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Items: 1 to 20 of 137

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137156copy number variation1nstd233human GRCh37.p13 chr17: 59,529,098-60,599,347 , GRCh38 chr17: 61,451,737-62,521,986 TBX4, MED13, 20 more genes
    nsv7095406copy number variation2nstd102humanUncertain significance GRCh37 chr17: 58,227,396-59,938,900 , GRCh38.p12 chr17: 60,150,035-61,861,539 LOC101927855, TBX2-AS1, 30 more genes
    nsv7075960inversion1nstd229human GRCh38 chr17: 60,858,614-62,154,479 , GRCh37.p13 chr17: 58,935,975-60,231,840 TBX2, MED13, 13 more genes
    nsv7070986inversion1nstd229human GRCh38 chr17: 59,331,393-62,738,993 , GRCh37.p13 chr17: 57,408,754-60,816,354 MIR21, LINC01476, 83 more genes
    nsv7070223inversion1nstd229human GRCh38 chr17: 61,482,736-62,369,304 , GRCh37.p13 chr17: 59,560,097-60,446,665 TBC1D3P2, TBX4, 12 more genes
    nsv7062151inversion1nstd229human GRCh38 chr17: 58,705,434-61,610,111 , GRCh37.p13 chr17: 56,782,795-59,687,472 RNU4-13P, LOC105371850, 74 more genes
    nsv6531920copy number variation1nstd223human GRCh38 chr17: 61,591,401-61,597,587 , GRCh37.p13 chr17: 59,668,762-59,674,948 NACA2
    nsv6315566copy number variation1nstd102humanLikely pathogenic GRCh37 chr17: 58,111,094-60,323,067 , GRCh38.p12 chr17: 60,033,733-62,245,706 CA4, TBX2, 42 more genes
    nsv6310393copy number variation1nstd102humanUncertain significance GRCh37 chr17: 54,671,585-59,938,900 , GRCh38.p12 chr17: 56,594,224-61,861,539 RNF43, LOC107985048, 132 more genes
    nsv6289794copy number variation1nstd102humanLikely pathogenic GRCh37 chr17: 58,076,721-60,362,868 , GRCh38.p12 chr17: 59,999,360-62,285,507 CA4, TBX2, 49 more genes
    nsv6133316copy number variation1nstd213human GRCh37 chr17: 53,930,000-62,410,001 , GRCh38.p12 chr17: 55,852,639-64,332,641 CA4, CD79B, 208 more genes
    nsv6133251copy number variation1nstd213human GRCh37 chr17: 59,650,000-59,730,001 , GRCh38.p12 chr17: 61,572,639-61,652,640 NACA2
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5010508copy number variation1nstd200human GRCh38 chr17: 61,591,401-61,597,587 , GRCh37.p13 chr17: 59,668,762-59,674,948 NACA2
    nsv4851574copy number variation1nstd200human GRCh37 chr17: 59,668,762-59,674,948 , GRCh38.p12 chr17: 61,591,401-61,597,587 NACA2
    nsv4457799copy number variation1nstd102humanPathogenic GRCh37 chr17: 57,869,604-67,078,443 , GRCh38.p12 chr17: 59,792,243-69,082,302 PECAM1, TBX2-AS1, 215 more genes
    nsv4349383copy number variation1nstd102humanPathogenic GRCh37 chr17: 57,357,088-66,306,668 , GRCh38.p12 chr17: 59,279,727-68,310,527 FAM136DP, HELZ, 214 more genes
    nsv4349356copy number variation1nstd102humanLikely pathogenic GRCh37 chr17: 58,121,190-60,140,614 , GRCh38.p12 chr17: 60,043,829-62,063,253 CA4, TBX2, 39 more genes
    nsv4330632inversion1nstd166human GRCh37.p13 chr17: 18,838,526-72,042,289 , GRCh38.p12 chr17: 18,935,213-74,046,150 , ACACA, 1499 more genes
    nsv3918670copy number variation1nstd102humanPathogenic GRCh37 chr17: 58,172,700-60,315,303 , GRCh38 chr17: 60,095,339-62,237,942 , NCBI36 chr17: 55,527,482-57,670,085 MED13, RPL36AP46, 37 more genes
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