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Items: 1 to 20 of 472

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098190copy number variation1nstd102humanUncertain significance GRCh37 chr8: 98,358,247-106,815,766 , GRCh38.p12 chr8: 97,346,019-105,803,538 RNU6-914P, RPL30, 159 more genes
    nsv7072181inversion1nstd229human GRCh38 chr8: 94,465,642-98,351,757 , GRCh37.p13 chr8: 95,477,870-99,363,985 SDC2, LOC100286997, 59 more genes
    nsv6858046copy number variation1nstd229human GRCh38 chr8: 97,841,699-97,842,367 , GRCh37.p13 chr8: 98,853,927-98,854,595 LAPTM4B
    nsv6857881copy number variation1nstd229human GRCh38 chr8: 97,853,343-97,856,673 , GRCh37.p13 chr8: 98,865,571-98,868,901 LAPTM4B, TMEM69P1, 1 more genes
    nsv6857365copy number variation1nstd229human GRCh38 chr8: 97,806,857-97,809,479 , GRCh37.p13 chr8: 98,819,085-98,821,707 LAPTM4B
    nsv6856771copy number variation1nstd229human GRCh38 chr8: 97,750,812-97,786,466 , GRCh37.p13 chr8: 98,763,040-98,798,694 LAPTM4B
    nsv6854755copy number variation1nstd229human GRCh38 chr8: 97,784,701-97,789,600 , GRCh37.p13 chr8: 98,796,929-98,801,828 LAPTM4B
    nsv6853763copy number variation1nstd229human GRCh38 chr8: 97,821,542-97,821,573 , GRCh37.p13 chr8: 98,833,770-98,833,801 LAPTM4B
    nsv6850840copy number variation1nstd229human GRCh38 chr8: 97,796,745-97,800,437 , GRCh37.p13 chr8: 98,808,973-98,812,665 LAPTM4B
    nsv6849583copy number variation1nstd229human GRCh38 chr8: 97,852,383-97,854,058 , GRCh37.p13 chr8: 98,864,611-98,866,286 TMEM69P1, LAPTM4B
    nsv6847850copy number variation1nstd229human GRCh38 chr8: 97,849,839-97,851,084 , GRCh37.p13 chr8: 98,862,067-98,863,312 LAPTM4B, TMEM69P1
    nsv6847159copy number variation1nstd229human GRCh38 chr8: 97,852,401-97,854,000 , GRCh37.p13 chr8: 98,864,629-98,866,228 LAPTM4B, TMEM69P1
    nsv6846133copy number variation1nstd229human GRCh38 chr8: 97,773,210-97,781,311 , GRCh37.p13 chr8: 98,785,438-98,793,539 LAPTM4B
    nsv6841551copy number variation1nstd229human GRCh38 chr8: 97,844,252-97,849,438 , GRCh37.p13 chr8: 98,856,480-98,861,666 LAPTM4B
    nsv6840961copy number variation1nstd229human GRCh38 chr8: 97,812,912-97,816,136 , GRCh37.p13 chr8: 98,825,140-98,828,364 LAPTM4B
    nsv6840313copy number variation1nstd229human GRCh38 chr8: 97,789,350-97,792,532 , GRCh37.p13 chr8: 98,801,578-98,804,760 LAPTM4B
    nsv6839535copy number variation1nstd229human GRCh38 chr8: 97,825,155-97,851,395 , GRCh37.p13 chr8: 98,837,383-98,863,623 LAPTM4B, TMEM69P1
    nsv6838460copy number variation1nstd229human GRCh38 chr8: 97,785,352-97,785,464 , GRCh37.p13 chr8: 98,797,580-98,797,692 LAPTM4B
    nsv6636450copy number variation1nstd102humanPathogenic GRCh37 chr8: 79,409,349-119,040,631 , GRCh38.p12 chr8: 78,497,114-118,028,392 MIR2053, RPS2P33, 507 more genes
    nsv6634360copy number variation1nstd102humanPathogenic GRCh37 chr8: 68,912,432-146,295,771 , GRCh38.p12 chr8: 68,000,197-145,070,385 WASHC5, LOC100132280, 1028 more genes
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