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Items: 1 to 20 of 168

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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
    nsv7042771inversion1nstd229human GRCh38 chr5: 149,108,299-149,109,140 , GRCh37.p13 chr5: 148,487,862-148,488,703 SH3TC2-DT
    nsv7038217inversion1nstd229human GRCh38 chr5: 142,898,166-151,101,968 , GRCh37.p13 chr5: 142,277,731-150,481,529 RPS20P4, PPARGC1B, 126 more genes
    nsv6788183copy number variation1nstd229human GRCh38 chr5: 149,088,828-149,097,485 , GRCh37.p13 chr5: 148,468,391-148,477,048 SH3TC2-DT
    nsv6783075copy number variation1nstd229human GRCh38 chr5: 149,104,412-149,104,786 , GRCh37.p13 chr5: 148,483,975-148,484,349 SH3TC2-DT
    nsv6780096copy number variation1nstd229human GRCh38 chr5: 149,077,459-149,171,120 , GRCh37.p13 chr5: 148,457,022-148,550,683 RN7SKP145, ABLIM3, 1 more genes
    nsv6779184copy number variation1nstd229human GRCh38 chr5: 149,063,489-149,066,560 , GRCh37.p13 chr5: 148,443,052-148,446,123 SH3TC2, SH3TC2-DT
    nsv6778231copy number variation1nstd229human GRCh38 chr5: 149,059,688-149,064,646 , GRCh37.p13 chr5: 148,439,251-148,444,209 SH3TC2-DT, SH3TC2, 1 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
    nsv6407834copy number variation1nstd223human GRCh38 chr5: 149,093,561-149,093,987 , GRCh37.p13 chr5: 148,473,124-148,473,550 SH3TC2-DT
    nsv6407817copy number variation1nstd223human GRCh38 chr5: 149,063,489-149,066,559 , GRCh37.p13 chr5: 148,443,052-148,446,122 SH3TC2-DT, SH3TC2
    nsv6400022copy number variation1nstd223human GRCh38 chr5: 149,074,701-149,075,900 , GRCh37.p13 chr5: 148,454,264-148,455,463 SH3TC2-DT
    nsv6399218copy number variation1nstd223human GRCh38 chr5: 149,059,688-149,064,644 , GRCh37.p13 chr5: 148,439,251-148,444,207 SH3TC2, MIR584, 1 more genes
    nsv6398556copy number variation1nstd223human GRCh38 chr5: 149,105,414-149,105,839 , GRCh37.p13 chr5: 148,484,977-148,485,402 SH3TC2-DT
    nsv6312093copy number variation1nstd102humanUncertain significance GRCh37 chr5: 148,384,274-148,442,585 , GRCh38.p12 chr5: 149,004,711-149,063,022 SH3TC2-DT, RNU6-732P, 2 more genes
    nsv6244960mobile element insertion1nstd215human GRCh38 chr5: 149,083,289-149,083,289 , GRCh37.p13 chr5: 148,462,852-148,462,852 SH3TC2-DT
    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
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