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Items: 1 to 20 of 138

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097027copy number variation1nstd102humanUncertain significance GRCh37 chr5: 150,885,126-151,304,110 , GRCh38.p12 chr5: 151,505,565-151,924,549 CLMAT3, LOC100652758, 14 more genes
    nsv7053998inversion1nstd229human GRCh38 chr5: 148,749,982-154,424,819 , GRCh37.p13 chr5: 148,129,545-153,804,379 HMGXB3, RN7SL868P, 102 more genes
    nsv7040531inversion1nstd229human GRCh38 chr5: 151,482,879-155,518,141 , GRCh37.p13 chr5: 150,862,440-154,897,701 RN7SL803P, MRPL22, 56 more genes
    nsv6797961copy number variation1nstd229human GRCh38 chr5: 151,584,471-151,688,362 , GRCh37.p13 chr5: 150,964,032-151,067,923 FAT2, LOC105378231, 2 more genes
    nsv6793956copy number variation1nstd229human GRCh38 chr5: 151,667,600-151,669,663 , GRCh37.p13 chr5: 151,047,161-151,049,224 SPARC
    nsv6791587copy number variation1nstd229human GRCh38 chr5: 151,620,776-151,686,940 , GRCh37.p13 chr5: 151,000,337-151,066,501 SPARC, CLMAT3, 1 more genes
    nsv6786765copy number variation1nstd229human GRCh38 chr5: 151,663,540-151,664,048 , GRCh37.p13 chr5: 151,043,101-151,043,609 SPARC
    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
    nsv6414130copy number variation1nstd223human GRCh38 chr5: 151,620,776-151,686,940 , GRCh37.p13 chr5: 151,000,337-151,066,501 LOC105378231, CLMAT3, 1 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
    nsv6244969mobile element insertion1nstd215human GRCh38 chr5: 151,660,622-151,660,622 , GRCh37.p13 chr5: 151,040,183-151,040,183 SPARC
    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
    nsv6135120copy number variation1nstd213human GRCh37 chr5: 143,910,000-152,670,001 , GRCh38.p12 chr5: 144,530,437-153,290,441 ADRB2, ANXA6, 143 more genes
    nsv5473248copy number variation1nstd206human GRCh38 chr5: 151,681,189-151,682,503 , GRCh37.p13 chr5: 151,060,750-151,062,064 CLMAT3, SPARC
    nsv5340686translocation1nstd200human GRCh37 chr5: 151,066,424-151,066,424 , GRCh37 chr5: 151,055,764-151,055,764 , GRCh38.p12 chr5: 151,676,203-151,676,203 , GRCh38.p12 chr5: 151,686,863-151,686,863 CLMAT3, SPARC
    nsv5328731translocation1nstd204human GRCh37.p13 chr5: 151,055,763-151,055,763 , GRCh37.p13 chr5: 151,066,424-151,066,424 , GRCh38.p13 chr5: 151,686,863-151,686,863 , GRCh38.p13 chr5: 151,676,202-151,676,202 SPARC, CLMAT3
    nsv5322787translocation1nstd204human GRCh38.p13 chr15: 48,468,536-48,468,536 , GRCh37.p13 chr15: 48,760,733-48,760,733 , GRCh37.p13 chr5: 151,055,694-151,055,694 , GRCh38.p13 chr5: 151,676,133-151,676,133 FBN1, SPARC, 1 more genes
    nsv5316459copy number variation1nstd204human GRCh37.p13 chr5: 151,054,144-151,065,792 , GRCh38.p13 chr5: 151,674,583-151,686,231 SPARC, CLMAT3
    nsv5231404copy number variation1nstd204human GRCh38.p13 chr5: 151,674,485-151,680,915 , GRCh37.p13 chr5: 151,054,046-151,060,476 SPARC, CLMAT3
    nsv5231023copy number variation1nstd204human GRCh38.p13 chr5: 151,678,429-151,679,665 , GRCh37.p13 chr5: 151,057,990-151,059,226 CLMAT3, SPARC
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