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Items: 1 to 20 of 86

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097513copy number variation1nstd102humanUncertain significance GRCh37 chr5: 147,774,340-149,681,936 , GRCh38.p12 chr5: 148,394,777-150,302,373 CSNK1A1, SLC26A2, 39 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
    nsv7053584inversion1nstd229human GRCh38 chr5: 144,534,922-150,861,041 , GRCh37.p13 chr5: 143,914,485-150,240,603 SMIM3, NAMPTP2, 102 more genes
    nsv7045608inversion1nstd229human GRCh38 chr5: 142,902,498-151,105,008 , GRCh37.p13 chr5: 142,282,063-150,484,569 FBXO38-DT, POU4F3, 126 more genes
    nsv7038217inversion1nstd229human GRCh38 chr5: 142,898,166-151,101,968 , GRCh37.p13 chr5: 142,277,731-150,481,529 RPS20P4, PPARGC1B, 126 more genes
    nsv6798035copy number variation1nstd229human GRCh38 chr5: 149,932,242-149,938,781 , GRCh37.p13 chr5: 149,311,805-149,318,344 PDE6A, MFFP2
    nsv6790669copy number variation1nstd229human GRCh38 chr5: 149,922,397-149,930,021 , GRCh37.p13 chr5: 149,301,960-149,309,584 PDE6A, MFFP2
    nsv6781880copy number variation1nstd229human GRCh38 chr5: 149,709,401-149,948,000 , GRCh37.p13 chr5: 149,088,964-149,327,563 PDE6A, MIR378A, 4 more genes
    nsv6636986copy number variation1nstd102humanPathogenic GRCh37 chr5: 147,164,969-149,315,489 , GRCh38.p12 chr5: 147,785,406-149,935,926 GRPEL2-AS1, PDE6A, 43 more genes
    nsv6413992copy number variation1nstd223human GRCh38 chr5: 149,932,601-149,938,600 , GRCh37.p13 chr5: 149,312,164-149,318,163 PDE6A, MFFP2
    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
    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
    nsv5549028insertion1nstd206human GRCh38 chr5: 149,932,224-149,932,224 , GRCh37.p13 chr5: 149,311,787-149,311,787 MFFP2, PDE6A
    nsv5036421inversion1nstd200human GRCh38 chr5: 85,193,812-162,906,830 , GRCh37.p13 chr5: 84,489,630-162,333,836 , PRR16, 1116 more genes
    nsv4947215copy number variation1nstd200human GRCh38 chr5: 93,957,557-155,223,076 , GRCh37.p13 chr5: 93,293,262-154,602,636 , TGFBI, 937 more genes
    nsv4939156copy number variation1nstd200human GRCh38 chr5: 149,932,242-149,938,779 , GRCh37.p13 chr5: 149,311,805-149,318,342 MFFP2, PDE6A
    nsv4885569inversion1nstd200human GRCh37 chr5: 84,489,636-162,333,841 , GRCh38.p12 chr5: 85,193,818-162,906,835 , UBE2B, 1116 more genes
    nsv4814943copy number variation1nstd200human GRCh37 chr5: 149,311,805-149,318,342 , GRCh38.p12 chr5: 149,932,242-149,938,779 MFFP2, PDE6A
    nsv4675358copy number variation1nstd102humanUncertain significance GRCh37 chr5: 148,953,230-149,414,017 , GRCh38.p12 chr5: 149,573,667-150,034,454 PPARGC1B, RPS20P4, 10 more genes
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