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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
    nsv5901718copy number variation1nstd209human GRCh38 chr5: 172,153,284-177,326,767 , GRCh37.p13 chr5: 171,580,288-176,753,768 , LOC107986487, 114 more genes
    nsv5472974copy number variation1nstd206human GRCh38 chr5: 175,487,179-175,487,236 , GRCh37.p13 chr5: 174,914,182-174,914,239 SFXN1
    nsv5469468copy number variation1nstd206human GRCh38 chr5: 175,369,549-175,617,319 , GRCh37.p13 chr5: 174,796,552-175,044,322 SFXN1, DRD1
    nsv5171024mobile element insertion1nstd203human GRCh38 chr5: 175,501,232-175,501,249 , GRCh37.p13 chr5: 174,928,235-174,928,252 SFXN1
    nsv4949239copy number variation1nstd200human GRCh38 chr5: 175,527,908-175,537,324 , GRCh37.p13 chr5: 174,954,911-174,964,327 SFXN1
    nsv4949238copy number variation1nstd200human GRCh38 chr5: 175,492,918-175,499,119 , GRCh37.p13 chr5: 174,919,921-174,926,122 SFXN1
    nsv4947425copy number variation1nstd200human GRCh38 chr5: 175,502,757-175,503,817 , GRCh37.p13 chr5: 174,929,760-174,930,820 SFXN1
    nsv4947424copy number variation1nstd200human GRCh38 chr5: 175,495,972-175,500,776 , GRCh37.p13 chr5: 174,922,975-174,927,779 SFXN1
    nsv4825977copy number variation1nstd200human GRCh37 chr5: 174,922,975-174,927,779 , GRCh38.p12 chr5: 175,495,972-175,500,776 SFXN1
    nsv4824398copy number variation1nstd200human GRCh37 chr5: 174,919,921-174,926,122 , GRCh38.p12 chr5: 175,492,918-175,499,119 SFXN1
    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
    nsv4495537mobile element insertion1nstd166human GRCh37.p13 chr5: 174,913,244-174,913,244 , GRCh38.p12 chr5: 175,486,241-175,486,241 SFXN1
    nsv4124586copy number variation1nstd166human GRCh37.p13 chr5: 174,922,969-174,927,779 , GRCh38.p12 chr5: 175,495,966-175,500,776 SFXN1
    nsv4123747copy number variation1nstd166human GRCh37.p13 chr5: 174,921,702-174,927,106 , GRCh38.p12 chr5: 175,494,699-175,500,103 SFXN1
    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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