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Items: 1 to 20 of 132

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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
    nsv7040173inversion1nstd229human GRCh38 chr5: 161,553,790-164,538,923 , GRCh37.p13 chr5: 160,980,796-163,965,929 NUDCD2, LOC102724458, 23 more genes
    nsv7038458inversion1nstd229human GRCh38 chr5: 163,444,240-163,444,851 , GRCh37.p13 chr5: 162,871,246-162,871,857 CCNG1, NUDCD2
    nsv6794033copy number variation1nstd229human GRCh38 chr5: 163,403,337-163,477,662 , GRCh37.p13 chr5: 162,830,343-162,904,668 HMMR, CCNG1, 2 more genes
    nsv6789571copy number variation1nstd229human GRCh38 chr5: 163,449,320-164,407,694 , GRCh37.p13 chr5: 162,876,326-163,834,700 LSM1P2, LINC03000, 7 more genes
    nsv6784047copy number variation1nstd229human GRCh38 chr5: 162,954,466-164,681,920 , GRCh37.p13 chr5: 162,381,472-164,108,926 LOC100419716, CCNG1, 14 more genes
    nsv6782347copy number variation1nstd229human GRCh38 chr5: 163,443,185-163,452,418 , GRCh37.p13 chr5: 162,870,191-162,879,424 CCNG1, NUDCD2
    nsv6780091copy number variation1nstd229human GRCh38 chr5: 163,413,470-163,547,863 , GRCh37.p13 chr5: 162,840,476-162,974,869 MAT2B, HMMR-AS1, 4 more genes
    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
    nsv6414791copy number variation1nstd223human GRCh38 chr5: 163,403,337-163,477,662 , GRCh37.p13 chr5: 162,830,343-162,904,668 NUDCD2, LOC105377700, 2 more genes
    nsv6404373copy number variation1nstd223human GRCh38 chr5: 163,428,366-163,472,178 , GRCh37.p13 chr5: 162,855,372-162,899,184 HMMR, LOC105377700, 2 more genes
    nsv6396816copy number variation1nstd223human GRCh38 chr5: 163,443,060-163,455,514 , GRCh37.p13 chr5: 162,870,066-162,882,520 CCNG1, NUDCD2
    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
    nsv6141369copy number variation1nstd206human GRCh38 chr5: 163,425,070-163,470,265 , GRCh37.p13 chr5: 162,852,076-162,897,271 CCNG1, LOC105377700, 2 more genes
    nsv6136090copy number variation1nstd213human GRCh37 chr5: 161,030,000-172,600,001 , GRCh38.p12 chr5: 161,602,994-173,172,998 BNIP1, CCNG1, 130 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
    nsv6019880copy number variation1nstd212human GRCh38 chr5: 163,445,141-163,445,271 , GRCh37.p13 chr5: 162,872,147-162,872,277 NUDCD2, CCNG1
    nsv5677194mobile element insertion1nstd211human GRCh38 chr5: 163,448,274-163,448,274 , GRCh37.p13 chr5: 162,875,280-162,875,280 CCNG1, NUDCD2
    nsv5675980mobile element insertion2nstd211human GRCh38 chr5: 163,446,471-163,446,471 , GRCh37.p13 chr5: 162,873,477-162,873,477 NUDCD2, CCNG1
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