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Items: 1 to 20 of 129

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097134copy number variation1nstd102humanPathogenic GRCh37 chr5: 172,089,144-172,774,583 , GRCh38.p12 chr5: 172,662,141-173,347,580 RNA5SP200, MIR5003, 22 more genes
    nsv7096765copy number variation1nstd102humanUncertain significance GRCh37 chr5: 171,765,373-172,939,426 , GRCh38.p12 chr5: 172,338,369-173,512,423 MIR5003, LOC285591, 31 more genes
    nsv7057944inversion1nstd229human GRCh38 chr5: 172,134,356-176,589,266 , GRCh37.p13 chr5: 171,561,360-176,016,267 MIR10523, NIFKP2, 92 more genes
    nsv7038290inversion1nstd229human GRCh38 chr5: 172,489,078-179,485,008 , GRCh37.p13 chr5: 171,916,082-178,912,009 ZFP2, NHP2, 168 more genes
    nsv6797237copy number variation1nstd229human GRCh38 chr5: 173,140,401-173,386,000 , GRCh37.p13 chr5: 172,567,404-172,813,003 STC2, BNIP1, 8 more genes
    nsv6785664copy number variation1nstd229human GRCh38 chr5: 173,081,701-173,191,100 , GRCh37.p13 chr5: 172,508,704-172,618,103 CREBRF, BNIP1, 1 more genes
    nsv6782955copy number variation1nstd229human GRCh38 chr5: 172,218,701-173,333,400 , GRCh37.p13 chr5: 171,645,705-172,760,403 ATP6V0E1, MIR10523, 31 more genes
    nsv6781511copy number variation1nstd229human GRCh38 chr5: 170,662,244-174,111,903 , GRCh37.p13 chr5: 170,089,248-173,538,906 LOC101928093, LOC107986482, 79 more genes
    nsv6780365copy number variation1nstd229human GRCh38 chr5: 173,163,795-173,167,966 , GRCh37.p13 chr5: 172,590,798-172,594,969 BNIP1
    nsv6636891copy number variation1nstd102humanPathogenic GRCh37 chr5: 150,535,183-172,906,793 , GRCh38.p12 chr5: 151,155,622-173,479,790 EFCAB9, LOC112267936, 287 more genes
    nsv6634369copy number variation1nstd102humanPathogenic GRCh37 chr5: 170,350,336-180,719,789 , GRCh38.p12 chr5: 170,923,332-181,292,788 GFPT2, FOXO1B, 287 more genes
    nsv6630119copy number variation1nstd224human GRCh37 chr5: 172,346,648-172,590,824 , GRCh38.p12 chr5: 172,919,645-173,163,821 BNIP1, ATP6V0E1, 7 more genes
    nsv6315448copy number variation1nstd102humanPathogenic GRCh37 chr5: 149,010,383-180,719,789 , GRCh38.p12 chr5: 149,630,820-181,292,788 GRM6, MIR1229, 554 more genes
    nsv6256488mobile element insertion1nstd215human GRCh38 chr5: 173,159,504-173,159,504 , GRCh37.p13 chr5: 172,586,507-172,586,507 BNIP1
    nsv6136090copy number variation1nstd213human GRCh37 chr5: 161,030,000-172,600,001 , GRCh38.p12 chr5: 161,602,994-173,172,998 BNIP1, CCNG1, 130 more genes
    nsv6135205copy number variation1nstd213human GRCh37 chr5: 91,690,000-180,740,001 , GRCh38.p12 chr5: 92,354,293-181,313,000 ADRA1B, ASS1P10, 1378 more genes
    nsv6134989copy number variation1nstd213human GRCh37 chr5: 172,060,000-172,600,001 , GRCh38.p12 chr5: 172,632,997-173,172,998 BNIP1, DUSP1, 17 more genes
    nsv6009174copy number variation1nstd212human GRCh38 chr5: 173,145,433-173,145,540 , GRCh37.p13 chr5: 172,572,436-172,572,543 BNIP1
    nsv5901718copy number variation1nstd209human GRCh38 chr5: 172,153,284-177,326,767 , GRCh37.p13 chr5: 171,580,288-176,753,768 , LOC107986487, 114 more genes
    nsv5090568mobile element insertion1nstd203human GRCh38 chr5: 173,145,686-173,145,717 , GRCh37.p13 chr5: 172,572,689-172,572,720 BNIP1
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