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Items: 1 to 20 of 149

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5903705copy number variation1nstd209human GRCh38 chr5: 174,044,767-174,044,823 , GRCh37.p13 chr5: 173,471,770-173,471,826 NSG2
    nsv5901718copy number variation1nstd209human GRCh38 chr5: 172,153,284-177,326,767 , GRCh37.p13 chr5: 171,580,288-176,753,768 , LOC107986487, 114 more genes
    nsv5580202copy number variation1nstd207human GRCh38 chr5: 174,068,676-174,068,728 , GRCh37.p13 chr5: 173,495,679-173,495,731 NSG2
    nsv5454574copy number variation1nstd206human GRCh38 chr5: 174,096,399-174,099,419 , GRCh37.p13 chr5: 173,523,402-173,526,422 NSG2
    nsv5312249copy number variation1nstd204human GRCh38.p13 chr5: 174,091,556-174,093,969 , GRCh37.p13 chr5: 173,518,559-173,520,972 NSG2
    nsv5233699copy number variation1nstd204human GRCh38.p13 chr5: 174,079,106-174,113,503 , GRCh37.p13 chr5: 173,506,109-173,540,506 LOC102724551, NSG2
    nsv5229611copy number variation1nstd204human GRCh38.p13 chr5: 174,091,601-174,094,000 , GRCh37.p13 chr5: 173,518,604-173,521,003 NSG2
    nsv5223583copy number variation1nstd204human GRCh38.p13 chr5: 174,091,568-174,093,984 , GRCh37.p13 chr5: 173,518,571-173,520,987 NSG2
    nsv5222353copy number variation1nstd204human GRCh38.p13 chr5: 174,091,443-174,092,584 , GRCh37.p13 chr5: 173,518,446-173,519,587 NSG2
    nsv4947364copy number variation1nstd200human GRCh38 chr5: 174,091,559-174,093,967 , GRCh37.p13 chr5: 173,518,562-173,520,970 NSG2
    nsv4825945copy number variation1nstd200human GRCh37 chr5: 173,518,562-173,520,970 , GRCh38.p12 chr5: 174,091,559-174,093,967 NSG2
    nsv4768375copy number variation1nstd102humanPathogenic GRCh37 chr5: 170,805,664-180,719,789 , GRCh38.p12 chr5: 171,378,660-181,292,788 LINC01863, PRDX2P3, 279 more genes
    nsv4763538inversion1nstd199human GRCh37 chr5: 170,260,689-178,183,120 , GRCh38.p12 chr5: 170,833,685-178,756,119 , BNIP1, 194 more genes
    nsv4736871copy number variation1nstd199human GRCh37 chr5: 173,495,698-173,495,755 , GRCh38.p12 chr5: 174,068,695-174,068,752 NSG2
    nsv3937748copy number variation1nstd167human GRCh37 chr5: 173,495,679-173,495,732 , GRCh38.p12 chr5: 174,068,676-174,068,729 NSG2
    nsv3924705copy number variation1nstd102humanPathogenic GRCh38 chr5: 173,237,772-176,614,618 , GRCh37 chr5: 172,664,775-176,041,619 , NCBI36 chr5: 172,597,381-175,974,225 RNF44, OR1X1P, 62 more genes
    nsv3924400copy number variation1nstd102humanPathogenic NCBI36 chr5: 156,185,101-180,629,412 , GRCh37 chr5: 156,252,523-180,696,806 , GRCh38 chr5: 156,825,512-181,269,805 CEP192P1, ARL2BPP6, 443 more genes
    nsv3921186copy number variation1nstd102humanPathogenic GRCh38 chr5: 164,386,701-181,269,805 , GRCh37 chr5: 163,813,707-180,696,806 , NCBI36 chr5: 163,746,285-180,629,412 TENM2, LOC107986479, 347 more genes
    nsv3921182copy number variation1nstd102humanPathogenic GRCh37 chr5: 149,094,155-180,699,152 , GRCh38 chr5: 149,714,592-181,272,151 , NCBI36 chr5: 149,074,348-180,631,758 RN7SKP148, TCOF1, 553 more genes
    nsv3920339copy number variation1nstd102humanPathogenic NCBI36 chr5: 164,323,950-180,629,412 , GRCh37.p13 chr5: 164,391,372-180,696,806 , GRCh38.p12 chr5: 164,964,366-181,269,805 MIR1229, LOC105377713, 343 more genes
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