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Items: 1 to 20 of 116

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7045293inversion1nstd229human GRCh38 chr5: 73,247,847-76,069,477 , GRCh37.p13 chr5: 72,543,674-75,365,302 LOC107986423, NSA2, 48 more genes
    nsv6777325copy number variation1nstd229human GRCh38 chr5: 73,559,160-73,559,553 , GRCh37.p13 chr5: 72,854,985-72,855,378 ANKRA2
    nsv6770190copy number variation1nstd229human GRCh38 chr5: 73,545,001-73,551,600 , GRCh37.p13 chr5: 72,840,826-72,847,425 ANKRA2
    nsv6763618copy number variation1nstd229human GRCh38 chr5: 66,450,908-74,585,645 , GRCh37.p13 chr5: 65,746,736-73,881,470 LOC107986372, LOC105379027, 146 more genes
    nsv6575532inversion1nstd223human GRCh38 chr5: 73,557,810-73,558,695 , GRCh37.p13 chr5: 72,853,635-72,854,520 ANKRA2
    nsv6574398inversion1nstd223human GRCh38 chr5: 73,561,498-73,562,107 , GRCh37.p13 chr5: 72,857,323-72,857,932 ANKRA2
    nsv6136131copy number variation1nstd213human GRCh37 chr5: 70,130,000-73,760,001 , GRCh38.p12 chr5: 70,834,173-74,464,176 , BTF3, 69 more genes
    nsv6135436copy number variation1nstd213human GRCh37 chr5: 70,260,000-91,630,001 , GRCh38.p12 chr5: 70,964,173-92,334,184 , ARSB, 300 more genes
    nsv6135435copy number variation1nstd213human GRCh37 chr5: 69,990,000-73,820,001 , GRCh38.p12 chr5: 70,694,173-74,524,176 , BTF3, 71 more genes
    nsv6135198copy number variation1nstd213human GRCh37 chr5: 70,130,000-76,140,001 , GRCh38.p12 chr5: 70,834,173-76,844,176 , BTF3, 117 more genes
    nsv4675667copy number variation1nstd102humanPathogenic GRCh37 chr5: 72,790,061-97,478,870 , GRCh38.p12 chr5: 73,494,236-98,143,166 LOC101929380, LIX1-AS1, 318 more genes
    nsv4675088copy number variation1nstd102humanUncertain significance GRCh37 chr5: 72,829,994-74,076,751 , GRCh38.p12 chr5: 73,534,169-74,780,926 NSA2, RNU7-196P, 17 more genes
    nsv4436202copy number variation1nstd102humanUncertain significance GRCh37 chr5: 14,685,137-149,511,942 , GRCh38.p12 chr5: 14,685,028-150,132,379 RNU1-150P, RNU6-727P, 1757 more genes
    nsv3912593copy number variation1nstd102humanUncertain significance NCBI36 chr5: 332,389-180,837,866 , GRCh37.p13 chr5: 279,389-180,905,260 , GRCh38.p12 chr5: 279,274-181,478,259 LOC105378993, LOC107986375, 2492 more genes
    nsv3911585copy number variation1nstd102humanPathogenic NCBI36 chr5: 75,149-73,744,306 , GRCh38 chr5: 22,149-74,412,725 , GRCh37 chr5: 22,149-73,708,550 LINC02241, ATPSCKMT, 878 more genes
    nsv3889848copy number variation1nstd102humanPathogenic GRCh37 chr5: 17,628,741-176,575,720 , GRCh38.p12 chr5: 17,628,632-177,148,719 MEGF10, LOC100128407, 2080 more genes
    nsv3886374copy number variation1nstd102humanPathogenic GRCh37 chr5: 13,648-180,905,029 , GRCh38.p12 chr5: 13,648-181,478,028 LOC105374618, HARS1, 2499 more genes
    nsv3875235copy number variation2nstd102humanPathogenic GRCh37 chr5: 113,577-180,719,789 , GRCh38.p12 chr5: 113,462-181,292,788 SPEF2, NDST1, 2490 more genes
    nsv3871533copy number variation1nstd102humanPathogenic GRCh37 chr5: 25,328-180,693,344 , GRCh38.p12 chr5: 25,329-181,266,343 PCDHGC5, RGS14, 2492 more genes
    nsv3136522copy number variation2nstd151human GRCh37 chr5: 72,856,952-72,868,454 , GRCh38.p12 chr5: 73,561,127-73,572,629 ANKRA2, UTP15
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