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Items: 1 to 20 of 646

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097139copy number variation1nstd102humanUncertain significance GRCh37 chr5: 33,944,753-39,364,566 , GRCh38.p12 chr5: 33,944,648-39,364,464 RNU7-75P, UGT3A1, 77 more genes
    nsv7052596inversion1nstd229human GRCh38 chr5: 33,502,543-34,969,892 , GRCh37.p13 chr5: 33,502,648-34,969,997 TTC23L, DNAJC21, 22 more genes
    nsv7048548inversion1nstd229human GRCh38 chr5: 34,021,798-34,024,029 , GRCh37.p13 chr5: 34,021,903-34,024,134 C1QTNF3-AMACR, C1QTNF3
    nsv7039407inversion1nstd229human GRCh38 chr5: 32,373,124-34,861,255 , GRCh37.p13 chr5: 32,373,230-34,861,360 TTC23L, LOC105374715, 31 more genes
    nsv6777237copy number variation1nstd229human GRCh38 chr5: 34,017,101-34,033,700 , GRCh37.p13 chr5: 34,017,206-34,033,805 C1QTNF3, C1QTNF3-AMACR
    nsv6776527copy number variation1nstd229human GRCh38 chr5: 34,047,001-34,065,100 , GRCh37.p13 chr5: 34,047,106-34,065,205 C1QTNF3, C1QTNF3-AMACR
    nsv6775216copy number variation1nstd229human GRCh38 chr5: 34,020,340-34,020,594 , GRCh37.p13 chr5: 34,020,445-34,020,699 C1QTNF3, C1QTNF3-AMACR
    nsv6773565copy number variation1nstd229human GRCh38 chr5: 34,053,861-34,053,915 , GRCh37.p13 chr5: 34,053,966-34,054,020 C1QTNF3-AMACR, C1QTNF3
    nsv6772679copy number variation1nstd229human GRCh38 chr5: 34,142,713-34,142,755 , GRCh37.p13 chr5: 34,142,818-34,142,860 C1QTNF3
    nsv6771881copy number variation1nstd229human GRCh38 chr5: 34,056,261-34,058,177 , GRCh37.p13 chr5: 34,056,366-34,058,282 C1QTNF3, C1QTNF3-AMACR
    nsv6771061copy number variation1nstd229human GRCh38 chr5: 34,022,701-34,034,200 , GRCh37.p13 chr5: 34,022,806-34,034,305 C1QTNF3, C1QTNF3-AMACR
    nsv6770449copy number variation1nstd229human GRCh38 chr5: 34,018,101-34,048,400 , GRCh37.p13 chr5: 34,018,206-34,048,505 C1QTNF3, C1QTNF3-AMACR
    nsv6769884copy number variation1nstd229human GRCh38 chr5: 34,071,515-34,073,592 , GRCh37.p13 chr5: 34,071,620-34,073,697 C1QTNF3, C1QTNF3-AMACR
    nsv6769501copy number variation1nstd229human GRCh38 chr5: 34,073,901-34,086,500 , GRCh37.p13 chr5: 34,074,006-34,086,605 C1QTNF3, C1QTNF3-AMACR
    nsv6768437copy number variation1nstd229human GRCh38 chr5: 34,027,501-34,033,600 , GRCh37.p13 chr5: 34,027,606-34,033,705 C1QTNF3-AMACR, C1QTNF3
    nsv6766998copy number variation1nstd229human GRCh38 chr5: 34,018,110-34,048,370 , GRCh37.p13 chr5: 34,018,215-34,048,475 C1QTNF3-AMACR, C1QTNF3
    nsv6766889copy number variation1nstd229human GRCh38 chr5: 34,074,201-34,087,800 , GRCh37.p13 chr5: 34,074,306-34,087,905 C1QTNF3-AMACR, C1QTNF3
    nsv6766793copy number variation1nstd229human GRCh38 chr5: 34,018,039-34,019,651 , GRCh37.p13 chr5: 34,018,144-34,019,756 C1QTNF3, C1QTNF3-AMACR
    nsv6764896copy number variation1nstd229human GRCh38 chr5: 34,109,499-34,114,614 , GRCh37.p13 chr5: 34,109,604-34,114,719 C1QTNF3, C1QTNF3-AMACR
    nsv6764693copy number variation1nstd229human GRCh38 chr5: 33,302,234-34,039,432 , GRCh37.p13 chr5: 33,302,340-34,039,537 TARS1, SLC45A2, 12 more genes
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