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Items: 1 to 20 of 167

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5921287copy number variation1nstd209human GRCh38 chr7: 149,492,764-149,617,037 , GRCh37.p13 chr7: 149,189,855-149,314,128 TRC-GCA16-1, TRS-AGA5-1, 8 more genes
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv4685723copy number variation1nstd102humannot provided GRCh37 chr7: 147,897,705-149,874,566 , GRCh38.p12 chr7: 148,200,613-150,177,477 CUL1, RNY1, 63 more genes
    nsv4685715copy number variation1nstd102humannot provided GRCh37 chr7: 143,107,740-156,886,246 , GRCh38.p12 chr7: 143,410,647-157,093,552 CTAGE4, CDK5, 277 more genes
    nsv4675620copy number variation1nstd102humanPathogenic GRCh37 chr7: 109,251,060-159,119,707 , GRCh38.p12 chr7: 109,611,003-159,327,017 RPL26P23, ST13P17, 887 more genes
    nsv4675615copy number variation1nstd102humanPathogenic GRCh37 chr7: 131,414,604-159,126,310 , GRCh38.p12 chr7: 131,729,845-159,333,620 ATG9B, OR10AC1, 603 more genes
    nsv4675268copy number variation1nstd102humanPathogenic GRCh37 chr7: 145,962,558-159,119,707 , GRCh38.p12 chr7: 146,265,466-159,327,017 ABCB8, THAP5P1, 237 more genes
    nsv4609494copy number variation1nstd183human GRCh37 chr7: 149,281,386-149,300,912 , GRCh38.p12 chr7: 149,584,295-149,603,821 TRC-GCA3-1, TRC-GCA15-1, 3 more genes
    nsv4569957sequence alteration1nstd166human GRCh37.p13 chr7: 149,292,189-149,362,205 , GRCh38.p12 chr7: 149,595,098-149,665,114 ZNF767P, TRC-GCA12-1, 6 more genes
    nsv4524247copy number variation1nstd166human GRCh37.p13 chr7: 149,191,999-149,318,000 , GRCh38.p12 chr7: 149,494,908-149,620,909 TRC-GCA20-1, TRC-GCA16-1, 8 more genes
    nsv4455493copy number variation1nstd102humanPathogenic GRCh37 chr7: 130,592,554-159,119,707 , GRCh38.p12 chr7: 130,907,795-159,327,017 OR2A1, LOC101027084, 614 more genes
    nsv4455091copy number variation1nstd102humanPathogenic GRCh37 chr7: 10,365-159,119,707 , GRCh38.p12 chr7: 10,365-159,327,017 RPL23AP51, FLJ40288, 2684 more genes
    nsv4452353copy number variation1nstd102humannot provided GRCh37 chr7: 147,897,705-149,874,566 , GRCh38.p12 chr7: 148,200,613-150,177,477 RN7SL569P, ZNF746, 63 more genes
    nsv4436270complex substitution1nstd102humanUncertain significance GRCh37 chr7: 149,152,906-149,518,148 , GRCh38.p12 chr7: 149,455,815-149,821,059 SSPOP, ZNF777, 17 more genes
    nsv4410502copy number variation1nstd174human GRCh37 chr7: 149,282,376-149,312,157 , GRCh38.p12 chr7: 149,585,285-149,615,066 ZNF767P, TRC-GCA3-1, 5 more genes
    nsv4399423copy number variation1nstd174human GRCh37 chr7: 149,186,836-149,320,212 , GRCh38.p12 chr7: 149,489,745-149,623,121 TRC-GCA20-1, ZNF767P, 8 more genes
    nsv4387323copy number variation1nstd173human GRCh37 chr7: 149,285,755-149,318,921 , GRCh38.p12 chr7: 149,588,664-149,621,830 ZNF767P, TRC-GCA3-1, 4 more genes
    nsv4386275copy number variation1nstd173human GRCh37 chr7: 148,987,765-149,385,891 , GRCh38.p12 chr7: 149,290,674-149,688,800 TRC-GCA21-1, LOC101928733, 23 more genes
    nsv4383394copy number variation1nstd173human GRCh37 chr7: 149,280,911-149,318,933 , GRCh38.p12 chr7: 149,583,820-149,621,842 ZNF767P, TRC-GCA3-1, 5 more genes
    nsv4381716copy number variation1nstd173human GRCh37 chr7: 146,525,217-159,119,707 , GRCh38.p12 chr7: 146,828,125-159,327,017 , TRC-GCA17-1, 247 more genes
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