660copy number variation1nstd213human GRCh37 chr5: 158,750,000-159,990,001 , GRCh38.p12 chr5: 159,322,992-160,562,994 ADRA1B, FABP6, 25 more genes
    nsv6135388copy number variation1nstd213human GRCh37 chr5: 153,010,000-160,030,001 , GRCh38.p12 chr5: 153,630,440-160,602,994 ADRA1B, EBF1, 107 more genes
    nsv6135205copy number variation1nstd213human GRCh37 chr5: 91,690,000-180,740,001 , GRCh38.p12 chr5: 92,354,293-181,313,000 ADRA1B, ASS1P10, 1378 more genes
    nsv6003765copy number variation1nstd212human GRCh38 chr5: 160,423,177-160,423,236 , GRCh37.p13 chr5: 159,850,184-159,850,243 PTTG1
    nsv5898406copy number variation1nstd209human GRCh38 chr5: 160,423,168-160,423,225 , GRCh37.p13 chr5: 159,850,175-159,850,232 PTTG1
    nsv5301580copy number variation1nstd204human GRCh38.p13 chr5: 160,428,894-160,432,508 , GRCh37.p13 chr5: 159,855,901-159,859,515 PTTG1
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