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Items: 1 to 20 of 147

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7141187insertion1nstd232human GRCh37.p13 chr5: 162,939,202-162,939,202 , GRCh38.p12 chr5: 163,512,196-163,512,196 MAT2B
    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
    nsv6795894copy number variation1nstd229human GRCh38 chr5: 163,517,549-163,517,737 , GRCh37.p13 chr5: 162,944,555-162,944,743 MAT2B
    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
    nsv6788043copy number variation1nstd229human GRCh38 chr5: 163,505,190-163,505,213 , GRCh37.p13 chr5: 162,932,196-162,932,219 MAT2B
    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
    nsv6782986copy number variation1nstd229human GRCh38 chr5: 163,502,124-163,502,179 , GRCh37.p13 chr5: 162,929,130-162,929,185 MAT2B
    nsv6781395copy number variation1nstd229human GRCh38 chr5: 163,511,016-163,511,123 , GRCh37.p13 chr5: 162,938,022-162,938,129 MAT2B
    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
    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
    nsv6277659insertion1nstd214human GRCh38 chr5: 163,502,168-163,502,168 , GRCh37.p13 chr5: 162,929,174-162,929,174 MAT2B
    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
    nsv5952164insertion1nstd209human GRCh38 chr5: 163,502,168-163,502,168 , GRCh37.p13 chr5: 162,929,174-162,929,174 MAT2B
    nsv5628619insertion1nstd207human GRCh38 chr5: 163,502,168-163,502,168 , GRCh37.p13 chr5: 162,929,174-162,929,174 MAT2B
    nsv5536706insertion1nstd206human GRCh38 chr5: 163,502,179-163,502,219 , GRCh37.p13 chr5: 162,929,185-162,929,225 MAT2B
    nsv5469901copy number variation1nstd206human GRCh38 chr5: 163,501,679-163,502,008 , GRCh37.p13 chr5: 162,928,685-162,929,014 MAT2B
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