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Items: 1 to 20 of 265

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112833copy number variation1nstd186human GRCh37 chr16: 72,094,581-72,112,285 , GRCh38.p12 chr16: 72,060,682-72,078,386 HP, HPR, 1 more genes
    nsv5944119copy number variation1nstd209human GRCh38 chr16: 72,054,915-72,063,467 , GRCh37.p13 chr16: 72,088,814-72,097,366 HP, HPR, 1 more genes
    nsv5931506copy number variation1nstd209human GRCh38 chr16: 72,049,451-72,076,249 , GRCh37.p13 chr16: 72,083,350-72,110,148 HP, HPR, 1 more genes
    nsv5884456copy number variation4nstd209human GRCh38 chr16: 72,059,878-72,063,173 , GRCh37.p13 chr16: 72,093,777-72,097,072 HP, HPR, 1 more genes
    nsv5883847copy number variation3nstd209human GRCh38 chr16: 72,059,137-72,062,773 , GRCh37.p13 chr16: 72,093,036-72,096,672 TXNL4B, HP, 1 more genes
    nsv5881618copy number variation4nstd209human GRCh38 chr16: 72,075,403-72,078,198 , GRCh37.p13 chr16: 72,109,302-72,112,097 TXNL4B, HPR
    nsv5878270copy number variation2nstd209human GRCh38 chr16: 72,059,037-72,061,873 , GRCh37.p13 chr16: 72,092,936-72,095,772 HPR, HP, 1 more genes
    nsv5872978copy number variation6nstd209human GRCh38 chr16: 72,060,816-72,076,890 , GRCh37.p13 chr16: 72,094,715-72,110,789 HP, HPR, 1 more genes
    nsv5669930inversion1nstd207human GRCh38 chr16: 70,123,796-74,346,113 , GRCh37.p13 chr16: 70,157,699-74,380,011 , AARS1, 83 more genes
    nsv5653420insertion1nstd207human GRCh38 chr16: 72,061,419-72,061,419 , GRCh37.p13 chr16: 72,095,318-72,095,318 HP, HPR, 1 more genes
    nsv5557110sequence alteration1nstd206human GRCh38 chr16: 70,117,371-74,396,141 , GRCh37.p13 chr16: 70,151,274-74,430,039 , TAT, 84 more genes
    nsv5432539copy number variation1nstd206human GRCh38 chr16: 72,060,682-72,078,386 , GRCh37.p13 chr16: 72,094,581-72,112,285 HP, HPR, 1 more genes
    nsv5299405copy number variation1nstd204human GRCh38.p13 chr16: 72,059,137-72,061,773 , GRCh37.p13 chr16: 72,093,036-72,095,672 HP, HPR, 1 more genes
    nsv5295165copy number variation1nstd204human GRCh38.p13 chr16: 72,049,173-72,065,046 , GRCh37.p13 chr16: 72,083,072-72,098,945 HP, HPR, 1 more genes
    nsv5291152copy number variation1nstd204human GRCh38.p13 chr16: 72,061,370-72,067,996 , GRCh37.p13 chr16: 72,095,269-72,101,895 HP, HPR, 1 more genes
    nsv5289534copy number variation1nstd204human GRCh38.p13 chr16: 72,059,237-72,061,973 , GRCh37.p13 chr16: 72,093,136-72,095,872 TXNL4B, HPR, 1 more genes
    nsv5287332copy number variation1nstd204human GRCh38.p13 chr16: 72,061,574-72,076,740 , GRCh37.p13 chr16: 72,095,473-72,110,639 TXNL4B, HPR
    nsv5286142copy number variation1nstd204human GRCh38.p13 chr16: 72,075,803-72,078,598 , GRCh37.p13 chr16: 72,109,702-72,112,497 TXNL4B, HPR
    nsv5285680copy number variation1nstd204human GRCh38.p13 chr16: 72,071,947-72,077,040 , GRCh37.p13 chr16: 72,105,846-72,110,939 TXNL4B, HPR
    nsv5283201copy number variation1nstd204human GRCh38.p13 chr16: 72,060,273-72,064,096 , GRCh37.p13 chr16: 72,094,172-72,097,995 TXNL4B, HPR, 1 more genes
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