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Items: 1 to 20 of 155

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7045576inversion1nstd229human GRCh38 chr5: 180,805,627-181,281,045 , GRCh37.p13 chr5: 180,232,627-180,708,046 RPL13P10, TRV-AAC1-3, 46 more genes
    nsv7044684inversion1nstd229human GRCh38 chr5: 181,222,491-181,283,985 , GRCh37.p13 chr5: 180,649,491-180,710,986 TRV-CAC1-5, TRIM52, 8 more genes
    nsv7044540inversion1nstd229human GRCh38 chr5: 180,832,761-181,281,244 , GRCh37.p13 chr5: 180,259,761-180,708,245 LOC100128762, SNORD95, 44 more genes
    nsv6791316copy number variation1nstd229human GRCh38 chr5: 181,241,639-181,242,172 , GRCh37.p13 chr5: 180,668,639-180,669,172 RACK1, SNORD96A, 1 more genes
    nsv6788959copy number variation1nstd229human GRCh38 chr5: 181,100,901-181,281,600 , GRCh37.p13 chr5: 180,527,901-180,708,601 TRV-AAC1-4, TRV-AAC1-2, 30 more genes
    nsv6636455copy number variation1nstd102humanUncertain significance GRCh37 chr5: 180,148,276-180,719,789 , GRCh38.p12 chr5: 180,721,276-181,292,788 OR2Y1, TRV-AAC1-2, 48 more genes
    nsv6634369copy number variation1nstd102humanPathogenic GRCh37 chr5: 170,350,336-180,719,789 , GRCh38.p12 chr5: 170,923,332-181,292,788 GFPT2, FOXO1B, 287 more genes
    nsv6630143copy number variation1nstd224human GRCh37 chr5: 180,535,802-180,687,526 , GRCh38.p12 chr5: 181,108,802-181,260,525 TRP-TGG3-1, TRV-AAC1-4, 27 more genes
    nsv6413193copy number variation1nstd223human GRCh38 chr5: 181,234,916-181,279,833 , GRCh37.p13 chr5: 180,661,916-180,706,834 RACK1, TRIM41, 5 more genes
    nsv6408274copy number variation1nstd223human GRCh38 chr5: 180,927,801-181,343,300 , GRCh37.p13 chr5: 180,354,801-180,770,301 TRK-CTT2-2, ARPP19P1, 47 more genes
    nsv6399064copy number variation1nstd223human GRCh38 chr5: 180,956,101-181,297,100 , GRCh37.p13 chr5: 180,383,101-180,724,101 FOXO1B, CTC-338M12.4, 40 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
    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
    nsv5464944copy number variation1nstd206human GRCh38 chr5: 181,241,690-181,241,978 , GRCh37.p13 chr5: 180,668,690-180,668,978 SNORD96A, RACK1, 1 more genes
    nsv5457328copy number variation1nstd206human GRCh38 chr5: 181,241,639-181,242,098 , GRCh37.p13 chr5: 180,668,639-180,669,098 SNORD96A, RACK1, 1 more genes
    nsv5231911copy number variation1nstd204human GRCh38.p13 chr5: 181,242,777-181,243,776 , GRCh37.p13 chr5: 180,669,777-180,670,776 RACK1, SNORD95
    nsv4768375copy number variation1nstd102humanPathogenic GRCh37 chr5: 170,805,664-180,719,789 , GRCh38.p12 chr5: 171,378,660-181,292,788 LINC01863, PRDX2P3, 279 more genes
    nsv4729100copy number variation1nstd102humanUncertain significance GRCh37 chr5: 180,533,007-180,719,789 , GRCh38.p12 chr5: 181,106,007-181,292,788 TRV-AAC1-4, TRIM7-AS2, 27 more genes
    nsv4728969copy number variation1nstd102humanUncertain significance GRCh37 chr5: 180,064,955-180,719,789 , GRCh38.p12 chr5: 180,637,955-181,292,788 TMEM69P2, OR2V1, 52 more genes
    nsv4675041copy number variation1nstd102humanUncertain significance GRCh37 chr5: 179,479,838-180,695,063 , GRCh38.p12 chr5: 180,052,838-181,268,062 OR2AI1P, SNORD96A, 64 more genes
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