tnfsf12[All Fields] AND 1[has_clinical] - dbVar

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Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv6310410	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr17: 7,452,471-7,454,315 , GRCh38.p12 chr17: 7,549,154-7,550,998	TNFSF12, TNFSF12-TNFSF13
nsv3913013	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr17: 162,016-7,697,012 , GRCh37 chr17: 45,835-7,600,330 , NCBI36 chr17: 11,807-7,541,055	TNFSF12, RPS4XP17, 289 more genes
nsv3910343	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 5,636,297-7,942,140 , NCBI36 chr17: 5,577,021-7,882,865 , GRCh38 chr17: 5,732,977-8,038,822	TNFSF12, RPL23AP73, 106 more genes
nsv3898050	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 7,241,916-8,692,213 , GRCh38.p12 chr17: 7,338,597-8,788,895	TNFSF12, NDEL1, 108 more genes
nsv1397967	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr17: 6,838,295-7,991,364 , GRCh37.p13 chr17: 6,897,571-8,050,639 , GRCh38.p12 chr17: 6,994,252-8,147,321	TNFSF12, TNFSF12-TNFSF13, 96 more genes
nsv7095414	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 7,123,304-8,193,254 , GRCh38.p12 chr17: 7,219,985-8,289,936	TNFSF12, CTC1, 103 more genes
nsv6314103	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 7,020,054-8,086,290 , GRCh38.p12 chr17: 7,116,735-8,182,972	TNFSF12, RPL7AP64, 87 more genes
nsv7094915	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 7,120,455-8,151,423 , GRCh38.p12 chr17: 7,217,136-8,248,105	TNFSF12, MIR324, 101 more genes
nsv3923531	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr17: 7,322,238-8,279,567 , GRCh37 chr17: 7,381,514-8,338,842 , GRCh38 chr17: 7,478,195-8,435,524	TNFSF12, SLC25A35, 82 more genes
nsv1398205	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr17: 7,033,635-7,977,678 , GRCh37.p13 chr17: 7,092,911-8,036,953 , GRCh38.p12 chr17: 7,189,592-8,133,635	TNFSF12, YBX2, 76 more genes
nsv7098895	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 7,004,894-7,766,789 , GRCh38.p12 chr17: 7,101,575-7,863,471	TNFSF12, LOC105371512, 61 more genes
nsv3903684	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 8,547-81,060,040 , GRCh38.p12 chr17: 158,756-83,102,004	TNFSF12, MIR3185, 2366 more genes
nsv3899740	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 7,214-81,058,310 , GRCh38.p12 chr17: 157,423-83,100,564	TNFSF12, P4HB, 2366 more genes
nsv3906245	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 12,344-81,057,996 , GRCh38.p12 chr17: 162,553-83,100,251	TNFSF12, MIR21, 2366 more genes
nsv3907261	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr17: 526-81,041,938 , GRCh38.p12 chr17: 150,733-83,084,062	TNFSF12, SMURF2, 2366 more genes
nsv3897625	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 525-15,027,737 , GRCh38.p12 chr17: 150,732-15,124,420	TNFSF12, GP1BA, 439 more genes
nsv3915354	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr17: 150,732-14,764,202 , NCBI36 chr17: 525-14,608,244 , GRCh37 chr17: 525-14,667,519	TNFSF12, KIF1C-AS1, 433 more genes
nsv3917059	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 45,835-12,247,218 , NCBI36 chr17: 11,807-12,187,943 , GRCh38 chr17: 162,016-12,343,901	TNFSF12, PSMB6, 409 more genes
nsv7148254	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr17: 165,730-11,404,096 , GRCh37.p13 chr17: 396,627-11,307,413	TNFSF12, RFLNB, 401 more genes
nsv3904771	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 525-11,186,432 , GRCh38.p12 chr17: 150,732-11,283,115	TNFSF12, SLC2A4, 401 more genes

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Number of Variants: 20

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dbVar

Result Filters

Object Type

Organism

Variant Type

Method Type

Clinical Interpretation

Has Clinical Interpretation

Sex of Subject

Origin

Study Type

Subject Phenotype Status

Additional filters

Search results

Items: 1 to 20 of 33

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Number of Variants: 20

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Supplemental Content

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